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94665

Sigma-Aldrich

D-Valine methyl ester hydrochloride

≥99.0% (AT)

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About This Item

Linear Formula:
(CH3)2CHCH(NH2)COOCH3 · HCl
CAS Number:
7146-15-8
Molecular Weight:
167.63
Beilstein/REAXYS Number:
3912091
EC Number:
230-454-7
MDL number:
MFCD00237309
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57653635
NACRES:
NA.22

Quality Level

100

assay

≥99.0% (AT)

form

crystals

optical activity

[α]20/D −15.5±2°, c = 2% in H2O

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

SMILES string

Cl.COC(=O)[C@H](N)C(C)C

InChI

1S/C6H13NO2.ClH/c1-4(2)5(7)6(8)9-3;/h4-5H,7H2,1-3H3;1H/t5-;/m1./s1

InChI key

KUGLDBMQKZTXPW-NUBCRITNSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

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
BCCD9369
BCBQ5962V
BCBF1007V
1394012
1357976

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Jan Labuta et al.
Nature communications, 4, 2188-2188 (2013-07-19)
Enantiomeric excess of chiral compounds is a key parameter that determines their activity or therapeutic action. The current paradigm for rapid measurement of enantiomeric excess using NMR is based on the formation of diastereomeric complexes between the chiral analyte and

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