2C-T-8

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| verifiedrevid = 477216775

| ImageFile1 = 2C-T-82DACS.svg

| ImageSize1 = 180px

| ImageFile2 = 2C-T-8-3d-sticks.png

| ImageSize2 = 200px

| PIN = 2-{4-[(Cyclopropylmethyl)sulfanyl]-2,5-dimethoxyphenyl}ethan-1-amine

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| Section1 = {{Chembox Identifiers

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChemSpiderID = 21106234

| InChI = 1/C14H21NO2S/c1-16-12-8-14(18-9-10-3-4-10)13(17-2)7-11(12)5-6-15/h7-8,10H,3-6,9,15H2,1-2H3

| InChIKey = AHMSSHCYIDBVQB-UHFFFAOYAR

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| ChEMBL = 127995

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| StdInChI = 1S/C14H21NO2S/c1-16-12-8-14(18-9-10-3-4-10)13(17-2)7-11(12)5-6-15/h7-8,10H,3-6,9,15H2,1-2H3

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| StdInChIKey = AHMSSHCYIDBVQB-UHFFFAOYSA-N

| CASNo_Ref = {{cascite|changed|??}}

| CASNo = 207740-27-0

| PubChem = 44350055

| UNII = 50U317Z43G

| SMILES = COc2cc(SCC1CC1)c(cc2CCN)OC

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| Section2 = {{Chembox Properties

| Formula =

| C=14 | H=21 | N=1 | O=2 | S=1

| MolarMass = 267.39 g/mol

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2C-T-8, also known as 4-cyclopropylmethylthio-2,5-dimethoxyphenethylamine, is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin, sometimes used as an entheogen.

Chemistry

The full name of the chemical is 2,5-dimethoxy-4-cyclopropylmethylthiophenethylamine. The compound is reported to have a bad taste and smell.{{citation needed|date=November 2012}}

Effects

In his book PiHKAL, Shulgin lists the dosage range as 30 to 50 mg.{{CitePiHKAL}} [http://www.erowid.org/library/books_online/pihkal/pihkal044.shtml 2C-T-8 Entry in PiHKAL] 2C-T-8 is generally taken orally and effects typically last 10 to 15 hours. Experiences have varied between insight and creativity at low doses to hypersensitivity and paranoia at higher doses. A "thinking-connection" that is characteristic of the 2C-T group is evident in this chemical in stark contrast to the "pure euphoria" of phenethylamines such as MDMA.

Legality

2C-T-8 is unscheduled and uncontrolled in the United States, but possession and sales of 2C-T-8 will probably be prosecuted under the Federal Analog Act because of its structural similarities to 2C-T-7. However, 2C-T-8, unlike many other phenethylamines has not been sold by internet retailers. In the wake of Operation Web Tryp in July 2004, the issue of possession and sales of 2C-T-8 and other similar chemicals will probably be resolved in the courtroom as will the fate of this rare but unique psychedelic.{{needs update|date=June 2019}}

=Canada=

As of October 31, 2016, 2C-T-8 is a controlled substance (Schedule III) in Canada.{{Cite web|url=http://gazette.gc.ca/rp-pr/p2/2016/2016-05-04/html/sor-dors72-eng.php|title=Canada Gazette – Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)|date=4 May 2016}}

Pharmacology

{{original research|date=September 2019}}

The mechanism that produces 2C-T-8's hallucinogenic and entheogenic effects has not been specifically established, however it is most likely to result from action as a 5-HT2A serotonin receptor agonist in the brain, a mechanism of action shared by all of the hallucinogenic tryptamines and phenethylamines for which the mechanism of action is known.

Dangers

The toxicity of 2C-T-8 is not well documented. 2C-T-8 is somewhat less potent than 2C-T-7, but it may be expected that at higher doses it would display similar toxicity to that of other phenethylamines of the 2C-T family.

There have been no confirmed deaths due to 2C-T-8,{{Citation needed|date=March 2008}} though this may in part be due to its rarity and limited usage. Of the 2C-T family, there have been a few confirmed deaths due to 2C-T-7, which involved either insufflating large (>30 mg) doses[http://www.erowid.org/chemicals/2ct7/2ct7_death1.shtml Erowid.org][http://www.erowid.org/chemicals/2ct7/2ct7_death2.shtml Erowid.org] and in one case an unknown oral dose was combined with 200 mg MDMA.[http://www.erowid.org/chemicals/2ct7/2ct7_death3.shtml Erowid.org]

Popularity

2C-T-8 is unknown on the black market. Limited accounts of 2C-T-8 can be found in the book PiHKAL.

See also

References