77928-59-7

Basic information

• Product Name: triacetoxyoctylstannane
• Synonyms: triacetoxyoctylstannane;Octyltri(acetoxy)tin(IV);Octyltriacetoxystannane;Tris(acetyloxy)octyltin(IV)
• CAS NO: 77928-59-7
• Molecular Formula: C₁₄H₂₆O₆Sn
• Molecular Weight: 409.06264
• EINECS: 278-796-6
• Mol File: 77928-59-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: triacetoxyoctylstannane(CAS DataBase Reference)
• NIST Chemistry Reference: triacetoxyoctylstannane(77928-59-7)
• EPA Substance Registry System: triacetoxyoctylstannane(77928-59-7)

Safety Data

• Hazardous Substances Data: 77928-59-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H23O6.Sn/c1-10(19-12(3)16)14(20-13(4)17)8-6-5-7-9-18-11(2)15;/h10,14H,1,5-9H2,2-4H3;/rC14H23O6Sn/c1-10(15)18-8-6-4-5-7-13(19-11(2)16)14(9-21)20-12(3)17/h13-14H,4-9H2,1-3H3

Upstream product

• 952316-56-2 1,1,3,3-tetraoctyl-1,3-bis(3-methylbutyloxy)distannoxane 
• 108-24-7 acetic anhydride 
• 1020100-76-8 tri-(n-octyl)-(3-methylbutoxy) tin 
• 64-19-7 acetic acid 

Downstream Products

• 17586-94-6 1,2-bis(acetyloxy)dioctylstannane 
• 123-92-2 3-methyl-1-butyl acetate 
• 952316-32-4 di-(n-octyl)-bis-(3-methylbutoxy) tin 

Relevant articles and documents

PROCESS FOR PRODUCTION OF ALKYL TIN ALKOXIDE COMPOUND, AND PROCESS FOR PRODUCTION OF CARBONATE ESTER USING THE COMPOUND

The present invention provides a process for producing : a compound represented by XOR2; a dialkyl tin dialkoxide compound having one tin atom, two Sn-R1 bonds and two Sn-OR2 bonds; and/or a tetraalkyl dialkoxy distannoxane compound having one Sn-O-Sn bond, in which each tin atom of the tetraalkyl dialkoxy distannoxane compound has two Sn-R1 bonds and one Sn-OR2 bond, the process comprising reacting in the absence of a catalyst at least one alkyl tin compound selected from the group consisting of i) and ii) below: i) a dialkyl tin compound having one tin atom, two Sn-R1 (wherein R1 represents an alkyl group) bonds, and two Sn-OX bonds (wherein OX is a group in which HOX that is a conjugate acid of OX is a Bronsted acid having a pKa of from 0 to 6.8); and ii) a tetraalkyl distannoxane compound having one Sn-O-Sn bond, in which each tin atom of the tetraalkyl distannoxane compound has two Sn-R1 bonds and one Sn-OX bond (wherein OX is a group in which HOX that is a conjugate acid of OX is a Bronsted acid having a pKa of from 0 to 6.8); and a carbonic acid ester represented by R2OCOOR2 (wherein R2 represents a linear or branched, saturated or unsaturated hydrocarbon group, a hydrocarbon group having a saturated or unsaturated cyclic hydrocarbon substituent, or a Y-CH2- group (wherein Y represents an alkyl polyalkylene group, an aromatic group or a cyclic saturated or unsaturated alkylene ether group)), and/or an alcohol represented by R2OH (wherein R2 is the same as defined above).

PROCESS FOR PRODUCTION OF DIALKYLTIN DIALKOXIDES

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.