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Merck
CN

A7627

L-Alanine

≥98% (TLC), suitable for cell culture

Synonym(s):

(S)-2-Aminopropionic acid, L-α-Aminopropionic acid

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About This Item

Empirical Formula (Hill Notation):
C3H7NO2
CAS Number:
56-41-7
Molecular Weight:
89.09
NACRES:
NA.26
PubChem Substance ID:
24891260
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
200-273-8
MDL number:
MFCD00064410
Beilstein/REAXYS Number:
1720248

Key Documents

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Product Name

L-Alanine, ≥98% (TLC)

InChI key

QNAYBMKLOCPYGJ-REOHCLBHSA-N

InChI

1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m0/s1

SMILES string

C[C@H](N)C(O)=O

assay

≥98% (TLC)

form

powder

technique(s)

cell culture | mammalian: suitable

color

, Colorless or White

solubility

H2O: 50 mg/mL, clear, colorless

application(s)

peptide synthesis

Quality Level

200

Gene Information

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

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Application

L-Alanine has been used as a supplement in complete medium for cell culture.

General description

L-Alanine, a non-essential amino acid, is produced enzymatically from L-aspartate using aspartate β-decarboxylase. It is the smallest among all the aminoacids.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000462487
0000462487
0000334045
0000505995
0000505995

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Generation of a defined and uniform population of CNS progenitors and neurons from mouse embryonic stem cells
Bibel M, et al.
Nature Protocols, 2(5), 1034-1034 (2007)
Amino Acid Biosynthesis ? Pathways, Regulation and Metabolic Engineering, 147-152 (2007)
The Prokaryotes: Vol. 6: Proteobacteria: Gamma Subclass, 2663-2679 (2006)
Berg JM
Biochemistry (2002)
Mauro G. Di Pasquale
Amino Acids and Proteins for the Athlete: The Anabolic Edge, 297-297 (2007)
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