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    OTC Solvents FAQ

    v1.0

    The following artical was copied and pasted from Erowid.com

    This is version 1.00 of the OTC Solvents FAQ. It was preceded bytwo

    draft versions, one of which has been widely distributed. This

    version has been significantly updated, expanded, and corrected

    Please destroy any earlier drafts of this document, as the

    corrections and clarifications in this version may help avert

    potential disasters which could result if the older information is

    relied upon.

    Significant effort has gone into the preparation of this FAQ, but itis still lacking in a few areas. I need help with improving the

    "solvents" section, especially what these solvents will and will not

    dissolve. Some of the solvents listed are missing information on how

    polar they are. It would also be nice to know which are the best

    solvents for various substances.

    Also, I would like to expand the "other substances" section,

    specifically adding information on what will and will not dissolve

    various interesting substances (or substances contained in) including

    but not limited to: cinnamon, cannabinoids, citrus oils, DMT and

    relatives, hot peppers, psilocybin/psilocin, aromatic oriental

    mushrooms, LAA, garlic, opiates, ginkgo biloba, coca/cocaine,

    ephedra,

    pseudoephedrine, ginsen, kava, and anything else you have information

    on. (Information on any controlled substances would be just for the

    purpose of satisfying curiosity; not to do anything illegal, of

    course.)

    I only took about 1 year of general chemistry in college, so I am notexactly an expert on organic chemistry. It would be wonderful if

    someone who is more knowledgable would suggest massive

    improvements

    to the FAQ, or, better yet, if they would take over maintenance of

    this FAQ altogether. Just keep in mind that the intended audience is

    the not-too-much-above-average kitchen chemist. (Sometimes, it

    seems

    that the more knowledgable people get a little too impatient with the

    less knowledgable ones. Please don't be arrogant.) It wouldn't

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    hurt, however, to add extra information that would be useful to more

    experienced chemists.

    Please post any comments/additions/corrections to alt.drugs.chemistry

    (or e-mail them to me by replying to the anonymous remailer if youcan figure out how to do it). Unfortunately, my news feed sucks, so

    I may not see the comments posted to the alt.drugs.chemistry. If

    you

    feel your comments have not been addressed within a week or two,

    please post again so I will have a greater chance of seeing it. All

    additions to this FAQ derived from comments, etc. will remain

    anonymous unless otherwise requested.

    Many thanks to those who have already contributed to this work.

    ========================= OTC* Solvents FAQ

    =========================

    * OTC = over-the-counter

    First draft: by "The Goose" on September 29, 1994

    Draft version 0.1: by "The Goose" on October 25, 1994

    Version 1.00: by "The Goose", last updated on May 19, 1995

    PURPOSE: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    This document is intended to provide information on solvents and

    other substances to people who have less than an expert knowledge of

    chemistry. This information can be used as an aid and a reference

    by

    kitchen chemists, etc. who desire to do relatively simple organic

    extractions (e.g. THC from pot, DMT from whatever, LAA from

    morning

    glory, psilocybin/psilocin from shrooms, etc. for those who don'tmind breaking the law. Mint oil, citrus oils, and essences from

    various herbs, for those like myself who would rather stay legal.)

    Recipes for organic extractions are not provided here. There is an

    extensive file on organic extractions at hyperreal.com (in

    /drugs/misc/chemistry-extracting).

    DISCLAIMER/WARNING: . . . . . . . . . . . . . . . . . . . . . . . . .

    I do not advocate breaking the law. References to illegal substances

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    are included, however, for informational purposes only (just to

    satisfy everyone's curiosity). The authors of this document assume

    no responsibility for the actions or consequences of what anyone may

    do with this information. Even though efforts have been made to

    assure accuracy, the information presented here is not guaranteed tobe accurate or complete. The use of any information contained in

    this

    document constitutes an agreement to release the authors from any

    and

    all liability for the said use of this information no matter what the

    outcome of that use may be.

    Most of the substances discussed in this FAQ are toxic to one degree

    or another. Usually, after sufficient evaporation/separation/etc.,such small quantities remain, that there is not a great risk of

    poisoning, but you still need to watch out for contaminants. Many of

    these substances contain contaminants of unknown toxicity. DO NOT

    ingest unless you know what you are doing! You have been warned!

    Also, it is not a good idea to breath the fumes from most of these

    substances. You could get poisoned that way too. When evaporating

    or boiling off solvents, make sure there is adequate ventilation.

    Most of these solvents are flammable (or explosive). When working

    with flamable solvents, avoid sparks (e.g. from electrical switches)and open flames (e.g. from gas stoves). Using a hot plate with an

    extension cord to get it away from the house is a good idea. Good

    ventilation is the key to preventing both poisoning by inhalation,

    and explosions resulting from the build-up of flamable fumes.

    ALWAYS read the label of the products before you purchase them to

    make sure they contain what you are looking for, and are not mixed

    with a lot of other unwanted things. (See section on PURITY)

    P.S. This information is incomplete, Never assume that something is

    safe just because the information is not there!

    P.P.S. Only you are responsible for your own actions!!

    P.P.P.S. Use your head, damn it!!!

    ---------------- Answers to Frequently Asked Questions

    ----------------

    1) What is petroleum ether?

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    A: Petroleum ether refers generically to the lower boiling fractions

    of petroleum. Analytical grades may be quite pure, containing

    only hexane and/or pentane, and having a boiling point no higher

    than 69 degrees centigrade. The lower boiling fractions are mostuseful when the solvent is to be evaporated or boiled off. The

    petroleum ethers most often mentioned on the 'net usually consist

    of somewhat higher boiling fractions of petroleum (e.g. 100 to

    175 degrees centigrade). These are more useful when the solvent

    is to be separated and discarded (e.g. when removing oil soluble

    contaminants from water soluble extracts).

