🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
08797
CAS Number:
28671-28-5
Leu-Gly-NH2·HBr
Purity:
≥ 99% (TLC)
Synonym(s):
L-Leucylglycine amide hydrobromide
Documents
$86.23 /250MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Leu-Gly-NH2·HBr, also known as Leucylglycine hydrobromide, 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 for its potential use in peptide synthesis and as a building block for more complex molecules. Its unique structure allows it to serve as a substrate in enzymatic reactions, making it a valuable tool for researchers exploring protein interactions and metabolic pathways.

In addition to its applications in research, Leu-Gly-NH2·HBr is also utilized in the development of peptide-based therapeutics, where its stability and solubility enhance the efficacy of drug formulations. The hydrobromide salt form improves its handling and storage properties, making it easier for professionals to incorporate into their workflows. With its diverse applications in both academic and industrial settings, Leu-Gly-NH2·HBr stands out as a versatile compound that can significantly contribute to advancements in peptide research and development.

Synonyms
L-Leucylglycine amide hydrobromide
CAS Number
28671-28-5
Purity
≥ 99% (TLC)
Molecular Formula
C8H17N3O2·HBr
Molecular Weight
268.15
MDL Number
MFCD00190943
PubChem ID
91976726
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
L-Leucylglycine amide hydrobromide
CAS Number
28671-28-5
Purity
≥ 99% (TLC)
Molecular Formula
C8H17N3O2·HBr
Molecular Weight
268.15
MDL Number
MFCD00190943
PubChem ID
91976726
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Leu-Gly-NH2·HBr is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, which are crucial for developing new drugs and therapies in pharmaceuticals.
  • Biochemical Studies: It is used in studies examining protein interactions and enzyme functions, providing insights into cellular processes and disease mechanisms.
  • Nutrition and Dietary Supplements: Leu-Gly-NH2·HBr can be incorporated into supplements aimed at enhancing muscle recovery and growth, appealing to athletes and fitness enthusiasts.
  • Cosmetic Formulations: The compound is included in skincare products for its potential to promote skin health and hydration, making it attractive for cosmetic manufacturers.
  • Research in Neurobiology: It is explored for its effects on neurotransmitter activity, which can lead to advancements in treatments for neurological disorders.

Citations