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ChemicalBook--->CAS DataBase List--->84-96-8

84-96-8

84-96-8 Structure

84-96-8 Structure
IdentificationBack Directory
[Name]

Trimeprazine
[CAS]

84-96-8
[Synonyms]

Teralen
Teralene
Alimezine
Bayer 1219
ALIMENAZINE
alimemazine
TRIMEPRAZINE
Trimeperazine
Methylpromazine
dl-Trimeprazine
Trimeprazine USP/EP/BP
Alimemazine-d6 MALEATE SALT
Trimeprazine (base and/or unspecified salts)
10H-Phenothiazine-10-propanaMine,N,N,b-triMethyl-
10H-Phenothiazine-10-propanamine, N,N,β-trimethyl-
10-[2-Methyl-3-(dimethylamino)propyl]phenothiazine
10-[3-(Dimethylamino)-2-methylpropyl]phenothiazine
n,n,2-trimethyl-3-phenothiazin-10-yl-propan-1-amine
dimethyl-(2-methyl-3-phenothiazin-10-yl-propyl)amine
Phenothiazine, 10-[3-(dimethylamino)-2-methylpropyl]-
10H-Phenothiazine-10-propanamine, N,N,beta-trimethyl-
N,N,2-Trimethyl-3-(10H-phenothiazin-10-yl)-1-propanamine
N,N,2-triMethyl-3-(10H-phenothiazin-10-yl)propan-1-aMine
Phenothiazine, 10-[3-(dimethylamino)-2-methylpropyl]- (6CI, 8CI)
[EINECS(EC#)]

201-577-3
[Molecular Formula]

C18H22N2S
[MDL Number]

MFCD00242597
[MOL File]

84-96-8.mol
[Molecular Weight]

298.45
Chemical PropertiesBack Directory
[Melting point ]

68°C
[Boiling point ]

bp0.3 150-175°
[density ]

1.1163 (rough estimate)
[refractive index ]

1.6000 (estimate)
[pka]

pKa 9.00 (Uncertain)
[Water Solubility ]

0.942 mg/L
[CAS DataBase Reference]

84-96-8
[NIST Chemistry Reference]

Trimeprazine(84-96-8)
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Trimeprazine(84-96-8).msds
Safety DataBack Directory
[Hazardous Substances Data]

84-96-8(Hazardous Substances Data)
Hazard InformationBack Directory
[Originator]

Temaril,SKF,US,1958
[Uses]

antipruritic
[Uses]

Trimeprazine is used for treating itching during dermatitis of both allergic and nonallergic origin.
[Definition]

ChEBI:Trimeprazine is a member of phenothiazines.
[Manufacturing Process]

95% sodamide (2.77 grams) is added to a solution of phenthiazine (9.6 grams) in xylene (140 cc) at a temperature of 130°C and the mixture is heated with reflux for 2 hours.
A 0.61 N solution (90 cc) of 1-chloro-2-methyl-3-dimethylaminopropane in xylene is then added over 50 minutes and heating with reflux is continued for 20 hours. After cooling, the mixture is treated with water (40 cc) and N methanesulfonic acid (70 cc). The aqueous layer is washed with ether, treated with aqueous sodium hydroxide (density = 1.33; 10 cc) and extracted with ether.
The extract is dried over potassium carbonate and evaporated and the residue is distilled in vacuo. 3-(10-phenthiazinyl)-2-methyl-1-dimethylaminopropane (12.6 grams) is collected, distilling between 150° and 175°C under a pressure of about 0.3 mm Hg. By dissolving this base in acetone and adding ethereal hydrogen chloride, a hydrochloride is obtained, MP 216° to 217°C.
[Brand name]

Temaril (Allergan).
[Therapeutic Function]

Antipruritic
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