    2) Are ether and petroleum ether the same?

    A: No! Petroleum ether is a petroleum product. "Real" ether is

    more commonly known as diethyl ether or ethyl ether. Its

    chemical

    formula is C2H5-O-C2H5, and it is not a petroleum product.

    Diethy ether is the "ether" that was traditionally used as an

    anesthetic the early 1900's. Petroleum ether is sometimes

    referred to as "ether" because its solvent properties are similar

    to that of diethyl ether (i.e. it dissolves similar types of

    substances and has a low boiling point). Often (but not always),petroleum ether and diethyl ether can be used interchangeably.

    It is usually easier for the layman to obtain petroleum ether.

    3) Where can I get petroleum ether?

    A: Chemical supply houses usually can provide petroleum ether. Ask

    for it by boiling fraction or specific component (e.g. hexane,

    pentane, etc.). It is best to have a reasonable knowledge of

    chemistry when purchasing chemicals or solvents from professionalestablishments. Many substances are controlled to some extent.

    Often they will ask you to show identification, and sign a

    statement explaining what your intended use is. This information

    can be provided to government agencies such as the DEA. Since

    most laymen would have a difficult time bluffing their way in a

    chem supply shop, they probably would be tempted to use an

    industrial grade which may be more easily obtained from local

    retailers. These may take the forms of mineral spirits,

    petroleum spirits, naptha, automobile starter fluid, etc. See

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    the SOLVENTS section below for more information on these

    products

    and where to obtain them.

    4) Where can I get solvent ?

    A: Most solvents can be obtained from chemical supply houses. Just

    keep in mind the precautions mentioned in #3 above. Many

    solvents

    may be obtained from local retail establishments in industrial

    grades either semi-pure or mixed with other (possibly useful)

    solvents. For over-the-counter sources, see the SOLVENTS

    section

    below.

    5) What are polar and non-polar solvents?

    A: The easy answer: Polar solvents dissolve substances that are

    water soluble, but do not dissolve oily substances. Non-Polar

    solvents dissolve oily substances, but do not dissolve water

    soluble substances. Moderately polar solvents have a tendency to

    dissolve both types of substances. Petroleum distillates are

    non-polar, alcohols are moderately polar, and water is polar.

    The better (but not necessarily more helpful) answer: Polarity

    is a somewhat vague notion which gives a general idea of what

    will dissolve what. The chemistry-extracting file at hyperreal

    states the following:

    Polarity and solubility is a nebulous concept. If you actually

    look at what is dissolved by what, you can only find vague

    general principles, and plenty of exceptions. Some authorshave tried to make 3 and 4 dimensional polarity or solubility

    graphs, and put various solvents in various points as having

    a combination of different types of solvent power.

    See the SOLVENTS section below for more information on the

    polarity

    of specific solvents.

    6) What is the advantage of using a polar (or non-polar) solvent?

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    A: The advantage is that you are able to dissolve what you are

    after, leaving behind the things you don't want. (e.g. petroleum

    ether will dissolve cannabinoids but leave behind chlorophyll and

    sugars. Alcohols and acetone will dissolve cannabinoids,

    chlorophyll and sugars.)

    7) What type of solvent should I use for extracting substance ?

    A: Don't ask me. This FAQ was never intended to be a compilation

    of

    recipes. Look at the various extraction techniques which have

    been posted on the 'net or look in the chemistry-extracting file

    at hyperreal.com. (hint: oily substances dissolve in non-polar

    solvents, most other useful substances will dissolve in water.)

    8) What is an acid-base extraction?

    A: This is a technique in which alkaloids are extracted by taking

    advantage of common solubility properties of most alkaloids. In

    general, alkaloids are soluble in an acidic water solution, and

    become insoluble when the solution is made basic. The solubility

    rules for alkaloids are reversed for non-polar organic solvents.

    The basic form (precipitate) is soluble in non-polar solvents,and the acidic form is insoluble in non-polar solvents. Most

    other materials in plants do not have these same solubility

    properties. This allows for the isolation of alkaloids from most

    of the other unwanted junk. For more information on specific

    extractions, see the various extraction techniques on the 'net or

    look at the chemistry-extracting file at hyperreal.com.

    9) Why does my extracted material still smell like solvent?

    A: Your extract may still smell like solvent because it still has

    some solvent left in it or because some of the aromatic

    components of the solvent are overstaying their welcome. Some

    solvents have a high boiling point which makes it difficult to

    separate it from your extract by boiling it off. Even if most of

    the solvent solution boils off at a lower temperature, there may

    have been a portion of it that has a higher boiling point. One

    way to reduce the amount of excess solvent is to heat up theextract even more. Be careful because higher heat may destroy

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    some extracts. Another way to lessen the smell is to to let the

    excess solvent evaporate on its own by leaving your extract

    exposed to the air for an extended period of time (anywhere from

    overnight to several days). The down side of this is that the

    longer your extract is exposed to air, the more it can bedestroyed by oxidation. Warmer temperatures encourage both

    evaporation and oxidation while cooler temperatures do the

    opposite. Room temperature is probably ok for most purposes. It

    may well be next to impossible to get all of the residue out,

    however. Picking a good solvent from the start can help you

    avoid these problems to a large extent.

    10) How dangerous are over-the-counter solvents?

