TRIBUTYLPHENYLTIN

Product Information

Molecular Formula:
C18H32Sn
Molecular Weight:
367.16
Description
TRIBUTYLPHENYLTIN is a widely used biomedical compound. It offers a glimmer of hope in the fight against many forms of cancer and inflammatory diseases.
Synonyms
PHENYLTRI-N-BUTYLTIN; PHENYLTRIBUTYLSTANNANE; PHENYLTRIBUTYLTIN; TRIBUTYLPHENYLTIN; Tributyl-phenyl-stannane; Phenyltributylstannane, Phenyltributyltin, Tributylphenyltin; 1-(Tributylstannyl)benzene; Tributylphenyltin(IV)
IUPAC Name
tributyl(phenyl)stannane
Canonical SMILES
CCCC[Sn](CCCC)(CCCC)C1=CC=CC=C1
InChI
InChI=1S/C6H5.3C4H9.Sn/c1-2-4-6-5-3-13*1-3-4-2/h1-5H3*1,3-4H2,2H3
InChI Key
SYUVAXDZVWPKSI-UHFFFAOYSA-N
Boiling Point
125-128ºC0.14 mm Hg(lit.)
Flash Point
235.4 °F - closed cup
Purity
95%
Density
1.125 g/mL at 25 °C(lit.)
Refractive Index
n20/D 1.516 (lit.)

Safety Information

Hazards
H301 - H312 - H315 - H319 - H372 - H410
Precautionary Statement
P273 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P305 + P351 + P338 - P314

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
10
Exact Mass
368.152604 g/mol
Monoisotopic Mass
368.152604 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
184
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-112679532-A Boron-nitrogen-benzene shunt thiophene derivative, conjugated high-molecular polymer, preparation method of conjugated high-molecular polymer and application of conjugated high-molecular polymer in fluorine ion detection 2020-11-11
CN-112679532-B Boron-nitrogen-benzene shunt thiophene derivative, conjugated high-molecular polymer, preparation method of conjugated high-molecular polymer and application of conjugated high-molecular polymer in fluorine ion detection 2020-11-11
CN-112111069-A Preparation method and application of palladium nanoparticle-supported benzothiazole-linked covalent organic framework material 2020-09-30
WO-2022047230-A1 Compounds, compositions and methods for histone lysine demethylase inhibition 2020-08-28
CN-111187399-A Near-infrared light-controlled bistable field effect transistor polymer and preparation method and application thereof 2020-02-26
CN-111187399-B Near-infrared light-controlled bistable field effect transistor polymer and preparation method and application thereof 2020-02-26
ES-2824324-A1 PREPARATION OF METAL CERAMIC HETEROGENEOUS CATALYSTS WITH THREE-DIMENSIONAL STRUCTURE OBTAINED BY 3D PRINTING 2019-11-08
ES-2824324-B2 PREPARATION OF METAL CERAMIC HETEROGENEOUS CATALYSTS WITH THREE-DIMENSIONAL STRUCTURE OBTAINED BY 3D PRINTING 2019-11-08
WO-2021089901-A1 Preparation of heterogeneous ceramic metal catalysts with three-dimensional structure obtained by 3d printing 2019-11-08
WO-2021066059-A1 Compound, material for organic electroluminescent element, organic electroluminescent element, and electronic device 2019-10-01
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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