3/12/2020 acetanilida | c8h9no - pubchem

3122020 Acetanilida | C8H9NO - PubChem

httpspubchemncbinlmnihgovcompoundAcetanilide 146

RESUMEN COMPUESTO

AcetanilidaPubChem CID 904

Estructura

Encuentra estructuras similares

Seguridad quiacutemica

Hoja de datos del resumen de seguridad quiacutemica de laboratorio (LCSS)

Foacutermula molecular C H N O

Sinoacutenimos

acetanilidaN-fenilacetamida103-84-4AntifebrinaAcetanil

Maacutes

Peso molecular 13516 g mol

Fecha sModificar2020-11-29

Crear2004-09-16

La acetanilida es un soacutelido de color blanco a gris (NTP 1992)

Quiacutemicos CAMEO

La N-fenilacetamida es un miembro de la clase de acetamidas que es la acetamida en la que uno de los hidroacutegenos unidos al nitroacutegeno estaacute sustituido por un grupo fenilo Tiene un papelcomo analgeacutesico Es miembro de acetamidas y anilida Deriva de un aacutecido aceacutetico

CHEBI

2D 3D Crystal

Irritant

8 9



1 Estructuras

11 Estructura 2D

PubChem

12 conformador 3D

PubChem

13 Estructuras de cristalMostrando 1 de 3 Ver maacutes

Nuacutemero CCDC 614360

Datos de estructuracristalina

DOI 105517 ccnm92m

Representacioacuten de laestructura cristalina

Artiacuteculo asociado DOI 101107 S0365110X54002174

The Cambridge Structural Database

Representacioacuten de laestructura quiacutemica

Modelo interactivo deestructura quiacutemica

Bola y palo

Palos

Marco de alambre

Llena el espacio

Mostrar Hidroacutegenos

Animar



2 Names and Identifiers

21 Computed Descriptors

211 IUPAC Name

N-phenylacetamideComputed by LexiChem 266 (PubChem release 20190618)

PubChem

212 InChI

InChI=1SC8H9NOc1-7(10)9-8-5-3-2-4-6-8h2-6H1H3(H910)Computed by InChI 105 (PubChem release 20190618)

PubChem

213 InChI Key

FZERHIULMFGESH-UHFFFAOYSA-NComputed by InChI 105 (PubChem release 20190618)

PubChem

214 Canonical SMILES

CC(=O)NC1=CC=CC=C1Computed by OEChem 215 (PubChem release 20190618)

PubChem

22 Molecular Formula

C8H9NOComputed by PubChem 21 (PubChem release 20190618)

PubChem

23 Other Identifiers

231 CAS

103-84-4

CAMEO Chemicals ChemIDplus DTPNCI EPA Chemicals under the TSCA EPA DSSTox European Chemicals Agency (ECHA) Hazardous Substances Data Bank (HSDB) The National Institute for Occupational Safety and Healt

15826-91-2

European Chemicals Agency (ECHA)

55576-55-1

Human Metabolome Database (HMDB)

232 European Community (EC) Number

203-150-7


239-928-8


233 NSC Number

757879

DTPNCI

7636

DTPNCI

234 RTECS Number



AD7350000

The National Institute for Occupational Safety and Health (NIOSH)

235 UNII

SP86R356CC

FDASPL Indexing Data

236 DSSTox Substance ID

DTXSID2022543

EPA DSSTox

237 Wikipedia

Acetanilide

Wikipedia

24 Synonyms

241 MeSH Entry Terms

acetanilidacetanilide

MeSH

242 Depositor-Supplied Synonyms

PubChem

acetanilideN-Phenylacetamide103-84-4AntifebrinAcetanilAcetamidobenzeneAcetanilidAcetamide N-phenyl-N-AcetylanilineAcetylanilineAcetic acid anilideAcetoanilide

PhenalgeneAcetylaminobenzenePhenalginAniline N-acetyl-N-acetylarylamineBenzenamine N-acetyl-USAF EK-3NSC 7636AN [Analgesic]Caswell No 003EEthananilideUNII-SP86R356CC

N-Phenyl-acetamideN-AcetylaminobenzeneAcetic acid amide N-phenyl-CCRIS 4452HSDB 2665Acetanilide (Antifebrin)EINECS 203-150-7MFCD00008674AI3-01045SP86R356CCCHEBI28884NSC7636

N-PhenylacetamideN-PhenylacetamideAcetanilide 99+NCGC00091326-01DSSTox_CID_2543DSSTox_RID_76620DSSTox_GSID_2254355576-55-1N-Phenylacetamide (Acetanilide)Acetamide N-(phenyl-d5)-N-phenylethanamideAcetanilide [NF]CAS-103-84-4

SMR001306799N-[23456-2H5]phenylacetamidePhNHAcN-phenyl acetamideAcetanilide 99Spectrum_000178Spectrum2_001434Spectrum3_000935Spectrum4_001034Spectrum5_000989WLN 1VMRACMC-1AR90

Ethanimidic acid N-phenyl-SCHEMBL24681KBioGR_001587KBioSS_000658KSC492K1LMLS002207284MLS002415707DivK1c_000073SPECTRUM1501173SPBio_001568ARONIS003513CHEMBL269644

DTXSID2022543SCHEMBL14255226Acetanilide LR gt=98CTK3B8627CTK3J2515HMS500D15KBio1_000073KBio2_000658KBio2_003226KBio2_005794KBio3_001970KS-00003WHS



3 Chemical and Physical Properties

31 Computed Properties

Property Name Property Value Reference

Molecular Weight 13516 gmol Computed by PubChem 21 (PubChem release 20190618)

XLogP3 12 Computed by XLogP3 30 (PubChem release 20190618)

Hydrogen Bond Donor Count 1 Computed by Cactvs 34611 (PubChem release 20190618)

Hydrogen Bond Acceptor Count 1 Computed by Cactvs 34611 (PubChem release 20190618)

Rotatable Bond Count 1 Computed by Cactvs 34611 (PubChem release 20190618)

Exact Mass 135068414 gmol Computed by PubChem 21 (PubChem release 20190618)

Monoisotopic Mass 135068414 gmol Computed by PubChem 21 (PubChem release 20190618)

Topological Polar Surface Area 291 Aringsup2 Computed by Cactvs 34611 (PubChem release 20190618)

Heavy Atom Count 10 Computed by PubChem

Formal Charge 0 Computed by PubChem

Complexity 116 Computed by Cactvs 34611 (PubChem release 20190618)

Isotope Atom Count 0 Computed by PubChem

Defined Atom Stereocenter Count 0 Computed by PubChem

Undefined Atom Stereocenter Count 0 Computed by PubChem

Defined Bond Stereocenter Count 0 Computed by PubChem

Undefined Bond Stereocenter Count 0 Computed by PubChem

Covalently-Bonded Unit Count 1 Computed by PubChem

Compound Is Canonicalized Yes Computed by PubChem (release 20190104)

PubChem

32 Experimental Properties

321 Physical Description

Acetanilide is a white to gray solid (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

Solid


322 ColorForm

ORTHORHOMBIC PLATES OR SCALES FROM WATERBudavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 10

Hazardous Substances Data Bank (HSDB)

WHITE SHINING CRYSTALLINE SCALESSax NI Dangerous Properties of Industrial Materials 5th ed New York Van Nostrand Rheinhold 1979 p 332


White shining crystalline leaflets or white crystalline powderLewis RJ Sr (Ed) Hawleys Condensed Chemical Dictionary 12th ed New York NY Van Nostrand Rheinhold Co 1993 p 6


Colorless glossy crystalline materialGerhartz W (exec ed) Ullmanns Encyclopedia of Industrial Chemistry 5th edVol A1 Deerfield Beach FL VCH Publishers 1985 to Present p VA2 310


323 Odor

ODORLESSLewis RJ Sr (Ed) Hawleys Condensed Chemical Dictionary 12th ed New York NY Van Nostrand Rheinhold Co 1993 p 6


324 Taste

SLIGHTLY BURNINGBudavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 10




325 Boiling Point

579 degF at 760 mm Hg (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

3040 degC

EPA DSSTox

304 degC 760 MM HGLide DR (ed) CRC Handbook of Chemistry and Physics 76th ed Boca Raton FL CRC Press Inc 1995-1996 p 3-5


326 Melting Point

2377 degF (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

1143 degC

EPA DSSTox Hazardous Substances Data Bank (HSDB)

327 Flash Point


CAMEO Chemicals

337 degF 169 degC (OPEN CUP)Fire Protection Guide to Hazardous Materials 12 ed Quincy MA National Fire Protection Association 1997 p 325-10


328 Solubility

less than 1 mgmL at 72deg F (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

005 MYALKOWSKYSH amp DANNENFELSERRM (1992)

EPA DSSTox

1 G SOL IN 185 ML WATER 34 ML ALC 20 ML BOILING WATER 3 ML METHANOL 4 ML ACETONE 06 ML BOILING ALCOHOL IN 37 ML CHLOROFORM 5 ML GLYCEROL 8 ML DIOXANE 47 MLBENZENE 18 ML ETHER VERY SPARINGLY SOL IN PETROLEUM ETHER CHLORAL HYDRATE INCREASES SOLUBILITY IN WATER

Budavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 10


SOL IN TOLUENE VERY SOL IN HOT TOLUENE IN CARBON TETRACHLORIDEWeast RC (ed) Handbook of Chemistry and Physics 60th ed Boca Raton Florida CRC Press Inc 1979 p C-85


Water solubility= 693X10+3 mgl at 25 degCYalkowsky SH Dannenfelser RM The Aquasol Database of Aqueous Solubility Fifth ed Tucson AZ Univ AZ College of Pharmacy PC Ver (1992)


Slightly soluble in water very soluble in ethanol and acetone soluble in ethyl etherLide DR (ed) CRC Handbook of Chemistry and Physics 76th ed Boca Raton FL CRC Press Inc 1995-1996 p 3-5


639 mgmL at 25 degC


gt203 [ugmL]

Sanford-Burnham Center for Chemical Genomics



329 Density

1219 at 59 degF (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

12190 15 degCLide DR (ed) CRC Handbook of Chemistry and Physics 76th ed Boca Raton FL CRC Press Inc 1995-1996 p 3-5


3210 Vapor Density

465 (NTP 1992) (Relative to Air)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

465Fire Protection Guide to Hazardous Materials 12 ed Quincy MA National Fire Protection Association 1997 p 325-10


3211 Vapor Pressure

1 mm Hg at 237 degF (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

200e-04 mmHg

EPA DSSTox

122X10-3 mm Hg at 25 degCPerry RH Green D Perrys Chemical Handbook 6th ed NY NY McGraw Hill p 3-50 (1984)


3212 LogP

116 (LogP)HANSCHC ET AL (1995)

EPA DSSTox

Log Kow= 116Hansch C Leo A D Hoekman Exploring QSAR - Hydrophobic Electronic and Steric Constants Washington DC American Chemical Society 1995 p 42


