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M1641

Sigma-Aldrich

Methoxyphenamine hydrochloride

≥99%

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Synonym(s):
2-Methoxy-N,α-dimethylbenzeneethanamine hydrochloride, NSC 65644
Empirical Formula (Hill Notation):
C11H17NO · HCl
CAS Number:
Molecular Weight:
215.72
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Assay

≥99%

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

SMILES string

Cl.CNC(C)Cc1ccccc1OC

InChI

1S/C11H17NO.ClH/c1-9(12-2)8-10-6-4-5-7-11(10)13-3;/h4-7,9,12H,8H2,1-3H3;1H

InChI key

FGSJNNQVSUVTPW-UHFFFAOYSA-N

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This Item
65390B8703479314
Benzoin methyl ether 96%

Sigma-Aldrich

B8703

Benzoin methyl ether

Benzoin methyl ether 99%

Sigma-Aldrich

479314

Benzoin methyl ether

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

drug control

-

drug control

-

drug control

-

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Y Nakahara et al.
Forensic science international, 63(1-3), 109-119 (1993-12-01)
The excretion of methoxyphenamine (MOP) and methamphetamine (MA) into beards has been studied. Six healthy male subjects orally took 50 mg of MOP at a single dose and 7 doses for a successive 7 days. Their beard hairs were collected
Hajime Miyaguchi et al.
Journal of chromatography. A, 1129(1), 105-110 (2006-07-29)
A microchip-based liquid-liquid extraction for the gas chromatography analysis of urine for amphetamine-type stimulants has been developed. Partially modified microchannels with the capillarity restricted modification (CARM) method were employed for stabilizing the interface consisting of 1-chlorobutane and alkalized urine. Reliability
S D Roy et al.
Clinical pharmacology and therapeutics, 38(2), 128-133 (1985-08-01)
Urine and plasma concentrations of methoxyphenamine (MP) and three of its metabolites were determined after a single oral 60.3 mg dose of MP hydrochloride to healthy subjects of known debrisoquin (D) phenotype. Urine was collected from five extensive (EM) and
Separation of optical isomers of methoxyphenamine and its metabolites as N-heptafluorobutyryl-L-prolyl derivatives by fused-silica capillary gas chromatography.
S D Roy et al.
Journal of chromatography, 431(1), 210-215 (1988-09-23)
S Geertsen et al.
Xenobiotica; the fate of foreign compounds in biological systems, 25(9), 895-906 (1995-09-01)
1. Control and P4502D6-transfected human B-lymphoblastoid cell lines (cHol and h2D6v2 respectively) were used to study 2D6-mediated metabolism of methoxyphenamine (MPA) and 2-methoxyamphetamine (2MA). The main metabolites were products of O-dealkylation and aromatic hydroxylation at the 5-position. In addition, N-desmethyl-methoxyphenamine

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