2C–H
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| Names | |||
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| IUPAC name
2-(2,5-Dimethoxyphenyl)ethanamine
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| Other names
2,5-Dimethoxy-phenethylamine
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| Identifiers | |||
(free base) ; 3166-74-3 (HCl salt) 3600-86-0 (free base) ; 3166-74-3 (HCl salt)  |
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| ChEMBL | ChEMBL287047 |
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| ChemSpider | 69096 |
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| Jmol 3D model | Interactive image | ||
| PubChem | 76632 | ||
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| Properties | |||
| C10H15NO2 | |||
| Molar mass | 181.23 g/mol | ||
| Melting point | 138 to 139 °C (280 to 282 °F; 411 to 412 K) (hydrochloride) | ||
| Vapor pressure | {{{value}}} | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |||
2C–H, or 2,5-dimethoxyphenethylamine, is a lesser-known substituted phenethylamine of the 2C family.
Contents
History
2C–H was first synthesized in 1932 by Johannes S. Buck.[1]
Usage
2C-H is used as a precursor in the synthesis of other substituted phenethylamines.[citation needed] 2C–H has been found in trace amounts by the DEA's south central laboratory in tablets that were suspected of containing MDMA.[citation needed]
Pharmacology
There is no record of 2C–H trials in humans, as it would likely be destroyed by monoamine oxidase enzymes before causing any significant psychoactive effects.[2] In the book PiHKAL (Phenethylamines i Have Known And Loved), Alexander Shulgin lists both the dosage and duration of 2C–H effects as unknown.[3] Very little data exists about the pharmacological properties, metabolism, and toxicity of 2C–H.
Research
It exhibits agonist activity at human trace amine associated receptor 1 expressed in RD-HGA16 CHO-K1 cells coexpressed with Galpha16 protein assessed as internal calcium mobilization.[4] 2C-H was found to be inactive in NCI In Vivo Anticancer Drug Screens for tumor model L1210 Leukemia.[5] It was found to be an active Alpha-1 adrenergic receptor agonist in rabbit ear arteries.[6] It has binding affinity towards 5-HT2C and 5-HT2A receptors in rats.[7] It features competitive antagonist activity at 5-HT serotonin receptor in Sprague-Dawley rat stomachs.[8] It exhibits binding affinity against rat 5-hydroxytryptamine 2C receptors using [3H]mesulergine as a radioligand.[9]
Legal Status
United States
As of July 9, 2012, 2C–H is a Schedule I controlled substance in the United States, under the Synthetic Drug Abuse Prevention Act of 2012.[10] 2C-H's DEA Drug Code is 7517.
See also
References
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