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52319-97-8

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52319-97-8 Usage

General Description

5-Tert-butyl-1,3-diiminoisindoline is a chemical compound with the molecular formula C16H20N2. It is a dark blue solid that is used as a solvent dye and a coloring agent, primarily in the plastics and coatings industries. 5-TERT-BUTYL-1,3-DIIMINOISOINDOLINE is known for its high color strength and resistance to fading, making it an ideal choice for applications that require long-lasting, vibrant colors. Additionally, it is also used in the manufacture of inks, paints, and textiles. Its unique chemical structure and properties make it an important component in various industrial processes where durable and intense coloring is required.

Check Digit Verification of cas no

The CAS Registry Mumber 52319-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,1 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52319-97:
(7*5)+(6*2)+(5*3)+(4*1)+(3*9)+(2*9)+(1*7)=118
118 % 10 = 8
So 52319-97-8 is a valid CAS Registry Number.

52319-97-8SDS

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 5-tert-Butyl-1,3-diiminoisoindoline

1.2 Other means of identification

Product number -
Other names 5-tert-butyl-3-iminoisoindol-1-amine

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:52319-97-8 SDS

52319-97-8Upstream product

52319-97-8Relevant articles and documents

Highly organized phthalocyanine assembly onto gold surface through spontaneous polymerization

Ishikawa, Masaaki,Fujiki, Michiya,Naito, Masanobu

, p. 304 - 305 (2007)

Soluble μ-dihydroxysilicon-tetra-t-butylphthalocyanine was immobilized onto OH-coated gold surface. The phthalocyanine was immobilized in a sigmoidal manner with two threshold times, and the process was successfully analyzed with QCM and AFM studies. UV-vis studies indicated the highly organized polymer structure deposited onto the surface. Copyright

Syntheses of Monometalated and Unsymmetrically Substituted Binuclear Phthalocyanines and a Pentanuclear Phthalocyanine by Solution and Polymer Support Methods

Leznoff, Clifford C.,Svirskaya, Polina I.,Khouw, Ben,Cerny, Ronald L.,Seymour, Penny,Lever, A. B. P.

, p. 82 - 90 (2007/10/02)

Binuclear phthalocyanines in which two different phthalocyanine nuclei are covalently linked through five-atom bridges, derived from 2-ethyl-2-methylpropane-1,3-diol, are prepared.In the examples, one phthalocyanine ring is always substituted with neopentyloxy substitutents, while the other phthalocyanine rin is unsubstituted or contains tert-butyl substituents or a neopentoxy-substituted copper phthalocyanine, constituting a binuclear phthalocyanine in which only one ring is metalated.The precursor, 2-(2-hydroxymethyl)-2-methylbutoxy)-9,16,23-trineopentoxyphthalocyanine was prepared in solution and also by solid-phase methods, using polymer-bound trityl chloride derived from a 1percent divinylbenzene-co-styrene copolymer.In some experiments some rare examples of demetalation of some zinc phthalocyanines are noted during phthalocyanine formation.A modified flash chromatography procedure proved to be useful for separating similarly substituted mononuclear phthalocyanines.

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