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3228-99-7

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3228-99-7 Usage

Description

PENTAERYTHRITYL TETRACHLORIDE, also known as PETC, is an organic compound with the chemical formula C5H4Cl4O4. It is a light beige, fluffy powder that is non-mutagenic to 7 strains of Salmonella typhimurium, indicating its potential safety in certain applications.

Uses

Used in Chemical Synthesis:
PENTAERYTHRITYL TETRACHLORIDE is used as a synthetic intermediate for the production of various chemicals and materials. Its unique structure allows it to be a versatile building block in the synthesis of different compounds.
Used in Pharmaceutical Industry:
PENTAERYTHRITYL TETRACHLORIDE is used as a reagent in the pharmaceutical industry for the synthesis of drugs and drug candidates. Its non-mutagenic properties make it a suitable candidate for use in the development of new medications.
Used in Plastics and Resins Industry:
PENTAERYTHRITYL TETRACHLORIDE is used as a monomer in the production of plastics and resins. Its chemical properties contribute to the formation of polymers with specific characteristics, such as durability and resistance to various environmental conditions.
Used in Coatings and Adhesives Industry:
PENTAERYTHRITYL TETRACHLORIDE is used as a component in the formulation of coatings and adhesives. Its light beige color and fluffy texture make it suitable for use in these applications, where it can improve the performance and properties of the final products.
Used in Flame Retardants Industry:
PENTAERYTHRITYL TETRACHLORIDE is used as a flame retardant additive in various industries, such as plastics, textiles, and electronics. Its chemical properties help to reduce the flammability of materials, enhancing their safety in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3228-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3228-99:
(6*3)+(5*2)+(4*2)+(3*8)+(2*9)+(1*9)=87
87 % 10 = 7
So 3228-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H8Cl4/c6-1-5(2-7,3-8)4-9/h1-4H2

3228-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dichloro-2,2-bis(chloromethyl)propane

1.2 Other means of identification

Product number -
Other names 1,3-dichloro-2,2-bis-chloromethyl-propane

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:3228-99-7 SDS

3228-99-7Relevant articles and documents

Generation of radical species in surface reactions of chlorohydrocarbons and chlorocarbons with fluorinated gallium(III) oxide or indium(III) oxide

Thomson

, p. 1881 - 1885 (2007/10/03)

The reactions of C1 and C2 chlorohydrocarbons and chlorocarbons have been studied with the Lewis acid catalysts fluorinated gallium(III) oxide and fluorinated indium(III) oxide, respectively. Product analysis shows chlorine-for-fluorine exchange reactions together with the formation of 2-methylpropane and its chlorinated analogues 2-chloromethyl-1,3-dichloropropane and 2-chloromethyl-1,2,3-trichloropropane. Reactivities of the chlorohydrocarbon probe molecules show fluorinated gallium(III) oxide to be a stronger Lewis acid than fluorinated indium(III) oxide. The formation of the symmetrical butyl compounds is consistent with the generation of surface radical species and is also consistent with a 1,2-migration mechanism operating within radical moieties at the Lewis acid surface.

Improved Preparations of 3-Chloro-2-(chloromethyl)-1-propene and 1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane: Intermediates in the Synthesis of Propellane

Lynch, Kathleen Mondanaro,Dailey, William P.

, p. 4666 - 4668 (2007/10/02)

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KINETICS OF THE TRANSFORMATION OF 5-R-5-CHLOROMETHYL-2-THIA-2-OXO-1,3-DIOXANES TO 1,3-DICHLORO-2-R-2-CHLOROMETHYLPROPANES

Bolotov, A. S.,V'yunov, K. A.

, p. 187 - 191 (2007/10/02)

Investigation of the kinetics of the formation of 1,3-dichloro-2-R-2-chloromethylpropanes from 5-R-5-chloromethyl-2-thia-2-oxo-1,3-dioxane by the action of an equimolecular mixture of thionyl chloride and dimethylformamide (the Vilsmeier-Haack reagent) led to the conclusion that the low activation energies and the large negative entropy values indicate the participation of a stable intermediate in the investigated complex many-stage reaction.

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