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5891-53-2

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5891-53-2 Usage

Uses

H-Glu-Lys-Oh can be used for sustained-release external pharmaceutical composition.

Check Digit Verification of cas no

The CAS Registry Mumber 5891-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5891-53:
(6*5)+(5*8)+(4*9)+(3*1)+(2*5)+(1*3)=122
122 % 10 = 2
So 5891-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H21N3O5/c12-6-2-1-3-8(11(18)19)14-10(17)7(13)4-5-9(15)16/h7-8H,1-6,12-13H2,(H,14,17)(H,15,16)(H,18,19)/t7-,8-/m0/s1

5891-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-2-[(2-amino-4-carboxybutanoyl)amino]hexanoic acid

1.2 Other means of identification

Product number -
Other names GLU-LYS

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:5891-53-2 SDS

5891-53-2Relevant articles and documents

Modelling of prebiotic synthesis and selection of peptides under isothermal conditions and thermal cycling mode

Demina,Kononikhin,Laptev,Khodonov,Nikolaev,Varfolomeev

, p. 422 - 441 (2013/06/27)

The model peptide synthesis from mixtures of amino acids was carried out under the thermal cycling and isothermal modes. The compositions of the obtained mixtures of products and the primary amino acid sequence of the synthesized peptides were determined by Fourier transform ion cyclotron resonance mass spectrometry and tandem mass spectrometry in combination with high-performance liquid chromatography with the application of de novo sequencing of the synthesized products. The processes of abiogenous synthesis of peptides were shown to occur under relatively mild temperature conditions and give a substantially less number of peptides as compared with the possible statistical set. The evolution of the system takes place in the process of the synthesis in solid phase with the disappearance of a series of the most unstable peptides. The selection process with the formation of complementary peptides takes place in peptide synthesis under the thermal cyclic mode.

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