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Dodecane, 1,1,1-trifluoro-, also known as 1,1,1-Trifluorododecane or C12F3H25, is a colorless, volatile liquid with a molecular formula of C12H25F3. It is a halogenated hydrocarbon, specifically a fluorinated alkane, and is characterized by the presence of three fluorine atoms attached to the terminal carbon atom of a dodecane chain. Dodecane, 1,1,1-trifluoro- is primarily used as a solvent, a blowing agent in the production of foams, and as a refrigerant in various industrial applications. Due to its low toxicity and high thermal stability, 1,1,1-trifluorododecane is considered a safer alternative to traditional chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs) in certain applications. However, it is important to note that like other fluorinated compounds, it can contribute to global warming due to its high global warming potential (GWP), and thus its use is subject to environmental regulations and restrictions.

764-84-1

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764-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 764-84-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 764-84:
(5*7)+(4*6)+(3*4)+(2*8)+(1*4)=91
91 % 10 = 1
So 764-84-1 is a valid CAS Registry Number.

764-84-1SDS

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-trifluoro-dodecane

1.2 Other means of identification

Product number -
Other names 1,1,1-Trifluor-dodecan

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:764-84-1 SDS

764-84-1Downstream Products

764-84-1Relevant academic research and scientific papers

Synthetic uses of thioesters of trifluoromethylated acids. Part 2: Reactions with alkenes

Billard, Thierry,Roques, Nicolas,Langlois, Bernard R.

, p. 3069 - 3072 (2000)

The photolysis of trifluoromethanethiosulfonates (CF3SO2SR) or trifluorothioacetates (CF3COSR) in the presence of alkenes provides (trifluoromethyl)alkanes or β-sulfanyl (trifluoromethyl)alkanes. The formation of these compounds can be controlled by the nature and the ratio of the reactants. (C) 2000 Published by Elsevier Science Ltd.

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