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Sku CI33615_250_MG
Chem Impex
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Product Information

Product Name
L-2,6-Dimethyltyrosine
Brand Name
Chem Impex
Product Number
33615
CAS
123715-02-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
124247
IUPAC Name
(2S)-2-amino-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid
InChI Key
LSNDLIKCFHLFKO-JTQLQIEISA-N
SMILES
CC1=CC(=CC(=C1CC@@H(C(=O)O)N)C)O

Application

L-2,6-Dimethyltyrosine is widely utilized in research focused on:

Pharmaceutical Development: This compound is often used in the synthesis of novel drugs, particularly in the development of treatments for neurological disorders, due to its structural similarity to natural amino acids.

Protein Engineering: It serves as a valuable building block in the design of proteins with enhanced stability and functionality, making it essential for researchers in biotechnology and synthetic biology.

Biochemical Research: L-2,6-Dimethyltyrosine is employed in studies investigating enzyme activity and protein interactions, helping scientists understand complex biological processes.

Food Industry: Its antioxidant properties make it a candidate for use in food preservation, providing a natural alternative to synthetic preservatives.

Agricultural Applications: The compound is explored for its potential in developing plant growth regulators, which can enhance crop yield and resistance to environmental stressors.

References Data Source From Pubchem

VDAC1-interacting proteins: binding site mapping and their derived peptides induce apoptosis and multifaceted cellular effects

Publication Name: Apoptosis : an international journal on programmed cell death
Publication Date: 2025-09-26
DOI: 10.1007/s10495-025-02185-y

Nociceptin Receptor-Related Agonists as Safe and Non-addictive Analgesics

Publication Name: Drugs
Publication Date: 2023-05-20
DOI: 10.1007/s40265-023-01878-5

Synthesis of 2,6-Dimethyltyrosine-Like Amino Acids through Pinacolinamide-Enabled C–H Dimethylation of 4-Dibenzylamino Phenylalanine

Publication Name: The Journal of Organic Chemistry
Publication Date: 2022-02-09
DOI: 10.1021/acs.joc.1c02527

Analgesic Opioid Ligand Discovery Based on Nonmorphinan Scaffolds Derived from Natural Sources

Publication Name: Journal of Medicinal Chemistry
Publication Date: 2022-01-07
DOI: 10.1021/acs.jmedchem.0c01915