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Perfluorodecane, with the chemical formula C10F22, is a member of the perfluorocarbon family. It is a colorless, odorless liquid at room temperature, characterized by its high stability and non-reactivity. Being insoluble in water, perfluorodecane is recognized for its non-flammable and non-toxic properties, making it a safe and compatible choice for various applications.

307-45-9

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307-45-9 Usage

Uses

Used in Pharmaceutical Industry:
Perfluorodecane is used as a solvent in drug delivery systems for its inert and non-toxic nature, which ensures the safety and compatibility of the pharmaceutical formulations.
Used in Medical Imaging:
In the field of medical imaging, perfluorodecane serves as a contrast agent to enhance the visibility of internal structures, improving the diagnostic accuracy of imaging procedures.
Used in Electronics Industry:
Perfluorodecane is utilized in heat transfer applications within the electronics industry, thanks to its stable and non-reactive properties, which are essential for maintaining the performance and longevity of electronic components.
Environmental Considerations:
Given the long persistence of perfluorodecane in the environment, there is an ongoing effort to research and develop more environmentally-friendly alternatives to PERFLUORODECANE, aiming to reduce its ecological impact while maintaining the benefits it provides in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 307-45-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 307-45:
(5*3)+(4*0)+(3*7)+(2*4)+(1*5)=49
49 % 10 = 9
So 307-45-9 is a valid CAS Registry Number.

307-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name perfluorodecane

1.2 Other means of identification

Product number -
Other names 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-docosafluorodecane

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:307-45-9 SDS

307-45-9Downstream Products

307-45-9Relevant academic research and scientific papers

Nucleophilic Displacement of Bis(perfluoroalkanoyl) Peroxides with Perfluoroalkanoate

Yoshida, Masato,Sasage, Shyuichi,Kamigate, Nobumasa,Sawada, Hideo,Nakayama, Masaharu

, p. 2416 - 2418 (1989)

Bis(perfluoroalknoyl) peroxide ((RFCO2)2) suffered a nucleophilic displacement with perfluoroalkanoate (RF'CO2(1-)) to give new mixed peroxide (RF(CO)OO(CO)RF').When thiophene was reacted with bis(perfluoroalkanoyl) peroxide in the presence of pyridinium perfluoroalkanoate, not only the perfluoroalkyl group (RF) of the peroxide, but also perfluoroalkyl group (RF') of perfluoroalkanoate, was introduced into thiophene.

THERMAL DECOMPOSITION OF PERFLUOROALKANESULFONYL FLUORIDES: THE PYROLYSIS OF PERFLUORO-n-OCTANE-1-SULFONYL FLUORIDE

Napoli, M.,Fraccaro, C.,Scipioni, A.,Armelli, R.

, p. 377 - 386 (2007/10/02)

The preliminary data obtained from thermal decompositions of perfluoro-n-octane-1-sulfonyl fluoride in a continuous tubular-flow reactor are reported.The pyrolysis results in a radical reaction producing fluorocarbons, with high conversions and with yields depending on the experimental conditions.The reaction mixture composition also depends on the experimental conditions, so it is possible to obtain a prevalent formation of either light or heavy fluorocarbons.

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