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Distannoxane, also known as 1,1,3,3-tetrabutyl-1,3-dimethoxy, is a chemical compound with the molecular formula C18H38O2Sn. It is a colorless liquid that is soluble in organic solvents and has a density of 1.22 g/cm3. Distannoxane, 1,1,3,3-tetrabutyl-1,3-dimethoxy- is primarily used as a catalyst in various chemical reactions, particularly in the production of polyurethane foams and as a stabilizer for polyvinyl chloride (PVC). Due to its tin content, it is important to handle Distannoxane with care, as it can be toxic and has potential environmental impacts.

5926-85-2

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5926-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5926-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5926-85:
(6*5)+(5*9)+(4*2)+(3*6)+(2*8)+(1*5)=122
122 % 10 = 2
So 5926-85-2 is a valid CAS Registry Number.

5926-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethoxy-1,1,3,3-tetrabutyldistannoxane

1.2 Other means of identification

Product number -
Other names tetra butyl dimethoxide distannoxane

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:5926-85-2 SDS

5926-85-2Relevant academic research and scientific papers

PROCESS FOR PRODUCING CARBONIC ESTER

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Page 31, (2008/06/13)

A method for producing a carbonic ester, comprising (1) performing a reaction between an organometal compound having a metal-oxygen-carbon linkage and carbon dioxide to obtain a reaction mixture containing a carbonic ester formed by the reaction, (2) separating the carbonic ester from the reaction mixture to obtain a residual liquid, and (3) reacting the residual liquid with an alcohol to form an organometal compound having a metal-oxygen-carbon linkage and form water and removing the water from the organometal compound, wherein the organometal compound obtained in step (3) is recovered for recycle thereof to step (1).

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