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Sku CI03081_25_G
Chem Impex
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Product Information

Product Name
Na-Benzoyl-L-histidine
Brand Name
Chem Impex
Product Number
03081
CAS
5354-94-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
152263
IUPAC Name
(2S)-2-benzamido-3-(1H-imidazol-5-yl)propanoic acid
InChI Key
AUDPUFBIVWMAED-NSHDSACASA-N
SMILES
C1=CC=C(C=C1)C(=O)NC@@H(CC2=CN=CN2)C(=O)O

Description

Na-Benzoyl-L-histidine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy.

Biochemistry Research: It is used in studies involving enzyme activity and protein interactions, helping researchers understand complex biological processes and develop new therapeutic strategies.

Cosmetic Formulations: The compound is incorporated into skincare products for its potential antioxidant properties, contributing to formulations aimed at reducing skin aging and improving overall skin health.

Food Industry: It acts as a preservative in certain food products, helping to maintain freshness and extend shelf life by inhibiting microbial growth.

Analytical Chemistry: Na-Benzoyl-L-histidine is utilized as a standard in chromatographic techniques, aiding in the accurate analysis of amino acids and peptides in various samples.

References Data Source From Pubchem

Photo-Degradation of Therapeutic Proteins: Mechanistic Aspects

Publication Name: Pharmaceutical Research
Publication Date: 2020-02-03
DOI: 10.1007/s11095-020-2763-8

Photocyclization of diarylethenes: the effect of imidazole on the oxidative photodegradation process

Publication Name: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
Publication Date: 2019-05-15
DOI: 10.1039/c8pp00507a

Relationship between the structure of compounds and the effect of Pluronic L61 on their permeation through lipid membranes

Publication Name: Polymer Science, Series A
Publication Date: 2007-09
DOI: 10.1134/s0965545x07090118

Peptide ozonolysis: Product structures and relative reactivities for oxidation of tyrosine and histidine residues

Publication Name: Journal of The American Society for Mass Spectrometry
Publication Date: 2006-09-01
DOI: 10.1016/j.jasms.2006.05.009