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L-Lysine, L-lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21743-34-0

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21743-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21743-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,4 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21743-34:
(7*2)+(6*1)+(5*7)+(4*4)+(3*3)+(2*3)+(1*4)=90
90 % 10 = 0
So 21743-34-0 is a valid CAS Registry Number.

21743-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-2,6-diaminohexanoyl]amino]hexanoyl]amino]hexanoyl]amino]hexanoyl]amino]hexanoyl]amino]hexanoyl]amino]hexanoyl]amino]hexanoic acid

1.2 Other means of identification

Product number -
Other names L-Lysine,L-lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysyl

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:21743-34-0 SDS

21743-34-0Downstream Products

21743-34-0Relevant academic research and scientific papers

Trypsin-catalyzed Oligomerization of L-Lysine Esters

Aso, Keiichi,Kodaka, Hiroaki

, p. 755 - 758 (2007/10/02)

The oligomerization of L-lysine esters with a free α-amino group was done using trypsin as a catalyst in aqueous media, and some reaction parameters were examined.The pH-dependence of the reaction suggested that aminolysis by the substrate species having non-protonated α- and ε-amino groups was a dominant factor governing the reaction progress.At the beginning of the reaction lysine oligomers containing up to 8 residues were observed, but much of the dimer was accumulated during prolonged incubation due to secondary hydrolysis of highly polymerized products.The reaction yield depends on the ratio of enzyme and substrate; an overall reaction yield higher than 70 percent was attained after 2 hr of reaction when 1,000 mM of L-lysine ethyl ester was treated with 200 μM of trypsin at pH 10.0.The oligomerization was apparently enhanced by an addition of NaCl and by using the longer alkyl esters.

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