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About This Item
Linear Formula:
(CH3)2CHCH(NH2)COOCH3 · HCl
CAS Number:
Molecular Weight:
167.63
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
230-454-7
MDL number:
Beilstein/REAXYS Number:
3912091
Product Name
D-Valine methyl ester hydrochloride, ≥99.0% (AT)
InChI key
KUGLDBMQKZTXPW-NUBCRITNSA-N
InChI
1S/C6H13NO2.ClH/c1-4(2)5(7)6(8)9-3;/h4-5H,7H2,1-3H3;1H/t5-;/m1./s1
SMILES string
Cl.COC(=O)[C@H](N)C(C)C
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
Quality Level
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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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