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- From: malcolm@cltr.uq.oz.au (Malcolm Gillies)
- Subject: Re: impurities in mdma
- Message-ID: <1993Jan19.044037.23958@cltr.uq.OZ.AU>
- Sender: news@cltr.uq.OZ.AU (Mr. Time Waster)
- Nntp-Posting-Host: lingua.cltr.uq.oz.au
- Organization: Centre for Language Teaching and Research, Uni of Queensland, AUSTRALIA.
- References: <1993Jan15.033437.22406@cltr.uq.OZ.AU> <wHcLXB2w166w@hogbbs.scol.pa.us>
- Date: Tue, 19 Jan 1993 04:40:37 GMT
- Lines: 63
-
- wce@hogbbs.scol.pa.us (Bill Eichman) writes:
-
- >malcolm@cltr.uq.oz.au (Malcolm Gillies) writes:
-
- >>
- >> Safrole and isosafrole, which are common precursons for MDA and MDMA,
- >> polymerise very easily, forming brown tarry crud. This is quite strongly
- >> coloured, and even a small amount will stain an otherwise reasonable looking
- >> product. Not to mention glassware, hands etc etc.
- >>
- >> Malcolm
-
- >How does it get into the final product? Attempting to answer my own
- >question, I've read enough to gather that these illegal chemicals are
- >vacuum distilled at several points to produce a 'pure' product. Perhaps
- >the black market chemists are using some other proceedure?
-
- Vacuum distillation is a pain, but can be useful to purify an
- intermediate. I doubt that many illicit syntheses would use such
- a technique, especially on the final product since there are
- simpler ways. The first stage is an acid-base amine
- extraction which isolates the crude product from a reaction
- mixture. This will generally contain small amounts of synthetic
- by-products, including those which will colour the product.
- Generally, this product (which would be an oil in the case
- of MDMA) would then be converted to a salt, and precipitated
- as crystals from an organic solvent. This would still contain
- small amounts of impurites, trapped in the crystals, but is
- probably as far as most illicit chemists would go.
- Coloured impurities may often be removed effectively by boiling a
- crude product in a solvent with activated charcoal.
- Further purification could be obtained at the cost of a loss
- of yield by recrystalisation (one dissolves the product in
- hot solvent, then allows it to cool, forming quite pure
- crystals) or in an extreme case by chromatography.
-
- >How carcinogenic, or otherwise dangerous, is the 'brown tarry crud'? Is
- >it fairly easily filtered out of the body by the kidneys and liver? Once
- >polymerized, does the safrole retain is carcinogenic status?
-
- The short answer is nobody knows. But consider that you eat such
- compounds frequently - e.g. in burnt toast or BBQ'd steak.
- Polyaromatic hydrocarbons do pose a significant risk to
- coal workers, for example. Personally, I'd be more worried
- about being near cigarette smoke.
-
- >How carcinogenic is that benzene ring, anyway? (this is a side question)
-
- Carcinogenicity is a very complex topic. For example, successive
- methylation of benzene decreases its carcinogenicity. It is not the
- benzene ring which may be considered carcinogenic, it is the
- entire molecule. The carcinogenicity of safrole was established
- (at great expense) because it was a food additive. Very few
- compounds go through such a procedure unless there is a good
- reason. It is impossible to extrapolate the data on safrole
- to MDMA or the kinds of impurities which may contaminate it.
-
- >Thanks to everyone for the many answers to my question.
-
- >Later, Bill
-
- Jeremy
- jeremy@rsc3.anu.edu.au
-