CAS 107-95-9|Beta-Alanine|3-aminopropanoic acid|β-alanine|β-ALANINE|3-Aminopropanoic acid|bAla|3-Aminopropionic acid|β-Ala|β-丙氨酸|β alanine|3-氨基丙酸|β-Ala|β-Alanine|3-Aminopropano...

InChI=1S/C3H7NO2/c4-2-1-3(5)6/h1-2,4H2,(H,5,6)

UCMIRNVEIXFBKS-UHFFFAOYSA-N

LogD (pH = 7.4)

-3.17

LogD (pH = 5.5)

-3.19

Log P

-3.17

Rotatable Bonds

H Donor

H Acceptors

Lipinski's Rule of Five

true

Acid pKa

4.08

Polar Surface Area

63.32

Polarizability

8.61

Molar Refractivity

20.70

LOG S

0.73

Beta-Alanineβ-ALANINE3-Aminopropanoic acid3-Aminopropionic acidβ-Alaβ-丙氨酸3-氨基丙酸β-Alaβ-Alanine3-Aminopropanoic acidβ-Alanineβ-Aminopropionic AcidAbufeneβ-Aminopropanoic Acidω-Aminopropionic Acidβ-AlanineNSC 76032-CarboxyethylamineH-beta-Ala-OHbeta-Alaninebeta-alaninebeta-Alanine3-aminopropanoic acidomega-aminopropionic acidH-beta-Ala-OHbAlabeta-aminopropionic acid3-Aminopropionic acidBETA-ALANINE

3-aminopropanoic acid

IUPAC Traditional name

β-alanine bAla β alanine

Unique Ingredient Identifier

MetaboLights Database

PubMed Citation Links

BRENDA Ligand Database

VirtualMetabolicHuman Database

Pharmacology Properties

no known allergens

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• Xia, J.-F. et al.: J. Chrom. B Anal. Technol. Biomed. Life Sci., 977, 1930 (2007)

• Artioli, G.G. et al.: Med. Sci. Sports Exer.,42, 1162 (2007)

• Derave, W. et al.: J. Appl. Physiol., 103, 1736 (2007)

• Effective catalyst for the Knoevenagel condensation, for example of ethyl cyanoacetate with 2-butanone: Org. Synth. Coll., 4, 93 (1963), and of malononitrile with various substrates, where stronger bases would cause self-condensation of the nitrile: J. Org. Chem., 38, 1512 (1973); Synthesis, 669 (1974).

Names and Identifiers

Synonyms

IUPAC name

3-aminopropanoic acid

IUPAC Traditional name

β-alanine bAla β alanine

References

PubChem Literature

From Data Sources

• Xia, J.-F. et al.: J. Chrom. B Anal. Technol. Biomed. Life Sci., 977, 1930 (2007)

• Artioli, G.G. et al.: Med. Sci. Sports Exer.,42, 1162 (2007)

• Derave, W. et al.: J. Appl. Physiol., 103, 1736 (2007)

Bioactivity

PubChem BioAssay

Room Temperature (15-30°C)

Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter

1.437 g/cm³ (19 °C)

1.437

fruity; sweet

German water hazard class

Personal Protective Equipment

Molecule Details

DrugBank

DB03107

Drug Groups

experimental

Description

An amino acid formed in vivo by the degradation of dihydrouracil and carnosine. Since neuronal uptake and neuronal receptor sensitivity to beta-alanine have been demonstrated, the compound may be a false transmitter replacing GAMMA-AMINOBUTYRIC ACID. A rare genetic disorder, hyper-beta-alaninemia, has been reported. [PubChem]

MP Biomedicals

02100929

Crystalline

02194618

Cell Culture Reagent
Crystalline

05210409

MP Biomedicals Rare Chemical collection

Wikipedia

Beta-Alanine

Sigma Aldrich

239720

Packaging
50 g in glass bottle
Biochem/physiol Actions
β-Alanine, a β-amino acid, is a component of pantothenic acid and the rate-limiting amino acid in the biosynthesis of the histidinyl antioxidant dipeptides carnosine and anserine. Endogenous β-amino acid that is a nonselective agonist at glycine receptors and a ligand for the G protein-coupled orphan receptor, TGR7 (MrgD). β-Alanine flux plays a cytoprotective role by supporting the osmotic stability of marine organisms, preimplantation mouse embryos and mammalian cells exposed to hypoxic stress.

146064

Packaging
2 kg in poly bottle
25, 500 g in poly bottle
Biochem/physiol Actions
β-Alanine, a β-amino acid, is a component of pantothenic acid and the rate-limiting amino acid in the biosynthesis of the histidinyl antioxidant dipeptides carnosine and anserine. Endogenous β-amino acid that is a nonselective agonist at glycine receptors and a ligand for the G protein-coupled orphan receptor, TGR7 (MrgD). β-Alanine flux plays a cytoprotective role by supporting the osmotic stability of marine organisms, preimplantation mouse embryos and mammalian cells exposed to hypoxic stress.

W325201

Packaging
1 kg in poly bottle
1 sample in glass bottle
5, 10 kg in fiber drum
Biochem/physiol Actions
β-Alanine, a β-amino acid, is a component of pantothenic acid and the rate-limiting amino acid in the biosynthesis of the histidinyl antioxidant dipeptides carnosine and anserine. Endogenous β-amino acid that is a nonselective agonist at glycine receptors and a ligand for the G protein-coupled orphan receptor, TGR7 (MrgD). β-Alanine flux plays a cytoprotective role by supporting the osmotic stability of marine organisms, preimplantation mouse embryos and mammalian cells exposed to hypoxic stress.

A7752

TRC

A637320

β-Alanine is a naturally occurring beta amino acid. β-Alanine is formed in vivo by the degradation of dihydrouracil (D449990) and carnosine. β-Alanine is also the rate-limiting precursor of carnosine, as a result supplementation with β-alanine increases t

ChEBI

CHEBI:16958

A naturally-occurring beta-amino acid comprising propionic acid with the amino group in the 3-position.

Biochem/physiol Actions
β-Alanine, a β-amino acid, is a component of pantothenic acid and the rate-limiting amino acid in the biosynthesis of the histidinyl antioxidant dipeptides carnosine and anserine. Endogenous β-amino acid that is a nonselective agonist at glycine receptors and a ligand for the G protein-coupled orphan receptor, TGR7 (MrgD). β-Alanine flux plays a cytoprotective role by supporting the osmotic stability of marine organisms, preimplantation mouse embryos and mammalian cells exposed to hypoxic stress.

A9920

General description
An N-blocked form of alanine.
Packaging
10 mg in autosmp vl
Biochem/physiol Actions
β-Alanine, a β-amino acid, is a component of pantothenic acid and the rate-limiting amino acid in the biosynthesis of the histidinyl antioxidant dipeptides carnosine and anserine. Endogenous β-amino acid that is a nonselective agonist at glycine receptors and a ligand for the G protein-coupled orphan receptor, TGR7 (MrgD). β-Alanine flux plays a cytoprotective role by supporting the osmotic stability of marine organisms, preimplantation mouse embryos and mammalian cells exposed to hypoxic stress.

Molecule

ID:2810