| Identification | Back Directory | [Name]
2,5-Dimethoxy-4-Methylamphamin | [CAS]
15588-95-1 | [Synonyms]
DOM (exempt preparation)
2,5-Dimethoxy-4-Methylamphamin
2,5-Dimethoxy-4-Methylamphetamine
Benzeneethanamine, 2,5-dimethoxy-α,4-dimethyl- | [Molecular Formula]
C12H19NO2 | [MOL File]
15588-95-1.mol | [Molecular Weight]
209.28 |
| Chemical Properties | Back Directory | [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 | [pka]
9.77±0.10(Predicted) |
| Hazard Information | Back Directory | [Uses]
2,5-Dimethoxy-4-methylamphetamine (DOM, STP) | [Uses]
DOM 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 |
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