Jump to content

2C-C: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous editNext edit →
Content deleted Content added
VisualWikitext
Removed misleading information
Myxsoma (talk | contribs)
195 edits
→Sweden: added US law section
Line 56: Line 56:
===Sweden===
===Sweden===
[[Riksdag|''Sveriges riksdags'']] health ministry [[:sv:Statens folkhälsoinstitut|''Statens folkhälsoinstitut'']] classified 2C-C as "health hazard" under the act [[:sv:Lagen om förbud mot vissa hälsofarliga varor|''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.<ref>http://www.notisum.se/rnp/sls/sfs/20050026.pdf</ref>
[[Riksdag|''Sveriges riksdags'']] health ministry [[:sv:Statens folkhälsoinstitut|''Statens folkhälsoinstitut'']] classified 2C-C as "health hazard" under the act [[:sv:Lagen om förbud mot vissa hälsofarliga varor|''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.<ref>http://www.notisum.se/rnp/sls/sfs/20050026.pdf</ref>

===USA===
As of July 9, 2012, in the [[United States]] 2C-C is a [[Controlled Substances Act#Schedule I controlled substances|Schedule I]] substance under the [[Food and Drug Administration Safety and Innovation Act of 2012]], making possession, distribution and manufacture illegal.<ref name="erowid-law">[http://www.erowid.org/chemicals/2cc/2cc_law.shtml Erowid.org, Legal Status of 2C-C]</ref>


==See also==
==See also==

Revision as of 02:21, 1 June 2014

2C-C
Names
IUPAC name
1-(4-Chloro-2,5-dimethoxyphenyl)-2-aminoethane 1-(4-Chloro-2,5-dimethoxyphenyl)-2-ethanamine
Other names
4-Chloro-2,5-dimethoxy-phenethylamine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
  • 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 checkY
    Key: CGKQFIWIPSIVAS-UHFFFAOYSA-N checkY
  • 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
  • COc1cc(CCN)c(cc1Cl)OC
Properties
C10H14ClNO2
Molar mass 215.6778 g/mol
Melting point 220–221 °C (hydrochloride)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Blotter paper containing 2C-C

2C-C is a psychedelic drug of the 2C family. It was first synthesized by Alexander Shulgin, sometimes used as an entheogen. The full name of the chemical is 2,5-dimethoxy-4-chlorophenethylamine. 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. Many users report that 2C-C is gentler and more sedating than other closely related psychedelic phenethylamines.[citation needed]

Effects

  • The visual effects of 2C-C are similar to those of LSD or psilocybin mushrooms, though much less intense at commonly taken doses. Unique among the psychedelics, 2C-C is intensely relaxing, almost sedating.[citation needed] Nasal insufflation (extremely painful) or rectal administration bypasses first pass metabolism, requiring about half the dose normally used orally; the effects occur within 2–30 minutes via these routes and tend to last about an hour or two. There are very few known negative side effects attributed to 2C-C and nearly no hangover period except headaches after repeated doses.[citation needed]
  • The effects can take up to two hours to manifest.
  • Over the approximate dose range 20–40 mg, effects last respectively, approximately, 4 to 8 hours. Increased dosages increase the duration of the trip.[1]

Drug prohibition laws

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.[3]

USA

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.[4]

See also

References

  1. ^ a b Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
  2. ^ "S. 3187: Food and Drug Administration Safety and Innovation Act, Subtitle D-Synthetic Drugs". FDA. June 27, 2012. Retrieved July 12, 2012.
  3. ^ http://www.notisum.se/rnp/sls/sfs/20050026.pdf
  4. ^ Erowid.org, Legal Status of 2C-C

Template:PiHKAL

Retrieved from "https://en.wikipedia.org/enwiki/w/index.php?title=2C-C&oldid=611014301"