CAS 5959-29-5
:(s)-(+)-2-aminobutyric acid hydrochloride
Description:
(S)-(+)-2-Aminobutyric acid hydrochloride, with the CAS number 5959-29-5, is a chiral amino acid derivative characterized by its specific stereochemistry, which is essential for its biological activity. This compound is a hydrochloride salt of (S)-2-aminobutyric acid, exhibiting a white crystalline appearance and high solubility in water due to the presence of the hydrochloride group. It plays a significant role in various biochemical processes and is often utilized in research and pharmaceutical applications, particularly in the study of neurotransmitter systems and as a potential therapeutic agent. The presence of the amino group (-NH2) and the carboxylic acid group (-COOH) in its structure allows it to participate in various chemical reactions, including peptide bond formation. Additionally, its chirality can influence its interaction with biological receptors, making it an important compound in the field of medicinal chemistry. Proper handling and storage conditions are essential to maintain its stability and efficacy in laboratory settings.
Formula:C4H10ClNO2
InChI:InChI=1/C4H9NO2.ClH/c1-2-3(5)4(6)7;/h3H,2,5H2,1H3,(H,6,7);1H
SMILES:CCC(C(=O)O)N.Cl
Synonyms:- H-2-Abu-OH x HCl
- L-2-Aminobutyric acid hydrochloride
- (S)-2-amino-butyric acid HCL
- 2-Aminobutanoic Acid Hydrochloride (1:1)
- L-2-Aminobutanoic acid hydrochloride
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Found 6 products.
L-2-Aminobutyric acid, HCl
CAS:Formula:C4H10ClNO2Purity:95%Color and Shape:SolidMolecular weight:139.5807(S)-2-Aminobutanoic acid hydrochloride
CAS:<p>(S)-2-Aminobutanoic acid hydrochloride is a non-essential amino acid widely used in biochemical experiments and drug synthesis research.</p>Formula:C4H10ClNO2Purity:99.85%Color and Shape:SolidMolecular weight:139.58(S)-2-Aminobutanoic acid hydrochloride
CAS:(S)-2-Aminobutanoic acid hydrochloridePurity:98%Molecular weight:139.58g/mol(S)-2-Aminobutanoic Acid Hydrochloride
CAS:Controlled Product<p>Applications (S)-2-Aminobutanoic Acid Hydrochloride is an intermediate in the synthesis of Levetiracetam (L331500), which is used as an anticonvulsant.<br>References Gower, A.J., et al.: Eur. J. Pharmacol., 222, 193 (1992); Kasteleijn-Noist Trenite, D.G.A., et al.: Epilepsy Res., 25, 225 (1996); Patsalos, P.N., et al.: Pharmacol. Ther., 85, 77 (2000)<br></p>Formula:C4H10ClNO2Color and Shape:NeatMolecular weight:139.58Homoalanine hydrochloride
CAS:Formula:C4H10ClNO2Purity:97%Color and Shape:SolidMolecular weight:139.58





