CID 13751184

Base Information

• Chemical Name: CID 13751184
• CAS No.: 56-35-9
• Molecular Formula: C24H54OSn2
• Molecular Weight: 596.112
• Hs Code.: 29310095
• Mol file: 56-35-9.mol

Synonyms:

Chemical Property of CID 13751184

Chemical Property:

• Appearance/Colour: Clear colorless liquid
• Vapor Pressure: <0.01 mm Hg ( 25 °C)
• Melting Point: -45 °C
• Refractive Index: n20/D 1.486(lit.)
• Boiling Point: 474.847 °C at 760 mmHg
• Flash Point: 240.979 °C
• PSA: 9.23000
• Density: 1.17g/mLat 25°C(lit.)
• LogP: 9.69460
• Storage Temp.: +4°C
• Sensitive.: Air & Moisture Sensitive
• Solubility.: Chloroform (Soluble), Methanol (Slightly)
• Water Solubility.: INSOLUBLE
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 18
• Exact Mass: 596.22128
• Heavy Atom Count: 27
• Complexity: 197

Purity/Quality:

99.0% ^*data from raw suppliers

Bis(tributyltin) oxide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T,N
• 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

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCC[Sn](=O)CCCC.CCCC[Sn](CCCC)(CCCC)CCCC
• Description: TBTO (bis(tri-n-butyltin)oxide) appears as thin, colourless to pale yellow, flammable and combustible liquid. It is soluble in organic solvents. TBTO, or bis(tri-n-butyltin)oxide, is an organotin compound used as a biocide, fungicide, and molluscicide. Uses of tributyltin also include as an anti-fouling chemical in marine paints for boats, anti-fungal agent in textiles and industrial water systems, in cooling tower and refrigeration water systems, wood pulp preservative in paints and paper mill systems, inner surfaces of cardboard, and in the manufacturing processes of leather goods, textiles, wood, plastics, and mothproof stored garments. In fact, TBT compounds are considered the most hazardous of all tin compounds.
• Uses: Bis(tributyltin) Oxide is an organotin compound used as a fungicide and molluscicide, particularly in wood preservation. Bis(tributyltin) Oxide was used as an active component in marine antifouling paints but is not longer used due to its toxicity and is considered a severe marine pollutant. Bis(tributyltin) oxide is widely used in Europe for the preservation of timber, millwork, and wood joinery, eg, window sashes and door frames. It is applied from organic solution by dipping or vacuum impregnation. It imparts resistance to attack by fungi and insects but is not suitable for underground use. An advantage of bis(tributyltin) oxide is that it does not interfere with subsequent painting or decorative staining and does not change the natural color of the wood. Tributyltin oxide is used as an antifouling and biocide agent against fungi, algae and bacteria in paints and is an irritant.

Technology Process of CID 13751184

There total 57 articles about CID 13751184 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: 100.0%

bis(tributyltin) carbonate (5035-69-8) → carbon dioxide (124-38-9,18923-20-1) + bis(tri-n-butyltin)oxide (56-35-9)

Guidance literature:

In not given; tin compd. was heated at 65°C under vac.;

DOI:10.1021/om000397f

Reference yield: 75.3%

(C4H9)3SnOCH(N(C2H5)2)CHCHC6H5 → C6H5CH(N(C2H5)2)CHCHN(C2H5)2 + 3-phenyl-propenal (104-55-2) + bis(tri-n-butyltin)oxide (56-35-9)

Guidance literature:

decompn. at 25°C within 8 h;

DOI:10.1016/S0022-328X(00)85507-2

Reference yield: 56.0%

tributylethynyltin (994-89-8) + μ-oxobis[(trifluoromethanesulfonato)(phenyl)iodine] (88016-29-9) → ethynylphenyl-iodonium-1,1,1-trifluoromethanesulfonate (125803-61-4) + bis(tri-n-butyltin)oxide (56-35-9)

Guidance literature:

In dichloromethane; at 0 ℃; for 0.5h;

upstream raw materials:

tributyltin chloride

tributylethynyltin

μ-oxobis[(trifluoromethanesulfonato)(phenyl)iodine]

β-(cyclohexylthio)ethyl tri-n-butyltin sulfide

Downstream raw materials:

tributyl(1-chloro-3-phenoxy-2-propanyloxy)stannane

Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{4-[4-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-phenylethynyl]-phenoxy}-tetrahydro-pyran-3-yl ester

5-(3,5-Dichlorophenylthio)-4-isopropyl-1-methyl-2-(N-methylcarbamoyl)oxymethyl-1H-imidazole

3-Phenoxycarbonyl-3,4,5,6-tetrahydro-2H-1,3-oxazin-2-one

Refernces

• 1、 Jousseaume, B.,Noiret, N.,Pereyre, M.,Frances, J. M.. "Unexpected Temperature-dependent Stereoselectivity in the Thermolysis of 2-Trialkylstannyl Alcohols". . p. 739 - 740. Retrieved 1992.
• 2、 Kai, Yuichi,Oku, Shinya,Sakurai, Kyoko,Tani, Tomohiro,Tsuchimoto, Teruhisa. "A Drastic Effect of TEMPO in Zinc-Catalyzed Stannylation of Terminal Alkynes with Hydrostannanes via Dehydrogenation and Oxidative Dehydrogenation". supporting information. . Retrieved 2019/08/21.
• 3、 Arias-Ugarte, Renzo,Sharma, Hemant K.,Morris, Andrew L.C.,Pannell, Keith H.. "Metal-catalyzed reduction of HCONR'2, R' = Me (DMF), et (DEF), by silanes to produce R'2NMe and disiloxanes: A mechanism unraveled". . p. 848 - 851. Retrieved 2012/03/07.