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Catalog Number:
05875
CAS Number:
74863-12-0
Arg-Tyr-OH·AcOH
Purity:
≥ 98% (HPLC)
Synonym(s):
L-Arginyl-L-tyrosine acetate
Documents
$103.56 /100MG
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Product Information

Arg-Tyr-OH·AcOH, also known as Acetyl-Arginine-Tyrosine, 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 in peptide synthesis and as a building block for more complex molecules. Its unique structure allows it to participate in a variety of reactions, making it an essential component in the development of therapeutic agents and research applications.

Researchers and industry professionals utilize Arg-Tyr-OH·AcOH for its ability to enhance the solubility and stability of peptides, which is crucial in drug formulation. Additionally, its role in signaling pathways and cellular functions makes it a valuable candidate for studies related to neurobiology and metabolic processes. The compound's compatibility with various analytical techniques further supports its use in research settings, providing insights into peptide behavior and interactions. With its diverse applications, Arg-Tyr-OH·AcOH stands out as a versatile tool for advancing scientific knowledge and developing innovative solutions in the pharmaceutical industry.

Synonyms
L-Arginyl-L-tyrosine acetate
CAS Number
74863-12-0
Purity
≥ 98% (HPLC)
Molecular Formula
C15H23N5O4·C2H4O2
Molecular Weight
397.43
MDL Number
MFCD00190754
PubChem ID
13017549
Optical Rotation
[a]D24 = +31.5 ± 2º (C=1 in Water)
Conditions
Store at 0-8°C
General Information
Synonyms
L-Arginyl-L-tyrosine acetate
CAS Number
74863-12-0
Purity
≥ 98% (HPLC)
Molecular Formula
C15H23N5O4·C2H4O2
Molecular Weight
397.43
MDL Number
MFCD00190754
PubChem ID
13017549
Optical Rotation
[a]D24 = +31.5 ± 2º (C=1 in Water)
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

Arg-Tyr-OH·AcOH 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 Research: It is used in studies investigating protein interactions and functions, aiding researchers in understanding cellular processes and disease mechanisms.
  • Cosmetic Formulations: The compound finds application in the cosmetic industry, particularly in anti-aging products, due to its potential skin-rejuvenating properties.
  • Drug Development: It plays a role in the formulation of new therapeutic agents, especially in targeting specific biological pathways, enhancing efficacy compared to traditional compounds.
  • Analytical Chemistry: Utilized in various analytical techniques, it helps in the detection and quantification of biomolecules, providing valuable data for research and quality control.

Citations