116HANSCHC ET AL (1995)


3213 StabilityShelf Life

REARRANGES UNDER INFLUENCE OF UV LIGHT ACETYL GROUP FORMS NEW BOND ON RING IN ORTHO OR PARA POSITIONKearney PC and D D Kaufman (eds) Herbicides Chemistry Degredation and Mode of Action Volumes 1 and 2 2nd ed New York Marcel Dekker Inc 1975 p 863


APPRECIABLY VOLATILE 95 degCThe Merck Index 9th ed Rahway New Jersey Merck amp Co Inc 1976 p 6


STABLE IN AIRHawley GG The Condensed Chemical Dictionary 9th ed New York Van Nostrand Reinhold Co 1977 p 4


3214 Autoignition Temperature


CAMEO Chemicals



985 + or - 10 degFFire Protection Guide to Hazardous Materials 12 ed Quincy MA National Fire Protection Association 1997 p 325-10


3215 Decomposition

SEE ANILINE WHEN HEATED TO DECOMP EMITS HIGHLY TOXIC FUMESSax NI Dangerous Properties of Industrial Materials 5th ed New York Van Nostrand Rheinhold 1979 p 333


3216 Refractive Index

INDEX OF REFRACTION 1515 (ALPHA) 1620 (BETA) GREATER THAN 1733 (GAMMA) PKA 1Sunshine I (ed) CRC Handbook of Analytical Toxicology Cleveland The Chemical Rubber Co 1969 p 292


3217 Dissociation Constants

KB 1X10-13 AT 28 degCBudavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 10


pKa = 050 at 25 degC (conjugate acid)Perrin DD Dissociation constants of organic bases in aqueous solution IUPAC Chem Data Ser Buttersworth London (1965)


3218 Collision Cross Section

12417 Aringsup2 [M-H] [CCS Type DT Method single field calibrated with Agilent tune mix (Agilent)]httpspubsacsorgdoiabs101021acsanalchem6b03091

CCSbase

125 Aringsup2 [M+H] [CCS Type TW Method calibrated with polyalanine and drug standards]httpspubsacsorgdoiabs101021acsanalchem7b01709

CCSbase

3219 Kovats Retention Index

Standard non-polar 1362 1362 1358

Semi-standard non-polar 13659

NIST Mass Spectrometry Data Center

3220 Other Experimental Properties

IT FORMS EUTECTIC MIXTURE WITH PHENOL RESORCINOL amp THYMOLOsol A and JE Hoover et al (eds) Remingtons Pharmaceutical Sciences 15th ed Easton Pennsylvania Mack Publishing Co 1975 p 1053


VAPOR PRESSURE 1 MM HG 1140 degCSax NI Dangerous Properties of Industrial Materials 5th ed New York Van Nostrand Rheinhold 1979 p 332


33 SpringerMaterials Properties

13C nuclear magnetic resonance spectrum15N nuclear magnetic resonance spectrumSchoenflies notationAngular frequencyBoiling pointChemical shiftCrystal structureDensityDiamagnetic susceptibilityExternal quantum efficiencyFormula unitFusion temperatureHeat of sublimation

LineshapeLuminescenceLuminescence emission linewidthMagnetic anisotropyMagnetic susceptibilityMelting temperatureMolecular structurePhase transitionPoint groupPolarization degreeReaction coordinateSpace groupSpin-spin coupling constant

Surface tensionTransition enthalpyUnit cellUnit cell parameterVapor pressureViscosity

-

+



SpringerMaterials



4 Spectral Information

41 1D NMR Spectra1D NMR Spectra MAX ABSORPTION (ALCOHOL) 242 NM (LOG E= 416) SADTLER REFERENCE NUMBER 160 (IR PRISM) 49 (IR GRATING) 63 (UV) 5235 (NMR)


1D NMR Spectra NMRShiftDB Link

NMRShiftDB

411 1H NMR Spectra

Showing 2 of 3 View More

Instrument Name BRUKER AC-300

Source of Sample The Matheson Company Inc East Rutherford New Jersey

Copyright Copyright copy 1991-2018 Bio-Rad Laboratories Inc All Rights Reserved

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SpectraBase

Instrument Name Varian A-60



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SpectraBase

412 13C NMR Spectra


Source of Sample M Zanger Philadelphia College of Pharmacy amp Science Philadelphia Pennsylvania

Copyright Copyright copy 1980 1981-2018 Bio-Rad Laboratories Inc All Rights Reserved

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SpectraBase

Technique APT DEPT INEPT


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SpectraBase

413 15N NMR Spectra

Copyright Copyright copy 2016-2018 W Robien Inst of Org Chem Univ of Vienna All Rights Reserved

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SpectraBase

414 17O NMR Spectra


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SpectraBase



42 Mass Spectrometry


Source of Spectrum Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences

Copyright Copyright copy 2012-2018 Bio-Rad Laboratories Inc Portions provided by AAFS Toxicology Section All Rights Reserved

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SpectraBase



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SpectraBase

421 GC-MS


GC-MS

GC-MS Spectrum 29717 - N-Acetylarylamine (HMDB0001250)GC-MS Spectrum 31744 - N-Acetylarylamine (HMDB0001250)GC-MS Spectrum 31745 - N-Acetylarylamine (HMDB0001250)GC-MS Spectrum 31746 - N-Acetylarylamine (HMDB0001250)GC-MS Spectrum 99675 - N-Acetylarylamine (HMDB0001250)GC-MS Spectrum 99676 - N-Acetylarylamine (HMDB0001250)GC-MS Spectrum 99677 - N-Acetylarylamine (HMDB0001250)GC-MS Spectrum 99678 - N-Acetylarylamine (HMDB0001250)


MoNA ID FiehnLib000055

MS Category Experimental

MS Type GC-MS

MS Level MS1

Instrument Leco Pegasus IV

Instrument Type GC-EI-TOF

Ionization Mode positive

Splash splash10-0006-9100000000-4122036cecde322748ea

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Submitter Oliver Fiehn University of California Davis

MassBank of North America (MoNA)

422 MS-MS

MS-MS

MS-MS Spectrum 437226 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 437227 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 437228 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 437229 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 437230 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 445696 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 445697 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 445698 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 445699 - N-Acetylarylamine (HMDB0001250)MS-MS Spectrum 445700 - N-Acetylarylamine (HMDB0001250)


423 LC-MS


MoNA ID FiehnHILIC000151


MS Type LC-MS

MS Level MS2

Precursor Type [M+H]+

precursor mz 1360757

Instrument Thermo Q Exactive HF

Instrument Type LC-ESI-QFT


Collision Energy HCD (NCE 20-30-40)

Splash splash10-0006-9200000000-ff83d4bfea9eb02cf890

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Submitter Megan Showalter University of California Davis




MS Type LC-MS

MS Level MS2


precursor mz 136075

Instrument SCIEX TripleTOF 6600

Instrument Type LC-ESI-QTOF


Collision Energy 35 eV



Splash splash10-0006-9000000000-e95de445e93356b68915

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424 Other MS

Other MS MASS 304 (National Bureau of Standards EPA-NIH Mass Spectra Data Base NSRDS-NBS-63)


43 UV Spectra

UV 599 (Sadtler Research Laboratories Spectral Collection)Weast RC and MJ Astle CRC Handbook of Data on Organic Compounds Volumes I and II Boca Raton FL CRC Press Inc 1985 p V2 79


44 IR SpectraIR Spectra IR 2230 (Sadtler Research Laboratories Prism Collection)


441 FTIR Spectra

Technique KBr WAFER

Source of Sample The Matheson Company Inc


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Technique KBr WAFER



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SpectraBase

442 Vapor Phase IR Spectra

Instrument Name DIGILAB FTS-14

Technique Vapor Phase


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45 Other Spectra

Intense mass spectral peaks 93 mz 135 mzPfleger K H Maurer and A Weber Mass Spectral and GC Data of Drugs Poisons and their Metabolites Parts I and II Mass Spectra Indexes Weinheim Federal Republic of Germany 1985 p 174




5 Related Records

51 Related Compounds with Annotation

PubChem

52 Related CompoundsSame Connectivity 22 Records

Same Parent Connectivity 96 Records

Same Parent Exact 75 Records

Mixtures Components andNeutralized Forms 284 Records

Similar Compounds 1681 Records

Similar Conformers 16961 Records

PubChem

53 Substances

531 Related Substances

All 609 Records

Same 263 Records

Mixture 346 Records

PubChem

532 Substances by Category

PubChem

54 Entrez CrosslinksPubMed 302 Records

OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem



7 Drug and Medication Information

71 Therapeutic Uses

IT IS PARTICULARLY EFFECTIVE AS AN ANALGESIC IN PAIN OF THE NEURALGIC TYPEOsol A and JE Hoover et al (eds) Remingtons Pharmaceutical Sciences 15th ed Easton Pennsylvania Mack Publishing Co 1975 p 1053


MEDICATION (VET) ANALGESIC ANTIPYRETIC AGENTBudavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 10


72 Drug Warnings

ACETANILID IS ESPECIALLY DANGEROUS IN ANEMIA AFTER HEMORRHAGE AND DURING MENSTRUATIONThienes C and TJ Haley Clinical Toxicology 5th ed Philadelphia Lea and Febiger 1972 p 81


ITS USE AS AN ANALGESIC IS CONDEMNED BECAUSE SAFER amp EQUALLY EFFECTIVE DRUGS ARE AVAILABLEAmerican Medical Association Council on Drugs AMA Drug Evaluations 2nd ed Acton Mass Publishing Sciences Group Inc 1973 p 262


NECROSIS OF RENAL PAPILLAE amp TERMINAL TUBULES HAS BEEN ASSOCIATED WITH EXCESSIVE DOSES OF DRUG MIXTURES CONTAINING ACETOPHENETIDIN WITHACETANILIDThienes C and TJ Haley Clinical Toxicology 5th ed Philadelphia Lea and Febiger 1972 p 81


ACETANILIDPRODUCES HEMOLYTIC ANEMIA IN INDIVIDUALS WITH GENETIC DEFICIENCY OF ERYTHROCYTIC GLUCOSE-6-PHOSPHATE DEHYDROGENASE DARK SKINNED RACES HAVE HIGHERINCIDENCE THAN LIGHT SKINNED BUT DISEASE HAS NOT BEEN NOTED IN NORTH AMERICAN INDIANS OR ESKIMOS

Thienes C and TJ Haley Clinical Toxicology 5th ed Philadelphia Lea and Febiger 1972 p 232


For more Drug Warnings (Complete) data for ACETANILIDE (6 total) please visit the HSDB record page


