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1,1,1,3-tetrachloropropene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15022-22-7

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15022-22-7 Usage

Physical state

Colorless liquid

Odor

Sharp, sweet

Classification

Chlorinated hydrocarbon

Primary uses

Intermediate in the production of chemicals
Herbicides
Pesticides
Flame retardants
Solvent
Fumigant

Toxicity

Considered toxic and potentially harmful to human health and the environment

Handling precautions

Caution should be taken when handling and using 1,1,1,3-tetrachloropropene

Environmental impact

Persistent organic pollutant

Bioaccumulation

Can bioaccumulate in living organisms

Ecosystem impacts

Long-term impacts on ecosystems

Check Digit Verification of cas no

The CAS Registry Mumber 15022-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,2 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15022-22:
(7*1)+(6*5)+(5*0)+(4*2)+(3*2)+(2*2)+(1*2)=57
57 % 10 = 7
So 15022-22-7 is a valid CAS Registry Number.

15022-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,3,3-Tetrachloroprop-1-ene

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:15022-22-7 SDS

15022-22-7Relevant academic research and scientific papers

PROCESS FOR MAKING TETRAFLUOROPROPENE

-

Paragraph 0018, (2013/08/28)

The present invention describes a process for making CF3CH═CHF (HFO-1234ze). The process involves the addition of carbon tetrachloride (CCl4) to 1,2-dichloroethylene to form CCl3CHClCHCl2. The compound CCl3CHClCHCl2 thus can then either be treated with HF to produce CF3CHClCHClF as the main product, or it can be converted to CCl2═CHCHCl2 (1230za) by dechlorination. CCl2═CHCHCl2 can be treated with HF such that the main product obtained is CF3CHClCHClF. CF3CH═CHCl may be produced as a by-product, but upon treatment with HF, it affords the compound CF3CHClCHClF. The desired compound, CF3CH═CHF (HFO-1234ze), is obtained as a trans/cis mixture by dehydrochlorination of CF3CH2CHClF or by dechlorination of CF3CHClCHClF.

ArF laser photolytic deposition and thermal modification of an ultrafine chlorohydrocarbon

Pola, Josef,Galikova, Anna,Subrt, Jan,Ouchi, Akihiko

experimental part, p. 625 - 629 (2011/10/19)

MW ArF laser irradiation of gaseous cis-dichloroethene results in fast decomposition of this compound and in deposition of solid ultrafine Cl- and H-containing carbonaceous powder which is of interest due to its sub-microscopic structure and possible reactive modification of the C-Cl bonds. The product was characterized by electron microscopy, and FTIR and Raman spectra and it was revealed that HCl, H2, and C/H fragments are lost and graphitic features are adopted upon heating to 700°C.

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