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Key Documents

W381829

Sigma-Aldrich

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:
1720248
EC Number:
MDL number:
UNSPSC Code:
12164502
eCl@ss:
32160406
PubChem Substance ID:
Flavis number:
17.002
NACRES:
NA.21

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

Gene Information

human ... CA1(759) , CA2(760)

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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 Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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