73 Reported Fatal Dose

BETWEEN 4 amp 5 4= VERY TOXIC PROBABLE ORAL LETHAL DOSE (HUMAN) 50-500 MGKG BETWEEN 1 TEASPOONFUL amp 1 OZ FOR A 70 KG PERSON (150 LB) 5= EXTREMELY TOXIC PROBABLEORAL LETHAL DOSE (HUMAN) 5-50 MGKG BETWEEN 7 DROPS amp 1 TEASPOONFUL FOR 70 KG PERSON (150 LB)

Gosselin RE HC Hodge RP Smith and MN Gleason Clinical Toxicology of Commercial Products 4th ed Baltimore Williams and Wilkins 1976 p II-139




8 Food Additives and Ingredients

81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan

Columbidae (Dove Pigeon)

FooDB



9 Pharmacology and Biochemistry

91 Absorption Distribution and Excretion

IT IS READILY EXCRETED IN THE URINE AS SULFATE OR GLUCURONATE CONJUGATE OF THE PHENOL N-ACETYL-P-AMINOPHENOLPatty F (ed) Industrial Hygiene and Toxicology Volume II Toxicology 2nd ed New York Interscience Publishers 1963 p 1835


36 OF ACETANILIDE DISSOLVED IN 01 N HCL (PKA 03) WAS ABSORBED FROM RAT STOMACH IN ONE HOUR FROM TABLELaDu BN HG Mandel and EL Way Fundamentals of Drug Metabolism and Disposition Baltimore Williams and Wilkins 1971 p 27


GREATER THAN 999 OF ACETANILIDE REMAINS UN-IONIZED BODY PH FACILITATING ABSORPTION FROM BLOOD TO CEREBROSPINAL FLUID THE BLOOD-CEREBROSPINAL FLUIDPERMEABILITY COEFFICIENT IS 0039MIN FROM TABLE

LaDu BN HG Mandel and EL Way Fundamentals of Drug Metabolism and Disposition Baltimore Williams and Wilkins 1971 p 82


ACETANILID IS READILY ABSORBED FROM GASTROINTESTINAL TRACTThienes C and TJ Haley Clinical Toxicology 5th ed Philadelphia Lea and Febiger 1972 p 80


For more Absorption Distribution and Excretion (Complete) data for ACETANILIDE (14 total) please visit the HSDB record page


92 MetabolismMetabolites

RESEARCHERS FOUND THAT STARVATION DECREASED RATE OF METABOLISM OFACETANILIDE STARVATION REDUCED OXIDATIVE PATHWAYS OF MALE RATSLaDu BN HG Mandel and EL Way Fundamentals of Drug Metabolism and Disposition Baltimore Williams and Wilkins 1971 p 529


STRAIN DIFFERENCES WITHIN THE SAME SPECIES WERENOTED IN ACETANILIDEMETABOLISMLaDu BN HG Mandel and EL Way Fundamentals of Drug Metabolism and Disposition Baltimore Williams and Wilkins 1971 p 530


HEPATIC MICROSOMES FROM RABBITS WITH OBSTRUCTIVE JAUNDICE SHOW IMPAIRED METABOLISM OF ACETANILIDELaDu BN HG Mandel and EL Way Fundamentals of Drug Metabolism and Disposition Baltimore Williams and Wilkins 1971 p 530


2 NEW URINARY METABOLITES OF ACETANILIDE IN RATS THAT HAVE BEEN IDENTIFIED AS N-ACETYL-S-(5-ACETAMIDO-2-HYDROXYPHENYL)CYSTEINE amp N-ACETYL-S-(3-ACETAMIDOPHENYL)CYSTEINE MAY HAVE BEEN FORMED VIA AN INTERMEDIATE EPOXIDE

The Chemical Society Foreign Compound Metabolism in Mammals Volume 4 A Review of the Literature Published during 1974 and 1975 London The Chemical Society 1977 p 182


YIELDS O-ACETAMIDOPHENOL P-ACETAMIDOPHENOL amp ANILINE IN RABBIT DALY J JERINA D amp WITKOP B ARCHS BIOCHEM BIOPHYS 128 517 (1968) YIELDS O-ACETAMIDOPHENOL IN RATDALY J amp JERINA D ARCHS BIOCHEM BIOPHYS 134 266 (1969) YIELDS P-ACETAMIDOPHENOL IN MAN HAMMAR CH amp PRELLWITZ W KLIN WSCHR 44 1010 (1966) FROM TABLE

Goodwin BL Handbook of Intermediary Metabolism of Aromatic Compounds New York Wiley 1976 p A-12


YIELDS O-ACETAMIDOPHENOL amp P-ACETAMIDOPHENOL IN CAT amp DOG POSNER HS MITOMA C amp UDENFRIEND S ARCHS BIOCHEM BIOPHYS 94 269 (1961) YIELDS P-ACETAMIDOPHENOL INRAT GUINEA PIG MOUSE DALY J JERINA D FARNSWORTH J amp GUROFF G ARCHS BIOCHEM BIOPHYS 131 238 (1969) FROM TABLE



YIELDS P-ACETAMIDOPHENOL IN PIG HEINZE E HLAVICA P KIESE M amp LIPOWSKY G BIOCHEM PHARMAC 19 641 (1970) YIELDS ANILINE IN RAT GUINEA PIG CAT DOG HORSE MOUSE BRAYHG JAMES SP THORPE WV amp WASDELL MR BIOCHEM J 47 483 (1950) FROM TABLE



YIELDS ANILINE IN CHICK NIMMO-SMITH RH BIOCHEM J 75 284 (1960) YIELDS ANILINE IN PIG FRANZ W amp KRISCH K BIOCHEM BIOPHYS RES COMMUN 23 816 (1966) YIELDS GLYCOLLANILIDEIN RABBIT KIESE M amp LENK W BIOCHEM PHARMAC 18 1325 (1969) FROM TABLE



MYOGLOBIN AND HEMOGLOBIN ENHANCED RAT LIVER MICROSOMAL P-HYDROXYLATION OF ACETANILIDEJONEN HG ET AL XENOBIOTICA 6(5) 307 (1976)


INTESTINAL MICROFLORA CONTRIBUTE TO METABOLISM OF ACETANILIDE BY DEGRADING N-ACETYL-P-AMINOPHENYL GLUCURONIDE



SMITH GE GRIFFITHS LA EXPERIENTIA 32(12) 1556 (1976)


HEPATIC MICROSOMES OR RECONSTITUTED CYTOCHROME MONOXYGENASE SYSTEMS FROM RATS CONVERTED RADIOACTIVE ACETANILIDE TO RING-HYDROXYLATED PRODUCTS PRIMARILY 4-HYDROXYACETANILIDE

SELANDER HG ET AL ARCH BIOCHEM BIOPHYS 164(1) 241 (1974)


OXIDN OF 500 MG ORAL ACETANILID BY AROMATIC HYDROXYLATION IN 8 HEALTHY ADULT MALES (AGE 22-42) WITH GENETIC DEFECT DESCRIBED CONCLUDED THAT GENETIC DEFECT DOES NOTOCCUR FOR HYDROXYLATION amp THE REACTION IS CONTROLLED BY DIFFERENT GENE COMPLEX

WAKILE LA ET AL J PHARM PHARMACOL 31(MAY) 350 (1979)


EFFECT OF AGE ON ACTIVITY OF LIVER MICROSOMAL ENZYMES INVESTIGATED BY MEASURING HEPATIC OXIDATION AND PLASMA CONCN OF METABOLITES OF ACETANILID IN 15 YOUNG PEOPLE(MEAN AGE 23 YR) AS COMPARED WITH 15 ELDERLY PT (MEAN AGE 81 YR) NO CHANGE IN BIOTRANSFORMATION NOTED

PLAYFER JR ET AL BR J CLIN PHARMACOL 6(DEC) 529 (1978)


WHEN CYTOCHROME P-450 IS ISOLATED FROM LIVER MICROSOMES OF ADULT MALE RABBITS TREATED WITH TCDD THEN RECONSTITUTED WITH HIGHLY PURIFIED NADPH-CYTOCHROME P-450REDUCTASE IT CATALYZES HYDROXYLATION OF ACETANILIDE

JOHNSON EF MULLER-EBERHARD U BIOCHEM BIOPHYS RES COMMUN 76(3) 652 (1977)


3-[(5-ACETA MIDO-2-HYDROXYPHENYL)THIO]-N-ACETYLALANINE amp 3-[(5-ACETAMIDOPHE NYL)THIO]-N-ACETYLALANINE WERE URINARY METABOLITES OF 3H-LABELED ACETANILIDE IN RATSTHEY ACCOUNTED FOR 7-10 AND 1-3 OF URINARY RADIOACTIVITY RESPECTIVELY MODE OF FORMATION MAY INVOLVE INT EPOXIDE

GRANTHAM PH ET AL XENOBIOTICA 4(2) 69 (1974)


THE DRUG METABOLIZING ACTIVITY AND DRUG AND STEROID BINDING BY CYTOCHROME P-450 WAS STUDIED IN HUMAN TERM PLACENTAL MICROSOMES THE MICROSOMES DID NOTMETABOLIZE ACETANILIDE

BERGHEIM P ET AL BIOCHEM PHARMACOL 22(13) 1633 (1973)


METAB OF (3)H-ACETANILIDE STUDIED IN RATS AFTER SINGLE IP DOSE (200 MGKG) 1-5 DAYS OF CONTINUOUS FEEDING 08 OF DIET amp WEEKLY INTERVALS DURING 4 WK OF SUCH FEEDING4-HYDROXYACETANILIDE MAJOR METABOLITE FOUND FREE amp ALSO CONJUGATED WITH GLUCURONIC amp SULFURIC ACIDS



METAB OF (3)H-ACETANILIDE STUDIED IN RATS 4-HYDROXYACETANILIDE GLUCURONIDE INCR FROM 46 (SINGLE IP DOSE 200 MGKG) amp 60 (1 DAY FEEDING 08 OF DIET) TO 16 OF DOSE 1 WK (08 OF DIET) 4-HYDROXYACETANILIDE SULFATE DECR FROM 70 OF DOSE 24 HR TO 43 AFTER 1 WK



TIME COURSE OF OXIDATIVE METAB OF PENTOBARBITAL amp ACETANILIDE BY RAT LIVER MICROSOMES IN VITRO WAS LINEAR FOR RELATIVELY SHORT PERIODS OF TIME amp ACCOMPANIED BY HIGHRATE OF NADPH-DEPENDENT LIPID PEROXIDATION amp BREAKDOWN OF HEME OF CYTOCHROME P-450

JACOBSON MM ET AL DRUG METAB DISPOS 1(6) 766 (1973)