    A: It is always best to acquire reagent grade solvents, but since

    this IS an over-the-counter solvents FAQ . . .

    Some solvents are very dangerous by themselves while others are

    almost harmless. Some contaminants in industrial grade solvents

    could be quite dangerous (poisonous, carcinogenic, flammable,

    etc.), while others are not. Most contaminants are not highly

    toxic, and the government imposes some regulations on

    manufacturers to prevent highly hazardous contaminants from

    beingdistributed, so one could assume that the risks posed by

    contaminants is fairly low. However, if you choose to use an

    industrial grade, you always run some risk. Research and common

    sense can help reduce this risk. See the section on PURITY below

    for a more lengthy discussion on this topic. See the SOLVENTS

    section below for information on the hazards of specific

    solvents. See the OTHER SUBSTANCES section below for

    information

    on the hazards of other miscellaneous substances.

    ------------------- REFERENCE & GENERAL INFORMATION

    -------------------

    TERMS: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    "bp" = boiling point (or boiling fraction in some cases)

    note: boiling points are slightly lower at high altitudes

    "C" = degrees centigrade

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    "dens" = density (in grams per ml unless otherwise specified)

    "dis:" = what it dissolves

    "F" = degrees Fahrenheit

    "LD50" = (lethal dose 50%) dosage at which 50% of test subjects

    (rats, dogs, etc.) died."mis" = miscible with

    "mp" = melting point

    "otc:" = (over-the-counter) where to find it, etc.

    "pol:" = polarity ( > = more polar than, < = less polar than )

    "prop:" = physical properties

    "sol:" = what it is soluble in

    "tox:" = data on toxicity. if not listed, DON'T assume it is safe!

    "uses:" = common uses. this is nice to know when you are asking a

    store clerk to help you find it.

    SOLVENTS: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    ACETONE (dimethyl ketone, ketone propanone, propanone)

    prop: mp -94.6 C, bp 56.48 C, dens 0.80

    dis: water solubles, oils; mis: water, alcohols, chloroform, oils

    pol: polar?/moderately polar?

    tox: oral LD50 (rat) 9750 mg/kg

    otc: hardware stores (acetone)uses: thinning fiberglass resins, dissolving 2 part epoxies,

    cleaning brushes and tools used with resins or epoxies,

    cleaning greasy stuff

    otc: some drug stores (pure, small quantities, expensive)

    uses: dissolving fats, waxes, etc.

    caution: flamable, reacts with some solvents

    note: acetone is also used in fingernail polish remover, but

    it is mixed with water, fragrance, etc.

    note: may react with some alkaloids, may extract more organic

    compounds than is desirable

    ALCOHOL see ethyl alcohol, methyl alcohol, isopropyl alcohol

    BENZENE (C6H6, benzol, phenyl hydride, coal naptha)

    (included for comparison and cautions)

    prop: mp 5.51 C, bp 80.1 C, dens 0.8794

    dis: oils; mis: alcohols, chloroform, ether, acetone

    sol: slightly soluble in water (1 part per 1403 parts H2O)pol: non-polar

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    tox: 3000 ppm vapor considered high concentration, toxic via

    inhalation or skin absorption as well as oral ingestion,

    prolonged inhalation of low concentrations also toxic

    otc: none known (you wouldn't want it anyway)

    note: do not confuse with benzine which is a petroleum distillatecaution: a recognized leukemogen (causes leukemia)!

    caution: highly flamable

    caution: can react vigorously with oxidizing materials

    BUTANE (C4H10, n-butane, methylethyl methane, butyl hydride)

    prop: bp -0.5 C

    dis: oils

    pol: non-polar

    sol: ether, alcohol, waterotc: anywhere (butane cigarette lighters)

    uses: lighter fuel, butane torches, curling irons (yes, really)

    caution: extremely flamable

    note: if you use this, you will have to work with sub-freezing

    temperatures or at least higher pressures like a small jar

    with a tight lid (higher pressures tend to raise boiling

    points thus improving solvent capabilities). the advantage

    is that you could boil it off at room temperature!

    CHLOROFORM (CHCL3, trichloromethane)

    (included for comparison and cautions)

    prop: mp -63.5 C, bp 62.26 C, dens 1.498

    dis: oils, fats, rubber, alkaloids, waxes, resins

    sol: 1mL in 200 mL water; mis: alcohols, ether, petroleum ether

    pol: non-polar

    tox: oral LD50 (rat) 800 mg/kg, prolonged inhalation can cause

    unconsciousness and poisoning (or even death)

    otc: none knownnote: non-flamable

    caution: reacts violently with acetone + base, methyl alcohol +

    sodium hydroxide or potassium hydroxide

    DICHLOROMETHANE see methylene chloride

    DIESEL FUEL (fuel oil #2)

    composed of heavier hydrocarbons than gasoline

    prop: bp higher than gasoline

    dis: oils

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    pol: non-polar

    tox: recognized carcinogen, see also petroleum distillates

    DECANE (CH3(CH2)8CH3)

    a minor component of kerosene, may be a minor component of gasolineprop: mp aprox -29 C, bp aprox 174 C

    dis: oils

    pol: non-polar

    tox: see petroleum distillates

    otc: see kerosene, gasoline

    caution: flamable

    DIETHYL ETHER (C2H5-O-C2H5, ether, ethyl ether, anesthesia

    ether,

    ethyl oxide)

    prop: bp 35 C

    dis: oils, etc.

