ChemicalBook >> CAS DataBase List >>10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride

10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride

CAS No.
2975-36-2
Chemical Name:
10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride
Synonyms
Mepazine hydrochloride;10-((1-methylpiperidin-3-yl)methyl)-10H-phenothiazine hydrochloride;10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride;10H-Phenothiazine, 10-[(1-methyl-3-piperidinyl)methyl]-,monohydrochloride
CBNumber:
CB3921722
Molecular Formula:
C19H23ClN2S
Molecular Weight:
346.91732
MDL Number:
MOL File:
2975-36-2.mol
Last updated:2023-05-21 10:59:17

10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Properties

Melting point 180-181 °C
Boiling point 180-183 °C(Press: 0.5 Torr)
storage temp. Store at -20°C
solubility DMSO: 50 mg/mL (144.13 mM)
FDA UNII TIW15Q5R21

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501

10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 5.00500 MALT1InhibitorII,MepazineHydrochloride-CAS2975-36-2-Calbiochem 2975-36-2 25mg $233 2023-01-07 Buy
ChemScene CS-0111531 Mepazine(hydrochloride) 98.29% 2975-36-2 100mg $255 2021-12-16 Buy
ChemScene CS-0111531 Mepazine(hydrochloride) 98.29% 2975-36-2 250mg $455 2021-12-16 Buy
ChemScene CS-0111531 Mepazine(hydrochloride) 98.29% 2975-36-2 25mg $115 2021-12-16 Buy
ChemScene CS-0111531 Mepazine(hydrochloride) 98.29% 2975-36-2 50mg $175 2021-12-16 Buy
Product number Packaging Price Buy
5.00500 25mg $233 Buy
CS-0111531 100mg $255 Buy
CS-0111531 250mg $455 Buy
CS-0111531 25mg $115 Buy
CS-0111531 50mg $175 Buy

10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Chemical Properties,Uses,Production

Originator

Pacatal,Warner Lambert,US,1957

Manufacturing Process

A 500 cc flask equipped with a mechanical stirrer, reflux condenser and a soda-lime tube was filled with 230 cc of absolute xylene, 27.5 g of 1-methyl3-bromomethylpiperidine, 53.3 g of phenothiazine and 14.2 g of finely powdered sodium amide, and the solution was heated under reflux for 6 hours. After cooling water was added and the batch was extracted with ether. As the hydrochloric acid salt of the obtained phenothiazine derivative is difficultly soluble in water, the further processing was carried out by way of the acetate. The etheric solution was extracted several times in a separating funnel with dilute acetic acid. The combined aqueous extracts were basified, extracted with ether, dried with potassium carbonate and, after removal of the ether, distilled in vacuo.
Yield = 64%; boiling point 230°C to 235°C at 4 mm; melting point of hydrochloride is 180°C to 181°C.

Therapeutic Function

Tranquilizer

10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride 10-((1-methylpiperidin-3-yl)methyl)-10H-phenothiazine hydrochloride 10H-Phenothiazine, 10-[(1-methyl-3-piperidinyl)methyl]-,monohydrochloride Mepazine hydrochloride 2975-36-2