ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >Alanine derivatives >L-beta-Homoalanine hydrochloride

L-beta-Homoalanine hydrochloride

L-beta-Homoalanine hydrochloride Suppliers list
Company Name: Ningbo Chemrio Chemtech Co,.Ltd.  Gold
Tel: 0574-27891269 18667892864
Email: frank.xiaodong@chemriotech.com
Company Name: WuYan Pharmaceutical Technology (Shanghai) Co., Ltd.  Gold
Tel: 18621565901
Email: sales@wuyanpharm.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Shanghai HC Biotech Co., Ltd  
Tel: 021-20227858
Email: sale@hcbiotech.com.cn

L-beta-Homoalanine hydrochloride manufacturers

L-beta-Homoalanine hydrochloride Basic information
Product Name:L-beta-Homoalanine hydrochloride
Synonyms:L-BETA-HOMOALANINE-HCL;L-BETA-HOMOALANINE HYDROCHLORIDE;H-ALA-(C*CH2)OH HCL;H-BETA-HOMOALA-OH HCL;H-BETA-HOALA-OH HCL;(S)-3-AMINOBUTYRIC ACID HYDROCHLORIDE;(S)-B-AMINOBUTYRIC ACID HCL;(S)-BETA-HOMOALANINE HYDROCHLORIDE
CAS:58610-41-6
MF:C4H9NO2.ClH
MW:139.58
EINECS:
Product Categories:Amino Acid Derivatives;Unusual Amino Acids;β-Homo Amino Acids;Beta amino acids
Mol File:58610-41-6.mol
L-beta-Homoalanine hydrochloride Structure
L-beta-Homoalanine hydrochloride Chemical Properties
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Powder
color White to off-white
BRN 4754597
InChIInChI=1/C4H9NO2.ClH/c1-3(5)2-4(6)7;/h3H,2,5H2,1H3,(H,6,7);1H/t3-;/s3
InChIKeyUHYVVUABAWKTJJ-OQFXAWDINA-N
SMILESC(C(=O)O)[C@@H](N)C.Cl |&1:4,r|
CAS DataBase Reference58610-41-6(CAS DataBase Reference)
Safety Information
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
L-beta-Homoalanine hydrochloride Usage And Synthesis
Chemical PropertiesWhite powder
UsesL-beta-Homoalanine hydrochloride is an alanine derivative[1].
Synthesis1. Thermal Michael addition of ethyl (E)-but-2-enoate with benzylamine.
2. Lipase CAL-B is added to catalyze the reaction.
3. The reaction mixture is worked up. The organic phase is washed with sat. NaHCO solution to give an intermediate mixture.
4. An aqueous NaOH solution is added and the mixture is stirred for 16 hours.
5. The aqueous layer is treated with an ion exchanger (Merck-III), eluted with HCl, and evaporated under reduced pressure to yield the hydrochloride salt.
References[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1137. DOI:10.1080/10408398.2012.708368
L-beta-Homoalanine hydrochloride Preparation Products And Raw materials
Tag:L-beta-Homoalanine hydrochloride(58610-41-6) Related Product Information
L(+)-2-Aminobutyric acid Phenprobamate DL-2-Aminobutyric acid EC 2.6.1.2 Folic acid 3-Aminopyridine D-Alanine D-Glucosamine hydrochloride D-2-Aminobutyric acid Ethyl 2-(Chlorosulfonyl)acetate Aminoacetonitrile hydrochloride 4-Aminobutyric acid DL-3-Aminobutyric acid Topotecan hydrochloride Citric acid Aminoguanidine hydrochloride Ascoric Acid r-Amino Butryric Acid