    pol: moderately polar ( < water, alcohols; > petroleum

    distillates and toluene )

    tox: moderate oral toxicity, low inhalation toxicity, oral LD50

    (rat) 1700 mg/kg, oral LD50 (human) 420 mg/kg

    otc: found in automobile starter fluid

    caution: very flamable, can form explosive peroxides withprolonged exposure to air

    note: this is the ether that was used extensively as an

    anesthetic a few years back

    ETHANOL see ethyl alcohol

    ETHYL ALCOHOL (ethanol, methyl corbinol, spirit of wine, grain

    alcohol)

    prop: bp 78.32 C, dens 0.79

    dis: water solubles, oils; mis waterpol: polar? / moderately polar? ( < water; > isopropanol )

    tox: oral LD50 (rat) 21,000 mg/kg

    otc: liquor store (Everclear, 95%)

    uses: party, party, party!

    caution: flamable, could get you drunk :-)

    note: there have been reports of people using denatured alcohol

    as

    a solvent. this may be ok if it is denatured only with

    something that will be eliminated when the solvent is boiled

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    off (e.g. with methyl alcohol). if you don't think you can

    eliminate the denaturant, then don't use denatured alcohol!

    FUEL OIL (fuel oil #1 through fuel oil #6)

    increasingly viscous petroleum distillates, generally with increasingboiling fractions.

    dis: oils

    pol: non-polar

    tox: see petroleum distillates

    caution: flamable

    note: fuel oil #1 is kerosene, fuel oil #2 is diesel oil

    note: there are not many applications that could benefit from

    using fuel oils as solvents

    GASOLINE (petrol, gas, white gas)

    composed of octanes, some heavier hydrocarbons (nonanes, etc.),

    and some lighter hydrocarbons (heptanes, etc.)

    prop: bp aprox 35-180 C (depending on what it contains)

    dis: oils

    pol: non-polar

    tox: see petroleum distillates

    otc: gas stations

    uses: automobile, etc. fuelcaution: very flamable

    note: gasoline for automobiles contains additives, better to use

    white gas.

    KEROSENE (fuel oil #1, ultrasene)

    composed mostly of heavier hydrocarbons than gasoline (10 to 16

    carbon

    atoms per chain)

    prop: bp 175-325

    dis: oils

    pol: non-polar

    tox: oral LD50 (rat, rabbit) 28,000 mg/kg, oral toxicity is low,

    see also petroleum distillates

    otc: fuel distributors, hardware stores

    caution: flamable

    uses: stoves, heaters, lamps

    note: ultrasene is deodorized kerosene

    HEPTANE (C7H16)

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    a component of starter fluid, gasoline, and some petroleum ethers

    prop: bp aprox 98 C

    dis: oils

    pol: non-polar

    tox: see petroleum distillatesotc: found in starting fluid and some napthas

    caution: highly flamable

    HEXANE (C6H14)

    a component of starter fluid, and some petroleum ethers

    prop: bp aprox 69 C

    dis: oils

    pol: non-polar

    tox: see petroleum distillatesotc: found in automobile starting fluid and some napthas

    caution: highly flamable

    ISOPROPANOL se isopropyl alcohol

    ISOPROPYL ALCOHOL (dimethyl alcohol, sec-propyl alcohol,

    isopropanol)

    prop: mp -89 C, bp 80.3 C, dens 0.79

    dis: water solubles, oils; mis water

    pol: polar? (hydrogen bonded?), ( < ethanol; >> diethyl ether )tox: oral LD50 (rat) 5,840 mg/kg

    otc: automotive stores (fuel dryer, 99.9%)

    caution: flamable

    note: rubbing alcohol is usually only 70% alcohol, and 30% water

    METHANOL see methyl alcohol

    METHYL ALCOHOL (methanol, wood alcohol)

    prop: bp 64.8 C, dens 0.79dis: water solubles, oils; mis water

    pol: moderately polar? (hydrogen bonded), ( < water, > diethyl

    ether )

    tox: oral LD50 (rat) 13,000 mg/kg, eliminates slowly and can

    build up with repeated exposure/ingestion. toxic metabolites

    include formaldehyde and formic acid. damages optic nerve.

    otc: automotive stores

    uses: fuel dryer

    otc: hardware and paint storesuses: shellac thinner, alcohol stove fuel

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    caution: flamable

    note: often mixed with paint removers or varnish removers

    note: good at penetrating cell walls and membranes

    METHYLENE CHLORIDE (CH2Cl2, dichloromethane)prop: bp 39.8

    dis: oils

    pol: non-polar

    tox: oral LD50 (rat) 2136 mg/kg, VERY dangerous to eyes,

    produces highly toxic fumes when heated to decomposition

    (e.g. by open flames, etc.), may be carcinogenic in rats

    otc: paint and hardware stores (mixed with methyl alcohol, etc.)

    uses: paint and varnish remover

    note: fire hazard is low (by itself)

    MINERAL SPIRITS see petroleum spirits

    NAPTHA (see below for types)

    dis: oils

    pol: non-polar

    tox: see petroleum distillates

    otc: hardware and paint stores

    uses: paint thinner, some lighter fluids, some spot removers

    note: boiling fractions are similar to gasoline

    NAPTHA (coal tar, naptha solvent)

    prop: bp 149-216 C, dens 0.86-0.89

    tox: see petroleum distillates

    caution: flamable

    NAPTHA, V.M. & P. (benzine, 76 degree naptha)

    prop: bp 100-140 C, dens 0.67-0.80, flash point 20 F.

