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1-Chloro-1,2,3,3,3-pentafluoroprop-1-ene, with the molecular formula C3H2ClF5, is a colorless, flammable gas characterized by a faint odor. It is recognized as a hydrochlorofluorocarbon (HCFC) and has been utilized as a substitute for chlorofluorocarbons (CFCs) due to its reduced potential for ozone depletion. Despite its environmental advantages over CFCs, it is still being phased out because of its contribution to global warming and its overall environmental impact.

2804-49-1

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2804-49-1 Usage

Uses

Used in Air Conditioning and Refrigeration Industry:
1-Chloro-1,2,3,3,3-pentafluoroprop-1-ene is used as a refrigerant for its ability to maintain lower temperatures efficiently in air conditioning and refrigeration systems, providing a more environmentally friendly alternative to traditional chlorofluorocarbons.
Used in Industrial Processes:
In various industrial applications, 1-Chloro-1,2,3,3,3-pentafluoroprop-1-ene serves as a solvent, leveraging its chemical properties to facilitate processes that require specific conditions or reactions.
Used in Aerosol Products:
As a propellant in aerosol products, 1-Chloro-1,2,3,3,3-pentafluoroprop-1-ene aids in the dispensing of substances from aerosol cans, offering a more eco-friendly option compared to some traditional propellants.
Despite its utility in these areas, the compound is being phased out due to its contribution to global warming, reflecting a global effort to seek more sustainable and environmentally benign alternatives.

Check Digit Verification of cas no

The CAS Registry Mumber 2804-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2804-49:
(6*2)+(5*8)+(4*0)+(3*4)+(2*4)+(1*9)=81
81 % 10 = 1
So 2804-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C3ClF5/c4-2(6)1(5)3(7,8)9/b2-1-

2804-49-1SDS

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-Chloro-1,2,3,3,3-pentafluoroprop-1-ene

1.2 Other means of identification

Product number -
Other names 1-chloro-1,2,3,3,3-pentafluoro-1-propene

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:2804-49-1 SDS

2804-49-1Relevant academic research and scientific papers

HYDROGEN FLUORIDE-HFC-254EB AZEOTROPE AND ITS USES

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Page/Page column 15, (2011/05/11)

Described is a process for separating 1,1,1,2-tetrafluoropropane and hydrogen fluoride from a mixture comprising 1,1,1,2-tetrafluoropropane, 1,1,1,2,3-pentafluoropropane and hydrogen fluoride comprising: subjecting said 1,1,1,2-tetrafluoropropane, 1,1,1,2,3-pentafluoropropane and hydrogen fluoride mixture to a distillation step, forming a column distillate composition comprising an azeotropic or near-azeotropic composition of said 1,1,1,2-tetrafluoropropane and hydrogen fluoride, and a bottoms composition of 1,1,1,2,3-pentafluoropropane. The column distillate may optionally be made essentially free of 1,1,1,2,3-pentafluoropropane and the column bottoms composition may optionally be made essentially free of HF. Also described is a process for separating 1,1,1,2-tetrafluoropropane and hydrogen fluoride from a mixture of 1,1,1,2-tetrafluoropropane and hydrogen fluoride. Also described are azeotropic and azeotrope-like compositions comprising 1,1,1,2-tetrafluoropropane and hydrogen fluoride.

PROCESS FOR THE SYNTHESIS AND SEPARATION OF HYDROFLUOROOLEFINS

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Page/Page column 12-14, (2008/12/07)

A process for the synthesis of fluorinated olefins of the formula CF3CF=CHX, wherein X is F or H comprising contacting hexafluoropropene with hydrogen chloride in the vapor phase, in the presence of a catalyst, at a temperature in the range from about 200 °C to about 350 °C, wherein the mole ratio of hydrogen chloride to hexafluoropropene is from about 2:1 to about 4:1, separating the 1-chloro-1,2,3,3,3-pentafluoro-1-propene, 1,1-dichloro-2,3,3,3-tetrafluoro-1-propene and hydrogen fluoride products from unreacted hexafluoropropene, and hydrogen chloride by distillation, hydrogenating either the 1-chloro-1,2,3,3,3-pentafluoro-1-propene, 1,1-dichloro-2,3,3,3-tetrafluoro-1-propene or mixture thereof over a catalyst, and dehydrochlorinating the said hydrogenation product to produce either 1225ye or 1234yf.

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