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1,1,2,3,3,4,4-Heptafluoro-1-butene, with the molecular formula C4F7H, is a fluorocarbon compound characterized by its colorless gaseous form. It is highly stable and non-flammable, offering a suitable alternative to ozone-depleting substances. 1,1,2,3,3,4,4-HEPTAFLUORO-1-BUTENE is recognized for its low global warming potential, positioning it as an environmentally friendly option in various applications. However, caution is advised in handling due to its potential to cause irritation to the eyes, skin, and respiratory system upon excessive exposure.

680-54-6

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680-54-6 Usage

Uses

Used in Refrigeration Industry:
1,1,2,3,3,4,4-Heptafluoro-1-butene is used as a refrigerant for its non-flammable and stable properties, making it a preferred choice over substances that deplete the ozone layer.
Used in Propellant Applications:
In the propellant industry, 1,1,2,3,3,4,4-Heptafluoro-1-butene serves as a propellant due to its ability to provide a controlled release of substances, leveraging its stable and non-flammable nature.
Used as a Solvent:
1,1,2,3,3,4,4-Heptafluoro-1-butene is utilized as a solvent in various chemical processes, capitalizing on its stability and low reactivity with other compounds.
Used in Environmentally Friendly Applications:
Given its low global warming potential, 1,1,2,3,3,4,4-Heptafluoro-1-butene is employed in applications seeking to minimize environmental impact, offering a greener alternative to traditional substances with higher potential for global warming.

Check Digit Verification of cas no

The CAS Registry Mumber 680-54-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 680-54:
(5*6)+(4*8)+(3*0)+(2*5)+(1*4)=76
76 % 10 = 6
So 680-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C4HF7/c5-1(2(6)7)4(10,11)3(8)9/h3H

680-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,3,3,4,4-heptafluorobut-1-ene

1.2 Other means of identification

Product number -
Other names 4H-Heptafluor-but-1-en

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:680-54-6 SDS

680-54-6Downstream Products

680-54-6Relevant articles and documents

PRODUCTION METHOD OF PERFLUOROALKADIENE COMPOUND

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Paragraph 0046; 0056-0058, (2021/01/15)

PROBLEM TO BE SOLVED: To provide a method capable of obtaining a perfluoroalkandiene compound in a high yield while reducing the generation amount of impurities which are difficult to separate. SOLUTION: The production method is a method for producing a perfluoroalkandiene compound represented by the general formula (1): CF2=CF-(CF2)n-4-CF=CF2 (1) [in the formula, n represents an integer of 4 to 20.] and comprises a reaction step of reacting a compound represented by the general formula (2): CF2X1-CFX2-(CF2)n-4-CF2-CF2X3 (2) [in the formula, n is the same as defined above; X1, X2 and X3 are the same or different, X1 and X2 represent a halogen atom, and X3 represents a chlorine atom, a bromine atom or an iodine atom, provided that both X1 and X2 are not fluorine atoms] in the presence of a nitrogen-containing compound and zinc or a zinc alloy in an organic solvent in which the reaction step includes a mixing step of sequentially mixing a solution including zinc or a zinc alloy and an organic solvent, a nitrogen-containing compound and the compound represented by the general formula (2). SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Method of preparing perfluoroalkadiene

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Page/Page column 3, (2009/04/24)

Disclosed herein is a method of preparing a perfluoroalkadiene. A dihaloperfluorocarbon used as a starting material is added dropwise to a nonpolar organic solvent, a metal powder and an organic metal compound. The dihaloperfluorocarbon is slowly added dropwise in a temperature range from 30° C. to 150° C. for a certain period of time. Moreover, the nonpolar organic solvent used may be benzene, toluene, xylene, etc., and the organic metal compound is used by being dissolved in ethyl ether or tetrahydrofuran at a concentration of 1 to 3M. The metal powder used may be Mg, Zn, Cd, etc.

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