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378-76-7

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378-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 378-76-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 378-76:
(5*3)+(4*7)+(3*8)+(2*7)+(1*6)=87
87 % 10 = 7
So 378-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C3HF5O2.K/c4-2(5,1(9)10)3(6,7)8;/h(H,9,10);/q;+1/p-1

378-76-7SDS

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 potassium,2,2,3,3,3-pentafluoropropanoate

1.2 Other means of identification

Product number -
Other names Potassium perfluoropropionate

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:378-76-7 SDS

378-76-7Relevant articles and documents

Preparation of tetrafluoroethylene from the pyrolysis of pentafluoropropionate salts

Hercules, Daniel A.,Parrish, Cameron A.,Sayler, Todd S.,Tice, Kevin T.,Williams, Shane M.,Lowery, Lauren E.,Brady, Michael E.,Coward, Robert B.,Murphy, Justin A.,Hey, Trevyn A.,Scavuzzo, Anthony R.,Rummler, Lucy M.,Burns, Emory G.,Matsnev, Andrej V.,Fernandez, Richard E.,McMillen, Colin D.,Thrasher, Joseph S.

, p. 107 - 116 (2017/04/18)

The use of tetrafluoroethylene (TFE) in academic institutions beyond a few millimoles has often been inhibited by the compound's inherent danger and general lack of commercial availability. On the other hand, TFE is prepared industrially on a rather large scale by a number of major fluorochemical companies via the pyrolysis of chlorodifluoromethane at high temperatures, yielding TFE and HCl. For a few years at The University of Alabama and Clemson University, we have been preparing TFE on a 100+-gram scale by the pyrolysis under dynamic vacuum of pentafluoropropionate salts, which can be obtained from the neutralization of pentafluoropropionic acid with a M(OH)n (where M?=?Li, Na, K, and Cs for n?=?1 and Mg, Ca, and Ba for n?=?2). Additionally, potassium pentafluoropropionate can be prepared from the reaction of potassium trimethylsilanolate and ethyl pentafluoropropionate. The pentafluoropropionate salts and their decomposition products have been characterized by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), accelerating rate calorimetry (ARC), nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, Fourier transform-infrared (FTIR) spectrophotometry, scanning electron microscopy (SEM)/energy dispersive spectroscopy (EDAX), X-ray diffraction (XRD), and single-crystal X-ray crystallography, where applicable. Typical yields of TFE obtained from pyrolysis of potassium pentafluoropropionate obtained from the acid-base neutralization method are >98%, while yields of TFE from the same salt prepared by the silanolate method from ethyl pentafluoropropionate are ca. 80%.

Preparation of anhydrous organic acid salts

-

, (2008/06/13)

One-step process for preparing anhydrous, organic acid alkali or alkaline earth metal salts by contacting and reacting an organic or polymeric acid fluoride, anhydride or ester and an organic alkali or alkaline earth metal silanolate.

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