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87831-94-5

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87831-94-5 Usage

General Description

H-LEU-ALA-NH2 HCL is a chemical compound comprising of the amino acids leucine and alanine that are linked together to form a peptide chain. The "HCL" in its name indicates that it is in the form of a hydrochloride salt. H-LEU-ALA-NH2 HCL is commonly used in biochemical and pharmaceutical research as a building block for the synthesis of peptides and other complex molecules. It is also used in the study of protein structure and function, as well as in the development of new drugs and pharmaceutical products. Additionally, H-LEU-ALA-NH2 HCL may have potential applications in the treatment of various diseases and medical conditions, as it can be modified and engineered to exhibit specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 87831-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,3 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87831-94:
(7*8)+(6*7)+(5*8)+(4*3)+(3*1)+(2*9)+(1*4)=175
175 % 10 = 5
So 87831-94-5 is a valid CAS Registry Number.

87831-94-5SDS

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-LEU-ALA-NH2 HCL

1.2 Other means of identification

Product number -
Other names H-Leu-Ala-NH2*HCl

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:87831-94-5 SDS

87831-94-5Relevant articles and documents

Peptide Synthesis by Means of Immobilized Enzymes II. Immobilized Trypsin, Thermolysin and Papain

Koennecke, Andreas,Haensler, Marion,Schellenberger, Volker,Jakubke, Hans-Dieter

, p. 433 - 444 (1983)

Model studies were performed on the utility of covalently immobilized trypsin, thermolysin and papain for peptide bond formation.Trypsin and thermolysin catalyzed the formation of peptide bonds with nearly the same efficiency as the soluble proteases and they could be re-used successfully for further coupling experiments.The possibility of using immobilized trypsin and papain for kinetically controlled peptide bond formation was investigated.With the serine type enzyme trypsin excellent product yields were obtained starting with ester carboxyl components and an economical ratio of substrates.Experiments with the thiol protease papain were unsatisfactory because the once formed product is hydrolyzed as fact as the starting ester substrate used. - Keywords: Immobilized enzymes; Papain; Peptide synthesis; Thermolysin; Trypsin

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