2,5-Dimethoxy-4-Methylamphamin

2,5-Dimethoxy-4-Methylamphamin Basic information
Product Name:2,5-Dimethoxy-4-Methylamphamin
Synonyms:2,5-Dimethoxy-4-Methylamphamin;2,5-Dimethoxy-4-Methylamphetamine;DOM (exempt preparation);Benzeneethanamine, 2,5-dimethoxy-α,4-dimethyl-
CAS:15588-95-1
MF:C12H19NO2
MW:209.28
EINECS:
Product Categories:Amines;Aromatics
Mol File:15588-95-1.mol
2,5-Dimethoxy-4-Methylamphamin Structure
2,5-Dimethoxy-4-Methylamphamin Chemical Properties
Melting point 60.5-61°
Boiling point 312.6±37.0 °C(Predicted)
density 1.010±0.06 g/cm3(Predicted)
solubility DMF: 14 mg/ml
DMF: PBS (pH 7.2) (1:1): 0.5 mg/ml
DMSO: 5 mg/ml
Ethanol: 10 mg/ml
pka9.77±0.10(Predicted)
Safety Information
Hazardous Substances Data15588-95-1(Hazardous Substances Data)
DEA Controlled SubstancesCSCN: 7395
CSA SCH: Schedule I
NARC: No
MSDS Information
2,5-Dimethoxy-4-Methylamphamin Usage And Synthesis
Uses2,5-Dimethoxy-4-methylamphetamine (DOM, STP)
UsesDOM is an amphetamine with dose-dependent psychotomimetic and hallucinogenic effects. It potently binds and activates serotonin 5-HT2 receptors (pA2 = 7.12). DOM is classified as a Schedule I compound in the United States. This product is intended for research and forensic purposes.
References[1] THERESA M CARBONARO M B G Michael J Forster. Discriminative stimulus effects of N,N-diisopropyltryptamine.[J]. Psychopharmacology, 2013, 226 2: 241-246. DOI: 10.1007/s00213-012-2891-x
2,5-Dimethoxy-4-Methylamphamin Preparation Products And Raw materials
Tag:2,5-Dimethoxy-4-Methylamphamin(15588-95-1) Related Product Information
3,4,5-Trimethoxy-α-methylbenzeneethanamine hydrochloride 2,5-Dimethoxy-4-Methylamphamin (-MDA-d3 (hydrochloride) S(-)-cathinone hydrochloride 1-(3,4-Methylenedioxyphenyl)-2-butanamine 2,5-Dimethoxy-4-ethylamphetamin