Methoxyphenamine hydrochloride structure
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Common Name | Methoxyphenamine hydrochloride | ||
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CAS Number | 5588-10-3 | Molecular Weight | 215.720 | |
Density | 0.951 g/cm3 | Boiling Point | 252.3ºCat 760 mmHg | |
Molecular Formula | C11H18ClNO | Melting Point | 210°C | |
MSDS | Chinese USA | Flash Point | 102.6ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | Methoxyphenamine hydrochloride |
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Synonym | More Synonyms |
Density | 0.951 g/cm3 |
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Boiling Point | 252.3ºCat 760 mmHg |
Melting Point | 210°C |
Molecular Formula | C11H18ClNO |
Molecular Weight | 215.720 |
Flash Point | 102.6ºC |
Exact Mass | 215.107697 |
PSA | 21.26000 |
LogP | 3.03850 |
Storage condition | -20℃ |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn:Harmful |
Risk Phrases | R22 |
Safety Phrases | S36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | SH8050000 |
HS Code | 2942000000 |
HS Code | 2922299090 |
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Summary | 2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Quinidine but not quinine inhibits in man the oxidative metabolic routes of methoxyphenamine which involve debrisoquine 4-hydroxylase.
Eur. J. Clin. Pharmacol. 41(5) , 471-4, (1991) Healthy male volunteers (n = 13) took a single oral dose of 60.3 mg of methoxyphenamine HCl with and without prior administration of either quinidine (250 mg as bisulphate salt) or its diastereomer qu... |
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Influence of urinary pH on the disposition of methoxyphenamine and three metabolites in humans.
J. Pharm. Sci. 76(6) , 427-32, (1987) The disposition of methoxyphenamine (o-methoxy-N,alpha-dimethylphenethylamine) and three of its metabolites was studied in five healthy volunteers on three occasions, with the urine pH separately unde... |
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Metabolism of methoxyphenamine and 2-methoxyamphetamine in P4502D6-transfected cells and cell preparations.
Xenobiotica 25(9) , 895-906, (1995) 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).... |
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