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
- Product Categories:
-
- Amines
- Aromatics
- Mol File:
- 15588-95-1.mol
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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 - pka
- 9.77±0.10(Predicted)
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Safety Information
- Hazardous Substances Data
- 15588-95-1(Hazardous Substances Data)
- DEA Controlled Substances
- CSCN: 7395
CSA SCH: Schedule I
NARC: No
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2,5-Dimethoxy-4-Methylamphamin Usage And Synthesis
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.
Uses
2,5-Dimethoxy-4-methylamphetamine (DOM, STP)
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