    tox: see petroleum distillatesnote: do not confuse with benzene

    caution: flamable, autoignite 450 F

    NAPTHA, V.M. & P., 50 degree flash

    prop: bp 115-143 C, flash point 50 F

    tox: see petroleum distillates

    caution: flamable

    NAPTHA, V.M. & P., high flash

    prop: bp 138-165 C, flash point 50 F

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    tox: see petroleum distillates

    caution: flamable

    NONANE (C9H20, n-nonane)

    a component of gasoline, a component of some napthasprop: mp aprox -54 C, bp aprox 151 C

    dis: oils

    pol: non-polar

    tox: see petroleum distillates

    otc: see naptha, white gas, gasoline

    caution: flamable

    OCTANE (C8H18)

    a major component of gasoline

    prop: bp aprox 126 C

    dis: oils

    pol: non-polar

    tox: see petroleum distillates

    otc: hardware and paint stores (some napthas)

    otc: sporting goods stores (white gas)

    caution: highly flamable

    PAINT THINNER see petroleum spirits, turpentine

    PAINT and VARNISH REMOVER

    usually composed of methylene chloride and methyl alcohol. may also

    contain toluene and other solvents. see individual components for

    more information

    PENTANE (C5H12, n-pentane)

    a component of some light petroleum ethers

    prop: bp aprox 36 C

    dis: oilspol: non-polar

    tox: see petroleum distillates

    otc: see petroleum spirits

    caution: highly flamable

    PETROLEUM DISTILLATES (gasoline, naptha, petroleum ether,

    mineral

    spirits, petroleum spirits, fuel oils, xylene, etc.)

    dis: oilspol: non-polar

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    tox: generally low to moderate toxicity, laboratory experiments

    show a slight carcinogenic potential for most petroleum

    distillates. higher boiling fractions may be more

    carcinogenic.

    caution: flamable to highly flamablenote: petroleum distillates do not dissolve most water-solubles

    note: petroleum distillates include everything from pentane to

    heavy tars

    PETROLEUM ETHER see petroleum spirits, naptha, starter fluid

    note: generally (but not always) refers to the lower boiling

    fractions of petroleum distillates

    PETROLEUM SPIRITS (petroleum benzine, petroleum naptha, light

    ligroin, petroleum ether, mineral spirits)

    prop: bp 35-180 C, dens .64-.66

    dis: oils

    pol: non-polar

    tox: see petroleum distillates

    otc: hardware and paint stores

    uses: paint thinner

    caution: flamable

    note: "petroleum spirits" often refers to the lower boilingfractions of petroleum distillates. However, one "odorless

    paint thinner" claiming 100% mineral spirits had a boiling

    point of 175 C.

    note: do not confuse with benzene

    STARTER FLUID

    composed of hexane, diethyl ether, and heptane. see individual

    components for more information.

    otc: automotive stores

    uses: starting stubborn automobiles on cold days

    caution: very flamable

    note: some starter fluids may contain heavier lubricants

    alpha-TRICHLOROETHANE (CH3CCl3, 1,1,1-trichloroethane, methyl

    chloroform)

    prop: bp 74.1 C, dens 1.3492

    dis: oils, etc.?

    pol: non-polar?/moderately polar? (insoluble in water)

    tox: oral LD50 (dog) 750 mg/kg, avoid fumes

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    otc: super markets, hardware stores, etc.

    uses: spot remover (brand name: "Energine"), industrial uses

    include cleaning of metal parts and metal molds

    caution: can react violently with acetone

    note: non-flamable!

    TETRAHYDROFURAN (OCH2CH2CH2CH2, diethylene oxide,

    cyclotetramethylene

    oxide-1,4-epoxy butane)

    (included for comparison and cautions)

    dis: oils, etc.; mis: water, alcohols, ethers, hydrocarbons

    pol: moderately polar

    otc: none known

    note: peroxides may be removed by treating with strong ferroussulfate solution made slightly acidic with sodium bisulfate

    caution: same as diethyl ether (slightly more dangerous)

    TOLUENE (C6H5CH3, methylbenzene, phenylmethane, toluol)

    prop: mp -95 C to -94.5 C, bp 110.4 C

    dis: oils

    pol: non-polar

    tox: oral LD50 (rat) 5000 mg/kg, oral toxicity is moderate,

    inhalation of 100 ppm can cause psychotropic effects, 200 ppmcan produce CNS effects

    otc: paint and hardware stores (mixed with methyl alcohol, etc.)

    uses: furniture refinisher, liquid sandpaper, paint remover

    note: low fire hazard (by itself)

    TURPENTINE (spirit of turpentine, turpentine gum, turpentine oil)

    prop: bp 154-170 C

    dis: oils ?, etc.?

    pol: non-polar? (insoluble in water)

    sol: alcohols, chloroform, ether, glacial acetic acid

    tox: aspiration causes pheumonitis, oral ingestion causes damage

    to GI tract and kidneys, inhalation toxicity is high

    otc: paint and hardware stores

    uses: thinning varnish, paint, & enamel; cleaning brushes

    caution: moderately flamable

    WATER (H2O)

    prop: mp 0 C (32 F), bp 100 C (212 F), dens .99999 @ 4 C

    dis: anything that is water soluble

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    pol: polar

    tox: non-toxic unless contaminated with a toxic substance

    otc: your kitchen sink (contains chlorine, etc.)

    otc: grocery store (distilled water or purified water)

    uses: drinking, washing, etc.note: distilled water is better for most things (and it's cheap).

    water is ofter used with petroleum ether to separate water-

    solubles from non-water-solubles. i.e. combine and shake

    vigorously until your arm falls off, then separate.

