Name | 4-[2-(methylamino)ethyl]benzene-1,2-diol,hydrochloride |
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Synonyms |
4-[2-(Methylamino)ethyl]benzene-1,2-diol hydrochloride (1:1)
Pyrocatechol, 4-[2- (methylamino)ethyl]-, hydrochloride Ephinine hydrochloride 1,2-Benzenediol, 4-[2-(methylamino)ethyl]-, hydrochloride (1:1) MFCD00035074 1,2-Benzenediol, 4-[2-(methylamino)ethyl]-hydrochloride 1,2-Benzenediol, 4-[2- (methylamino)ethyl]-, hydrochloride N-Methyldopamine hydrochloride 3,4-Dihydroxyphenylethylmethylamine hydrochloride EPININE HCl 3,4-dihydroxyphenethylmethylammonium chloride 1,2-Benzenediol, 4-(2-(methylamino)ethyl)-, hydrochloride (9CI) Methyldopamine hydrochloride EINECS 200-528-3 4-[2-(Methylamino)ethyl]-1,2-benzenediol hydrochloride (1:1) Deoxyepinephrine hydrochloride Epinine hydrochloride |
Description | N-Methyldopamine hydrochloride is a precursor of adrenaline in the adrenal medulla. N-Methyldopamine hydrochloride is a modification of the dopamine (DA), and retains agonist activity at the DA1 receptor. N-Methyldopamine hydrochloride remains capable of universal surface coating and secondary reactions using the surface catechols. N-Methyldopamine hydrochloride can be used for heart failure research[1][2][3]. |
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Related Catalog | |
Target |
D1 Receptor |
In Vitro | N-Methyldopamine hydrochloride shows highly improved surface coating properties, and exhibits an accelerated coating rate. N-Methyldopamine hydrochloride coating makes solid surface cell adhesion possible, and postfunctionalization of the coating is also possible[1]. |
References |
Boiling Point | 328.6ºC at 760 mmHg |
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Melting Point | 174-176ºC |
Molecular Formula | C9H14ClNO2 |
Molecular Weight | 203.666 |
Flash Point | 154.3ºC |
Exact Mass | 203.071304 |
PSA | 52.49000 |
LogP | 2.05260 |
Appearance | solid | white |
Storage condition | 2-8°C |
Water Solubility | H2O: soluble |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Hazard Codes | Xi |
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WGK Germany | 3 |
RTECS | UX1925000 |
HS Code | 2922299090 |
~88% 62-32-8 |
Literature: Carpenter, Joel F. Journal of Organic Chemistry, 1993 , vol. 58, # 6 p. 1607 - 1609 |
~% 62-32-8 |
Literature: Carpenter, Joel F. Journal of Organic Chemistry, 1993 , vol. 58, # 6 p. 1607 - 1609 |
Precursor 2 | |
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DownStream 2 | |
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% |