:BOD (psychedelic)

{{chembox

| Name = BOD

| verifiedrevid = 401813792

| ImageFile1 = 4-methyl-2,5,beta-trimethoxy-phenethylamine.svg

| ImageSize1 =

| ImageFile2 = BOD-3d-sticks.png

| ImageSize2 =

| PIN = 2-(2,5-Dimethoxy-4-methylphenyl)-2-methoxyethan-1-amine

| OtherNames = 4-Methyl-2,5,β-trimethoxyphenethylamine
2-(4-Methyl-2,5,β-trimethoxyphenyl)ethanamine

|Section1={{Chembox Identifiers

| InChIKey = VTEIFHQUZWABDE-UHFFFAOYAC

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChI = 1S/C12H19NO3/c1-8-5-11(15-3)9(6-10(8)14-2)12(7-13)16-4/h5-6,12H,7,13H2,1-4H3

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = VTEIFHQUZWABDE-UHFFFAOYSA-N

| CASNo_Ref = {{cascite|correct|??}}

| CASNo = 98537-41-8

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = 9PXE981731

| PubChem = 44719486

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

| ChemSpiderID = 21106262

| SMILES = COc1cc(C)c(cc1C(CN)OC)OC

| InChI = 1/C12H19NO3/c1-8-5-11(15-3)9(6-10(8)14-2)12(7-13)16-4/h5-6,12H,7,13H2,1-4H3

}}

|Section2={{Chembox Properties

| C=12

| H=19

| N=1

| O=3

| Appearance =

| Density =

| MeltingPt =

| BoilingPt =

| Solubility = }}

|Section3={{Chembox Hazards

| MainHazards =

| FlashPt =

| AutoignitionPt = }}

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BOD (4-methyl-2,5,β-trimethoxyphenethylamine) is a lesser-known psychedelic drug of the BOx group. It is the beta-methoxy analog of 2C-D and was first synthesized by Alexander Shulgin. In his book PiHKAL, the dosage range is listed as 15–25 mg with a duration of 8–16 hours.[http://www.erowid.org/library/books_online/pihkal/pihkal014.shtml BOD Entry in PiHKAL] Its reported effects include mild open-eye and moderate closed-eye alterations in visual perception, enhancement of conversation and sense of humor, and unpleasant physical effects such as nausea and lethargy.{{CitePiHKAL}} Very little data exists about the pharmacological properties, metabolism, and toxicity of BOD.

Legality

=United States=

BOD is unscheduled in the United States, but purchase, sale, or possession for human consumption could be prosecuted under the Federal Analogue Act.{{Cite web |title=21 U.S. Code § 841 - Prohibited acts A |url=https://www.law.cornell.edu/uscode/text/21/841 |access-date=2016-08-02 |website=LII / Legal Information Institute |mode=cs2}}

=United Kingdom=

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.{{cite web | title = UK Misuse of Drugs act 2001 Amendment summary | url = http://isomerdesign.com/Cdsa/scheduleUK.php?schedule=1&ion=30&structure=C | access-date = 12 March 2014 | publisher = Isomer Design}}

See also

References