medrylamine

medrylamine Structure
CAS No.
524-99-2
Chemical Name:
medrylamine
Synonyms
Histaphene;medrylamine;Postafen Salve;2-(4-Methoxy-α-phenylbenzyloxy)-N,N-dimethylethanamine;2-[(4-methoxyphenyl)-phenyl-methoxy]ethyl-dimethyl-amine;2-[(4-methoxyphenyl)-phenylmethoxy]-N,N-dimethylethanamine;Ethanamine, 2-[(4-methoxyphenyl)phenylmethoxy]-N,N-dimethyl-;2-[(4-methoxyphenyl)-phenyl-methoxy]-N,N-dimethyl-ethanamine;2-((4-Methoxyphenyl)(phenyl)methoxy)-n,n-dimethylethan-1-amine
CBNumber:
CB8936497
Molecular Formula:
C18H23NO2
Molecular Weight:
285.38
MOL File:
524-99-2.mol
Modify Date:
2023/5/4 17:34:39

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

medrylamine Chemical Properties,Uses,Production

Originator

Medrylamine,Shanghai Lansheng Corporation

Manufacturing Process

A 116 parts by weight of phenyl-p-methoxy-chloromethane (4- methoxybenzhydryl chloride) were added to 500 parts by weight of toluene and to the resulting mixture 65 parts by weight of 2-dimethylaminoethanol was added. Then the entire mixture was refluxed for two hours. The refluxed mixture was cooled and 250 parts by weight of a 10% solution of sodium hydroxide were added. This alkaline mixture was then steam distilled until the distillate was only weakly alkaline, for example a pH 7.5-8.
The residue of this steam distillation was then mixed with 200 parts by weight of benzene and washed with water until the wash waters were practically neutral. The benzene solution was then evaporated to dryness until the resulting mixture was of constant weight (145 parts). This product was oily and was then dissolved in 3000 parts by weight of dry ether; and treated while being agitated with the theoretically equivalent amount of dry hydrochloric acid dissolved in ether. This product is an oily product, which solidified after standing overnight in an ice box. The ether solution was decanted off and the solidified residue was dissolved in 1500 parts by weight of dioxane, and then precipitated with 3000 parts by weight of ether while being continuously agitated. The resulting solid product was the hydrochloride of 2-(p-methoxy-α-phenylbenzyloxy)-N,N-dimethylethylamine 100 parts by weight of the desired product were obtained corresponding to a yield of 62% and having a melting point of 141°C.

Therapeutic Function

Antihistaminic

medrylamine Preparation Products And Raw materials

medrylamine 2-(4-Methoxy-α-phenylbenzyloxy)-N,N-dimethylethanamine Histaphene Postafen Salve 2-[(4-methoxyphenyl)-phenyl-methoxy]ethyl-dimethyl-amine 2-[(4-methoxyphenyl)-phenyl-methoxy]-N,N-dimethyl-ethanamine 2-[(4-methoxyphenyl)-phenylmethoxy]-N,N-dimethylethanamine Ethanamine, 2-[(4-methoxyphenyl)phenylmethoxy]-N,N-dimethyl- 2-((4-Methoxyphenyl)(phenyl)methoxy)-n,n-dimethylethan-1-amine 524-99-2