In an in vitro study hepatic microsomes prepared from male Sprague-Dawley rats were incubated with tritium (3)H labeled aniline or acetanilide Microsomal metabolism of radiolabeled anilineproduced p-aminophenol with a low retention of (3)H 1124 Radioactive acetanilide was converted to p-hydroxyacetanilide with a substantially greater retention of (3)H 489 Male Sprague-Dawley rats were injected ip with 15 milimoleskg (3)H labeled aniline or acetanilide 24 Hr urine samples were collected and analyzed for metabolites Following dosing with radiolabelled aniline p-aminophenol and p-hydroxyacetanilide were excreted in the urine with (3)H retentions of 15 and 38 respectively Similar results were obtained with acetanilide Pretreatment with 100 mgkg bis-(p-nitrophenyl)phosphate an inhibitor of amide deacetylation followed by 15 millimolekg (3)H labeled acetanilide was carried out Effects on blood aniline concn were determined 0 to 11 hrafter acetanilide Bis-(p-nitrophenyl)phosphate greatly reduced the formation of aniline in the blood from acetanilide In urine p-hydroxyacetanilide was recovered with a 53 retention f (3)H

Grossman SJ Jollow DJ Drug Metab Dispos 14 (6) 689-91 (11986)


Acetanilide has known human metabolites that include N-Hydroxy-N-phenylacetamide and acetaminophenS73 | METXBIODB | Metabolite Reaction Database from BioTransformer | DOI105281zenodo4056560

NORMAN Suspect List Exchange

93 Biological Half-Life

T2 OF ACETANILID MEASURED IN POPULATIONS OF YOUNG (AGED 20-35 YR) amp ELDERLY (AGED OVER 65 YR) PEOPLE (TOTAL= 93) T2 WERE SIGNIFICANTLY LONGER IN THE ELDERLYFARAH F ET AL HEPATIC DRUG ACETYLATION AND OXIDATION EFFECTS OF AGING IN MAN BR MED J 2(JUL 16) 155 (1977)


94 Human Metabolite Information



941 Cellular Locations

Membrane


95 Biochemical Reactions

PubChem

96 Transformations




10 Use and Manufacturing

101 Use Classification

Pharmaceuticals -gt Animal Drugs -gt Approved in TaiwanS72 | NTUPHTW | Pharmaceutically Active Substances from National Taiwan University | DOI105281zenodo3955664


Cosmetics -gt StabilizingS13 | EUCOSMETICS | Combined Inventory of Ingredients Employed in Cosmetic Products (2000) and Revised Inventory (2006) | DOI105281zenodo2624118


102 Uses

EPA CPDat Chemical and Product Categories

EPA Chemical and Products Database (CPDat)

MFR OF MEDICINALS DYES STABILIZER FOR HYDROGEN PEROXIDE AS ADDN TO CELLULOSE ESTER VARNISHESBudavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 10


RUBBER ACCELERATORPatty F (ed) Industrial Hygiene and Toxicology Volume II Toxicology 2nd ed New York Interscience Publishers 1963 p 1835


MFR OF INTERMEDIATES IN SYNTHETIC CAMPHOR PRECURSOR IN PENICILLIN MFRLewis RJ Sr (Ed) Hawleys Condensed Chemical Dictionary 12th ed New York NY Van Nostrand Rheinhold Co 1993 p 6


Intermediate for sulfa drugs hydrogen peroxide stabilizer azo dye manufactureKirk-Othmer Encyclopedia of Chemical Technology 4th ed Volumes 1 New York NY John Wiley and Sons 1991-Present p V2 439


Mfr of intermediates (p-nitroaniline p-nitroacetanilide p-phenylenediamine) synthetic camphor pharmaceutical chemicals dyestuffs precursor in penicillin mfr medicine (antiseptic) acetanisoleLewis RJ Sr (Ed) Hawleys Condensed Chemical Dictionary 12th ed New York NY Van Nostrand Rheinhold Co 1993 p 6


Used as a chemical intermediate for the synthesis of 4-acetamidobenzenesulphonyl chloride p-bromoaniline p-nitroacetanilideAshford RD Ashfords Dictionary of Industrial Chemicals London England Wavelength Publications Ltd 1994 p 11


Plasticizer intermediate for synthesis of sulfonamidesGerhartz W (exec ed) Ullmanns Encyclopedia of Industrial Chemistry 5th edVol A1 Deerfield Beach FL VCH Publishers 1985 to Present p VA2 310


MEDICATION (VET)


MEDICATION


103 Methods of Manufacturing



USUALLY PREPARED FROM ANILINE amp ACETIC ACIDS AI VOGEL PRACTICAL ORGANIC CHEMISTRY (LONDON 3RD ED 1959) PAGE 577 FROM ANILINE amp ACETYL CHLORIDE GATTERMANN-WIELAND PRAXIS DES ORGANISCHEN CHEMIKERS (BERLIN 40TH ED 1961) PAGE 114



FROM ANILINE ACETONE amp KETENE HURD ORG SYN COLL VOL I (NEW YORK 2ND ED 1941) PAGE 332Budavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 9


Heating aniline with acetic anhydrideGerhartz W (exec ed) Ullmanns Encyclopedia of Industrial Chemistry 5th edVol A1 Deerfield Beach FL VCH Publishers 1985 to Present p VA2 310


104 FormulationsPreparations

GRADES TECHNICAL CPLewis RJ Sr (Ed) Hawleys Condensed Chemical Dictionary 12th ed New York NY Van Nostrand Rheinhold Co 1993 p 6


105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data


108 General Manufacturing Information

EPA TSCA Commercial Activity Status

Acetamide N-phenyl- ACTIVEhttpswwwepagovtsca-inventory

EPA Chemicals under the TSCA

INCOMPATIBILITIES FERRIC SALTS (RED COLOR OR PRECIPITATE)Budavari S (ed) The Merck Index - An Encyclopedia of Chemicals Drugs and Biologicals Whitehouse Station NJ Merck and Co Inc 1996 p 10


INCOMPATIBILITIES ETHYL NITRATE AMYL NITRITE ACID SOLN OF NITRILES ALKALIES (ANILINE LIBERATED) ALKALI BROMIDE amp IODIDES IN AQ SOLN (INSOL COMPD FORMED) CHLORALHYDRATE PHENOL RESORCINOL THYMOL (THESE PRODUCE LIQ OR SOFT MASS ON TRITURATION)



ACETANILID IS PARENT MEMBER OF SO-CALLED COAL TAR ANALGESICS PHENACETIN amp ITSMETABOLITE ACETAMINOPHEN IT WAS INTRODUCED INTO MEDICINE IN 1886 UNDER NAME OFANTIFEBRINAFTER DISCOVERY OF ITS ANTIPYRETIC ACTION PROVED TO BE EXCESSIVELY TOXIC ampREPORTS OF POISONINGPROMPTED SEARCH FOR LESS TOXIC COMPD

Hardman JG LE Limbird PB Molinoff RW Ruddon AG Goodman (eds) Goodman and Gilmans The Pharmacological Basis of Therapeutics 9th ed New York NY McGraw-Hill 1996 p 631




11 Identification

111 Analytic Laboratory Methods

EXAMPLES ARE GIVEN OF SEPARATION OF COMBINATIONS OF ANALGESICS BY HIGH-PRESSURE LIQUID CHROMATOGRAPHYHARZER K BARCHET R SEPARATION AND DETECTION OF SOME COMMON ANALGESICS BY HIGH-PRESSURE LIQUID CHROMATOGRAPHY DTSCH APOTH-ZTG 116(34) 1229 (1976)


METHOD OF DETERMINATION OF ACETANILIDE IN MIXED PHARMACEUTICAL PREPNINOUE T ET AL COLORIMETRIC DETERMINATION OF ACETANILIDE WITH BETA-DIETHYLAMINOETHYL-ALPHA-NAPHTHYLAMINE OXALATE J HYG CHEM 16(1) 19 (1970)


AOAC Method Numbers 91602 - 91607 Acetanilidin DrugsAssociation of Official Analytical Chemists Official Methods of Analysis 15th ed and Supplements Washington DC Association of Analytical Chemists 1990 p 555


Microchemical Tests AOAC Method Number 96221 Barbituates in DrugsAssociation of Official Analytical Chemists Official Methods of Analysis 15th ed and Supplements Washington DC Association of Analytical Chemists 1990 p 536


112 Clinical Laboratory Methods

ACETANILIDE DETERMINED IN BLOOD BY GC LOWER LIMIT OF DETECTION WAS 60 NG IN 100 MU LCOOPER MJ ANDERS MW GAS CHROMATOGRAPHIC MICRODETERMINATION OF ACETANILIDE IN BLOOD J CHROMATOGR 104(1) 215 (1975)


A GS-MS METHOD FOR ANALYSIS OF ACETANILIDE IN PLASMA OR URINE USING D-LABELED ANALOGS IS DESCRIBEDBATY JD ET AL A METHOD FOR THE ESTIMATION OF ACETANILIDE PARACETAMOL AND PHENACETIN IN PLASMA AND URINE USING MASS FRAGMENTOGRAPHY BIOMED MASS SPECTROM 3(2) 60 (1976)




12 Safety and Hazards

121 Hazards Identification

1211 GHS Classification


Pictogram(s)

Signal Warning

GHS Hazard Statements

Aggregated GHS information provided by 1684 companies from 10 notifications to the ECHA CampL Inventory

Reported as not meeting GHS hazard criteria by 2 of 1684 companies For more detailed information please visit ECHA CampL website

Of the 9 notification(s) provided by 1682 of 1684 companies with hazard statement code(s)

H302 (100) Harmful if swallowed [Warning Acute toxicity oral]

Information may vary between notifications depending on impurities additives and other factors The percentage value in parenthesis indicates the notified classification ratio fromcompanies that provide hazard codes Only hazard codes with percentage values above 10 are shown

Precautionary StatementCodes

P264 P270 P301+P312 P330 and P501

(The corresponding statement to each P-code can be found at the GHS Classification page)


1212 Hazard Classes and Categories


Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)


1213 NFPA Hazard Classification

NFPA 704 Diamond

NFPA Health Rating 3 - Materials that under emergency conditions can cause serious or permanent injury

NFPA Fire Rating 1 - Materials that must be preheated before ignition can occur Materials require considerable preheating under all ambient temperature conditions before ignition and combustion canoccur

NFPA Instability Rating 0 - Materials that in themselves are normally stable even under fire conditions


1214 Health Hazards

SYMPTOMS Symptoms of exposure to this compound may include contact dermatitis and eczematous skin eruptions anemia and cyanosis ACUTECHRONIC HAZARDS This compound is an irritantIt emits toxic fumes when heated to decomposition (NTP 1992)

National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

1215 Fire Hazards

This chemical is combustible (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

122 First Aid Measures

1221 First Aid

EYES First check the victim for contact lenses and remove if present Flush victims eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poisoncontrol center Do not put any ointments oils or medication in the victims eyes without specific instructions from a physician IMMEDIATELY transport the victim after flushing eyes to a hospital evenif no symptoms (such as redness or irritation) develop SKIN IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing Gently wash all affected skin areas