    WHITE GAS (petrol, gasoline)

    prop: see gasoline

    dis:, pol:, and tox: see petroleum distillates

    otc: sporting goods storesuses: fuel for camp stoves and camp heaters

    caution: flamable

    XYLENE (C6H4(CH3)2)

    prop: (m-xylene) mp -47.9 C, bp 139 C

    (o-xylene) bp 144.4 C

    (p-xylene) bp 138.3 C

    dis: oils

    pol: non-polartox: oral LD50 (rat) 5000 mg/kg, see also petroleum distillates

    otc: super markets, hardware stores

    uses: some cleaners (e.g. for dissolving chewing gum,

    brand name: "Goof-off"), some lighter fluids

    caution: flamable

    OTHER SUBSTANCES: . . . . . . . . . . . . . . . . . . . . . . . . . .

    ACETIC ACID (CH3COOH, vinegar acid, methane carboxylic acid,ethanoic

    acid)

    prop: mp 16.7 C, bp 118.1 C

    sol: water

    tox: oral LD50 (rat) 3310 mg/kg

    otc: grocery stores (vinegar)

    uses: cooking, cleaning

    caution: dangerous in contact with: chromic acid, sodium peroxide,

    nitric acid, potassium hydroxide, sodium hydroxide, xylene,oleum. decomposition (at high temp.) evolves toxic fumes

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    note: normal vinegar is 5% acetic acid, vinegar concentrate is 18%

    acetic acid

    note: can be used for extracting some alkaloids from plant

    material

    AMMONIA see AMMONIUM HYDROXIDE

    AMMONIUM HYDROXIDE (NH4OH, ammonia, aqua ammonium, water

    of ammonia,

    ammonium hydrate)

    prop: mp -77 C

    sol: water

    tox: oral LD50 (rat) 350 mg/kg, oral LDlo (human) 43 mg/kg,

    inhale LClo (human) 5000 ppm

    otc: grocery & hardware stores

    uses: household cleaning ammonia

    note: ammonia is a gas at room temperature. it is sold otc

    dissolved in water (much as is done with hydrochloric acid).

    note: a weak base. can be used to precipitate some alkaloids

    from slightly acidic solutions.

    CANNABIDIOL (CBD)

    found in marijuana, organicly converted to THC, can be isomerized

    into THC by refluxing with dilute acidprop: mp 66-67 C, bp 187-190 C @ 2mm Hg

    sol: acetone, petroleum distillates, alcohols, etc.

    note: this is an oily substance, not water soluble

    CANNABINOL (CBN)

    found in marijuana, a degradation product of THC

    prop: mp 76-77 C, bp 185 C @ .05mm Hg

    sol: acetone, petroleum distillates, alcohols, aqueous alkaline

    note: this is an oily substance, not water soluble

    EPHEDRINE HYDROCHLORIDE (C6H5CHOHCH(CH3)NHCH3 HCL, a[1-

    (methylamino)

    ethyl]benzyl alcohol hydrochloride)

    prop: mp 187-188 C

    sol: water (1gm/4ml), (insoluble in diethyl ether)

    tox: oral LD50 (mouse) 400 mg/kg

    otc: truck stops (Mini Thins, MaxAlert, etc.)

    uses: bronchiodialator (for asthma)caution: decomposes into toxic fumes at higher temperatures

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    note: pure ephedrine is no longer available otc in the

    U.S. current

    otc varieties usually have guiafenesin

    note: slightly stronger that ephedrine sulfate

    note: pure ephedrine can be converted into methcathinonenote: now a controlled substance in the US

    EPHEDRINE SULFATE ((C6H5CHOHCH(CH3)NHCH3)2 H2SO4, 1-

    phenyl-2-

    (methylamino)propanol sulfite)

    prop: mp 247 C

    sol: water (1gm/20 ml), alcohol (1gm/0.2ml)

    tox: oral LD50 (rat) 600 mg/kg

    otc: same as for ephedrine hydrochloride?caution: decomposes into toxic fumes at higher temperatures

    note: slightly weaker than ephedrine HCl

    note: pure ephedrine can be converted into methcathinone

    note: now a controlled substance in the US

    HYDROCHLORIC ACID (HCl, muriatic acid, chlorohydric acid,

    hydrogen

    chloride)

    prop: mp -114.3 C, bp -84.8 C, dens 1.639 g/liter gas @ 0 Ctox: oral LD50 (rabbit) 900 mg/kg

    otc: hardware stores (muriatic acid)

    uses: cleaning calcium or lime deposits from cement, brick,

    swimming pools, and ceramic tile.

    caution: caustic

    note: useful in isomerizing CBD to THC. useful in extracting

    some alkaloids from plant material. HCl is found naturally in

    low concentrations in the digestive juices of your stomach.

    LYE see SODIUM HYDROXIDE

    PARAQUAT

    an herbicide used by Latin-American drug enforcers to kill marijuana

    crops in bulk

    tox: oral LD50 (rat) 57 mg/kg, dermal LD50 (rat) 80 mg/kg, can

    cause severe damage to lungs (nasty stuff!)

    note: avoid all marijuana that looks like it has any dye on it.

    unfortunately, not all paraquat is used with dye.

