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1219833-37-0

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1219833-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1219833-37-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,8,3 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1219833-37:
(9*1)+(8*2)+(7*1)+(6*9)+(5*8)+(4*3)+(3*3)+(2*3)+(1*7)=160
160 % 10 = 0
So 1219833-37-0 is a valid CAS Registry Number.

1219833-37-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tri-tert-butyl (((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tris(benzene-4,1-diyl))tricarbamate

1.2 Other means of identification

Product number -
Other names -

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:1219833-37-0 SDS

1219833-37-0Relevant articles and documents

Gelation of a highly fluorescent urea-containing triarylmelamine derivative: 2,4,6-tris(p-N'-octadecylureido-anilino)triazine in organic solvents

Lu, Cheng-Chi,Su, Shuenn-Kung

experimental part, p. 115 - 120 (2010/04/05)

A new gelator of urea-containing triazine derivatives was synthesized and tested in order to explore the gelation potential in different organic solvents. This compound has been found to form organogels with a variety of organic solvents such as decalin and other solvents. The resulting thermo-reversible gel was characterized by using the dropping ball method and a number of other instruments. The melting temperature of the gel increased with the gel concentration. The intermolecular hydrogen bonding of gelation was demonstrated through an FT-IR spectrometer. UV-Vis and fluorescence analysis showed that the gel displayed various optical effects in different organic solvents. The blue fluorescence of the gel in decalin and the quenched effect of gel in CHCl3 were displayed, respectively. Morphological features in decalin and CHCl3 were studied by applying atomic force microscopy (AFM), and the morphological features demonstrated that there were different aggregations in different solvents. In conductivity electrolyte experiments, the organogel electrolytes indicated high conductivity (?) comparable to the corresponding NaClO4/THF solution. The conductivity of gel electrolytes was increased with electrolyte salt.

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