Irritant

13 0

3-1-0



thoroughly with soap and water If symptoms such as redness or irritation develop IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment INHALATIONIMMEDIATELY leave the contaminated area take deep breaths of fresh air If symptoms (such as wheezing coughing shortness of breath or burning in the mouth throat or chest) develop call aphysician and be prepared to transport the victim to a hospital Provide proper respiratory protection to rescuers entering an unknown atmosphere Whenever possible Self-Contained BreathingApparatus (SCBA) should be used if not available use a level of protection greater than or equal to that advised under Protective Clothing INGESTION DO NOT INDUCE VOMITING If the victim isconscious and not convulsing give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center Be prepared to transport the victim to a hospital if advisedby a physician If the victim is convulsing or unconscious do not give anything by mouth ensure that the victims airway is open and lay the victim on hisher side with the head lower than the bodyDO NOT INDUCE VOMITING IMMEDIATELY transport the victim to a hospital (NTP 1992)


CAMEO Chemicals

123 Fire Fighting

Fires involving this compound can be controlled with a dry chemical carbon dioxide or Halon extinguisher (NTP 1992)National Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

124 Accidental Release Measures

1241 Disposal Methods

SRP At the time of review criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision Prior to implementing land disposal of waste residue (includingwaste sludge) consult with environmental regulatory agencies for guidance on acceptable disposal practices


Incineration Incineration at 1000 degC followed by treatment of the off-gas has been recommended Landfill burial has also been suggested But in light of the generation of more toxic persistentproducts this mode of disposal does not seem desirable

United Nations Treatment and Disposal Methods for Waste Chemicals (IRPTC File) Data Profile Series No 5 Geneva Switzerland United Nations Environmental Programme Dec 1985 p 68


125 Handling and Storage

1251 Nonfire Spill Response

SMALL SPILLS AND LEAKAGE Should a spill occur while you are handling this chemical FIRST REMOVE ALL SOURCES OF IGNITION then you should dampen the solid spill material with 60-70ethanol and transfer the dampened material to a suitable container Use absorbent paper dampened with 60-70 ethanol to pick up any remaining material Seal the absorbent paper and any ofyour clothes which may be contaminated in a vapor-tight plastic bag for eventual disposal Solvent wash all contaminated surfaces with 60-70 ethanol followed by washing with a soap and watersolution Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned STORAGE PRECAUTIONS You should keepthis material in a tightly-closed container under an inert atmosphere and store it at refrigerated temperatures (NTP 1992)


CAMEO Chemicals

126 Exposure Control and Personal Protection

1261 Personal Protective Equipment (PPE)

RECOMMENDED RESPIRATOR Where the neat test chemical is weighed and diluted wear a NIOSH-approved half face respirator equipped with an organic vaporacid gas cartridge (specific fororganic vapors HCl acid gas and SO2) with a dustmist filter (NTP 1992)


CAMEO Chemicals

127 Stability and Reactivity

1271 Air and Water Reactions

This compound is sensitive to prolonged exposure to air (NTP 1992) Water insolubleNational Toxicology Program Institute of Environmental Health Sciences National Institutes of Health (NTP) 1992 National Toxicology Program Chemical Repository Database Research Triangle Park North Carolina

CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals

1273 Reactivity Profile

ACETANILIDE is an amide Flammable gases are formed by the reaction of organic amides with strong reducing agents Amides are very weak bases (weaker than water) Imides are less basic yet andin fact react with strong bases to form salts That is they can react as acids Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile The combustion ofthese compounds generates mixed oxides of nitrogen (NOx)



CAMEO Chemicals

1274 Hazardous Reactivities and Incompatibilities

SEE ANILINECAN REACT VIGOROUSLY WITH OXIDIZING MATERIALSSax NI Dangerous Properties of Industrial Materials 5th ed New York Van Nostrand Rheinhold 1979 p 333




13 Toxicity

131 Toxicological Information

1311 NIOSH Toxicity Data


1312 Acute Effects

ChemIDplus

1313 Interactions

THIRTY-MOLAR EXCESS OF ACETANILIDE REDUCED CARCINOGENICITY OF N-2-FLUORENYLACETAMIDE ON LIVER amp SEVERAL OTHER TARGET ORGANS IN SEVERAL SPECIESDoull J CD Klaassen and M D Amdur (eds) Casarett and Doulls Toxicology 2nd ed New York Macmillan Publishing Co 1980 p 117


ACETANILID WILLPOTENTIATE ANALGESIC EFFECTS OF OPIATESOsol A and JE Hoover et al (eds) Remingtons Pharmaceutical Sciences 15th ed Easton Pennsylvania Mack Publishing Co 1975 p 1053


ENHANCING EFFECT OF METAPYRONE UPON THE P-HYDROXYLATION OF ACETANILIDE HAS BEEN CONFIRMEDLEIBMAN KC ORTIZ E DRUG METAB DISPOS 3(6) 507 (1975)


ACUTE EFFECT OF ORAL ADMIN OF BENZENE ON LIVER MICROSOMAL DRUG ENZYMES AND LIPID PEROXIDATION WAS INVESTIGATED IN RATS INCR IN HYDROXYLATION OF ACETANILIDE WASOBSERVED

MUNGIKAR AM PAWAR SS INDIAN J EXP BIOL 13(5) 439 (1975)


For more Interactions (Complete) data for ACETANILIDE (11 total) please visit the HSDB record page


1314 Human Toxicity Excerpts

IT IS WELL KNOWN TO PRODUCE CYANOSIS IN SOME HUMANS WHEN TAKEN REPEATEDLY POSSIBLY DUE TO FORMATION OF SULFHEMOGLOBIN LARGE DOSES IN ACUTE POISONING PRODUCEMETHEMOGLOBIN

Patty F (ed) Industrial Hygiene and Toxicology Volume II Toxicology 2nd ed New York Interscience Publishers 1963 p 1835




COAL TAR ANALGETICS INCL ACETANILID ARE DEPRESSANTS OF CNS SYMPTOMS OF NAUSEA amp VOMITING VERTIGO amp RINGING IN EARSOCCUR WITH LARGE DOSES OR IN SENSITIVEINDIVIDUALS WITH THERAPEUTIC DOSES SWEATING MAY BE PROFUSE LARGE DOSES LEAD TO MENTAL CONFUSION MUSCULAR INCOORDINATION amp COMA



CIRCULATORY COLLAPSE WITH COLD EXTREMITIES PALENESSFEEBLE RAPID PULSE amp DYSPNEA amp COMA WITH FIXED SEMI-DILATED PUPILS IS CHARACTERISTIC FINDING IN ACUTE ACETANILIDPOISONING



IT MAYCAUSE CONTACT DERMATITIS amp INHALATION OR INGESTION MAY CAUSE AN ECZEMATOUS ERUPTION OF THE SKINSax NI Dangerous Properties of Industrial Materials 5th ed New York Van Nostrand Rheinhold 1979 p 333


For more Human Toxicity Excerpts (Complete) data for ACETANILIDE (9 total) please visit the HSDB record page


1315 Non-Human Toxicity Excerpts

ACUTE TOXICITYIS VERY LOW--RATS amp MONKEYS TOLERATING DOSES OF 200-400 MGKG ORALLY PER DAY FOR MANY WEEKS WITH VERY LARGE DOSESMETHEMOGLOBIN amp SOMEHYPERPLASIA OF BONE MARROW CAN BE PRODUCED



IN MOUSE RAT GUINEA PIG AND RABBIT LIVER MICROSOMES GLUTATHIONE DEPLETION WAS NOT OBSERVED WITH ACETANILIDEAIKAWA K ET AL GLUTATHIONE DEPLETION BY ANILINE ANALOGS IN VITRO ASSOCIATED WITH LIVER MICROSOMAL CYTOCHROME P-450 JPN J PHARMACOL 28(5) 699 (1978)


At a single dose of 200 mgkg by gavage acetanilide oxidized hemoglobin to methemoglobin in dogs From tableClayton G D and F E Clayton (eds) Pattys Industrial Hygiene and Toxicology Volume 2A 2B 2C Toxicology 3rd ed New York John Wiley Sons 1981-1982 p 2416


If a value of 100 is assigned to the sensitivity of the cat with respect to methemoglobin formation then the sensitivities of other species are as follows for acetanilide man 56 dog 29 rat 5 rabbit0 and monkey 0

Clayton G D and F E Clayton (eds) Pattys Industrial Hygiene and Toxicology Volume 2A 2B 2C Toxicology 3rd ed New York John Wiley Sons 1981-1982 p 2416


For more Non-Human Toxicity Excerpts (Complete) data for ACETANILIDE (6 total) please visit the HSDB record page


132 Ecological Information

1321 Environmental FateExposure Summary

Acetanilide may be released into the environment in various waste streams from its production and use as an intermediate in drug and dye production as a stabilizer in hydrogen peroxide andcellulose esters as a plasticizer and as a rubber accelerator If released to the atmosphere acetanilide is expected to exist solely as a vapor in the ambient atmosphere based on an extrapolated vaporpressure of 12X10-3 mm Hg at 25 degC Vapor-phase acetanilide is expected to degrade rapidly by reaction with photochemically-produced hydroxyl radicals (estimated half-life of 13 days) If releasedto the soil acetanilide is expected to exhibit very high mobility based on a measured Koc of 27 Acetanilide is not expected to volatilize from either wet or dry soil based on an estimated Henrys Lawconstant of 62X10-9 atm-cu mmol and an extrapolated vapor pressure of 12X10-3 mm Hg respectively If released into water biodegradation of acetanilide is expected to be an important removalprocess An estimated BCF of 45 suggests that bioconcentration of acetanilide in aquatic organisms is low Hydrolysis adsorption to soil and sediment and volatilization are not expected to beenvironmentally important removal processes in aquatic systems Occupational exposure to acetanilide is expected to occur primarily through dermal contact with this compound in workplaceswhere it is produced and used The general population may be exposed to acetanilide through ingestion of contaminated drinking water (SRC)


1322 Artificial Pollution Sources

Acetanilides production and use as an intermediate in drug and dye manufacture(1) a stabilizer for hydrogen peroxide(1) and cellulose esters(2) a plasticizer(2) and a rubber accelerator(3) mayresult in its release to the environment through various waste streams(SRC) Acetanilide has been found to be a thermal decomposition product of epoxy powder paint(4)

(1) Billig E Kirk-Othmer Encycl Chem Technol 4th ed NY NY John Wiley and Sons Vol 2 439 (1992) (2) Lawrence FR et al Ullmanns Encycl Indust Chem A2 310 (1985) (3) Sax NI Dangerous Properties of Industrial Materials 5thed NYNY Van Nostrand Reinhold (1979) (4) Peltonen K J Anal Appl Pyrolysis 10 51-7 (1986)


1323 Environmental Fate

TERRESTRIAL FATE Based on a recommended classification scheme(1) a measured Koc value of 27(2SRC) indicates that acetanilide will have very high mobility in soil(SRC) Volatilization ofacetanilide from moist soil surfaces is not expected to be important(SRC) given an estimated Henrys Law constant of 62X10-9 atm-cu mmole(SRC) using a fragment constant estimation method(3)



