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10H-Phenothiazine,10-[(1-methyl-3-pyrrolidinyl)methyl]-, hydrochloride (1:1) (1229-35-2)

Identification
Name:10H-Phenothiazine,10-[(1-methyl-3-pyrrolidinyl)methyl]-, hydrochloride (1:1)
Synonyms:10H-Phenothiazine,10-[(1-methyl-3-pyrrolidinyl)methyl]-, monohydrochloride (9CI); Phenothiazine,10-[(1-methyl-3-pyrrolidinyl)methyl]-, monohydrochloride (8CI); Dilosyn;Disyncran; Methdilazine hydrochloride; Methdilazine monohydrochloride; NSC169091; Tacaryl; Tacaryl hydrochloride
CAS:1229-35-2
EINECS: 214-967-3
Molecular Formula: C18H20 N2 S . Cl H
Molecular Weight: 332.92
InChI: InChI=1/C18H20N2S/c1-19-11-10-14(12-19)13-20-15-6-2-4-8-17(15)21-18-9-5-3-7-16(18)20/h2-9,14H,10-13H2,1H3
Molecular Structure: (C18H20N2S.ClH) 10H-Phenothiazine,10-[(1-methyl-3-pyrrolidinyl)methyl]-, monohydrochloride (9CI); Phenothiazine,10-[...
Properties
Melting Point: 187.5-189 DEG C
Flash Point: 214.1°C
Boiling Point: 430.4°Cat760mmHg
Density:g/cm3
Refractive index:1.642
Solubility:1 G IN 2 ML WATER, 2 ML ALC, 6 ML CHLOROFORM, MORE THAN 10,000 ML ETHER
Specification:

Reactivity Profile: Methdilazine hydrochloride (200 MG) is sensitive to exposure to light. An acidic salt. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible.

Flash Point: 214.1°C
Color: LIGHT-TAN, CRYSTALLINE POWDER
CRYSTALS FROM ISOPROPYL ALCOHOL
Safety Data