Welcome to LookChem.com Sign In|Join Free

CAS

  • or

686-44-2

Post Buying Request

686-44-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

686-44-2 Usage

Description

H-THR-GLY-OH is a unique tripeptide composed of histidine, threonine, and glycine, with an additional hydroxyl group attached to the glycine molecule. H-THR-GLY-OH leverages the distinct functionalities of its constituent amino acids, which are vital for various biological processes in the human body. Histidine is pivotal for pH regulation and metal ion binding, threonine is essential for protein synthesis, immune function, and nervous system health, and glycine, being the simplest amino acid, contributes to the synthesis of critical molecules like heme and creatine. The hydroxyl group on glycine endows H-THR-GLY-OH with hydrophilic properties, potentially enhancing its solubility in water. The synergistic effect of these amino acids in H-THR-GLY-OH likely imparts it with versatile properties suitable for a range of biological and chemical applications.

Uses

Used in Pharmaceutical Industry:
H-THR-GLY-OH is used as a therapeutic agent for its potential role in modulating biological processes due to the combined effects of its constituent amino acids. The histidine component is particularly beneficial for pH regulation and metal ion binding, which can be crucial in various physiological and pathological conditions.
Used in Cosmetics Industry:
H-THR-GLY-OH is used as a hydrating and skin-conditioning agent, leveraging the hydrophilic nature imparted by the hydroxyl group on glycine. This property may enhance the compound's ability to improve skin moisture retention and overall skin health.
Used in Food and Beverage Industry:
H-THR-GLY-OH is used as a flavor enhancer and nutritional supplement, capitalizing on the taste-modifying properties of histidine and the nutritional benefits of threonine and glycine, which are essential for protein synthesis and various metabolic processes.
Used in Research and Development:
H-THR-GLY-OH serves as a valuable compound in scientific research, particularly in studies focused on the roles of amino acids in biological systems, the development of novel drug delivery systems, and the exploration of peptide-based therapeutics.
Each application of H-THR-GLY-OH is underpinned by the unique combination of its amino acid components and the hydroxyl group, which together confer a range of beneficial properties that can be harnessed across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 686-44-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 686-44:
(5*6)+(4*8)+(3*6)+(2*4)+(1*4)=92
92 % 10 = 2
So 686-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O4/c1-3(9)5(7)6(12)8-2-4(10)11/h3,5,9H,2,7H2,1H3,(H,8,12)(H,10,11)

686-44-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name H-THR-GLY-OH

1.2 Other means of identification

Product number -
Other names L-Threonyl-glycin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:686-44-2 SDS

686-44-2Relevant articles and documents

Total Synthesis of Bovine Pancreatic Ribonuclease A. Part 3. Synthesis of the Protected Hexapentacontapeptide Ester (Positions 69-124)

Fujii, Nobutaka,Yajima, Haruaki

, p. 804 - 810 (2007/10/02)

Commencing with the protected hexatriacontapeptide, corresponding to the sequence of bovine pancreatic RNase A, Z(OMe)-(RNase 89-124)-OBzl, chain elongation was carried out to the hexapentacontapeptide stage, Z(OMe)-(RNase 69-124)-OBzl, by six successive

Syntheses of ophthalmic acid and its analogues.

Ogata,Ishii

, p. 707 - 710 (2007/10/05)

-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 686-44-2