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Dipropionic acid dioctyltin(IV) salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21619-67-0

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21619-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21619-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,1 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21619-67:
(7*2)+(6*1)+(5*6)+(4*1)+(3*9)+(2*6)+(1*7)=100
100 % 10 = 0
So 21619-67-0 is a valid CAS Registry Number.

21619-67-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name di-n-octyl di(propionyloxy) tin

1.2 Other means of identification

Product number -
Other names di-n-octyldipropionyloxytin

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:21619-67-0 SDS

21619-67-0Downstream Products

21619-67-0Relevant academic research and scientific papers

PROCESS FOR PRODUCTION OF DIALKYLTIN DIALKOXIDES

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Page/Page column 38-39; 42, (2009/07/25)

An object of the present invention is to provide a process for producing a dialkyl tin compound from a composition of deactivated forms of a dialkyl tin catalyst, and to provide a process for producing the dialkyl tin catalyst from the dialkyl tin compound and using the dialkyl tin catalyst to produce a carbonic acid ester. According to the present invention, a process for producing a dialkyl tin compound is provided that subjects a composition of the deactivated forms of the dialkyl tin catalyst, formed when producing an ester compound, to an alkyl group redistribution reaction and/or dealkylation reaction.

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