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Sku CI01322_1_KG
Chem Impex
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Product Information

Product Name
Boc-L-alanine
Brand Name
Chem Impex
Product Number
01322
CAS
15761-38-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
85082
IUPAC Name
(2S)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoic acid
InChI Key
QVHJQCGUWFKTSE-YFKPBYRVSA-N
SMILES
CC@@H(C(=O)O)NC(=O)OC(C)(C)C

Description

Boc-L-alanine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing researchers to selectively modify amino acids without affecting others, which is crucial for creating complex proteins.

Drug Development: Boc-L-alanine is often used in the development of pharmaceutical compounds, particularly in designing new drugs that target specific biological pathways, enhancing efficacy and reducing side effects.

Biotechnology: In the field of biotechnology, it is employed in the production of recombinant proteins, aiding in the development of vaccines and therapeutic proteins that are vital for treating various diseases.

Research in Neuroscience: This chemical is utilized in studies related to neurotransmitter function, helping researchers understand the role of amino acids in brain chemistry and their implications for mental health.

Food Industry Applications: Boc-L-alanine can also be used in food science for flavor enhancement and as a building block in the synthesis of food additives, improving taste and nutritional value.

References Data Source From Pubchem

Crosslinking, salt-induced aging, and secondary structure formation in Peptide-containing coacervates inspired by spider silk

Publication Name: Communications Chemistry
Publication Date: 2025-08-28
DOI: 10.1038/s42004-025-01634-8

Rapid and practical synthesis of N-protected amino ketones in continuous flow via pre-deprotonation protocol

Publication Name: Journal of Flow Chemistry
Publication Date: 2024-09-18
DOI: 10.1007/s41981-024-00336-x

Synthesis of a highly thermostable insulin by phenylalanine conjugation at B29 Lysine

Publication Name: Communications Chemistry
Publication Date: 2024-07-23
DOI: 10.1038/s42004-024-01241-z

Exploitation of pyrazole C-3/5 carbaldehydes towards the development of therapeutically valuable scaffolds: a review

Publication Name: Chemical Papers
Publication Date: 2024-05-31
DOI: 10.1007/s11696-024-03534-y

Discovery from Hypericum elatoides and synthesis of hyperelanitriles as α-aminopropionitrile-containing polycyclic polyprenylated acylphloroglucinols

Publication Name: Communications Chemistry
Publication Date: 2024-01-02
DOI: 10.1038/s42004-023-01091-1