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N,N''-hexane-1,6-diylbis[N'-benzylurea] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39072-70-3

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39072-70-3 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 39072-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,7 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39072-70:
(7*3)+(6*9)+(5*0)+(4*7)+(3*2)+(2*7)+(1*0)=123
123 % 10 = 3
So 39072-70-3 is a valid CAS Registry Number.

39072-70-3SDS

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 N,N'-bis(benzylcarbamoyl)-1,6-hexamethylenediamine

1.2 Other means of identification

Product number -
Other names N,N''-hexane-1,6-diylbis(N'-benzylurea)

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:39072-70-3 SDS

39072-70-3Downstream Products

39072-70-3Relevant academic research and scientific papers

Detection of nerve agent via perturbation of supramolecular gel formation

Hiscock, Jennifer R.,Piana, Francesca,Sambrook, Mark R.,Wells, Neil J.,Clark, Alistair J.,Vincent, Jack C.,Busschaert, Nathalie,Brown, Richard C. D.,Gale, Philip A.

, p. 9119 - 9121 (2013)

The formation of tren-based tris-urea supramolecular gels in organic solvents is perturbed by the presence of the nerve agent soman providing a new method of sensing the presence of organophosphorus warfare agents.

Synthesis of bis-ureas from Bis(o-nitrophenyl) carbonate

Turoczi, Maria-Cristina,Simon, Monika,Badea, Valentin,Csunderlik, Carol

experimental part, p. 3192 - 3197 (2009/04/10)

A general method for the preparation of bis-ureas from bis(o-nitrophenyl) carbonate has been developed. Directional urea synthesis is achieved by sequential amine addition to bis(o-nitrophenyl) carbonate in two steps: in the first step bis(o-nitrophenyl) carbonate is reacted with benzylamine to form benzyl-o-nitrophenyl carbamate; in the second step the carbamate is reacted with a variety of diamines in toluene to yield bis-ureas.

Di-urea compounds as gelators for organic solvents

Van Esch, Jan,Kellogg, Richard M.,Feringa, Ben L.

, p. 281 - 284 (2007/10/03)

Simple diurea compounds form thermoreversible gels with several organic solvents. These gels are stable up to temperatures of 100°C, and can be stored for months. Electron microscopy reveals that in these solvents the gelation agents assemble into very thin rectangular sheets which are several tens of micrometers long.

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