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Perfluoroisoheptyl iodide, with the molecular formula C7F15I, is a chemical compound that falls under the category of perfluoroalkyl iodides. It is recognized for its high thermal and chemical stability, coupled with low toxicity. PERFLUOROISOHEPTYL IODIDE's exceptional water and oil repellent properties make it a crucial component in the creation of fluorinated materials.

3486-08-6

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3486-08-6 Usage

Uses

Used in Electronics Industry:
Perfluoroisoheptyl iodide is used as a material in the electronics industry for its thermal and chemical stability, which is essential for the production of various electronic components and devices.
Used in Pharmaceuticals Industry:
In the pharmaceutical sector, perfluoroisoheptyl iodide serves as a building block in organic synthesis, enabling the development of a broad spectrum of specialty chemicals and polymers that can be utilized in drug formulations and delivery systems.
Used in Agrochemicals Industry:
Perfluoroisoheptyl iodide is utilized in the agrochemicals industry, where its properties contribute to the development of effective and stable agrochemical products.
Used in Textile Production:
PERFLUOROISOHEPTYL IODIDE is used as a key ingredient in the textile industry, where it imparts water and oil repellent properties to fabrics, enhancing their durability and performance.
Used in Coatings and Finishes:
Perfluoroisoheptyl iodide is employed in the production of coatings and finishes, providing surfaces with enhanced resistance to water, oil, and other environmental factors.
Used in Non-stick Cookware:
It is a vital component in the manufacturing of non-stick cookware, offering improved food release and easy cleaning properties due to its inherent repellent characteristics.
Used in Organic Synthesis:
As a versatile building block in organic synthesis, perfluoroisoheptyl iodide is used for creating a wide range of specialty chemicals and polymers that find applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3486-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3486-08:
(6*3)+(5*4)+(4*8)+(3*6)+(2*0)+(1*8)=96
96 % 10 = 6
So 3486-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C7F15I/c8-1(5(15,16)17,6(18,19)20)2(9,10)3(11,12)4(13,14)7(21,22)23

3486-08-6SDS

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 1,1,1,2,3,3,4,4,5,5,6,6-dodecafluoro-6-iodo-2-(trifluoromethyl)hexane

1.2 Other means of identification

Product number -
Other names Perfluoroisoheptyl iodide

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:3486-08-6 SDS

3486-08-6Relevant academic research and scientific papers

Synthesis of telogens and optimization of tetrafluoroethene telomerization process

Lewandowski, Grzegorz,Meissner, Egbert,Milchert, Eugeniusz

, p. 337 - 344 (2007/10/03)

The most advantageous technological parameters of tetrafluoroethene telomerization using 1-chloro-2-iodohexafluoropropane (telogen) towards the telomers n2-n4 or n1-n4 were experimentally established. The telomers n1-n4 were prepared with the yield of 48 mol% under the following conditions: temperature 170°C, the molar ratio of 1-chloro-2-iodohexafluoropropane to tetrafluoroethene equal to 1.2, the autoclave filling of 1.5 kg dm-3. The maximum yield of telomers n2-n4 amounted to 27 mol% when the molar ratio of telogen to tetrafluoroethene was decreased to 0.7 and the other parameters of synthesis remained the same. The optimum parameters for the synthesis of telogens: 1-chloro-2-iodohexafluoropropane and 2-iodoheptafluoropropane have been also determined.

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