triphenyltin hydride

Product Information

Molecular Formula:
C18H16Sn
Molecular Weight:
351.030
Description
Triphenyltin hydride is an organotin compound. Tin is a chemical element with the symbol Sn and atomic number 50. It is a natural component of the earth's crust and is obtained chiefly from the mineral cassiterite, where it occurs as tin dioxide.
Synonyms
Stannane, triphenyl-; triphenyl-stannan; Triphenylstannyl hydride; triphenylstannylhydride; TRIPHENYLSTANNANE; TRIPHENYLTIN; TRIPHENYLTIN HYDRIDE; Triphenylhydridetin(IV)
Canonical SMILES
C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChI=1S/3C6H5.Sn/c3*1-2-4-6-5-3-1/h3*1-5H
InChI Key
SBXWFLISHPUINY-UHFFFAOYSA-N
Boiling Point
163-165°C0.3 mm Hg(lit.)
Melting Point
28°C(lit.)
Flash Point
235.4 °F - closed cup
Purity
95%
Density
1.374
Storage
0-6°C
Refractive Index
n20/D 1.632 (lit.)

Safety Information

Hazards
H301 + H311 + H331 - H410
Precautionary Statement
P273 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P304 + P340 + P311

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
351.019578 g/mol
Monoisotopic Mass
351.019578 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
202
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-114163927-A Waterproof material and preparation method and application thereof 2021-11-09
CN-113740465-A Method for detecting organic tin in children toy 2021-09-23
CN-113667070-A Low-smoke halogen-free flame-retardant cable compatilizer, maleic anhydride grafted modified polyolefin and preparation method thereof 2021-09-17
CN-113698903-A Molecular sieve based amine catalyst and rapidly-curable MS sealant 2021-08-25
CN-113429875-A Steel wool resistant paint without organotin and preparation method thereof 2021-08-09
CN-113603695-A Substituted pyrimidinamine compound or salt thereof acceptable as pesticide, composition and application thereof 2021-08-05
CN-113176369-A Method for determining organic tin in marine shellfish product 2021-04-09
RU-2765955-C1 Pulmonary metastasis inhibitor 2021-03-30
CN-113072465-A Carbodiimide modified polyisocyanate, preparation method thereof and catalyst system 2021-03-29
CN-113145142-A Preparation method of tin-based catalyst and application of tin-based catalyst in acetylene hydration reaction 2021-02-07

Literatures

PMID Publication Date Title Journal
35998708 2022-10-15 The organotin triphenyltin disrupts cholesterol signaling in mammalian ovarian steroidogenic cells through a combination of LXR and RXR modulation Toxicology and applied pharmacology
32504733 2020-09-01 Triphenyltin chloride reduces the development of rat adrenal cortex during puberty Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association
32525019 2020-08-15 The triphenyltin carboxylate derivative triphenylstannyl 2-(benzylcarbamoyl)benzoate impedes prostate cancer progression via modulation of Akt/FOXO3a signaling Toxicology and applied pharmacology
32173372 2020-05-01 Thyroid disruption and developmental toxicity caused by triphenyltin (TPT) in zebrafish embryos/larvae Toxicology and applied pharmacology
31927052 2020-04-01 Tributyltin and triphenyltin induce 11β-hydroxysteroid dehydrogenase 2 expression and activity through activation of retinoid X receptor α Toxicology letters
31765896 2020-03-01 Long-term triphenyltin exposure disrupts adrenal function in adult male rats Chemosphere
31634547 2020-01-01 Down-regulation of vimentin by triorganotin isothiocyanates-nuclear retinoid X receptor agonists: A proteomic approach Toxicology letters
32879257 2020-01-01 Tri-substituted organotin compounds, but not retinoic acid, are potent ligands of complement component 8 γ The Journal of toxicological sciences
30772500 2019-05-15 Stem Leydig cell regeneration in the adult rat testis is inhibited after a short-term triphenyltin exposure Toxicology letters
29549738 2018-07-30 Organotin exposure stimulates steroidogenesis in H295R Cell via cAMP pathway Ecotoxicology and environmental safety
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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