2C–H
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Names | |||
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IUPAC name
2-(2,5-Dimethoxyphenyl)ethanamine | |||
Other names
2,5-Dimethoxy-phenethylamine | |||
Identifiers | |||
(free base) ; 3166-74-3 (HCl salt) 3600-86-0 (free base) ; 3166-74-3 (HCl salt) | |||
ChEMBL | ChEMBL287047 | ||
ChemSpider | 69096 | ||
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) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
verify (what is ?) | |||
Infobox references | |||
2C–H, or 2,5-dimethoxyphenethylamine, is a lesser-known substituted phenethylamine of the 2C family.
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. 2C–H has been found in trace amounts by the DEA's south central laboratory in tablets that were suspected of containing MDMA.
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
- ↑ Buck, Johannes S. (1932). "Hydroxy- and Dihydroxyphenylethylmethylamines and their Ether". Journal of Chemical Society 54 (9): 3661–3665. doi:10.1021/ja01348a024.
- ↑ Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
- ↑ Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
- ↑ ""PubChem"".
- ↑ ""PubChem"".
- ↑ ""PubChem"".
- ↑ ""PubChem"".
- ↑ ""PubChem"".
- ↑ ""PubChem"".
- ↑ Portman. "Rules - 2013 - Establishment of Drug Codes for 26 Substances (SDAPA)". usdoj. Retrieved 22 July 2012.
External links
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