The potential for volatilization of acetanilide from dry soil surfaces may not exist(SRC) based on the extrapolated vapor pressure of 12X10-3 mm Hg(4SRC) Limited data suggest that acetanilide mayundergo microbial degradation in soil

(1) Swann RL et al Res Rev 85 23 (1983) (2) Briggs GG J Agric Food Chem 29 1050-9 (1981) (3) Meylan WM Howard PH Environ Toxicol Chem 10 1283-93 (1991) (4) Perry RH Green D Perrys Chemical Handbook 6th ed NYNY McGraw Hill p 3-50 (1984)


AQUATIC FATE Based on a recommended classification scheme(1) a measured Koc value of 27(2SRC)indicates that acetanilide is not expected to adsorb to suspended solids and sediment inwater(SRC) Acetanilide is not expected to volatilize from water surfaces(1SRC) based on an estimated Henrys Law constant of 62X10-9 atm-cu mmole(SRC) developed using a fragment constantestimation method(3) According to a classification scheme(5) an estimated BCF value of 45(1SRC) from an experimental log Kow(4SRC) suggests that bioconcentration in aquatic organisms islow(SRC) Acetanilide should biodegrade rapidly in aquatic systems Hydrolysis of acetanilide is not expected to be an environmentally important removal process in aquatic systems(SRC)

(1) Lyman WJ et al Handbook of Chemical Property Estimation Methods Washington DC Amer Chem Soc pp 4-9 5-4 5-10 15-1 to 15-29 (1990) (2) Briggs GG J Agric Food Chem 29 1050-9 (1981) (3) Meylan WM Howard PHEnviron Toxicol Chem 10 1283-93 (1991) (4) Hansch C et al Exploring QSAR Hydrophobic Electronic and Steric Constants ACS Professional Reference Book Heller SR consult ed Washington DC Amer Chem Soc p 42 (1995) (5)Franke C et al Chemosphere 29 1501-14 (1994)


ATMOSPHERIC FATE According to a model of gasparticle partitioning of semivolatile organic compounds in the atmosphere(1) acetanilide which has an extrapolated vapor pressure of 12X10-3mm Hg at 25 degC(2SRC) will exist solely as a vapor in the ambient atmosphere Vapor-phase acetanilide is degraded in the atmosphere by reaction with photochemically-produced hydroxylradicals(SRC) the half-life for this reaction in air is estimated to be about 13 days(3SRC)

(1) Bidleman TF Environ Sci Technol 22 361-367 (1988) (2) Perry RH Green D Perrys Chemical Handbook 6th ed NY NY McGraw Hill p 3-50 (1984) (3) Meylan WM Howard PH Chemosphere 26 2293-99 (1993)


1324 Environmental Biodegradation

Several tests indicate that acetanilide biodegrades rapidly under aerobic conditions(1-3) One screening test based on COD measurements using an activated sludge seed and an initial chemicalconcentration of 200 ppm reported a 94 COD removal after 5 days(1) A screening test using an acclimated riverwater seed based on BOD measurements reported an 80 BODT after 8 days(2) Agrab sample test from the Nile River using an initial chemical concentration of 6-7 ppm reported 100 degradation after 43 days incubation(3)

(1) Pitter P Water Res 10 231-5 (1976) (2) Mills EJ Stack VT Jr Eng Bull of Purdue U Ext Ser Purdue U Lafayette IN 9 449-64 (1955) (3) El-Dib MA Aly OA Water Res 101055-9 (1976)


1325 Environmental Abiotic Degradation

The rate constant for the vapor-phase reaction of acetanilide with photochemically-produced hydroxyl radicals has been estimated as 12X10-11 cu cmmolecule-sec at 25 degC(SRC) using a structureestimation method(1SRC) This corresponds to an atmospheric half-life of about 13 days at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1SRC) The rate constant for theaqueous-phase reaction with photochemically-produced hydroxyl radicals has been determined to be 52X10+9 Lmol-sec at pH 9(2) This corresponds to as aqueous half-life of approximately 154days at an aqueous hydroxyl radical concentration of 10X10-17 moll(2) Acetanilide is not expected to undergo hydrolysis or direct photolysis in the environment due to the lack of functional groupsto hydrolyze or absorb UV light

(1) Meylan WM Howard PH Chemosphere 26 2293-99 (1993) (2) Buxton GV et al J Phys Chem Ref Data 17 513-882 (1988)


1326 Environmental Bioconcentration

An estimated BCF value of 45 was calculated for acetanilide(SRC) using an experimental log Kow of 116(1SRC) and a recommended regression-derived equation(2) According to a classificationscheme(3) this BCF value suggests that bioconcentration in aquatic organisms is low(SRC)

(1) Hansch C et al Exploring QSAR Hydrophobic Electronic and Steric Constants ACS Profess Ref Book Heller SR consult ed Washington DC Amer Chem Soc p 42 (1995) (2) Lyman WJ et al Handbook of Chemical PropertyEstimation Methods Washington DC Amer Chem Soc pp 5-4 5-10 (1990) (3) Franke C et al Chemosphere 29 1501-14 (1994)


1327 Soil AdsorptionMobility

Soil Adsorption Coefficient

2692 Lkg

EPA DSSTox

The Koc of acetanilide is estimated as approximately 38(SRC) using an experimental log Kow of 116(1SRC) and a regression-derived equation(2SRC) A Koc of 27 was experimentally determined foracetanilide using silt loam and sandy loam with organic matter ranging from 109-592 (Kom was converted to Koc by multiplying by 1724) and pH ranging from 59-75(4) According to arecommended classification scheme(3) the estimated and measured Koc values suggest that acetanilide has very high mobility in soil(SRC)

(1) Hansch C et al Exploring QSAR Hydrophobic Electronic and Steric Constants ACS Profess Ref Book Heller SR consult ed Washington DC Amer Chem Soc p 42 (1995) (2) Lyman WJ et al Handbook of Chemical PropertyEstimation Methods Washington DC Amer Chem Soc pp 4-9 (1990) (3) Swann RL et al Res Rev 85 23 (1983) (4) Briggs GG J Agric Food Chem 29 1050-9 (1981)


1328 Volatilization from WaterSoil

The Henrys Law constant for acetanilide is estimated as 62X10-9 atm-cu mmole(SRC) using a fragment constant estimation method(1) This value indicates that acetanilide will be essentiallynonvolatile from water surfaces(2SRC) Acetanilides Henrys Law constant(1SRC) indicates that volatilization from moist soil surfaces may not occur(SRC) The potential for volatilization of acetanilidefrom dry soil surfaces may not exist(SRC) based on the extrapolated vapor pressure of 12X10-3 mm Hg(3SRC)

(1) Meylan WM Howard PH Environ Toxicol Chem 10 1283-93 (1991) (2) Lyman WJ et al Handbook of Chemical Property Estimation Methods Washington DC Amer Chem Soc pp 15-1 to 15-29 (1990) (3) Perry RH Green DPerrys Chemical Handbook 6th ed NY NY McGraw Hill (1984)


1329 Environmental Water Concentrations

DRINKING WATER Acetanilide was quantitatively detected in drinking water in Cincinnati OH on Jan 14 1980(1)



(1) Lucas SV GCMS Anal of Org in Drinking Water Concentrates and Advanced Treatment Concentrates Vol 1 USEPA-6001-84-020A (NTIS PB85-128239) p 321 (1984)


13210 Effluent Concentrations

Acetanilide was detected in one wastewater sample from an undisclosed specialty chemicals manufacturing plant at a level of 02 ppm between Nov 6 1975 and Sept 6 1976(1)(1) Jungclaus GA et al Environ Sci Technol 12 88-96 (1978)


13211 Probable Routes of Human Exposure

REACTION OF WORKERS WHO FILL BAGS OF ACETANILIDE AFTER DUTY HR MOSTCOMPLAINED OF CHEST PAIN GIDDINESS EPIGASTRIC PAIN amp HIGHLY COLORED URINE OCCASIONALLYTHERE WAS TINGE OF CYANOSIS HEMOGLOBIN VALUESWERE BETWEEN 70 amp 85



SYMPTOMS OF OCCUPATIONALLY CAUSED ACETANILIDE POISONING ARE PRESENTED WITH PARTICULAR EMPHASIS ON CYANOSIS GIDDINESS amp DELAYED ABSORPTION TREATMENT ANDPREVENTATIVE MEASURES ARE ALSO DESCRIBED

CUTHBERT J PRACTITIONER 207(1242) 807 (1971)


NIOSH (NOES Survey 1981-1983) has statistically estimated that 9000 workers (6100 of these are female) are potentially exposed to acetanilide in the US(1) Limited monitoring data indicate thatnon-occupational exposure can occur from the ingestion of contaminated drinking water The most probable human exposure would be occupational exposure which may occur through dermalcontact at workplaces where acetanilide is produced or used(SRC)

(1) NIOSH National Occupational Exposure Survey (NOES) (1983)




14 Associated Disorders and Diseases

Comparative Toxicogenomics Database (CTD)



15 Literature

151 NLM Curated PubMed Citations

PubChem

152 Springer Nature References

Springer Nature

153 Thieme References

Thieme Chemistry

154 Wiley References



Wiley

155 Depositor Provided PubMed Citations

PubChem

156 Metabolite References


157 General References

Nguyen et al Engaging unactivated alkyl alkenyl and aryl iodides in visible light-mediated free radical reactions Nature Chemistry doi 101038nchem1452 published online 24 September2012 httpwwwnaturecomnchem

Nature Chemistry

Liu et al From alkylarenes to anilines via site-directed carbon-carbon amination Nature Chemistry doi 101038s41557-018-0156-y published online 29 October 2018

Nature Chemistry

158 Chemical Co-Occurrences in Literature



PubChem

159 Chemical-Gene Co-Occurrences in Literature

PubChem

1510 Chemical-Disease Co-Occurrences in Literature

PubChem



16 Patents

161 Depositor-Supplied Patent Identifiers

PubChem

Link to all deposited patent identifiers

PubChem

162 WIPO PATENTSCOPE

Patents are available for this chemical structure

httpspatentscopewipointsearchenresultjsfinchikey=FZERHIULMFGESH-UHFFFAOYSA-N

PATENTSCOPE (WIPO)



17 Biomolecular Interactions and Pathways

171 Drug-Gene Interactions

Drug Gene Interaction database (DGIdb)

172 Pathways

PubChem



18 Biological Test Results

181 BioAssay Results

PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus

1915 CAMEO Chemicals

CAMEO Chemicals

1916 ChEMBL Target Tree

ChEMBL

1917 UN GHS Classification

UN Globally Harmonized System of Classification and Labelling of Chemicals (GHS)

