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4-Dimethylaminoheptafluorotoluene, commercially known as Fluorinert FC-3283, is a colorless liquid chemical compound with the molecular formula C10H9F7N. It is highly stable and inert, characterized by a very low boiling point and excellent dielectric properties. 4-DIMETHYLAMINOHEPTAFLUOROTOLUENE's non-flammability and low toxicity make it a versatile and safe solvent for a range of applications.

28012-10-4

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28012-10-4 Usage

Uses

Used in Electronics Industry:
4-Dimethylaminoheptafluorotoluene is used as a cooling and lubrication agent in the electronics industry due to its exceptional thermal and dielectric properties, as well as its non-flammability and low toxicity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Dimethylaminoheptafluorotoluene is utilized as a solvent for high-temperature reactions and processes, providing a stable and inert environment for sensitive chemical transformations.
Used in Chemical Industry:
Similarly, in the chemical industry, 4-Dimethylaminoheptafluorotoluene serves as a solvent for various organic and inorganic compounds, particularly in high-temperature applications, owing to its stability and inertness.

Check Digit Verification of cas no

The CAS Registry Mumber 28012-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,1 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28012-10:
(7*2)+(6*8)+(5*0)+(4*1)+(3*2)+(2*1)+(1*0)=74
74 % 10 = 4
So 28012-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F7N/c1-17(2)8-6(12)4(10)3(9(14,15)16)5(11)7(8)13/h1-2H3

28012-10-4SDS

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 2,3,5,6-tetrafluoro-N,N-dimethyl-4-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names CTK4G0628

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:28012-10-4 SDS

28012-10-4Relevant academic research and scientific papers

Interaction of N,N-dimethylperfluoroarylamines with nitric and nitrous acids

Platonov, Vyacheslav E.,Haas, Alois,Schelvis, Meinolf,Lieb, Max,Dvornikova, Kira V.,Osina, Ol'ga I.

, p. 3 - 8 (2007/10/03)

N,N-Dimethylpentafluoroaniline enters easily into reactions with a mixture of nitric and sulphuric acids or nitric acid with conversion of the side chain. In the reactions with mixtures of HNO3 and H2SO4, the formation of N-nitroso-N-methyl and N-nitro-N-methylpentafluoroanilines is observed. The ratio of these products was found to depend on the ratio of the acids: the formation of N-nitro-N-methylpentafluoroaniline increases with the quantity of sulphuric acid; N-nitroso-N-methylpentafluoroaniline is obtained when only nitric acid is employed. N,N-Dimethylperfluoro-p-toluidine, N,N-dimethylperfluoro-2,4-xylidine, N,N-dimethylperfluoro-5-aminoindane undergo similar transformations. N-Nitroso derivatives were converted by a mixture of HNO3 and H2SO4, HNO3 or NO2BF4 into the corresponding N-nitro derivatives. Formation of the corresponding N-nitroso-N-methyl derivatives occurs when N,N-dimethylpentafluoroaniline, N,N-dimethylperfluoro-p-toluidine are treated with HNO2.

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