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H-ALA-THR-OH is a dipeptide chemical compound formed by the condensation of the amino acids alanine (ALA) and threonine (THR) through peptide bonds. Alanine, a nonpolar, aliphatic amino acid, and threonine, a polar amino acid with a hydroxyl group, contribute to the unique properties of H-ALA-THR-OH. H-ALA-THR-OH is widely utilized in research and laboratory settings for the synthesis of peptides, proteins, and other biomolecules, and it may hold potential applications in pharmaceuticals due to its role in the structure and function of proteins and enzymes in the human body.

24032-50-6

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24032-50-6 Usage

Uses

Used in Research and Laboratory Settings:
H-ALA-THR-OH is used as a building block for the synthesis of peptides and proteins, facilitating the study of their structure, function, and interactions with other biomolecules.
Used in Pharmaceutical Development:
H-ALA-THR-OH is used as a potential component in the development of pharmaceuticals, leveraging the properties of its constituent amino acids to contribute to the structure and function of proteins and enzymes in the human body.
Used in the Exploration of Biological or Chemical Activities:
The dipeptide nature of H-ALA-THR-OH is utilized for investigating specific biological or chemical activities, potentially leading to novel applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 24032-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,3 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24032-50:
(7*2)+(6*4)+(5*0)+(4*3)+(3*2)+(2*5)+(1*0)=66
66 % 10 = 6
So 24032-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O4/c1-3(8)6(11)9-5(4(2)10)7(12)13/h3-5,10H,8H2,1-2H3,(H,9,11)(H,12,13)

24032-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-2-[[(2S)-2-aminopropanoyl]amino]-3-hydroxybutanoic acid

1.2 Other means of identification

Product number -
Other names L-Ala-L-Thr

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:24032-50-6 SDS

24032-50-6Upstream product

24032-50-6Relevant academic research and scientific papers

Amino Acids and Peptides. III. Synthesis of Model Peptides Related to Cytochrome P-450

Kawasaki, Koichi,Maeda, Mitsuko,Tamura, Hiromi,Ohashi, Sumiko,Yoshimura, Tetsuhiko,Hatayama Etsuji et al.

, p. 1717 - 1723 (2007/10/02)

Various tetra- and pentapeptides with Cys and Ser (Thr, Tyr, His) at the N- and C-terminals, respectively, were synthetized as model peptides of the apoprotein of cytochrome P-450.The optical spectra of synthetic peptide-hemin complexes were measured and the results are discussed.Keywords - cytochrome P-450; synthetic Cys-containing peptide; peptide-hemin complex; optical spectrum of peptide-hemin complex

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