metixene

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
MDL Number:
MFCD00867717
MOL File:
4969-02-2.mol
MSDS File:
SDS
Last updated:2023-05-04 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)
FDA UNII 32VY6L26ZW
NIST Chemistry Reference Piperidine, 1-methyl-3-(9h-thioxanthen-9-ylmethyl)-(4969-02-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
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 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0009179 METIXENE 95.00% 4969-02-2 5MG $550 2021-12-16 Buy
Product number Packaging Price Buy
API0009179 5MG $550 Buy

metixene Chemical Properties,Uses,Production

Originator

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

Definition

ChEBI: Metixene is a member of thioxanthenes and a member of piperidines. It has a role as an antiparkinson drug, a muscarinic antagonist and a histamine antagonist.

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( 14)Suppliers
Supplier Tel Email Country ProdList Advantage
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49390 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29016 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9116 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 14059 65
Shanghai Yolne Chemical Co., Ltd. 021-62960152 934678158@qq.com China 9906 55
Megchem Co., Ltd. +86 (21) 5471-7132 China 345 58

View Lastest Price from metixene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
metixene USP/EP/BP pictures 2021-07-28 metixene USP/EP/BP
4969-02-2
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
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