BOM (drug)

BOM
Names
	Preferred IUPAC name 2-Methoxy-2-(3,4,5-trimethoxyphenyl)ethan-1-amine
	Other names 3,4,5,beta-Tetramethoxyphenethylamine; 2-(3,4,5,beta-Tetramethoxyphenyl)ethanamine; β-methoxymescaline
Identifiers
CAS Number	98537-40-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	21106265 ;
PubChem CID	44719490;
UNII	ZYL4Q2506P ;
CompTox Dashboard (EPA)	DTXSID30660353 ;
	InChI InChI=1S/C12H19NO4/c1-14-9-5-8(11(7-13)16-3)6-10(15-2)12(9)17-4/h5-6,11H,7,13H2,1-4H3 Key: GAKIJEPUVBHWCK-UHFFFAOYSA-N ; InChI=1/C12H19NO4/c1-14-9-5-8(11(7-13)16-3)6-10(15-2)12(9)17-4/h5-6,11H,7,13H2,1-4H3 Key: GAKIJEPUVBHWCK-UHFFFAOYAE;
	SMILES COc1c(cc(cc1OC)C(CN)OC)OC;
Properties
Chemical formula	C12H19NO4
Molar mass	241.287 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

BOM (3,4,5,beta-tetramethoxyphenethylamine) is a lesser-known drug of the BOx group. It is the β-methoxy derivative of mescaline. BOM was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 200 mg, and the duration unknown.^[1] BOM produces few to no effects.^[2] Very little data exists about its pharmacological properties, metabolism, and toxicity.

Legality

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.^[3]

References

^ BOM Entry in PiHKAL
^ Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.

[1] BOM Entry in PiHKAL

[2] Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.

[3] "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.

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