|  | |  |  | Tributyl(vinyl)tin Basic information | 
|  |  | Tributyl(vinyl)tin Chemical Properties | 
 | Melting point | <0°C |  | Boiling point | 104-106 °C/3.5 mmHg (lit.) |  | density | 1.085 g/mL at 25 °C (lit.) |  | refractive index | n20/D 1.478(lit.) |  | Fp | >230 °F |  | storage temp. | Refrigerator |  | solubility | Chloroform (Soluble), Ethyl Acetate (Sparingly) |  | form | liquid |  | color | Colourless |  | Specific Gravity | 1.085 |  | Water Solubility | Not miscible or difficult to mix in water. |  | Hydrolytic Sensitivity | 1: no significant reaction with aqueous systems |  | BRN | 3537662 |  | Exposure limits | ACGIH: TWA 0.1 mg/m3; STEL 0.2 mg/m3 (Skin) NIOSH: IDLH 25 mg/m3; TWA 0.1 mg/m3
 |  | Stability: | Light sensitive |  | InChIKey | QIWRFOJWQSSRJZ-UHFFFAOYSA-N |  | CAS DataBase Reference | 7486-35-3(CAS DataBase Reference) |  | NIST Chemistry Reference | Stannane, tributylethenyl-(7486-35-3) | 
|  |  | Tributyl(vinyl)tin Usage And Synthesis | 
 | Chemical Properties | clear colorless to pale yellow liquid |  | Uses | Tributyl(vinyl)tin is used as a reagent in the palladium catalyzed synthesis of allyl and benzyl ethers. Tributyl(vinyl)tin is also a vinyl nucleophile for bromoacetylene and bromoaromatics. |  | Uses | Tributyl(vinyl)tin is used as a reagent in the palladium catalyzed synthesis of allyl and benzyl ethers. It is also a vinyl nucleophile for bromoacetylene and bromoaromatics. |  | Purification Methods | Fractionate the stannane under reduced pressure and taking the middle fraction to remove impurities such as (n-Bu)3SnCl. [Seyferth & Stone J Am Chem Soc 79 515 1957, Beilstein 16 III 1279.] | 
|  |  | Tributyl(vinyl)tin Preparation Products And Raw materials | 
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