13121-71-6

Usage

Safety Profile

Poison by ingestion. When heated to decomposition it emits toxic fumes of Sn.

InChI:InChI=1/3C6H11.C2H4O2.Sn/c3*1-2-4-6-5-3-1;1-2(3)4;/h3*1H,2-6H2;1H3,(H,3,4);/rC18H33Sn.C2H4O2/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-2(3)4/h16-18H,1-15H2;1H3,(H,3,4)

Upstream product

• 64-19-7 acetic acid 
• 563-63-3 silver(I) acetate 
• 13121-86-3 tris(cyclohexyl)tin iodide 
• 127-09-3 sodium acetate 
• 3091-32-5 tricyclohexyltin(IV) chloride 
• 130876-78-7 {(p-chloro-phenylthio)methyl}tricyclohexylstannane 
• 546-67-8 lead(IV) tetraacetate 
• 13121-70-5 cyhexatin 
• 130876-82-3 tricyclohexyl(iodomethyl)stannane 

Relevant academic research and scientific papers

RECYCLING OF ORGANOTIN COMPOUNDS

A method for the synthesis of a first organic molecule, said method comprising the steps of: a) Reacting a first reactant with an organotin reactant having at least one optionally substituted organic group having from 5 to 20 carbon atoms selected from alkyl, alkenyl, alkynyl, alkoxyalkyl, alkoxy, alkylthioalkyl, carboxylates and alkylaminoalkyl groups, thereby forming a mixture of a product and a tin-containing by-product, and b) Removing most of the tin-containing by-product from said mixture in such a way as to provide a purified product comprising less than 1000 ppm of remaining tin-containing by- product, wherein said step of removing most of said tin-containing by-product is either an extraction between a first liquid and a second liquid, said second liquid being more polar than said first liquid and at least partly immiscible therewith or is a reversed phase chromatography.

Recycling of organotin compounds

A method for the synthesis of a first organic molecule, said method comprising the steps of: a) Reacting a first reactant with an organotin reactant having at least one organic group having from 5 to 20 carbon atoms selected from alkyl, alkoxyalkyl, alkoxy, alkylthioalkyl, carboxylates and alkylaminoalkyl groups, thereby forming a mixture of a product and a tin-containing by-product, and b) Removing most of the tin-containing by-product from said mixture in such a way as to provide a purified product comprising less than 1000 ppm of remaining tin-containing by-product, wherein said step of removing most of said tin-containing by-product is either an extraction between a first liquid being an alkane or a mixture of alkanes having from 5 to 17 carbon atoms and a second liquid more polar than said first liquid or is a reversed phase chromatography.