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metixene

metixene Structure
CAS No.
4969-02-2
Chemical Name:
metixene
Synonyms
Trest;Tremonil;Tremaril;Methixene;Methixart;60 SJ 1977;Aids-001633;115511-20-1 (3S);115511-21-2 (3R);metixene USP/EP/BP
CBNumber:
CB7918610
Molecular Formula:
C20H23NS
Molecular Weight:
309.47
MOL File:
4969-02-2.mol
MSDS File:
SDS
Modify Date:
2023/5/4 17:34:39

metixene Properties

Melting point <25 °C
Boiling point bp0.07 171-175°
Density 1.118±0.06 g/cm3(Predicted)
pka 9.46±0.10(Predicted)
NIST Chemistry Reference Piperidine, 1-methyl-3-(9h-thioxanthen-9-ylmethyl)-(4969-02-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H410
Precautionary statements  P264-P270-P301+P312-P330-P501-P273-P391-P501
Toxicity LD50 oral in mouse: 430mg/kg

metixene Chemical Properties,Uses,Production

Originator

Tremarit Wander W. Germany,Wander ,W. Germany,1960

Manufacturing Process

To 4.9 g of finely pulverized sodium in 50 ml of absolute benzene add dropwise with stirring 12 g of chlorobenzene in 50 ml of absolute benzene. As soon as the exothermic reaction begins, maintain the temperature by cooling between 30° and 35°C, and continue stirring for 2 to 3 hours. To the resulting phenyl sodium add dropwise 19.8 g of thioxanthene in 120 ml of absolute benzene. The slightly exothermic reaction ceases after about 1 to 1? hours.
To this newly formed 9-thioxanthyl sodium add dropwise, with stirring and cooling, 13.1 g of N-methyl-3-chloromethyl-piperidine in 30 to 40 ml of absolute benzene, then continue stirring at about 25°C for 1? hours, and heat subsequently to 40°C for 1 hour. Decompose the resulting mixture by adding carefully a small amount of water, and then extract the newly formed base from the benzene solution by means of dilute hydrochloric acid. The aqueous hydrochloric solution is made alkaline by adding dilute sodium hydroxide, and the thioxanthene base is isolated by extraction with ether. This results in 22 g of a slightly yellow, viscous base of BP 171° to 175°C/0.07 mm.
The base is acidified with alcoholic hydrochloric acid. Alcohol-ether (1:2) is then added and the hydrochloride salt is crystallized as colorless flakes melting at 211° to 213°C.

Therapeutic Function

Spasmolytic

metixene Preparation Products And Raw materials

Raw materials

Preparation Products

metixene Suppliers

Global( 12)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49374 58 Inquiry
TargetMol Chemicals Inc. United States 38470 58 Inquiry
Amadis Chemical Company Limited 571-89925085 China 131957 58 Inquiry
BOC Sciences 1-631-485-4226; 16314854226 United States 14055 65 Inquiry
Service Chemical Inc. 888-895-6920 Germany 6350 71 Inquiry
Yick-Vic Chemicals & Pharmaceuticals (HK) Ltd (852)2541 2772 China 6206 58 Inquiry
Suchem Pharma Co., Ltd. 86 0577 85505511 13968864715 China 79 50 Inquiry
American Custom Chemicals Corporation 858 201 6118 United States 6820 51 Inquiry
Wonda Science +1 (514) 581-6866 United States 2192 50 Inquiry
ABI Chem United States 380 0 Inquiry
Methixene 1-Methyl-3-(9H-thioxanthen-9-ylmethyl)piperidine 1-Methyl-3-[(thioxanthen-9-yl)methyl]piperidine 60 SJ 1977 9H-Thioxanthene, piperidine deriv. Piperidine, 1-methyl-3-(9H-thioxanthen-9-ylmethyl)- (9CI) Piperidine, 1-methyl-3-(thioxanthen-9-ylmethyl)- (6CI, 7CI, 8CI) Tremaril Tremonil Trest 9-[(1-Methyl-3-piperidinyl)methyl]-9H-thioxanthene 115511-20-1 (3S) 115511-21-2 (3R) 1553-34-0 (Hydrochloride) 1-Methyl-3-(thioxanthen-9-ylmethyl)-1-piperidine 1-Pipecoline, 3-(thioxanthen-9-yl)methyl- 60 Sj 1977 (*hydrochloride*) 9-(1'-Methylpiperidine-3'-methyl)thioxanthene Aids-001633 metixene USP/EP/BP Methixart Piperidine, 1-methyl-3-(9H-thioxanthen-9-ylmethyl)- 4969-02-2