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41430-70-0

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41430-70-0 Usage

General Description

Ethyl perfluoroheptanoate is a fluorinated organic compound that is commonly used in the production of fluoropolymers, which are used in a wide range of applications, including non-stick coatings, waterproof fabrics, and firefighting foams. It is also used as a surfactant and as a solvent in various industrial processes. Ethyl perfluoroheptanoate is highly stable, non-flammable, and resistant to chemicals, making it a valuable ingredient in the production of durable and long-lasting materials. However, it is also considered to be a potential environmental pollutant and may have adverse effects on human health, so it is important to handle and dispose of this chemical with care.

Check Digit Verification of cas no

The CAS Registry Mumber 41430-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,3 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41430-70:
(7*4)+(6*1)+(5*4)+(4*3)+(3*0)+(2*7)+(1*0)=80
80 % 10 = 0
So 41430-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H5F13O2/c1-2-24-3(23)4(10,11)5(12,13)6(14,15)7(16,17)8(18,19)9(20,21)22/h2H2,1H3

41430-70-0SDS

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 Ethyl perfluoroheptanoate

1.2 Other means of identification

Product number -
Other names ethyl 2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptanoate

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:41430-70-0 SDS

41430-70-0Relevant articles and documents

Ozonolysis of alkenes and studies of reactions of polyfunctional compounds: LXV.* Ozonolysis of perfluoro-1-octene in Freon-113

Odinokov,Akhmetova,Bazunova,Savchenko,Paramonov,Khalilov

, p. 321 - 325 (2007/10/03)

Ozonization of perfluoro-1-octene in Freon-113 yields the corresponding ozonide whose catalytic hydrogenation over Pd/C or hydride reduction leads to formation of perfluoroheptanoic acid; the reduction with lithium aluminum hydride gives 2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoro-1-heptanol. Ozonization of perfluoro-1-octene in Freon-113 containing excess (≥3 equiv) alcohol affords the corresponding perfluoroheptanoic acid ester.

REACTIVITE DES PERFLUOROIODOALCANES AVEC LES CARBONATES ET PYROCARBONATES D'ALCOYLES EN PRESENCE DE COUPLE METALLIQUE ZINC-CUIVRE

Benefice, S.,Blancou, H.,Commeyras, A.

, p. 1541 - 1544 (2007/10/02)

Perpluoroalkyl iodides RFI, in dissociating solvents, in the presence of zinc-copper couple give perfluoroorganic compounds RFZnI, which reac with alkyl carbonates and pyrocarbonates to give perfluorocarboxylic acids and perfluorocarboxylis esters of industrial interest.

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