L-2-Aminobutanamide hydrochloride

Product Details

CAS No:7682-20-4

MF:C4H10N2O.HCl

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:MT

Synonyms:(S)-2-Aminobutyramide hydrochloride;2-AMINOBUTYRIC ACID AMIDE HYDROCHLORIDE;H-ALPHA-ABU-NH2 HCL;H-ABU(ALPHA)-NH2 HCL;H-ABU(2)-NH2 HCL;H-ABU-NH2 HCL;L-ALPHA-AMINOBUTYRIC ACID AMIDE HYDROCHLORIDE;L-2-AMINOBUTANAMIDE HCL

Product application:L-2-Aminobutanamide hydrochloride,7682-20-4,(S)-2-Aminobutanamide hydrochloride,L-alpha-Aminobutyramide HCl,(S)-2-Aminobutyramide hydrochloride,Levetiracetam intermediate,Brivaracetam intermediate,Antiepileptic drug building block,Anticonvulsant intermediate,Chiral amino acid amide derivative,Pharmaceutical intermediate CAS 7682-20-4,API synthesis raw material,Pyrrolidone derivative precursor,CNS drug building block,Chiral building block for peptide synthesis,Custom synthesis intermediate,Fine chemical raw material,High chiral purity L-2-aminobutanamide,L-2-Aminobutanamide hydrochloride manufacturer China,CAS 7682-20-4 supplier,Suzhou Health Chemicals pharma intermediates,Levetiracetam intermediate wholesale bulk export

 

L-2-Aminobutanamide hydrochloride serves as an indispensable, high-purity chiral building block and foundational intermediate extensively utilized across the pharmaceutical, central nervous system therapeutics, fine agrochemical, and asymmetric organic synthesis sectors. In the commercial chemical manufacturing of active pharmaceutical ingredients, it functions as the pivotal chiral precursor for synthesizing blockbuster antiepileptic and anticonvulsant therapeutics, most notably Levetiracetam and Brivaracetam; its well-defined (S)-enantiomeric configuration and active functional groups facilitate the precise stereospecific assembly of the 2-pyrrolidone core, ensuring high target binding affinity toward synaptic vesicle glycoprotein 2A (SV2A) for managing focal and generalized epileptic seizures. In medicinal chemistry and neurological drug discovery pipelines, this amino acid amide derivative is widely utilized as a rigid chiral scaffold to design novel neuroprotective agents, peptidomimetics, and enzyme inhibitors. In specialty agricultural chemistry, it is applied in the structural synthesis of bio-selective chiral fungicides and crop protection formulations. Furthermore, in academic and industrial laboratory research, L-2-Aminobutanamide hydrochloride remains a standard chiral reference reagent for investigating stereoselective reaction kinetics and developing novel asymmetric synthetic pathways.