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1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE is a chemical compound belonging to the perfluoroalkyl family, characterized by its eight carbon atoms, six chlorine atoms, and one fluorine atom. It is renowned for its exceptional stability, resistance to heat, water, and oil, which has made it a popular choice in various industrial applications.

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  • 335-68-2 Structure
  • Basic information

    1. Product Name: 1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE
    2. Synonyms: 1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE;1,1,3,5,7,8-Hexachloro-1,2,2,3,4,4,5,6,6,7,8,8-dodecafluorooctane
    3. CAS NO:335-68-2
    4. Molecular Formula: C8Cl6F12
    5. Molecular Weight: 536.78
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 335-68-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 338.5 °C at 760 mmHg
    3. Flash Point: 194.4 °C
    4. Appearance: /
    5. Density: 1.821 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE(335-68-2)
    11. EPA Substance Registry System: 1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE(335-68-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 335-68-2(Hazardous Substances Data)

335-68-2 Usage

Uses

Used in the Chemical Industry:
1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE is used as a surfactant for the production of non-stick coatings, such as those found in cookware, due to its heat and chemical resistance properties.
Used in the Textile Industry:
In the textile industry, 1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE is utilized as a surfactant in the creation of waterproofing fabrics, capitalizing on its water-repellent characteristics.
However, due to its persistence in the environment and potential to bioaccumulate, there are growing concerns about the impact of 1,1,3,5,7,8-HEXACHLOROPERFLUOROOCTANE on human health and the environment. Consequently, this chemical compound has faced regulatory restrictions in some countries to mitigate its environmental and health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 335-68-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 335-68:
(5*3)+(4*3)+(3*5)+(2*6)+(1*8)=62
62 % 10 = 2
So 335-68-2 is a valid CAS Registry Number.

335-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,5,7,8-Hexachloro-1,2,2,3,4,4,5,6,6,7,8,8-dodecafluorooctane

1.2 Other means of identification

Product number -
Other names Octane, 1,1,3,5,7,8-hexachloro-1,2,2,3,4,4,5,6,6,7,8,8-dodecafluoro-

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:335-68-2 SDS

335-68-2Relevant articles and documents

Reaction of 1,2-Dichloroiodotrifluoroethane With Zinc

Eapen, K. C.,Tamborski, C.

, p. 421 - 424 (2007/10/02)

The zinc coupling reaction of 1,2-dichloroiodotrifluoroethane (I) in acetic anhydride-methylene chloride has been reinvestigated in more detail than its original disclosure.The expected coupling product C4F6Cl4 was shown to be an isomeric mixture of three components, CF2ClCFClCFClCF2Cl (II, 80percent), CFCl2CF2CF2CFCl2 (IIa, 15percent) and CF2ClCFClCF2CFCl2 (IIb, 5percent).In addition, other products e.g.CF2-CFCl, C6F9Cl5 and C8F12Cl6 were formed in minor quantities.A probable mode of formation of various byproducts via initial formation of CF2-CFCl and subsequent telomerization is presented.

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