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61098-00-8

HOSTINERT 216 FOR X-RAY STRUCTURAL ANALY SIS is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61098-00-8

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61098-00-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61098-00-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,9 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61098-00:
(7*6)+(6*1)+(5*0)+(4*9)+(3*8)+(2*0)+(1*0)=108
108 % 10 = 8
So 61098-00-8 is a valid CAS Registry Number.

61098-00-8SDS

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 perfluoro-5,8,9,12-tetramethyl-4,7,10,13-tetraoxahexadecane

1.2 Other means of identification

Product number -
Other names Perfluoro-5,8,9,12-tetramethyl-4,7,10,13-tetaoxahexadecane

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:61098-00-8 SDS

61098-00-8Downstream Products

61098-00-8Relevant articles and documents

Study of liquid-phase photolysis of perfluorinated ketones

Starobin,Berenblit,Lebedev,Gubanov

body text, p. 1046 - 1051 (2011/09/12)

Liquid-phase photolysis of perfluorinated ketones under UV irradiation was examined.

Photolysis of perfluoroacyl fluorides

Tonelli, Claudio,Tortelli, Vito

, p. 117 - 123 (2007/10/03)

The photochemical decarbonylation and coupling of acyl fluorides containing perfluoroalkyl and perfluoro(oxa)alkyl chains have been re-examined. The reaction on either single acyl fluorides or on their binary mixtures has allowed the formation and isolation of macromolecular perfluoro(oxa)alkanes having interesting physical-chemical properties. These perfluoropolyethers are also useful as model compounds and standards to better characterize more complex mixtures of similar commercial products.

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