1918 EPA CPDat Classification




1919 NORMAN Suspect List Exchange Classification


19110 CCSBase Classification

CCSBase



20 Information Sources

FILTER BY SOURCE

1 CAMEO ChemicalsLICENSECAMEO Chemicals and all other CAMEO products are available at no charge to those organizations and individuals (recipients) responsible for the safe handling of chemicals However some of the chemical data itself is subject to the copyrightrestrictions of the companies or organizations that provided the datahttpscameochemicalsnoaagovhelpreferenceterms_and_conditionshtmd_f=false

ACETANILIDEhttpscameochemicalsnoaagovchemical19701

CAMEO Chemical Reactivity Classificationhttpscameochemicalsnoaagovbrowsereact

2 ChemIDplusLICENSEhttpswwwnlmnihgovcopyrighthtml

Acetanilide [NF]httpschemnlmnihgovchemidplussid0000103844

ChemIDplus Chemical Information Classificationhttpschemnlmnihgovchemidplus

3 DTPNCILICENSEhttpswwwcancergovpoliciescopyright-reuse

acetanilidehttpsdtpcancergovdtpstandardservletdwindexsearchtype=NSCampoutputformat=htmlampsearchlist=757879


4 EPA Chemicals under the TSCALICENSEhttpswwwepagovprivacyprivacy-act-laws-policies-and-resources

Acetamide N-phenyl-httpswwwepagovchemicals-under-tsca

5 EPA DSSToxLICENSEhttpswwwepagovprivacyprivacy-act-laws-policies-and-resources

AcetanilidehttpscomptoxepagovdashboardDTXSID2022543

6 European Chemicals Agency (ECHA)LICENSEUse of the information documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice and subject to other binding limitations provided for under applicable law the information documents and data madeavailable on the ECHA website may be reproduced distributed andor used totally or in part for non-commercial purposes provided that ECHA is acknowledged as the source Source European Chemicals Agency httpechaeuropaeu Suchacknowledgement must be included in each copy of the material ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions Links can only be made to webpages thatprovide a link to the Legal Notice pagehttpsechaeuropaeuwebguestlegal-notice

acetanilidehttpsechaeuropaeusubstance-information-substanceinfo100002864

N-[23456-2H5]phenylacetamidehttpsechaeuropaeusubstance-information-substanceinfo100036284

Acetanilidehttpsechaeuropaeuinformation-on-chemicalscl-inventory-database-disclidetails79085

N-[23456-2H5]phenylacetamidehttpsechaeuropaeuinformation-on-chemicalscl-inventory-database-disclidetails110520

7 Hazardous Substances Data Bank (HSDB)ACETANILIDEhttpspubchemncbinlmnihgovsourcehsdb2665

8 Human Metabolome Database (HMDB)LICENSEHMDB is offered to the public as a freely available resource Use and re-distribution of the data in whole or in part for commercial purposes requires explicit permission of the authors and explicit acknowledgment of the source material (HMDB)and the original publication (see the HMDB citing page) We ask that users who download significant portions of the database cite the HMDB paper in any resulting publicationshttpwwwhmdbcaciting

N-AcetylarylaminehttpwwwhmdbcametabolitesHMDB0001250

9 The National Institute for Occupational Safety and Health (NIOSH)LICENSEThe information provided using CDC Web site is only intended to be general summary information to the public It is not intended to take the place of either the written law or regulationshttpswwwcdcgovOtherdisclaimerhtml

Acetanilidehttpswwwcdcgovniosh-rtecsAD7026F0html

10 ChEBIN-phenylacetamidehttpwwwebiacukchebisearchIddochebiId=CHEBI28884

ChEBI OntologyhttpwwwebiacukchebiuserManualForwarddoChEBI20Ontology

11 Sanford-Burnham Center for Chemical GenomicsSID85148657

ALL SOURCES



httpspubchemncbinlmnihgovbioassay1996section=Data-Table

12 CCSbaseN-Phenylacetamide

13 Comparative Toxicogenomics Database (CTD)LICENSEIt is to be used only for research and educational purposes Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the MDI Biological Laboratory and NC State Universityhttpctdbaseorgaboutlegaljsp

httpctdbaseorgdetailgotype=chemampacc=C508827

14 Drug Gene Interaction database (DGIdb)LICENSEThe data used in DGIdb is all open access and where possible made available as raw data dumps in the downloads sectionhttpwwwdgidborgdownloads

httpswwwdgidborgdrugsACETANILIDE

15 EPA Chemical and Products Database (CPDat)LICENSEhttpswwwepagovprivacyprivacy-act-laws-policies-and-resources

acetanilidehttpscomptoxepagovdashboardDTXSID2022543exposure

EPA CPDat Classificationhttpswwwepagovchemical-researchchemical-and-products-database-cpdat

16 NITE-CMCAcetanilide - FY2012httpswwwnitegojpchemenglishghs12-mhlw-0010ehtml

17 FDASPL Indexing DataLICENSEUnless otherwise noted the contents of the FDA website (wwwfdagov) both text and graphics are not copyrighted They are in the public domain and may be republished reprinted and otherwise used freely by anyone without the need to obtainpermission from FDA Credit to the US Food and Drug Administration as the source is appreciated but not requiredhttpswwwfdagovabout-fdaabout-websitewebsite-policieslinking

SP86R356CChttpswwwfdagovForIndustryDataStandardsSubstanceRegistrationSystem-UniqueIngredientIdentifierUNII

18 FooDBLICENSEFooDB is offered to the public as a freely available resource Use and re-distribution of the data in whole or in part for commercial purposes requires explicit permission of the authors and explicit acknowledgment of the source material (FooDB)and the original publicationhttpsfoodbcaabout

N-AcetylarylaminehttpsfoodbcacompoundsFDB022512

19 NORMAN Suspect List ExchangeacetanilideNORMAN Suspect List Exchange Classificationhttpswwwnorman-networkcomndsSLE

20 NMRShiftDBhttpspubchemncbinlmnihgovsubstance588093

21 MassBank of North America (MoNA)LICENSEThe content of the MoNA database is licensed under CC BY 40httpsmonafiehnlabucdavisedudocumentationlicense

acetanilidehttpmonafiehnlabucdaviseduspectrabrowseinchikey=FZERHIULMFGESH-UHFFFAOYSA-N

22 NIST Mass Spectrometry Data CenterAcetamide N-phenyl-httpwwwnistgovsrdnist1acfm

23 Nature Chemistryhttpspubchemncbinlmnihgovsubstance144071704httpspubchemncbinlmnihgovsubstance375743888

24 SpectraBasehttpsspectrabasecomspectrum8vvjleQAGc5httpsspectrabasecomspectrumF5pDQt4Xx3Ahttpsspectrabasecomspectrum6Vqc117izTPhttpsspectrabasecomspectrumHwVORJJ6MMKhttpsspectrabasecomspectrum5GSPGugrDaphttpsspectrabasecomspectrumEGA70DXDq8HhttpsspectrabasecomspectrumHK9IkiLWgUZhttpsspectrabasecomspectrumBZrKkLzXdnUhttpsspectrabasecomspectrumHCxOGCeUIjwhttpsspectrabasecomspectrum7ryvBCtztN2httpsspectrabasecomspectrumBQHK4B39VFwhttpsspectrabasecomspectrum3arJOSBlEVhttpsspectrabasecomspectrum6PAaRAh2aHPhttpsspectrabasecomspectrumERU1CctaYKwhttpsspectrabasecomspectrumAKIVJlcI2q4httpsspectrabasecomspectrumFbaLDhHv2tMhttpsspectrabasecomspectrumI6S0FBUVgGShttpsspectrabasecomspectrum7MkIrUNIQe6httpsspectrabasecomspectrumHCq7SCPB7LhttpsspectrabasecomspectrumEySAwC4tm4ohttpsspectrabasecomspectrumJKWkkyKP2Iyhttpsspectrabasecomspectrum56mi6sxWYK4httpsspectrabasecomspectrumJXbSbsUXfxe



25 Springer Naturehttpspubchemncbinlmnihgovsubstance341141147

26 SpringerMaterialsN-phenylethanamidehttpsmaterialsspringercomsubstanceprofiledocssmsid_acuckchtwjbgfgcg

27 The Cambridge Structural DatabasehttpswwwccdccamacukstructuresSearchCcdcid=614360httpswwwccdccamacukstructuresSearchCcdcid=785065httpswwwccdccamacukstructuresSearchCcdcid=907077

28 Thieme ChemistryLICENSEThe Thieme Chemistry contribution within PubChem is provided under a CC-BY-NC-ND 40 license unless otherwise statedhttpscreativecommonsorglicensesby-nc-nd40

29 WikipediaAcetanilidehttpsenwikipediaorgwikiAcetanilide

30 Wileyhttpspubchemncbinlmnihgovsubstancesource=wileyampsourceid=122237

31 PubChemhttpspubchemncbinlmnihgov

32 MeSHacetanilidehttpswwwncbinlmnihgovmesh67508827

Aacuterbol MeSHhttpwwwnlmnihgovmeshmeshhomehtml

33 KEGGAditivos farmaceacuteuticos en Japoacutenhttpwwwgenomejpkegg-binget_htextbr08316keg

34 Sistema Globalmente Armonizado de Clasificacioacuten y Etiquetado de Productos Quiacutemicos (GHS) de las Naciones UnidasAacuterbol de clasificacioacuten GHShttpwwwuneceorgtransdangerpublighsghs_welcome_ehtml

35 CHEMBLAacuterbol objetivohttpswwwebiacukchembltargetbrowser

36 CCSBaseClasificacioacuten CCSBasehttpsccsbasenet

37 PATENTSCOPE (OMPI)SID 403031180httpspubchemncbinlmnihgovsubstance403031180

38 NCBIhttpswwwncbinlmnihgovprojectslinkout



1 Estructuras

11 Estructura 2D

PubChem

12 conformador 3D

PubChem

13 Estructuras de cristalMostrando 1 de 3 Ver maacutes

Nuacutemero CCDC 614360

Datos de estructuracristalina

DOI 105517 ccnm92m

Representacioacuten de laestructura cristalina

Artiacuteculo asociado DOI 101107 S0365110X54002174

The Cambridge Structural Database

Representacioacuten de laestructura quiacutemica

Modelo interactivo deestructura quiacutemica

Bola y palo

Palos

Marco de alambre

Llena el espacio

Mostrar Hidroacutegenos

Animar





211 IUPAC Name


PubChem

212 InChI


PubChem

213 InChI Key


PubChem



PubChem



PubChem


231 CAS

103-84-4


15826-91-2


55576-55-1



203-150-7


239-928-8


233 NSC Number

757879

DTPNCI

7636

DTPNCI

234 RTECS Number



AD7350000


235 UNII

SP86R356CC



DTXSID2022543

EPA DSSTox

237 Wikipedia

Acetanilide

Wikipedia

24 Synonyms



MeSH


PubChem































PubChem




CAMEO Chemicals

Solid


322 ColorForm









323 Odor



324 Taste





325 Boiling Point


CAMEO Chemicals

3040 degC

EPA DSSTox



326 Melting Point


CAMEO Chemicals

1143 degC


327 Flash Point


CAMEO Chemicals



328 Solubility


CAMEO Chemicals


EPA DSSTox










639 mgmL at 25 degC


gt203 [ugmL]




