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{{short description|Chemical compound}} |
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{{Drugbox |
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{{Infobox drug |
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| verifiedrevid = 443313080 |
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| Watchedfields = changed |
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| IUPAC_name = 1-(2-methyl-1H-indol-3-yl)propan-2-amine |
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| verifiedrevid = 443314047 |
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| IUPAC_name = 1-(2-methyl-1''H''-indol-3-yl)propan-2-amine |
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| image = 2,a-DMT.svg |
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| image = 2,a-DMT.svg |
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| width = 200 |
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| width = 200 |
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| image2 = 2,alpha-DMT_3d_structure.png |
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| image2 = 2,alpha-DMT_3d_structure.png |
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<!--Clinical data--> |
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| width = 200 |
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| tradename = |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CAS_number = 4966-28-3 |
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| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> |
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| pregnancy_US = <!-- A / B / C / D / X --> |
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| ATC_prefix = |
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| pregnancy_category = |
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| ATC_suffix = |
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| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> |
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| legal_CA = <!-- / Schedule I, II, III, IV, V, VI, VII, VIII --> |
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| legal_UK = <!-- GSL / P / POM / CD / Class A, B, C --> |
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| legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> |
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| legal_status = |
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| routes_of_administration = |
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<!--Pharmacokinetic data--> |
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| bioavailability = |
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| protein_bound = |
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| metabolism = |
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| elimination_half-life = |
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| excretion = |
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<!--Identifiers--> |
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| CAS_number_Ref = {{cascite|correct|CAS}} |
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| CAS_number = 4966-28-3 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = QAH3JR2679 |
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| ATC_prefix = |
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| ATC_suffix = |
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| PubChem = |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 23511903 |
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<!--Chemical data--> |
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| chemical_formula = |
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| C=12 | H=16 | N=2 |
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| molecular_weight = |
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| smiles = Cc1c(c2ccccc21)CC(C)N |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C12H16N2/c1-8(13)7-11-9(2)14-12-6-4-3-5-10(11)12/h3-6,8,14H,7,13H2,1-2H3 |
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| StdInChI = 1S/C12H16N2/c1-8(13)7-11-9(2)14-12-6-4-3-5-10(11)12/h3-6,8,14H,7,13H2,1-2H3 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = AXZQFXRPULJFQK-UHFFFAOYSA-N |
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| StdInChIKey = AXZQFXRPULJFQK-UHFFFAOYSA-N |
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| PubChem = |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 23511903 |
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| smiles = Cc1c(c2ccccc21)CC(C)N |
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| InChI = 1S/C12H16N2/c1-8(13)7-11-9(2)14-12-6-4-3-5-10(11)12/h3-6,8,14H,7,13H2,1-2H3 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = |
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| chemical_formula =|C=12|H=16|N=2 |
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| molecular_weight = |
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| bioavailability = |
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| protein_bound = |
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| metabolism = |
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| elimination_half-life = |
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| excretion = |
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| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> |
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| pregnancy_US = <!-- A / B / C / D / X --> |
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| pregnancy_category= |
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| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> |
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| legal_CA = <!-- / Schedule I, II, III, IV, V, VI, VII, VIII --> |
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| legal_UK = <!-- GSL / P / POM / CD / Class A, B, C --> |
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| legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> |
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| legal_status = |
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| routes_of_administration = |
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}} |
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}} |
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'''2,alpha-DMT''', or '''2,α-dimethyltryptamine''', is a ] and a lesser-known ]. It is the 2,a-di] ] of ]. 2,α-DMT was first synthesized by ]. In his book '']'' (''Tryptamines I Have Known and Loved''), Shulgin lists the dosage as 300-500 ], and the duration as 7-10 hours.<ref>{{CiteTiHKAL|pages=422}}</ref> 2,α-DMT causes ] and ]. It also produces a calm, ]-like feeling. Very little data exists about the pharmacological properties, metabolism, and toxicity of 2,α-DMT. |
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'''2,α-Dimethyltryptamine''' ('''2,α-DMT''') is a ] and a lesser-known ]. It is the 2,α-di] ] of ]. Its synthesis was first reported in 1965.<ref>{{cite journal | vauthors = Heath-Brown B, Philpott PG |title=Studies in the Indole Series. Part I. Indolylalkylamines |journal=Journal of the Chemical Society |date=1965 |issue=Dec |pages=7165–7178|doi=10.1039/jr9650007165 }}</ref> ] lists the dosage as 300-500 ], and the duration as 7–10 hours in his book '']'' (''Tryptamines I Have Known and Loved'').<ref>{{CiteTiHKAL|pages=422|name-list-style = vanc }}</ref> 2,α-DMT causes ] and ]. It also produces a calm, ]-like feeling. Very little data exists about the pharmacological properties, metabolism, and toxicity of 2,α-DMT. |
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==References== |
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==References== |
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==External links== |
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==External links== |
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{{TiHKAL}} |
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{{Tryptamines}} |
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{{DEFAULTSORT:DMT, 2,alpha-}} |
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{{DEFAULTSORT:DMT, 2, alpha-}} |
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{{Psychoactive-stub}} |
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{{Psychoactive-stub}} |