W381829

L-Alanine

≥99%

• Sinónimos: (S)-2-Aminopropionic acid, L-α-Aminopropionic acid
• Fórmula empírica (notación de Hill): C₃H₇NO₂
• Número de CAS: 56-41-7
• Peso molecular: 89.09
• FEMA Number: 3818
• Beilstein/REAXYS Number: 1720248
• EC Number: 200-273-8
• MDL number: MFCD00064410
• UNSPSC Code: 12164502
• eCl@ss: 32160406
• PubChem Substance ID: 24901893
• Flavis number: 17.002
• NACRES: NA.21

Propiedades

• biological source: synthetic
• assay: ≥99%
• form: chunks; crystalline powder; powder
• optical activity: [α]20/D +13.5 to +15.5°, c = 10 in 6 M HCl
• solubility: H₂O: soluble 89.1 g/L at 20 °C (completely)
• application(s): flavors and fragrances
• documentation: see Safety & Documentation for available documents
• food allergen: no known allergens
• organoleptic: sweet
• SMILES string: C[C@H](N)C(O)=O
• InChI: 1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m0/s1
• InChI key: QNAYBMKLOCPYGJ-REOHCLBHSA-N
• Gene Information: human ... CA1(759) , CA2(760)

Descripción

Application

• Exposure to synthesized tribromobisphenol A and critical effects: Metabolic pathways, disease signature, and benchmark dose derivation.: This study provides insight into the metabolic pathways and disease signatures associated with exposure to synthesized tribromobisphenol A, emphasizing the critical role of L-alanine in mediating these effects (Kuang et al., 2024).


• Prenylated indole diketopiperazine alkaloids as phosphatase inhibitors from the marine-derived fungus Talaromyces purpureogenus.: Identifies new prenylated indole diketopiperazine alkaloids from Talaromyces purpureogenus that act as potent phosphatase inhibitors, with L-alanine being key to their structure and bioactivity, offering potential for drug development (Liang et al., 2024).

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)