A1879

L-2-Aminobutyric acid

≥99% (titration), suitable for ligand binding assays

• Synonym(s): L-α-Aminobutyric acid
• Empirical Formula (Hill Notation): C₄H₉NO₂
• CAS Number: 1492-24-6
• Molecular Weight: 103.12
• NACRES: NA.26
• PubChem Substance ID: 24890595
• UNSPSC Code: 12352209
• EC Number: 216-083-3
• MDL number: MFCD00064415
• Beilstein/REAXYS Number: 1720935

Properties

• Product Name: L-2-Aminobutyric acid, ≥99% (titration)
• Quality Segment: 200
• assay: ≥99% (titration)
• form: powder
• technique(s): ligand binding assay: suitable
• color: white
• application(s): peptide synthesis
• SMILES string: CC[C@H](N)C(O)=O
• InChI: 1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1
• InChI key: QWCKQJZIFLGMSD-VKHMYHEASA-N

Description

Application

• Targeted metabolomics combined with machine learning to identify and validate new biomarkers for early SLE diagnosis and disease activity.: This study utilizes L-2-aminobutyric acid in targeted metabolomics, enhancing the predictive accuracy for Systemic Lupus Erythematosus (SLE), a crucial development in autoimmune disease diagnostics (Liang J et al., 2024).


• Alcoholamine enhanced fractionation of cellulose from lignocellulosic biomass in ionic liquids.: This research highlights the use of L-2-aminobutyric acid in the process of biomass conversion, offering insights into more efficient biofuel production techniques (Zhu Y et al., 2023).

Safety Information

• pictograms: GHS07
• signalword: Warning
• hcodes: H317
• pcodes: P280
• Hazard Classifications: Skin Sens. 1
• Storage Class: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Faceshields, Gloves