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Chem Impex
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Product Information

Product Name
N-Methyl-L-valine hydrochloride
Brand Name
Chem Impex
Product Number
02677
CAS
2480-23-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
444080
IUPAC Name
(2S)-3-methyl-2-(methylamino)butanoic acid
InChI Key
AKCRVYNORCOYQT-YFKPBYRVSA-N
SMILES
CC(C)C@@H(C(=O)O)NC

Application

N-Methyl-L-valine hydrochloride is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of peptide-based drugs, enhancing their stability and bioactivity.

Pharmaceutical Development: It plays a crucial role in drug formulation, especially in creating compounds that target specific biological pathways, which can lead to more effective treatments with fewer side effects.

Biochemical Research: Researchers use it to study protein interactions and enzyme activities, providing insights into metabolic processes and potential therapeutic targets.

Cosmetic Applications: The compound is also explored in cosmetic formulations for its potential to improve skin hydration and elasticity, making it a promising ingredient in skincare products.

Amino Acid Studies: It is utilized in academic and industrial research to investigate the properties of amino acids and their derivatives, contributing to advancements in nutrition and dietary supplements.

References Data Source From Pubchem

Comparative metabolomics reveals specific metabolic signatures in colorectal cancer cell line models

Publication Name: Discover Oncology
Publication Date: 2025-12-02
DOI: 10.1007/s12672-025-04183-7

Structure-informed design of an ultrabright RNA-activated fluorophore

Publication Name: Nature Chemistry
Publication Date: 2025-05-28
DOI: 10.1038/s41557-025-01832-w

Hazard characterization of the mycotoxins enniatins and beauvericin to identify data gaps and improve risk assessment for human health

Publication Name: Archives of Toxicology
Publication Date: 2025-03-26
DOI: 10.1007/s00204-025-03988-3

Mechanistic and enantioselectivity analysis of amino acid-catalyzed asymmetric aldol reactions: a theoretical study

Publication Name: Reaction Kinetics, Mechanisms and Catalysis
Publication Date: 2025-01-13
DOI: 10.1007/s11144-025-02799-y

Advancements in Microbioreactor Technology: High-Throughput Cultivation and Peptide Profiling in Microbial Research

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2025
DOI: 10.1007/978-1-0716-4562-8_11