3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride

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3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride Basic information
Product Name:3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride
Synonyms:3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride;(±)-3,4,5-Trimethoxyamphetamine hydrochloride (TMA);3,4,5-Trimethoxyamphetamine (hydrochloride) (exempt preparation);GOAXEHDWLMGWIV-UHFFFAOYSA-N;d,l-3,4,5-TMA.HCl;(±)-3,4,5-Trimethoxyamphetamine HCl (TMA);d,l-3,4,5-TMA.HCl, 1mg/ml in Methanol (as free base)
CAS:5688-80-2
MF:C12H20ClNO3
MW:261.745
EINECS:
Product Categories:
Mol File:5688-80-2.mol
3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride Structure
3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride Chemical Properties
Melting point 219-220 °C
solubility DMF: 13 mg/ml
DMSO: 5 mg/ml
Ethanol: 14 mg/mlPBS (pH 7.2): 10 mg/ml
Safety Information
MSDS Information
3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride Usage And Synthesis
Description3,4,5-Trimethoxyamphetamine (TMA), is a psychedelic hallucinogen which has appeared on the illicit drug market. Unlike amphetamines and cathinones, TMA has no effect on monoamine re-uptake. TMA has modest effects on the 5-HT2 serotonin receptors (pEC50 = 5.15 and 5.31 for phosphatidyl inositol release through 5-HT2A and 5-HT2C, respectively). This product is intended for research and forensic applications.
Uses3,4,5-Trimethoxyamphetamine (TMA), is a psychedelic hallucinogen that has appeared on the illicit drug market. Unlike amphetamines and cathinones, TMA has no effect on monoamine re-uptake. TMA has modest effects on the 5-HT2 serotonin receptors (pEC50s = 5.15 and 5.31 for phosphatidyl inositol release through 5-HT2A and 5-HT2C, respectively). This product is intended for research and forensic applications.[Cayman Chemical]
References[1] ARIANE WOHLFARTH  Sebastian D  Wolfgang Weinmann. LC-MS/MS screening method for designer amphetamines, tryptamines, and piperazines in serum[J]. Analytical and Bioanalytical Chemistry, 2010, 396 7: 2403-2414. DOI: 10.1007/s00216-009-3394-4
[2] PABLO R MOYA. Functional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A and 5-HT2C receptors.[J]. Journal of Pharmacology and Experimental Therapeutics, 2007, 321 3: 1054-1061. DOI: 10.1124/jpet.106.117507
[3] FUMIKO NAGAI  Kanako S H K  Ryouichi Nonaka. The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain[J]. European journal of pharmacology, 2007, 559 2: Pages 132-137. DOI: 10.1016/j.ejphar.2006.11.075
3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride Preparation Products And Raw materials
Tag:3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride(5688-80-2) Related Product Information
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