    TETRAHYDROCANNABINOL (THC)

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    found in marijuana, the psychoactive stuff

    prop: bp 200 C @ 0.02mm Hg (other cannabinoids may have bp's

    lower than 185 C)

    sol: polar solvents, acetone, alcohols, etc.

    note: this is an oily substance, not water soluble

    SODIUM HYDROXIDE (NaOH, caustic soda, sodium hydrate, lye,

    white caustic)

    prop: mp 318.4 C, bp 1390 C, dens 2.120

    tox: oral LDlo (rabbit) 500 mg/kg

    otc: hardware stores, etc. (Red Devil Lye, etc.)

    uses: unclogging drains

    caution: highly corrosive to body tissue

    caution: can react violently with acetic acid or tetrahydrofurannote: useful in precipitating some alkaloids from acid solutions

    SODIUM SULFATE (Na2SO4)

    by product of isomerization of CBD to THC when sulfuric acid is

    neutralized with baking soda

    sol: water

    note: insoluble in alcohol

    note: can be removed by dissolving resin in petroleum ether

    and shaking with waterSULFURIC ACID (H2SO4, oil of vitriol, dipping acid)

    prop: mp 10.49 C, bp 330 C, dens 1.83

    tox: oral LD50 (rat) 2,140 mg/kg

    otc: plumming supply stores (plummers' sulfuric acid)

    uses: unclogging drains

    otc: automotive supply stores (battery acid)

    caution: battery acid may have lead in it

    caution: caustic, use care when mixing with water as it heats

    rapidly when dissolved and causes spattering (add slowly to

    water drop by drop)

    note: useful in isomerizing CBD to THC

    VINEGAR see acetic acid

    SUBSTITUTIONS: . . . . . . . . . . . . . . . . . . . . . . . . . . .

    It is not always easy to come up with the exact solvent discussed in

    any particular recipe. Consequently, it may be advantageous to

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    consider substituting an over-the-counter solvent for a hard-to-get

    one. This can often be done successfully if you keep a few things in

    mind. The main thing to look for is what the solvent dissolves.

    If you are trying to dissolve an oily substance (such as cannabinoids

    from pot or oil from lemon peels), look for solvents that willdissolve oils (e.g. polar solvents, etc.). Be aware that some

    solvents may dissolve more than you bargained for. Alcohols and

    acetone will dissolve things that petroleum distillates won't, like

    sugars and chlorophyll. Another thing to look for is boiling point.

    Naptha solvent (coal tar naptha) has a boiling point so high that you

    wouldn't be able to boil it off to separate it from THC (the THC

    would boil off with it). Solvents with lower boiling points are

    much easier to boil off, and usually leave less residual solvent.

    Petroleum distillates are usually a mixture of various hydrocarbonswith a variety of boiling points. The boiling fraction of any

    particular petroleum distillate refers to the range of boiling points

    of its components.

    PURITY: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    There are basically two ways that impurities can get into solvents,

    etc. The first way is inherent in the manufacturing process. Very

    few products are pure at the time of manufacture. The general ideais to produce a product that meets certain minimum purity

    requirements. The product is refined to remove contaminants until

    the minimum purity level is reached. Most manufacturing methods

    favor low cost production over purity of product. Industrial grade

    products are used in applications that require only marginal purity.

    With reagent grade chemicals, however, a high degree of purity is

    required. Reagent grades are refined until they are ridiculously

    pure (e.g. something like 99.999% pure). This additional refining is

    costly, and as a result, reagent grades are usually many times the

    price of industrial grades. Industrial grades are used in a lot of

    commercial products, and are often available at hardware stores, etc.

    Reagent grades are generally only available at chemical supply

    stores. Unfortunately, most kitchen chemists would have a difficult

    time bluffing their way in a chem shop without arousing suspicion.

    Additionally, many reagent grade products are watched closely by

    certain government agencies, where the industrial grades are not.

    (e.g. acetone)

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    The other way impurities can be introduced is when the manufacturer

    intentionally places additives into a product to enhance its

    performance (or appearance) or to dilute an expensive component.

    Since the performance enhancing additives usually cost more, the

    expensive, big brand names are the ones most likely to use them.When performance enhancing additives are present, the product

    labels

    often boast a lot of features. The less expensive, more generic

    looking products are less likely to add performance enhancers but are

    more likely to dilute their product. Some additives may actually be

    useful, however. e.g. Paint and varnish removers often combine

    methylene chloride with methyl alcohol, and furniture refinishers

    often have toluene combined with methyl alcohol.

    When dealing with industrial grades, always read the label carefully

    to determine if it contains things you don't want. Unfortunately,

    not all products list every component on their labels. Try calling

    the emergency accidental poisoning numbers listed on the labels.

    Tell them your dog ingested some of their product, and that the vet

    asked you to call the number. Try to get as much information from

    them as you can about what the product contains. Work up a likely

    story (including symptoms) before you place the call. One crude

    method of testing for contaminants in solvents would be to place afew drops on some clean glass, and let it evaporate. The amount of

    residue remaining gives a very rough idea of how much other crud is

    in the solvent. Feed a generous amount of this residue to the

    neighbor's cat, and if it dies, the product may be too toxic. :-)

    Actually, the likelyhood that contaminants in an industrial grade

    product are highly toxic or carcinogenic is probably much lower than

    most people think. Relatively few substances are highly toxic and/or

    significantly carcinogenic. Many things in our everyday environmentare carcinogenic if you are exposed to massive quantities, but potent

    carcinogens are not all that common. Due to government regulations,

    many (if not most) industrial grade products are not allowed to

    contain significant amounts of dangerous substances, anyway. (Who

    wants a cleaner or solvent that will leave a highly hazardous

    residue?) Even with all of these assurances, there is always a

    certain amount of risk associated with the use of industrial grade

    products.

