Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

94665

Sigma-Aldrich

D-Valine methyl ester hydrochloride

≥99.0% (AT)

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

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

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCD9369
BCBQ5962V
BCBF1007V
1394012
1357976

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service