tybamate

tybamate Suppliers list
Company Name: GIHI CHEMICALS CO.,LIMITED
Tel: +8618058761490
Email: info@gihichemicals.com
Products Intro: Product Name:Tybamate
CAS:4268-36-4
Purity:99 Package:5KG;1KG,25kg
Company Name: LGC Science (Shanghai) Ltd.  
Tel: 17717235263
Email: cindy.yang@lgcgroup.com
Products Intro: Product Name:Tybamate
CAS:4268-36-4
Purity:>99%, 有含量赋值/不确定度, 检测方法: 定量核磁/质量平衡法(HPLC)/水含量/灰分分析/H-NMR/MS/I Package:10mg-500mg
Company Name: Shanghai Hao Zhun Biological Technology Co., Ltd.  
Tel: 15800340161
Email: info@zzsrm.com
Products Intro: Product Name:Tybamate
CAS:4268-36-4
Company Name: Lanospharma Laboratories Co.,Ltd  
Tel: 13440048448
Email: sales@lanospharma.com
Products Intro:
tybamate Basic information
Product Name:tybamate
Synonyms:tybamate;Nospan;Solacen;Solacin;Tybatran;W 713;[2-(aminocarbonyloxymethyl)-2-methyl-pentyl] N-butylcarbamate;[2-(carbamoyloxymethyl)-2-methylpentyl] N-butylcarbamate
CAS:4268-36-4
MF:C13H26N2O4
MW:274.36
EINECS:224-254-9
Product Categories:
Mol File:4268-36-4.mol
tybamate Structure
tybamate Chemical Properties
Melting point 49-51°
Boiling point bp0.06 150-152°
density 1.0790 (rough estimate)
refractive index 1.4365 (estimate)
pka12.80±0.46(Predicted)
Safety Information
Hazardous Substances Data4268-36-4(Hazardous Substances Data)
MSDS Information
tybamate Usage And Synthesis
OriginatorSolacen,Wallace,US,1965
UsesTranquilizer (minor).
DefinitionChEBI: Tybamate is a carbamate ester.
Manufacturing ProcessDiethylmethyl propylmalonate is reacted with LiAlH4, then H2SO4 to give 2- methyl-2-propyl-1,3-propanediol. That is reacted with phosgene in toluene to give the chlorocarbonate which is in turn reacted with butylamine to give N_x0002_butyl-2-methyl-2-propyl-3-hydroxy-propyl carbamate. 22.1 parts of N-butyl-2-methyl-2-propyl-3-hydroxy-propyl carbamate and 9.8 parts of urethane are dissolved in 300 parts of anhydrous xylene in a suitable vessel equipped with an efficient distillation column. Xylene is distilled to remove traces of water from the mixture. 2.3 parts of aluminum isopropylate are added and distillation is continued until substantially the theoretical quantity of ethanol has been distilled at about 78°C. The reaction mixture is then freed from xylene by distillation under reduced pressure. Approximately 100 parts of water are added and the mixture again freed of solvent by distillation under reduced pressure. 100 parts of trichloroethylene are added, the solution filtered to remove insoluble matter and the solution freed of solvent by evaporation. The residual oil is purified by molecular distillation at a pressure of about 0.01 mm. 8.7 parts (35% of theoretical yield) of purified N-butyl-2-methyl-2-propyl-1,3-propanediol dicarbamate are obtained.
Brand nameSolacen (Wallace).
Therapeutic FunctionTranquilizer
tybamate Preparation Products And Raw materials
Tag:tybamate(4268-36-4) Related Product Information
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