    In order to reduce the risks associated with contaminants, the

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    following precautions are in order:

    1) use reagent grades when possible

    2) if reagent grades cannot be obtained, then make every effort

    to acquire the purest product available (read labels, studymanufacturing methods, etc.)

    3) purify the product (if you can) before using it

    4) use minimal amounts of these products (a liter of solvent

    boiled down to a few cc's may still contain a liter's worth

    of contaminants)

    Some people recommend purifying petroleum distillates by adding

    water, shaking vigorously for a long time, and then discarding the

    water. This will only help remove water soluble contaminants. Abetter way to purify most liquids is to distill them. Unfortunately,

    this is not always easy to do if you don't have the right equipment.

    One thing I have been intending to try is to shake paint stripper

    (containing methyl alcohol and methylene chloride) with a generous

    quantity of water to see if I can separate the methylene chloride.

    If anyone has comments on whether this will work, please let me

    know.

    USEFUL HINTS: . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    Boiling off solvents with low boiling points (less than 100 C):

    Place the solvent into a small pan or shallow, wide mouth jar.

    Shallow containers with wide openings aid in allowing the vapors to

    escape quickly. Place the container with the solvent into a larger

    pan of simmering water. Don't allow the water to come to a full

    boil. Boiling water is really no hotter than simmering water.Rapidly boiling water can splash into your solvent, or cause the

    solvent container to tip over. Watch the level of the solvent as it

    boils away so that the container won't get too light, and tip over.

    If the level of the solvent is too low (i.e. 1 cm below the level of

    the water), then remove some of the water. Anchoring the solvent

    container in place may help. Use hot pads to avoid burning yourself.

    Remember to use good ventilation to avoid the build-up of toxic or

    flamable fumes. If the boiling point of your solvent is too close to

    100 C, you can add sugar or automobile antifreeze to the simmeringwater to raise it's boiling point a little, or use the method below

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    for higher boiling point solvents.

    Boiling off solvents with higher boiling points (greater than 100 C):

    Follow the method and precautions for lower boiling point solvents

    with the following differences: Use melted shortening (or vegetable

    oil if you don't have shortening) instead of simmering water. If

    your solvent container is glass, place it in the shortening as soon

    as it is melted, and then heat it up from there. This will help keep

    the jar from cracking. Elevate the solvent container slightly from

    the bottom of the larger pan to aid in even heating. A few nails in

    the bottom of the shortening works for me. Place a candy

    thermometer

    in the shortening to measure it's temperature. Heat the shortening

    until it is 20 or 30 degrees centigrade hotter than the highest

    boiling point of your solvent or until the solvent begins to boil at

    a comfortable rate. Always keep the temperature of the shortening

    well below the boiling point of the dissolved product you are trying

    to recover, or you may loose significant amounts of it to

    evaporation. Be careful to not let solvent or water splash into the

    hot shortening or you may get some spattering of hot grease. If

    your

    solvent container is glass, allow it to cool slowly when you are doneto keep it from cracking. If you are extracting cannabinoids or

    other oils of similar or higher boiling points, you may want to raise

    the temperature of the shortening to about 160 C for a minute or

    two

    to help eliminate solvent residue. (It can be tough to get rid of

    all of it, though.)

    Preventing boil-overs:

    Some solvents may have a tendency to boil over quite easily. Thiscan waste valuable product as well as pose fire hazards, etc. By

    making sure that the solvent level is well below the top of its

    container, many boil-overs may be avoided. It is common practice in

    chemistry to use boiling chips to control excessive boiling. Glass

    marbles can serve the same purpose, and they are easy to get. Put

    as

    many marbles into your solvent as needed to control the boiling.

    Marbles may be removed a few at a time as the solvent level drops.

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    Remember that valuable extract may coat the surface of the

    marbles.

    Wash them with a very small quantity of solvent and add this to the

    rest of the solvent when it is mostly boiled off.

    Refluxing in the kitchen:

    Find a pan with a lid that can be put on upside down, and still

    remain stable with a reasonable fit. Place your solvent, etc. into

    the pan, and put the lid on upside down. Place ice in the lid. Heat

    the solvent until it begins to boil gently. The heat may be applied

    directly, or for better temperature control, you may use a method

    similar to the ones listed above for boiling off solvents. If you

    use hot shortening to apply heat, be careful to not let water from

    melting ice or solvent condensing on the sides drip into the hot

    grease. Tying a rag around the top of the solvent pan can help. As

    the ice melts, scoop out the water and add more ice.

    Getting rid of water in oil extracts:

    Sometimes water can get into an oil extract when it is purified by

    dissolving in petroleum ether, and shaking with water. As the last

    of the solvent boils off, the water forms beads in the bottom of the

    extract. These beads of water begin to spatter when the extractgets

    too hot. By adding a small amount of acetone or alcohol, the water

    will tend to evaporate off as the alcohol or acetone is boiled off.

    Make sure that the alcohol or acetone is not contaminated with large

    amounts of water or this may be counterproductive. This process

    may

    be repeated until all of the water is gone.

    REFERENCES: . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    - Dangerous Properties of Industrial Materials, Litton Educational

    Publishing, Inc. (got a lot of good information here)

    - CRC Handbook of Chemistry and Physics

    - The Merck Index

    - Some dictionary of technical and scientific terms

    - Labels from numerous OTC products

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    - Comments from people on the 'net (many thanks to contributors)

    - The chemistry-extracting file at hyperreal.com

    - Things I remembered, but don't know where I read them

    - My own ingenuity and experience (nothing illegal, of course!)

    If a law is unjust, a man is not only right to disobey it, he is obligated to do so -

    Thomas Jefferson