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Catalog Number:
04478
CAS Number:
23404-09-3
Ala-Gly-OMe·HCl
Purity:
≥ 98 % (AgNO3)
Documents
$60.39 /1G
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Product Information

Ala-Gly-OMe·HCl, also known as methyl 2-[(2S)-2-aminopropanoyl]amino]acetate hydrochloride, is a valuable compound widely utilized in biochemical research and pharmaceutical applications. This dipeptide derivative features a methyl ester group, enhancing its solubility and stability, making it an excellent choice for various synthesis processes. Researchers often employ Ala-Gly-OMe·HCl in peptide synthesis, particularly in the development of bioactive peptides and as a building block in drug discovery. Its ability to mimic natural peptide structures allows for the exploration of novel therapeutic agents, especially in the fields of oncology and immunology.

The compound's unique properties, such as its favorable reactivity and compatibility with various coupling reagents, make it a preferred choice for peptide coupling reactions. Additionally, its hydrochloride form ensures optimal stability and ease of handling in laboratory settings. With its diverse applications and significant role in advancing peptide-based therapeutics, Ala-Gly-OMe·HCl stands out as a crucial tool for researchers and industry professionals alike.

CAS Number
23404-09-3
Purity
≥ 98 % (AgNO3)
Molecular Formula
C6H12N2O3 · HCl
Molecular Weight
196.63
MDL Number
MFCD00155457
PubChem ID
24201684
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = +17,0 ± 2º (1 % DMF)
Conditions
Conserver à 0-8°C
General Information
CAS Number
23404-09-3
Purity
≥ 98 % (AgNO3)
Molecular Formula
C6H12N2O3 · HCl
Molecular Weight
196.63
MDL Number
MFCD00155457
PubChem ID
24201684
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = +17,0 ± 2º (1 % DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ala-Gly-OMe·HCl is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, which are essential in drug development and biological research.
  • Biochemical Studies: It is used in studies examining protein interactions and enzyme activity, helping researchers understand cellular processes.
  • Drug Formulation: The compound can be incorporated into pharmaceutical formulations, enhancing the stability and efficacy of certain medications.
  • Diagnostic Applications: It plays a role in developing diagnostic tools, particularly in assays that measure enzyme activity or protein levels.
  • Research in Neuroscience: Ala-Gly-OMe·HCl is used in neurochemical studies, aiding in the exploration of neurotransmitter functions and potential therapeutic targets.

Citations