329 Density


CAMEO Chemicals



3210 Vapor Density


CAMEO Chemicals



3211 Vapor Pressure


CAMEO Chemicals

200e-04 mmHg

EPA DSSTox



3212 LogP


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3215 Decomposition













CCSbase


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-

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SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





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precursor mz 136075








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45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

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107 US Exports

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11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


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1221 First Aid


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13 0

3-1-0





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123 Fire Fighting


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1272 Reactive Group

Amides and Imides

Amines Aromatic

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13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES













































211 IUPAC Name


PubChem

212 InChI


PubChem

213 InChI Key


PubChem



PubChem



PubChem


231 CAS

103-84-4


15826-91-2


55576-55-1



203-150-7


239-928-8


233 NSC Number

757879

DTPNCI

7636

DTPNCI

234 RTECS Number



AD7350000


235 UNII

SP86R356CC



DTXSID2022543

EPA DSSTox

237 Wikipedia

Acetanilide

Wikipedia

24 Synonyms



MeSH


PubChem































PubChem




CAMEO Chemicals

Solid


322 ColorForm









323 Odor



324 Taste





325 Boiling Point


CAMEO Chemicals

3040 degC

EPA DSSTox



326 Melting Point


CAMEO Chemicals

1143 degC


327 Flash Point


CAMEO Chemicals



328 Solubility


CAMEO Chemicals


EPA DSSTox










639 mgmL at 25 degC


gt203 [ugmL]




329 Density


CAMEO Chemicals



3210 Vapor Density


CAMEO Chemicals



3211 Vapor Pressure


CAMEO Chemicals

200e-04 mmHg

EPA DSSTox



3212 LogP


EPA DSSTox














CAMEO Chemicals





3215 Decomposition













CCSbase


CCSbase














-

+



SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





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412 13C NMR Spectra




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413 15N NMR Spectra


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414 17O NMR Spectra


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421 GC-MS


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precursor mz 136075








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424 Other MS



43 UV Spectra





441 FTIR Spectra

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45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


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CAMEO Chemicals

1272 Reactive Group

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Amines Aromatic

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13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

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15 Literature


PubChem


Springer Nature


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Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



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CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































AD7350000


235 UNII

SP86R356CC



DTXSID2022543

EPA DSSTox

237 Wikipedia

Acetanilide

Wikipedia

24 Synonyms



MeSH


PubChem































PubChem




CAMEO Chemicals

Solid


322 ColorForm









323 Odor



324 Taste





325 Boiling Point


CAMEO Chemicals

3040 degC

EPA DSSTox



326 Melting Point


CAMEO Chemicals

1143 degC


327 Flash Point


CAMEO Chemicals



328 Solubility


CAMEO Chemicals


EPA DSSTox










639 mgmL at 25 degC


gt203 [ugmL]




329 Density


CAMEO Chemicals



3210 Vapor Density


CAMEO Chemicals



3211 Vapor Pressure


CAMEO Chemicals

200e-04 mmHg

EPA DSSTox



3212 LogP


EPA DSSTox














CAMEO Chemicals





3215 Decomposition













CCSbase


CCSbase














-

+



SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





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SpectraBase




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412 13C NMR Spectra




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45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES
































































PubChem




CAMEO Chemicals

Solid


322 ColorForm









323 Odor



324 Taste





325 Boiling Point


CAMEO Chemicals

3040 degC

EPA DSSTox



326 Melting Point


CAMEO Chemicals

1143 degC


327 Flash Point


CAMEO Chemicals



328 Solubility


CAMEO Chemicals


EPA DSSTox










639 mgmL at 25 degC


gt203 [ugmL]




329 Density


CAMEO Chemicals



3210 Vapor Density


CAMEO Chemicals



3211 Vapor Pressure


CAMEO Chemicals

200e-04 mmHg

EPA DSSTox



3212 LogP


EPA DSSTox














CAMEO Chemicals





3215 Decomposition













CCSbase


CCSbase














-

+



SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





Thumbnail

SpectraBase




Thumbnail

SpectraBase

412 13C NMR Spectra




Thumbnail



SpectraBase



Thumbnail

SpectraBase

413 15N NMR Spectra


Thumbnail

SpectraBase

414 17O NMR Spectra


Thumbnail

SpectraBase







Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES












































325 Boiling Point


CAMEO Chemicals

3040 degC

EPA DSSTox



326 Melting Point


CAMEO Chemicals

1143 degC


327 Flash Point


CAMEO Chemicals



328 Solubility


CAMEO Chemicals


EPA DSSTox










639 mgmL at 25 degC


gt203 [ugmL]




329 Density


CAMEO Chemicals



3210 Vapor Density


CAMEO Chemicals



3211 Vapor Pressure


CAMEO Chemicals

200e-04 mmHg

EPA DSSTox



3212 LogP


EPA DSSTox














CAMEO Chemicals





3215 Decomposition













CCSbase


CCSbase














-

+



SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





Thumbnail

SpectraBase




Thumbnail

SpectraBase

412 13C NMR Spectra




Thumbnail



SpectraBase



Thumbnail

SpectraBase

413 15N NMR Spectra


Thumbnail

SpectraBase

414 17O NMR Spectra


Thumbnail

SpectraBase







Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































329 Density


CAMEO Chemicals



3210 Vapor Density


CAMEO Chemicals



3211 Vapor Pressure


CAMEO Chemicals

200e-04 mmHg

EPA DSSTox



3212 LogP


EPA DSSTox














CAMEO Chemicals





3215 Decomposition













CCSbase


CCSbase














-

+



SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





Thumbnail

SpectraBase




Thumbnail

SpectraBase

412 13C NMR Spectra




Thumbnail



SpectraBase



Thumbnail

SpectraBase

413 15N NMR Spectra


Thumbnail

SpectraBase

414 17O NMR Spectra


Thumbnail

SpectraBase







Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES













































3215 Decomposition













CCSbase


CCSbase














-

+



SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





Thumbnail

SpectraBase




Thumbnail

SpectraBase

412 13C NMR Spectra




Thumbnail



SpectraBase



Thumbnail

SpectraBase

413 15N NMR Spectra


Thumbnail

SpectraBase

414 17O NMR Spectra


Thumbnail

SpectraBase







Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































SpringerMaterials







NMRShiftDB

411 1H NMR Spectra





Thumbnail

SpectraBase




Thumbnail

SpectraBase

412 13C NMR Spectra




Thumbnail



SpectraBase



Thumbnail

SpectraBase

413 15N NMR Spectra


Thumbnail

SpectraBase

414 17O NMR Spectra


Thumbnail

SpectraBase







Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES















































NMRShiftDB

411 1H NMR Spectra





Thumbnail

SpectraBase




Thumbnail

SpectraBase

412 13C NMR Spectra




Thumbnail



SpectraBase



Thumbnail

SpectraBase

413 15N NMR Spectra


Thumbnail

SpectraBase

414 17O NMR Spectra


Thumbnail

SpectraBase







Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































SpectraBase



Thumbnail

SpectraBase

413 15N NMR Spectra


Thumbnail

SpectraBase

414 17O NMR Spectra


Thumbnail

SpectraBase







Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES















































Thumbnail

SpectraBase



Thumbnail

SpectraBase

421 GC-MS


GC-MS





MS Type GC-MS

MS Level MS1





Thumbnail





422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES













































422 MS-MS

MS-MS



423 LC-MS




MS Type LC-MS

MS Level MS2








Thumbnail





MS Type LC-MS

MS Level MS2


precursor mz 136075








Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES












































Thumbnail



424 Other MS



43 UV Spectra





441 FTIR Spectra

Technique KBr WAFER



Thumbnail

SpectraBase

Technique KBr WAFER



Thumbnail



SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































SpectraBase





Thumbnail

SpectraBase

45 Other Spectra





5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































5 Related Records


PubChem







PubChem

53 Substances


All 609 Records

Same 263 Records

Mixture 346 Records

PubChem


PubChem


OMIM 1 Record

PubChem

55 NCBI LinkOut



NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































NCBI



6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































6 Chemical Vendors

PubChem




71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES












































71 Therapeutic Uses





72 Drug Warnings



















81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES












































81 Associated Foods

Bison

Wild boar

Buffalo

Chicken

Mule deer

Mallard duck

Elk

Emu

Greylag goose

Guinea hen

Horse

Ostrich

Velvet duck

Pheasant

European rabbit

Sheep (Mutton Lamb)

Squab

Turkey

Cattle (Beef Veal)

Deer

Rabbit

Domestic goat

Beefalo

Domestic pig

Quail

Anatidae

Mountain hare

Rock ptarmigan


FooDB




















































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES




























































































































Membrane



PubChem

96 Transformations










102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES

















































102 Uses

















MEDICATION (VET)


MEDICATION















105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES





















































105 US Production

(1986) No Data


106 US Imports

(1986) No Data


107 US Exports

(1986) No Data
















11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































11 Identification





















Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES















































Pictogram(s)

Signal Warning








P264 P270 P301+P312 P330 and P501





Acute Tox 4 (100)


Acute Tox 4 (100)

Skin Irrit 2 (100)

Eye Irrit 2 (100)

STOT SE 3 (100)



NFPA 704 Diamond





1214 Health Hazards



CAMEO Chemicals

1215 Fire Hazards


CAMEO Chemicals


1221 First Aid


Irritant

13 0

3-1-0





CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES













































CAMEO Chemicals

123 Fire Fighting


CAMEO Chemicals












CAMEO Chemicals





CAMEO Chemicals




CAMEO Chemicals

1272 Reactive Group

Amides and Imides

Amines Aromatic

CAMEO Chemicals





CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































CAMEO Chemicals






13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES











































13 Toxicity




1312 Acute Effects

ChemIDplus

1313 Interactions












































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES






































































































2692 Lkg

EPA DSSTox

































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES
































































15 Literature


PubChem


Springer Nature


Thieme Chemistry




Wiley


PubChem





Nature Chemistry


Nature Chemistry




PubChem


PubChem


PubChem



16 Patents


PubChem


PubChem




PATENTSCOPE (WIPO)






172 Pathways

PubChem





PubChem



19 Classification

191 Ontologies

1911 MeSH Tree

MeSH

1912 ChEBI Ontology

ChEBI

1913 KEGG Additive

KEGG

1914 ChemIDplus



ChemIDplus


CAMEO Chemicals


ChEMBL










CCSBase




FILTER BY SOURCE



























ALL SOURCES









































3/12/2020 acetanilida | c8h9no - pubchem

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