Skip to Content
Merck
All Photos(1)

Documents

15528

Sigma-Aldrich

Boc-Val-OH

≥99.0% (T)

Synonym(s):

(S)-2-(Boc-amino)-3-methylbutyric acid, N-(tert-Butoxycarbonyl)-L-valine, Boc-L-valine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)2CHCH(COOH)NHCOOC(CH3)3
CAS Number:
Molecular Weight:
217.26
Beilstein:
1711290
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

Assay

≥99.0% (T)

form

solid

optical activity

[α]20/D −6.2±0.5°, c = 1% in acetic acid

reaction suitability

reaction type: Boc solid-phase peptide synthesis
reaction type: C-H Activation
reagent type: ligand
reaction type: Peptide Synthesis

mp

77-80 °C (lit.)

application(s)

peptide synthesis

functional group

amine
carboxylic acid

SMILES string

CC(C)[C@H](NC(=O)OC(C)(C)C)C(O)=O

InChI

1S/C10H19NO4/c1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h6-7H,1-5H3,(H,11,14)(H,12,13)/t7-/m0/s1

InChI key

SZXBQTSZISFIAO-ZETCQYMHSA-N

Looking for similar products? Visit Product Comparison Guide

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Ye Sheng et al.
International journal of pharmaceutics, 487(1-2), 242-249 (2015-04-19)
Amino acid and dipeptide prodrugs have been developed to examine their potential in enhancing aqueous solubility and permeability as well as to bypass P-glycoprotein (P-gp) mediated cellular efflux of prednisolone. Prodrugs have been synthesized and identified with LC/MS/MS and NMR.

Articles

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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