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Catalog Number:
08280
CAS Number:
71431-66-8
Ala-Gly- NH2 ·HCl
Purity:
≥ 99 % (TLC)
Synonym(s):
Clorhidrato de L-alanil glicina amida
Documents
$176.76 /100 mg
Tamaño
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Product Information

Ala-Gly-NH2·HCl, also known as L-Alanylglycine hydrochloride, is a dipeptide derivative that plays a significant role in various biochemical applications. This compound is particularly valued in the fields of pharmaceuticals and biochemistry due to its ability to act as a building block for peptide synthesis. Its unique structure allows it to participate in the formation of more complex peptides, making it an essential component in drug development and research. Researchers often utilize Ala-Gly-NH2·HCl in studies related to protein synthesis, enzyme activity, and metabolic pathways, providing insights into cellular functions and therapeutic potentials.

In addition to its applications in research, Ala-Gly-NH2·HCl is also explored for its potential benefits in nutritional supplements and functional foods. Its properties may contribute to improved muscle recovery and overall health, appealing to both athletes and health-conscious consumers. The compound’s stability and solubility in aqueous solutions further enhance its usability in various formulations. With its diverse applications and benefits, Ala-Gly-NH2·HCl stands out as a valuable asset for researchers and industry professionals alike.

Synonyms
Clorhidrato de L-alanil glicina amida
CAS Number
71431-66-8
Purity
≥ 99 % (TLC)
Molecular Formula
C5H11N3O2 · HCl
Molecular Weight
181.62
MDL Number
MFCD00190742
PubChem ID
137704984
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
Synonyms
Clorhidrato de L-alanil glicina amida
CAS Number
71431-66-8
Purity
≥ 99 % (TLC)
Molecular Formula
C5H11N3O2 · HCl
Molecular Weight
181.62
MDL Number
MFCD00190742
PubChem ID
137704984
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

Ala-Gly-NH2·HCl is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, which are crucial in developing pharmaceuticals and biotechnological products.
  • Biochemical Research: It is used in studies involving enzyme activity and protein interactions, helping researchers understand biological processes at a molecular level.
  • Drug Development: The compound plays a role in the formulation of new drugs, particularly those targeting metabolic disorders, enhancing therapeutic efficacy.
  • Cell Culture Applications: Ala-Gly-NH2·HCl is utilized in cell culture media to support the growth of various cell lines, aiding in cancer research and regenerative medicine.
  • Diagnostics: It can be employed in diagnostic assays, improving the accuracy of tests for certain diseases by acting as a reagent in biochemical assays.

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