chlorphenamine hydrogen maleate
-
Molecular Structure
Detailed Description
Product Name: Chlorpheniramine maleate
Synonyms: 1-(p-Chlorophenyl)-1-(2-pyridyl)-3-dimethy-laminopropanebimaleate;1-(p-chlorphenyl)-1-(2-pyridyl)-3-dimethylaminopropanmaleat;2-(p-chloro-alpha-(2-(dimethylamino)ethyl)benzyl)-pyridinmaleate(1:1);allerclor;allergin;alunex;antagonate;carbinoxamidemaleate
CAS: 113-92-8
MF: C20H23ClN2O4
MW: 390.86
EINECS: 205-054-0
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Antagonists;Histaminergics;Neurotransmitters;TELDRIN
Mol File: 113-92-8.mol
Chemical Properties White Solid
Usage Antihistaminic
General Description Odorless white crystalline solid or white powder with a bitter taste. pH (2% aqueous solution) 5. pH (1% aqueous solution) 4-5.
Air & Water Reactions Water soluble.
Reactivity Profile A halogenated amine, ester. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Fire Hazard Flash point data for Chlorpheniramine maleate are not available; however, Chlorpheniramine maleate is probably combustible.
- chlorphenamine hydrogen maleate
View Contact Detail