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Benzamide, N-(5-aminopentyl)-, monohydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29833-52-1

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29833-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29833-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,3 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29833-52:
(7*2)+(6*9)+(5*8)+(4*3)+(3*3)+(2*5)+(1*2)=141
141 % 10 = 1
So 29833-52-1 is a valid CAS Registry Number.

29833-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzoyl-1,5-diaminopentane hydrochloride

1.2 Other means of identification

Product number -
Other names N-(5-amino-pentyl)-benzamide, hydrochloride

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:29833-52-1 SDS

29833-52-1Downstream Products

29833-52-1Relevant academic research and scientific papers

KINETICS AND MECHANISM OF ACID HYDROLYSIS OF N-BENZOYL-L-LYSINES

Muzalewski, Feliks,Ciurak, Marek

, p. 931 - 940 (2007/10/02)

Minor differences in acid hydrolysis rates of α- and ε-amide bonds in corresponding N-benzoyl-L-lysines have been found.The reaction is accelerated in the presence of free carboxyl group in the lysine-derivative molecule.The acid dissociation constants KAH of N - and Nε-benzoyl-L-lysines have been determined.Also the substituent effect in benzoyl group on the reaction rate has been examined.A mechanism of the acid hydrolysis of acyl derivatives of lysine is proposed.

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