2C-C
2C-C
Names
Preferred IUPAC name
2-(4-Chloro-2,5-dimethoxyphenyl)ethan-1-amine
Other names
(4-Chloro-2,5-dimethoxyphenethyl)amine
Identifiers
ChEMBL
ChemSpider
UNII
InChI=1S/C10H14ClNO2/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12/h5-6H,3-4,12H2,1-2H3
Y Key: CGKQFIWIPSIVAS-UHFFFAOYSA-N
Y InChI=1/C10H14ClNO2/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12/h5-6H,3-4,12H2,1-2H3
Key: CGKQFIWIPSIVAS-UHFFFAOYAM
Properties
C 10 H 14 Cl N O 2
Molar mass
215.6778 g/mol
Melting point
220 to 221 °C (428 to 430 °F; 493 to 494 K) (hydrochloride )
Pharmacology
Legal status
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
2C-C is a psychedelic drug of the 2C family . It was first synthesized by Alexander Shulgin , sometimes used as an entheogen . In his book PiHKAL (Phenethylamines i Have Known And Loved) , Shulgin lists the dosage range as 20–40 mg. 2C-C is usually taken orally, but may also be insufflated.[ 1] 2C-C is schedule I of section 202(c) of the Controlled Substances Act in the United States, signed into law as of July, 2012 under the Food and Drug Administration Safety and Innovation Act .[ 2]
Not much information is known about the toxicity of 2C-C.
Effects
Over the approximate dose range 20–40 mg, visual effects last approximately 4 to 8 hours.[ 1]
Drug prohibition laws
China
As of October 2015 2C-C is a controlled substance in China.[ 3]
Canada
As of October 31, 2016; 2C-C is a controlled substance (Schedule III) in Canada.[ 4]
Germany
2C-C is an Anlage I controlled drug.
Sweden
Sveriges riksdags health ministry Statens folkhälsoinstitut classified 2C-C as "health hazard" under the act Lagen om förbud mot vissa hälsofarliga varor (translated Act on the Prohibition of Certain Goods Dangerous to Health ) as of Mar 1, 2005, in their regulation SFS 2005:26 listed as 2,5-dimetoxi-4-klorfenetylamin (2C-C) , making it illegal to sell or possess.[ 5]
United States
As of July 9, 2012, in the United States 2C-C is a Schedule I substance under the Food and Drug Administration Safety and Innovation Act of 2012 , making possession, distribution and manufacture illegal.[ 6]
Analogues and derivatives
See also
References
External links
Psychedelics (5-HT2A agonists)
Benzofurans Lyserg‐ amides Phenethyl‐ amines
2C-x
3C-x 4C-x DOx HOT-x MDxx Mescaline (subst.) TMAs
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