22840-03-5

Basic information

• Product Name: H-ASP-TYR-OH
• Synonyms: CHOLECYSTOKININ 26-27 DESULFATED;CHOLECYSTOKININ OCTAPEPTIDE (1-2) (DESULFATED);H-ASP-TYR-OH;ASP-TYR;L-ASPARTIC ACID-L-TYROSINE;aspartyltyrosine
• CAS NO: 22840-03-5
• Molecular Formula: C₁₃H₁₆N₂O₆
• Molecular Weight: 296.28
• Mol File: 22840-03-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 673°Cat760mmHg
• Flash Point: 360.8°C
• Appearance: /
• Density: 1.46g/cm³
• Vapor Pressure: 4.93E-19mmHg at 25°C
• Refractive Index: 1.617
• Storage Temp.: -15°C
• CAS DataBase Reference: H-ASP-TYR-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-ASP-TYR-OH(22840-03-5)
• EPA Substance Registry System: H-ASP-TYR-OH(22840-03-5)

Safety Data

• Hazardous Substances Data: 22840-03-5(Hazardous Substances Data)

Usage

Description

H-ASP-TYR-OH, also known as Aspartate-Tyrosine, is a dipeptide composed of L-aspartic acid and L-tyrosine joined by a peptide linkage. It is a naturally occurring compound that plays a significant role in various biological processes.

Uses

Used in Pharmaceutical Industry:
H-ASP-TYR-OH is used as a pharmaceutical ingredient for its potential therapeutic effects. It has been studied for its potential role in treating various diseases and conditions, including neurological disorders, cardiovascular diseases, and metabolic disorders.
Used in Cosmetic Industry:
H-ASP-TYR-OH is used as an active ingredient in cosmetic products for its skin-protecting and anti-aging properties. It helps to improve skin elasticity, reduce the appearance of fine lines and wrinkles, and promote a more youthful and radiant complexion.
Used in Food and Beverage Industry:
H-ASP-TYR-OH is used as a flavor enhancer and a functional ingredient in food and beverage products. It contributes to the taste and texture of various dishes and beverages, while also providing potential health benefits.
Used in Research and Development:
H-ASP-TYR-OH is used as a research tool in the development of new drugs, therapies, and diagnostic methods. It helps scientists to better understand the mechanisms of various diseases and conditions, and to develop more effective treatments and interventions.

InChI:InChI=1/C13H16N2O6/c14-9(6-11(17)18)12(19)15-10(13(20)21)5-7-1-3-8(16)4-2-7/h1-4,9-10,16H,5-6,14H2,(H,15,19)(H,17,18)(H,20,21)/t9-,10-/m0/s1

Upstream product

• 42406-77-9 L-tyrosine benzyl ester 
• 23124-24-5 N-(O-benzyl-N-benzyloxycarbonyl-L-α-aspartyl)-L-tyrosine benzyl ester