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Tetraisobutyltin

Base Information
  • Chemical Name:Tetraisobutyltin
  • CAS No.:3531-43-9
  • Molecular Formula:C16H36 Sn
  • Molecular Weight:347.172
  • Hs Code.:2931900090
  • European Community (EC) Number:222-565-4
  • NSC Number:65526,22329
  • UNII:N8PR00IW5U
  • DSSTox Substance ID:DTXSID00188817
  • Mol file:3531-43-9.mol
Tetraisobutyltin

Synonyms:Tetraisobutyltin;Tetraisobutylstannane;STANNANE, TETRAISOBUTYL-;Stannane, tetrakis(2-methylpropyl)-;Tetrakis(isobutyl)stannane;3531-43-9;NSC 22329;Tin, tetraisobutyl-;EINECS 222-565-4;NSC 65526;BRN 3903677;N8PR00IW5U;NSC-22329;NSC-65526;tetrakis(2-methylpropyl)stannane;(iso-C4H9)4Sn;UNII-N8PR00IW5U;NCIOpen2_008224;DTXSID00188817;Tin, tetraisobutyl- (6CI,7CI);NSC22329;NSC65526;AKOS024338719;LS-146610

Suppliers and Price of Tetraisobutyltin
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • TETRAISOBUTYLTIN 95.00%
  • 5MG
  • $ 495.72
Total 9 raw suppliers
Chemical Property of Tetraisobutyltin
Chemical Property:
  • Vapor Pressure:0.000734mmHg at 25°C 
  • Melting Point:-12.9°C 
  • Boiling Point:317°C at 760 mmHg 
  • Flash Point:149.5°C 
  • PSA:0.00000 
  • Density:1.0500 
  • LogP:6.05920 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:8
  • Exact Mass:348.183904
  • Heavy Atom Count:17
  • Complexity:146
Purity/Quality:

99% *data from raw suppliers

TETRAISOBUTYLTIN 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C[Sn](CC(C)C)(CC(C)C)CC(C)C
Technology Process of Tetraisobutyltin

There total 9 articles about Tetraisobutyltin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With dibutylether;
Guidance literature:
With magnesium; In tetrahydrofuran; a soln. of ditin oxide in dry THF was added dropwise to a suspn. of a magnesium powder, activated by BrCH2CH2Br or I2, in dry THF, mixt. was heated at reflux for 15 h; petroleum ether was added, filtered, solvents evapd., residue was distilled;
DOI:10.1021/om00137a042
Guidance literature:
With formic acid; In not given; byproducts: CO2, H2O; 100°C, stirring (4 h), then 200°C (200 Torr, 4 h), addn. of further formic acid, 100°C (30 min); cooling to room temp., addn. of MeOH, decantation, addn. of petroleum ether, filtration, evapn., distn.; mixt. of products detd. by (119)Sn-NMRspectroscopy and liquid chromy.;
DOI:10.1016/0022-328X(85)87458-1
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