2,5-Dimethoxyphenethylamine
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| File:2C-H.svg | |
| Clinical data | |
|---|---|
| Pregnancy category |
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| Dependence liability | None |
| Routes of administration | None |
| Legal status | |
| Legal status |
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| Pharmacokinetic data | |
| Bioavailability | ?% (transdermal) ?% (buccal) |
| Protein binding | ?% |
| Metabolism | hepatic, primarily by CYP3A4 |
| Elimination half-life | hours (range ? h) |
| Excretion | Urine |
| Identifiers | |
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| CAS Number | |
| E number | {{#property:P628}} |
| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C10H15NO2 |
| Molar mass | 181.234 g/mol |
| 3D model (JSmol) | |
| Melting point | 160°C at 10 mm Hg °C (Expression error: Unrecognized punctuation character "°". °F) |
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2,5-Dimethoxyphenethylamine or 2C-H is a phenethylamine, first synthesized by Dr. Alexander & Ann Shulgin (PiHKAL). 2,5-Dimethoxyphenethylamine is an oily viscous liquid at room temperature. The LD50 in humans is not known.
Usage
2C-H is the normal starting point in the synthesis of the 2C compounds, including 2C-B, 2C-E, and others. It is not believed to be active, as it is likely rapidly metabolized by MAO.
See also
External links
Template:Amine-stub Template:Hallucinogenic phenethylamines Template:PiHKAL
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