M1641
甲氧那明 盐酸盐
≥99%
别名:
2-甲氧基-N,α-二甲基苯乙胺 盐酸盐, NSC 65644
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关于此项目
经验公式（希尔记法）:
C11H17NO · HCl
化学文摘社编号:
分子量:
215.72
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-993-2
MDL number:
Assay:
≥99%
InChI key
FGSJNNQVSUVTPW-UHFFFAOYSA-N
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
SMILES string
Cl.CNC(C)Cc1ccccc1OC
assay
≥99%
drug control
regulated under CDSA - not available from Sigma-Aldrich Canada
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
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
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)
A Guttman
Electrophoresis, 16(10), 1900-1905 (1995-10-01)
A systematic approach is described for methods development of chiral separations of weak acidic and basic compounds by capillary electrophoresis, using several natural and derivatized neutral cyclodextrins as chiral selectors. Following the methods development scheme suggested here, the appropriate pH
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