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Catalog Number:
03943
CAS Number:
3744-87-4
Boc-DL-alanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-DL-Ala-OH
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Product Information

Boc-DL-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyloxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Researchers often employ Boc-DL-alanine in the preparation of peptides, where it serves as a key building block due to its ability to facilitate selective reactions while protecting the amino group. Its unique properties allow for efficient coupling reactions, leading to high yields and purity in peptide products.

In addition to its role in peptide synthesis, Boc-DL-alanine is also valuable in the development of drug candidates and in the study of biological processes. Its structural characteristics enable it to mimic natural amino acids, making it a useful tool in the design of enzyme inhibitors and other bioactive compounds. The compound's compatibility with various coupling reagents and its ease of deprotection further enhance its utility in research and industrial applications, providing a reliable option for chemists and researchers seeking to streamline their synthesis processes.

Synonyms
Boc-DL-Ala-OH
CAS Number
3744-87-4
Purity
≥ 99% (HPLC)
Molecular Formula
C8H15NO4
Molecular Weight
189.2
MDL Number
MFCD00063124
PubChem ID
268471
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-DL-Ala-OH
CAS Number
3744-87-4
Purity
≥ 99% (HPLC)
Molecular Formula
C8H15NO4
Molecular Weight
189.2
MDL Number
MFCD00063124
PubChem ID
268471
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a protecting group for amino acids in peptide synthesis, allowing for the selective modification of amino groups without affecting the carboxyl groups.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, particularly in creating prodrugs that enhance bioavailability and reduce side effects.
  • Bioconjugation: Boc-DL-alanine is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules for applications in diagnostics and therapeutics.
  • Research in Neuroscience: This compound is utilized in studies related to neurotransmitter synthesis and metabolism, aiding in the understanding of various neurological conditions.
  • Protein Engineering: It is employed in the modification of proteins to enhance their stability and functionality, which is essential in biotechnology and industrial applications.

Citations