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Product Information

Product Name
4-Methyl-L-phenylalanine
Brand Name
Chem Impex
Product Number
07069
CAS
1991-87-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
151513
IUPAC Name
(2S)-2-amino-3-(4-methylphenyl)propanoic acid
InChI Key
DQLHSFUMICQIMB-VIFPVBQESA-N
SMILES
CC1=CC=C(C=C1)CC@@H(C(=O)O)N

Application

4-Methyl-L-phenylalanine is widely utilized in research focused on

Protein Engineering: This compound is used to create modified proteins with enhanced properties, making it valuable in biotechnology and pharmaceutical development.

Drug Development: It serves as a building block in the synthesis of novel therapeutic agents, particularly in the design of drugs targeting neurological disorders.

Research on Amino Acid Metabolism: Scientists study its effects on metabolic pathways, helping to understand various metabolic disorders and potential treatments.

Biochemical Studies: It is employed in experiments to investigate the structure-function relationship of proteins, aiding in the development of more effective enzymes and catalysts.

Food Industry Applications: This compound can be used to enhance the flavor profile of certain food products, appealing to manufacturers looking for natural flavor enhancers.

References Data Source From Pubchem

Structural insights into two thiamine diphosphate-dependent enzymes and their synthetic applications in carbon–carbon linkage reactions

Publication Name: Nature Chemistry
Publication Date: 2025-05-14
DOI: 10.1038/s41557-025-01822-y

Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory

Publication Name: Microbial Cell Factories
Publication Date: 2021-01-09
DOI: 10.1186/s12934-020-01506-x

Reprogramming the genetic code

Publication Name: Nature reviews. Genetics
Publication Date: 2020-12-14
DOI: 10.1038/s41576-020-00307-7

Reevaluating the Substrate Specificity of the L-Type Amino Acid Transporter (LAT1)

Publication Name: Journal of Medicinal Chemistry
Publication Date: 2018-07-26
DOI: 10.1021/acs.jmedchem.8b01007

Development of Peptide-Based Inhibitors of Amylin Aggregation Employing Aromatic and Electrostatic Repulsion

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2018
DOI: 10.1007/978-1-4939-8630-9_2