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860271

Sigma-Aldrich

L-Valine methyl ester hydrochloride

99%

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Synonym(s):
(S)-Valine methyl ester hydrochloride, Methyl (S)-2-amino-3-methylbutanoate hydrochloride
Linear Formula:
(CH3)2CHCH(NH2)COOCH3 · HCl
CAS Number:
6306-52-1
Molecular Weight:
167.63
Beilstein:
3594960
EC Number:
228-620-9
MDL number:
MFCD00012497
eCl@ss:
32160406
PubChem Substance ID:
24888503

Assay

99%

form

crystals

optical activity

[α]/D +15°, c = 2 in H2O

reaction suitability

reaction type: solution phase peptide synthesis

mp

171-173 °C (lit.)

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-;/m0./s1

InChI key

KUGLDBMQKZTXPW-JEDNCBNOSA-N

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Related Categories

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

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Beibei Hu et al.
International journal of pharmaceutics, 547(1-2), 637-647 (2018-06-23)
Thermogels, used as multi-functional drug-loading materials, have properties that mainly rely on their gelator structure. Although a large variety of organogel systems are used as drug delivery carriers, relatively few have been investigated in terms of their structure-property correlations based
Sonu Kumar et al.
Macromolecular bioscience, 20(6), e2000048-e2000048 (2020-04-15)
The synthesis and self-assembly of peptide-polymer conjugates into fibrillar nanostructures are reported, based on the amyloidogenic peptide KLVFF. A strategy for rational synthesis of polymer-peptide conjugates is documented via tethering of the amyloidogenic peptide segment LVFF (Aβ17-20 ) and its
Griet Van Zeebroeck et al.
Nature chemical biology, 5(1), 45-52 (2008-12-09)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

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