BOH (drug)

BOH
Clinical data
Other names	3,4-methylenedioxy-β-methoxyphenethylamine
MedlinePlus	a609035
Routes of; administration	Oral
ATC code	none;
Legal status
Legal status	In general: uncontrolled;
Identifiers
	IUPAC name 2-(1,3-Benzodioxol-5-yl)-2-methoxyethanamine;
CAS Number	73304-06-0 ;
PubChem CID	44719487;
ChemSpider	21106264 ;
UNII	W7KI9V2RCE;
CompTox Dashboard (EPA)	DTXSID10660351 ;
Chemical and physical data
Formula	C10H13NO3
Molar mass	195.218 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES NCC(OC)c1ccc2OCOc2c1;
	InChI InChI=1S/C10H13NO3/c1-12-10(5-11)7-2-3-8-9(4-7)14-6-13-8/h2-4,10H,5-6,11H2,1H3 ; Key:KUTKTMOZFCYDLZ-UHFFFAOYSA-N ;
	(verify)

BOH, also known as 3,4-methylenedioxy-β-methoxyphenethylamine, is a drug of the phenethylamine class.^[1] It is the β-methoxy analog of methylenedioxyphenethylamine (MDPEA) and is also more distantly related to methylone. On account of its similarity to norepinephrine, the effects of BOH may be of a purely adrenergic nature.^[1]

BOH was first synthesized by Alexander Shulgin.^[1] In his book PiHKAL, the dosage range is listed as 80–120 mg, and the duration listed as 6–8 hours. Shulgin reports that BOH causes slight warmth, mydriasis, anorexia, mild nausea, and cold feet, with no psychedelic, entactogen, or euphoriant effects.^[1] He gives it a ++ on the Shulgin Rating Scale.^[1]

Legality

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.^[2]

References

^ ^a ^b ^c ^d ^e Shulgin A, Shulgin A (1991). Pihkal: A Chemical Love Story. Transform Press. ISBN 0-9630096-0-5.
^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.

[isbn0-9630096-0-5-1] Shulgin A, Shulgin A (1991). Pihkal: A Chemical Love Story. Transform Press. ISBN 0-9630096-0-5.

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

[1]

[2]

BOH (drug)

Legality

United Kingdom

See also

References