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Methyl 4-aminobutyrate hydrochloride

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CAS:13031-60-2
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Methyl 4-aminobutyrate hydrochloride manufacturers

  • L-4-Abu-Ome.Hcl
  • L-4-Abu-Ome.Hcl pictures
  • $0.00 / 1kg
  • 2026-04-24
  • CAS:13031-60-2
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
Methyl 4-aminobutyrate hydrochloride Basic information
Product Name:Methyl 4-aminobutyrate hydrochloride
Synonyms:4-aminobutanoic acid methyl ester hydrochloride;L-γ-Abu-OMe·HCl;Methyl 4-aminobutyrate hydrochloride≥ 99%(Titration);butyricacid,4-amino-,methylester,hydrochloride;4-AMINO-N-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE;4-AMINOBUTYRIC ACID METHYL ESTER, HYDROCHLORIDE;4-METHOXY-4-OXOBUTAN-1-AMINIUM CHLORIDE;METHYL 4-AMINOBUTANOATE HYDROCHLORIDE
CAS:13031-60-2
MF:C5H12ClNO2
MW:153.61
EINECS:629-526-4
Product Categories:Others;Peptide Synthesis;Unnatural Amino Acid Derivatives;bc0001
Mol File:13031-60-2.mol
Methyl 4-aminobutyrate hydrochloride Structure
Methyl 4-aminobutyrate hydrochloride Chemical Properties
Melting point 120-125 °C(lit.)
storage temp. Inert atmosphere,Room Temperature
form powder to crystal
color White to Almost white
BRN 3558996
Major Applicationpeptide synthesis
InChIInChI=1S/C5H11NO2.ClH/c1-8-5(7)3-2-4-6;/h2-4,6H2,1H3;1H
InChIKeyWPGPRLVPWACBHW-UHFFFAOYSA-N
SMILESC(=O)(OC)CCCN.Cl
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37
WGK Germany 3
RTECS ES7065000
3
HazardClass IRRITANT
HS Code 2922498590
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
Methyl 4-aminobutyrate hydrochloride Usage And Synthesis
Chemical PropertiesWhite crystalline powder
UsesMethyl 4-aminobutyrate, HCl
reaction suitabilityreaction type: solution phase peptide synthesis
Synthesis
Methanol

67-56-1

4-Aminobutyric acid

56-12-2

Methyl 4-aminobutyrate hydrochloride

13031-60-2

GENERAL METHOD: Thionyl chloride (20 mmol) was added slowly and dropwise to a 20 mL methanol solution of gamma-aminobutyric acid (10 mmol) under ice bath conditions. The reaction mixture was stirred at room temperature for about 2 h before the solvent was removed by rotary evaporator to give methyl 4-aminobutyrate hydrochloride (11a). The product was a white solid in 96.0% yield.1H NMR (400 MHz, D2O) δ 3.46 (s, 3H), 2.79 (t, J = 7.6 Hz, 2H), 2.28 (t, J = 7.3 Hz, 2H), 1.77-1.67 (m, 2H).ESI-MS analysis showed that the calculated value of [M + H-HCl]+ m/z was 118.1 and the measured value was 118.1.

References[1] Journal of Medicinal Chemistry, 1984, vol. 27, # 10, p. 1263 - 1267
[2] Synthetic Communications, 1998, vol. 28, # 3, p. 471 - 474
[3] Tetrahedron Letters, 2005, vol. 46, # 47, p. 8137 - 8140
[4] Chemistry - A European Journal, 2012, vol. 18, # 18, p. 5767 - 5776
[5] Journal of Medicinal Chemistry, 2006, vol. 49, # 20, p. 6094 - 6103
Methyl 4-aminobutyrate hydrochloride Preparation Products And Raw materials
Raw materials4-[[(1,1-dimethylethoxy)carbonyl]amino]Butanoic acid methyl ester
Tag:Methyl 4-aminobutyrate hydrochloride(13031-60-2) Related Product Information
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