Cas no 7342-47-4 (iodotributyltin)

Iodotributyltin (C12H27ISn) is an organotin compound primarily used as an intermediate in organic synthesis and catalytic applications. Its key advantages include high reactivity in Stille coupling reactions, facilitating carbon-carbon bond formation in complex molecule construction. The compound exhibits stability under controlled conditions, making it suitable for use in specialized chemical processes. Its iodine substituent enhances selectivity in cross-coupling reactions, while the tributyltin group contributes to efficient transmetallation steps. Iodotributyltin is also employed in polymer stabilization and as a precursor for other organotin derivatives. Proper handling is essential due to its toxicity and moisture sensitivity.
iodotributyltin structure
iodotributyltin structure
Product Name:iodotributyltin
CAS No:7342-47-4
MF:C12H27ISn
MW:416.957255601883
CID:978061
PubChem ID:24860097
Update Time:2025-05-30

iodotributyltin Chemical and Physical Properties

Names and Identifiers

    • iodotributyltin
    • Tri-n-butyltin iodide
    • tributyl(iodo)stannane
    • Iodotributylstannane
    • Stannane,iodotributyl
    • Stannane,tributyliodo
    • Tin,tri-n-butyl-,iodide
    • Tributyltin iodide
    • tri-n-Butyliodotin
    • tri-n-butylstannyl iodide
    • Tri-n-butyl tin iodide
    • Bu3SnI
    • Tributyliodostannane
    • Tin, tri-n-butyl-, iodide
    • NS00126918
    • 7342-47-4
    • Stannane, iodotributyl-
    • MFCD00074996
    • DTXSID20223653
    • Tributyltin iodide, technical grade, 90%
    • Stannane, tributyliodo-
    • DTXCID50146144
    • MDL: MFCD00074996
    • Inchi: 1S/3C4H9.HI.Sn/c3*1-3-4-2;;/h3*1,3-4H2,2H3;1H;/q;;;;+1/p-1
    • InChI Key: YHHVXVNXTMIXOL-UHFFFAOYSA-M
    • SMILES: I[Sn](CCCC)(CCCC)CCCC

Computed Properties

  • Exact Mass: 418.01800
  • Monoisotopic Mass: 418.01795g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 104
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 0?2

Experimental Properties

  • Color/Form: Not determined
  • Density: 1.46?g/mL?at 25?°C(lit.)
  • Melting Point: Not available
  • Boiling Point: 172?°C/10?mmHg(lit.)
  • Flash Point: Degrees Fahrenheit:235.4°F
    Degrees Celsius:113°C
  • Refractive Index: n20/D 1.53(lit.)
  • PSA: 0.00000
  • LogP: 5.76720
  • Sensitiveness: Light Sensitive
  • Solubility: Not determined
  • Vapor Pressure: Not available

iodotributyltin Security Information

iodotributyltin Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd.
333034-10G
iodotributyltin
7342-47-4 90%
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A FA AI SHA , SAI MO FEI SHI ER KE JI QI XIA GONG SI
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iodotributyltin Production Method

Additional information on iodotributyltin

Introduction to Iodotributyltin (CAS No. 7342-47-4)

Iodotributyltin, also known as tributyltin iodide, is a versatile organotin compound with the CAS number 7342-47-4. This compound has garnered significant attention in various fields due to its unique chemical properties and wide-ranging applications. In recent years, advancements in synthetic methodologies and its utilization in cutting-edge research have further solidified its importance in both academic and industrial settings.

The molecular structure of iodotributyltin consists of a tin atom bonded to three butyl groups and one iodine atom. This configuration imparts it with distinct reactivity, making it a valuable reagent in organic synthesis. Recent studies have highlighted its role in catalytic processes, particularly in the formation of biologically active molecules and advanced materials. Its ability to act as a Lewis acid has been exploited in asymmetric catalysis, contributing to the development of enantioselective reactions.

In the realm of materials science, iodotributyltin has found applications in the synthesis of low-dimensional nanomaterials. Researchers have utilized its tin core to fabricate tin-based quantum dots and nanoparticles, which exhibit promising properties for optoelectronic devices. These materials have potential applications in solar cells, light-emitting diodes (LEDs), and sensors, underscoring the compound's versatility across disciplines.

The synthesis of tributyltin iodide has undergone significant refinement in recent years. Traditional methods involving the reaction of tin with alkyl halides have been complemented by more efficient protocols that minimize waste and enhance yield. For instance, the use of microwave-assisted synthesis has been reported to accelerate the formation of iodotributyltin, offering a greener alternative to conventional methods.

In terms of environmental impact, while iodotributyltin itself is not classified as hazardous under standard conditions, its application in industrial processes necessitates careful handling to prevent unintended releases into the environment. Recent research has focused on understanding its fate in aquatic ecosystems and developing remediation strategies should contamination occur.

The toxicological profile of tributyltin iodide has also been a subject of interest. Studies indicate that exposure to high concentrations can lead to adverse effects on aquatic organisms, particularly marine species. However, ongoing research aims to develop safer alternatives and improve risk assessment methodologies to mitigate potential hazards associated with its use.

Looking ahead, the future of iodotributyltin lies in its integration into emerging technologies such as bio-inspired materials and energy storage systems. Its role as a precursor in the synthesis of tin-based alloys for lithium-ion batteries is an area gaining traction due to the growing demand for high-capacity energy storage solutions.

In conclusion, iodotributyltin (CAS No. 7342-47-4) stands as a testament to the ingenuity of modern chemistry, offering a myriad of applications across diverse fields. As research continues to uncover new avenues for its utilization, this compound is poised to remain a cornerstone in both academic exploration and industrial innovation.

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