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Sku CI06163_1_G
Chem Impex
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Product Information

Product Name
4-Bromo-DL-phenylalanine
Brand Name
Chem Impex
Product Number
06163
CAS
14091-15-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
85681
IUPAC Name
2-amino-3-(4-bromophenyl)propanoic acid
InChI Key
PEMUHKUIQHFMTH-UHFFFAOYSA-N
SMILES
C1=CC(=CC=C1CC(C(=O)O)N)Br

Application

4-Bromo-DL-phenylalanine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a building block in the synthesis of novel pharmaceuticals, particularly in the development of drugs targeting neurological disorders.

Biochemical Research: It is used to study the effects of brominated amino acids on protein function and enzyme activity, providing insights into metabolic pathways.

Neuroscience Studies: Researchers employ this compound to investigate its role as a neurotransmitter precursor, aiding in the understanding of brain chemistry and potential treatments for mental health conditions.

Analytical Chemistry: It is utilized in the development of analytical methods for detecting and quantifying amino acids in biological samples, enhancing the accuracy of biochemical assays.

Food Industry Applications: The compound is explored for its potential use as a flavor enhancer or additive, contributing to the development of new food products with improved taste profiles.

References

Nontargeted Metabolomics Using the Sciex ZenoTOF 7600

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2025
DOI: 10.1007/978-1-0716-4534-5_1

High-throughput identification of gut microbiome-dependent metabolites

Publication Name: Nature Protocols
Publication Date: 2024-05-13
DOI: 10.1038/s41596-024-00980-6

A Ratio Fluorescence Method Based on Dual Emissive Copper Nanoclusters for the Detection of Vanillin

Publication Name: Journal of Fluorescence
Publication Date: 2024-01-17
DOI: 10.1007/s10895-024-03582-3

Aldehyde-catalysed carboxylate exchange in α-amino acids with isotopically labelled CO2

Publication Name: Nature Chemistry
Publication Date: 2022-11-07
DOI: 10.1038/s41557-022-01074-0

Approaches to α-Amino Acids Based on Deracemization and Stereoinversion

Publication Name: Science of Synthesis
Publication Date: 2019