Mescaline

Mescaline
Clinical data
Other names	3,4,5-Trimethoxyphenethylamine, TMPEA, Peyote
AHFS/Drugs.com	mescaline
Routes of; administration	Oral, intravenous
ATC code	None;
Legal status
Legal status	AU: S9 (Prohibited substance); BR: Class F2 (Prohibited psychotropics); CA: Schedule III; DE: Anlage I (Authorized scientific use only); UK: Class A (Plants containing mescaline legal); US: Schedule I; UN: Psychotropic Schedule I;
Pharmacokinetic data
Elimination half-life	6 hours
Identifiers
	IUPAC name 2-(3,4,5-trimethoxyphenyl)ethanamine;
CAS Number	54-04-6 ;
PubChem CID	4076;
ChemSpider	3934 ;
UNII	RHO99102VC;
KEGG	C06546 ;
ChEBI	CHEBI:28346 ;
ChEMBL	ChEMBL26687 ;
CompTox Dashboard (EPA)	DTXSID80202303 ;
ECHA InfoCard	100.000.174
Chemical and physical data
Formula	C11H17NO3
Molar mass	211.261 g·mol−1
3D model (JSmol)	Interactive image;
Melting point	35 to 36 °C (95 to 97 °F)
Boiling point	180 °C (356 °F) at 12 mmHg
	SMILES O(c1cc(cc(OC)c1OC)CCN)C;
	InChI InChI=1S/C11H17NO3/c1-13-9-6-8(4-5-12)7-10(14-2)11(9)15-3/h6-7H,4-5,12H2,1-3H3 ; Key:RHCSKNNOAZULRK-UHFFFAOYSA-N ;
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Mescaline or mescalin (3,4,5-trimethoxyphenethylamine) is a naturally occurring psychedelic protoalkaloid of the substituted phenethylamine class, known for its hallucinogenic effects comparable to those of LSD and psilocybin.

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