Triphenyltin hydroxide acetate

Base Information

• Chemical Name: Triphenyltin hydroxide acetate
• CAS No.: 900-95-8
• Molecular Formula: C20H18O2Sn
• Molecular Weight: 409.072
• UNII: 70M92GQA9T
• Mol file: 900-95-8.mol

Synonyms:triphenylstannylium acetate;FENTIN ACETATE [ISO];FENTIN ACETATE [HSDB];TRIPHENYLTIN HYDROXIDE ACETATE;AKOS015837514;AS-57344;TRIPHENYLTIN HYDROXIDE ACETATE [MI]

Chemical Property of Triphenyltin hydroxide acetate

Chemical Property:

• Appearance/Colour: white crystalline solid
• Vapor Pressure: 1.9 x 10-3 Pa (60 °C)
• Melting Point: 118-122 °C
• Boiling Point: 60 °C
• PSA: 26.30000
• Density: 1.55 g/cm³
• LogP: 2.21660
• Storage Temp.: APPROX 4°C
• Water Solubility.: 28 mg/L (20 ºC)
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 410.032882
• Heavy Atom Count: 23
• Complexity: 227

Purity/Quality:

99% ^*data from raw suppliers

TriphenyltinAcetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): N,T+
• Hazard Codes: T+;N,N,T+
• Statements: 24/25-26-37/38-40-41-48/23-50/53-63
• Safety Statements: 26-28-36/37/39-45-60-61

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)[O-].C1=CC=C(C=C1)[Sn+](C2=CC=CC=C2)C3=CC=CC=C3
• Uses: Triphenyltin Acetate is an organotin compound. Triphenyltin Acetate much like its hydroxide analogue is used as a fungicide and antifeeding compound for insect control. Recent studies show that Triphenyltin Acetate may have adverse effects on the reproductive and immune systems and may disrupt the endocrine system. Fentin is a non-systemic fungicide with protective and curative action. It is used to control early and late blight in potatoes and a range of diseases in vegetables, sugar beet, peanuts, wheat, coffee, cocoa and pecans. It is also used to control algae and snails in rice fields. Fentin has previously been used as an antifoulant in marine paint.

Technology Process of Triphenyltin hydroxide acetate

There total 25 articles about Triphenyltin hydroxide acetate 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: 85.0%

triphenylstannane (892-20-6) + acetic acid (64-19-7,77671-22-8) → triphenyltin acetate (900-95-8)

Guidance literature:

In n-heptane; reaction of excess (C6H5)3SnH on refluxing for 3 h;;

Reference yield:

(C6H5)3SnCH(CH3)CH(CH3)OH (24509-93-1) → triphenyltin acetate (900-95-8)

Guidance literature:

With acetic acid; In methanol; byproducts: CH3CHCHCH3; Kinetics;

DOI:10.1021/jo00830a011 DOI:10.1016/S0022-328X(00)80222-3

Reference yield:

(C6H5)3SnCH2C(CH3)2OH (23604-58-2) → triphenyltin acetate (900-95-8)

Guidance literature:

With acetic acid; In methanol; byproducts: CH2C(CH3)2; Kinetics;

DOI:10.1021/jo00830a011 DOI:10.1016/S0022-328X(00)80222-3

upstream raw materials:

acetic acid

triphenylstannane

tributyllead acetate

triphenyl(4-t-butylphenoxo)tin(IV)

Downstream raw materials:

Ph₃SnOAl(OPrⁱ)₂

(C₆H₅)3Sn(S₂CN(C₂H₅)2)

(C₆H₅)3Sn(C₅H₅FeC₅H₄CHNNCO(C₆H₄Cl))

[(triphenyltin(IV))2 piperazine bis(dithiocarbamate)]