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260054-47-5

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260054-47-5 Usage

Use

Stabilizer in polyvinyl chloride (PVC) and other polymers

Physical state

White, crystalline solid

Molecular weight

407.78 g/mol

Function

Prevents degradation and discoloration of PVC and other polymers caused by heat and ultraviolet radiation

Mechanism

Scavenges hydrogen chloride and other acidic degradation products

Additional uses

Stabilizer in adhesives, coatings, and sealants

Safety precautions

Toxic if ingested or absorbed through the skin; handle with care and follow proper safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 260054-47-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,0,5 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 260054-47:
(8*2)+(7*6)+(6*0)+(5*0)+(4*5)+(3*4)+(2*4)+(1*7)=105
105 % 10 = 5
So 260054-47-5 is a valid CAS Registry Number.

260054-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(trichloromethyl)-1,3-bis(2,4,6-trimethylphenyl)imidazolidine

1.2 Other means of identification

Product number -
Other names AS1023

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:260054-47-5 SDS

260054-47-5Relevant articles and documents

C-H insertion reactions of nucleophilic carbenes

Arduengo III, Anthony J.,Calabrese,Davidson, Fredric,Rasika Dias,Goerlich, Jens R.,Krafezyk, Roland,Marshall, William J.,Tamm, Matthias,Schumtzler, Reinhard

, p. 2348 - 2364 (1999)

Syntheses and characterizations are described for C-H insertion products derived from 1,3-dimesityldihydroimidazol-2-ylidene (1) with acetylene, acetonitrile, methyl phenyl sulfone, and chloroform. In the reaction with acetylene, both acetylenic H-atoms a

Synthesis and NMR study of N-heterocyclic carbenes (NHC) precursors derived from troger's base

Musengimana, Eric,Fatakanwa, Claver

, p. 1489 - 1496 (2014/05/06)

Since the discovery of olefin metathesis reactions, various catalysts have been developed but those based on Ruthenium and N-heterocyclic carbenes (NHC) ligands are particularly more efficient. Herein, we report a synthesis of NHC precursors derived from

High activity metal carbene metathesis catalysts generated using a thermally activated N-heterocyclic carbene precursor

-

, (2008/06/13)

The invention provides a method for converting a less active or slower to initiate system to a higher activity system so that at the end of a polymerization the most active species is present in the system. The invention generally relates to a process for

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