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)
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 |
