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| Research Chemicals Piperazines, Phenethylamines, Tryptamines & other Research Chemicals or designer drugs. |
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#1
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XTC testing kits to test Research Chemicals?
Is it possible to use any of the following reagents to test
research chems? Mecke Reagent, Simon’s reagent and Marquis Reagent Where can I find the expected results? Thanks. |
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#3
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i have tested most things around the lab and the house with Marquis and Mandelin.
methylone and cousins, many of the 2C-s, all tryptamines produce a reaction of note, if one is observant of nuances, accurate record may be assembled. as a first defence / ID measure (ie you spaced what powder is what) the 2 tests mentioned are accurate enough to tell what class you are dealing with. |
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#4
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BUMP
and Nanobrain, I don't suppose you kept logs of what the reactions were, did you? I'd like to begin compiling in one place, for the benefit of members & all humankind, how common (and not so common) RCs react with various reagents. Once I got enough data I'd make a nice easy-to-read chart & post it ... & keep updating. As of right now, the Erowid chart linked to by radiometer is the best we have, though it hardly reflects the substances that are most in circulation right now. (Particularly in regards to the highly potent stuff that people are trying to pass off on blotters as "acid.") I'll keep digging here & on other forums & post what I find; I seem to recall a BL member had done some systematic testing, but I can't find it just at the moment.... Anyone with information, please come forward & send me your results via PM or posting. Thanks muchly. |
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#5
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From a post in another thread by the ever-informative Illuminati Boy:
Color Test Reagents Ehrlich’s Reagent : 0.5 g of para-dimethylaminobenzaldehyde (p-DMAB) in a mixture containing 50 mL of ethyl alcohol and 50 mL concentrated hydrochloric acid [5]. Marquis Reagent: 100 mL formaldehyde in 1000 mL concentrated sulfuric acid [5]. Color Testing Testing each of the tryptamine analogues with the Ehrlich’s reagent produced the same change in color from purple to blue, except for DPT HCl, which produced a violet color change and 5-MeO-MIPT which changed from purple to a faint blue. In the presence of the Marquis reagent, each tryptamine analogue produced the same color change from yellow to black, except for DPT HCl which gave a yellow color only, as shown in Table 1. Table 1: Results of Color Testing. “Designer” Tryptamine | Ehrlich’s Reagent | Marquis Reagent N,N-DPT HCl | violet | yellow 5-MeO-DMT | purple to blue | yellow to black 5-MeO-MIPT | purple to faint blue | yellow to black 5-MeO-DIPT HCl | purple to blue | yellow to black 5-MeO-AMT HCl | purple to blue | yellow to black From Microgram Journal Volume 3, Numbers 1-2 ------------------------------------------------------------------------------------- Color Tests A purple color was observed when the sample was subjected to the para-dimethylaminobenzaldehyde (PDMAB) reagent test. [This result, along with the fact that sugar cubes were used as the supporting media, explain why the submitting agency believed the exhibits contained LSD.] However, a cherry red color was observed when the sample was subjected to the sodium nitroprusside reagent test, suggesting a tryptamine. This result was then compared to three tryptamine standards (Table 1). The results suggested the presence of a primary amine with an alpha-methyltryptamine moiety (Figure 2) - and not a secondary amine with an N-methyltryptamine moiety (Figure 3). Tryptamine | Sodium Nitroprusside Test alpha-Methyltryptamine | Cherry Red N-Methyltryptamine | Purple 5-Methoxy-alpha-methyltryptamine | Cherry Red |
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#6
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I think this may be the link that radiometer was referring to: http://www.erowid.org/chemicals/mdma/mdma_faq_testing_kits.shtml
In case it moves, Erowid has the following data points listed: Marquis 2-AminoIndan Orange to Red (slightly rusty) 2C-C Starting brown going to Dark Lime Green (similar to 2C-B) 2C-D Very light pink 2C-E No reaction (!?) 2C-I Dark Green to Black 2C-T-2 Orange to Red (usually a sort of salmon color) 2C-T-4 Orange to Red (usually a sort of salmon color) 2C-T-7 Orange to Red (salmon, again; also, there is less tendency towards orange than 2C-T-2 shows) 3C-P Orange 4-Acetoxy-DiPT Dirty (blackish) olive 4-Methyl-Aminorex (u4euh) no color change 4-MTA no color change 5-MeO-DiPT Fizzes then turns yellow quickly changing to a slightly rusty orange Alpha-Methyl-DiPT Fizzes then turns brown AMT Dark brownish-yellow BDB Dark brown, nearly black Benzylpiperazine No color change, but it causes the reagent to fizz. Looks like when you pour hydrogen peroxide on a cut. DiPT Fizzes strongly then turns a neon yellow DPT Dirty olive Harmine Fizzes slightly, much less so than BZP, and turns a brown-orange rust color. IAP Immediate reaction to salmon/red, slowly intensifies to a darker red over 1min. MBDB Dark Brown to Black Methylone Yellow Opiates Pink to Purple Phenolphthalein Crimson PMA No color change TMA-2 Lime Green (similar to 2C-B) TMA-6 Yellow to Orange Yohimbine Fizzes slightly, much less so than BZP. Slowly (up to a minute), it will turn an olive green color. Mecke 2C-E light yellow/green within 10 seconds 2C-I Immediate reaction to a reddish brown similar to drying blood 2C-T-21 Dark blood red which turns to an imperial purple over 30 seconds 4-Methyl-Aminorex (u4euh) no color change IAP No Reaction MBDB Yellow TMA-6 Dirty olive, gradually develops orange on the edges of the liquid puddle after about a minute Simons 2C-E No reaction 2C-I No reaction 2C-T-21 Greenish blue IAP No Reaction TMA-6 Purple Hopefully this is helpful.I B |
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#7
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Quote:
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#8
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Quote:
if anyone is interested still, i could dig up some logs for Easy 1 and 2 (Marquis and Mandelin) |
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#9
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Thanks I_B - I happened to spot this thread's reappearance yesterday, and fixed the link in my post as well. |
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#11
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Quote:
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