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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

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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

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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’.

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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.

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