DL-2-Aminobutyric acid

Product Details

CAS No:2835-81-6

MF:C4H9NO2

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

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

Supply Capacity:MT

Synonyms:DL-2-AMINOBUTYRIC ACID;DL-2-AMINO-N-BUTYRIC ACID;DL-ALPHA-AMINOBUTYRIC ACID;DL-ALPHA-AMINO-N-BUTYRIC ACID;H-DL-ABU-OH;(+/-)-2-AMINOBUTANOIC ACID;2-AMINOBUTANOIC ACID;2-AMINOBUTYRIC ACID; 2835-81-6; 2-Aminobutyric acid; 2-Aminobutanoic acid; ALPHA-AMINOBUTYRIC ACID; Butyrine; Butanoic acid, 2-amino-; DL-2-Amino-n-butyric acid; AABA; alpha-Amino-n-butyric acid; DL-alpha-Amino-n-butyric acid; Butyric acid, 2-amino-, DL-; 2-AMINO-N-BUTYRIC ACID; NSC3251; 8306QPJ19P; 2-aminobutyric acid, dl; NSC-3251; Homoalanine; CHEBI:35621; DTXSID90862679; butyrine, (+-)-; RefChem:555386; DTXCID30811409; 201-296-6; 220-616-5; DL-2-Aminobutyric acid; H-DL-ABU-OH; Butanoic acid, amino-; 80-60-4; (Phenyl-d5); 2-amino-butyric acid; L-.alpha.-Aminobutyrate; DL-2-Aminobutanoic acid; Butyric acid, 2-amino-; MFCD00008093; L-.alpha.-Aminobutyric acid; DL-.alpha.-Aminobutyric acid; DL-2- AMINOBUTYRIC ACID; L-.alpha.-Amino-n-butyric acid; DL-.alpha.-Amino-n-butyric acid; (R)-Norfluoxetine-d5 Phthalimide; 28805-76-7; M01290; DL-.alpha.-Amino-n-butyric acid (.beta.-form); Butyric acid, 2-amino-, L-; DL-A-Amino-n-Butyric Acid; D-a-aminobutyric acid; L-a-aminobutyric acid; l-2-aminobutanoic acid; 1346617-46-6; UNII-8306QPJ19P; 2-Aminobutyric; NSC-97060; s6203; NSC 3251; EINECS 201-296-6; EINECS 220-616-5; AMINOBUTYRIC ACID,-2-, ALPHA; Butanoic acid, 2-amino-, (.+-.)-; L-2-Aminobutyric aCld; 2-Amino-n-butyric-acid; AI3-15284; d,l-2-aminobutyric acid; DL-alpha-Amino-n-butyric acid (beta-form); dl-alpha-aminobutyric acid; bmse000390; DL-AMINOBUTYRIC ACID; SCHEMBL23958; CHEMBL55242; SCHEMBL597552; SCHEMBL910577; DL-| cent-Aminobutyric acid; orb1680011; orb1705044; orb3023235; orb3141119; SCHEMBL3940973; SCHEMBL5165007; SCHEMBL7350591; AMINOBUTYRIC ACID, ALPHA; .ALPHA.-AMINOBUTYRIC ACID; 2-Aminobutanoic acid, (L)- #; 2-AMINOBUTYRIC ACID, DL-; ALBB-016221; NSC97060; BBL012213; MSK001362; s6330; STL163554; TN9817; AKOS000201117; AKOS016050533; AB00928; CS-W011306; EBC-253059; FA09857; HY-W010590; SB33762; .ALPHA.-AMINOBUTYRIC ACID [MI]; .ALPHA.-AMINOBUTYRIC ACID, DL-; AS-11292; DA-69742; SY005223; A0280; NS00014651; NS00096417; EN300-21289; A-5210; DL-2-Aminobutyric acid, ReagentPlus(R), 99%; T21466; Q285687; DL-2-Aminobutyric acid, puriss., >=99.0% (NT); DL-2-Aminobutyric acid, Vetec(TM) reagent grade, 98%; F8889-0487; L(+)-2-Aminobutyric acid;(S)-(+)-2-Aminobutyric acid; Z104495144; 4D86307C-8B58-428C-BB29-5FE70D44669A

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DL-2-Aminobutyric Acid serves as a versatile non-proteinogenic amino acid and pivotal organic building block across pharmaceutical manufacturing, chemical biology, and advanced fine chemical synthesis. It is extensively utilized as a vital key intermediate in the commercial production and development of pharmaceutical agents, notably in the synthesis route of antitubercular medications such as ethambutol derivatives, novel anticonvulsant and antiepileptic candidates, and targeted central nervous system regulators. In biochemical and peptide engineering, it functions as an essential synthetic tool for incorporating unnatural residues into peptidomimetics, evaluating enzymatic substrate kinetics, and designing chiral auxiliaries. Furthermore, it finds robust applications in agrochemical formulations, custom stereoselective synthesis, and specialized biochemical research, providing high synthetic reactivity and broad process adaptability.