W381829
L-Alanine
≥99%
Synonym(s):
(S)-2-Aminopropionic acid, L-α-Aminopropionic acid
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About This Item
Empirical Formula (Hill Notation):
C3H7NO2
CAS Number:
Molecular Weight:
89.09
FEMA Number:
3818
Beilstein/REAXYS Number:
1720248
EC Number:
MDL number:
UNSPSC Code:
12164502
eCl@ss:
32160406
PubChem Substance ID:
Flavis number:
17.002
NACRES:
NA.21
Recommended Products
biological source
synthetic
Quality Level
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
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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.
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)
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Vancomycin resistance in Gram-positive bacteria is due to production of cell-wall precursors ending in D-Ala-D-Lac or D-Ala-D-Ser, to which vancomycin exhibits low binding affinities, and to the elimination of the high-affinity precursors ending in D-Ala-D-Ala. Depletion of the susceptible high-affinity
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