Tributylstannanylium;iodide

Base Information Edit

Chemical Name:Tributylstannanylium;iodide
CAS No.:7342-47-4
Molecular Formula:C12H27ISn
Molecular Weight:416.961
Hs Code.:
Mol file:7342-47-4.mol

Synonyms:SCHEMBL578857;AKOS032949947;H10834

Suppliers and Price of Tributylstannanylium;iodide

Supply Marketing:Edit

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

Sigma-Aldrich
Tributyltin iodide technical grade, 90%
10g
$ 78.40

Alfa Aesar
Tri-n-butyltin iodide, tech. 90% stab. with copper
5g
$ 76.20

Total 12 raw suppliers

Chemical Property of Tributylstannanylium;iodide Edit

Chemical Property:

Vapor Pressure:0.000588mmHg at 25°C
Refractive Index:n20/D 1.53(lit.)
Boiling Point:172 °C10 mm Hg(lit.)
Flash Point:>230 °F
PSA：0.00000
Density:1.46 g/mL at 25 °C(lit.)
LogP:5.76720
Sensitive.:Light Sensitive
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:9
Exact Mass:418.01795
Heavy Atom Count:14
Complexity:72.1

Purity/Quality:

98%,99%, ^*data from raw suppliers

Tributyltin iodide technical grade, 90% ^*data from reagent suppliers

Safty Information:

Pictogram(s): A poison by ingestion and skin contact. Moderately toxic by inhalation. Tributyl tin compounds are extremely toxic to marine life. TWA 0.1 mg(Sn)/m³; STEL 0.2 mg(Sn)/m³(skin).
Hazard Codes:T,N
Statements: 21-25-36/38-48/23/25-50/53
Safety Statements: 35-36/37/39-45-60-61

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC[Sn+](CCCC)CCCC.[I-]

Technology Process of Tributylstannanylium;iodide

There total 36 articles about Tributylstannanylium;iodide 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:

Reference yield: 98.0%

: 4282-44-4
1-iodo-n-undecane

: 688-73-3
tri-n-butyl-tin hydride

: 1120-21-4
n-Undecane

: 7342-47-4
tributyltin iodide

Guidance literature:: With 2,2'-azobis(isobutyronitrile); In benzene; Refluxing in benzene (8 h, N2) after addn. of AIBN as a free radical initiator, quenching of react. mixt. by cooling in ice bath.; GLC anal. with n-dodecane as an added integration std.;
DOI:10.1021/om00100a021

Reference yield: 98.0%

: 813-19-4
bis(tri-n-butyltin)

: 7342-47-4
tributyltin iodide

: 1528-01-4
methyltributyltin

Guidance literature:: With methyl iodide; dichloro bis(acetonitrile) palladium(II); In N,N,N,N,N,N-hexamethylphosphoric triamide; 20°C, molar ratio distannane/halide 1.3:1, 5 min;
DOI:10.1007/BF01141722

Reference yield: 95.0%

: 3437-95-4,149762-92-5
2-Iodothiophene

: 813-19-4
bis(tri-n-butyltin)

: 7342-47-4
tributyltin iodide

: 54663-78-4
tributyl(thien-2-yl)stannane

Guidance literature:: dichloro bis(acetonitrile) palladium(II); In N,N,N,N,N,N-hexamethylphosphoric triamide; 20°C, molar ratio distannane/halide 2:1, 80 min;
DOI:10.1007/BF01141722