Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Alanine derivatives >  AC-BETA-ALA-OH

AC-BETA-ALA-OH

Basic information Safety Supplier Related

AC-BETA-ALA-OH Basic information

Product Name:
AC-BETA-ALA-OH
Synonyms:
  • N-BETA-ACETYL-BETA-ALANINE
  • N-ACETYL-B-ALANINE
  • N-ACETYL-BETA-ALANINE
  • AC-GLY(C*CH2 )-OH
  • ACETYL-BETA-ALANINE
  • AC-BETA-ALA-OH
  • n-acetyl-á-alanine
  • 3-Acetylamino-propionic acid
CAS:
3025-95-4
MF:
C5H9NO3
MW:
131.13
EINECS:
221-185-6
Product Categories:
  • Amino Acids & Derivatives, Metabolites & Impurities
  • Amino Acids
  • Amino Acids & Derivatives
  • Metabolites & Impurities
Mol File:
3025-95-4.mol
More
Less

AC-BETA-ALA-OH Chemical Properties

Melting point:
105-106℃
Boiling point:
392.0±25.0 °C(Predicted)
Density 
1.174
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO, Methanol, Water
form 
Solid
pka
pK1: 4.445 (25°C)
color 
White
CAS DataBase Reference
3025-95-4(CAS DataBase Reference)
More
Less

Safety Information

HS Code 
2924.19.8000
HazardClass 
IRRITANT

MSDS

  • Language:English Provider:ALFA
More
Less

AC-BETA-ALA-OH Usage And Synthesis

Chemical Properties

White Cyrstalline Solid

Uses

Abnormal amino acid metbolite formed in patients with isovaleric acidemia (IVA)

Definition

ChEBI: The N-acetyl derivative of beta-alanine.

Synthesis

108-24-7

107-95-9

3025-95-4

In a 250 mL three-necked flask, 180 mL of chloroform was added as a solvent and 30 g of β-alanine (0.337 mol) and 37.8 g of acetic anhydride (0.371 mol) were added sequentially. The reaction system was heated to 60 °C and the reaction was stirred at this temperature for 5 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) or ninhydrin colorimetry during the reaction until β-alanine was completely converted. Upon completion of the reaction, the reaction mixture was cooled to 4 °C and stirring was continued at this temperature for 1 h to promote product precipitation. Subsequently, the solid product was collected by diafiltration and washed with cold chloroform. The resulting solid was dried to constant weight in a vacuum drying oven to afford 42 g of white crystalline N-acetyl-β-alanine (I) in 95.4% yield. The purity of the product was analyzed by high performance liquid chromatography (HPLC) and was ≥99.3%.

IC 50

Human Endogenous Metabolite

Purification Methods

The β-alanine crystallises from acetone. [King & King J Am Chem Soc 78 1089 1956, Beilstein 4 IV 2526, 2548.]

References

[1] European Journal of Organic Chemistry, 2012, # 29, p. 5774 - 5788,15
[2] European Journal of Organic Chemistry, 2012, # 29, p. 5774 - 5788
[3] Journal of the American Chemical Society, 2017, vol. 139, # 39, p. 13596 - 13599
[4] Patent: CN105461632, 2016, A. Location in patent: Paragraph 0030
[5] Journal of Polymer Science, 11946>124,

AC-BETA-ALA-OHSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com