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Tin(4+) diethane-1,2-bis(thiolate), also known as diethyltin(IV) dithionate, is an organotin compound with the chemical formula C4H10O4SSn. It is a colorless crystalline solid that is soluble in water and organic solvents. tin(4+) diethane-1,2-bis(thiolate) is formed by the coordination of two ethanethiolate (HSCH2CH3) ligands to a central tin(IV) ion. It is used in various applications, including as a catalyst, a stabilizer for PVC, and a fungicide in agriculture. Due to its potential environmental and health risks, the use of organotin compounds like tin(4+) diethane-1,2-bis(thiolate) is regulated in many countries.

176-56-7

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176-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176-56-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,7 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 176-56:
(5*1)+(4*7)+(3*6)+(2*5)+(1*6)=67
67 % 10 = 7
So 176-56-7 is a valid CAS Registry Number.

176-56-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,2-ethanedithiol)2Sn(IV)

1.2 Other means of identification

Product number -
Other names (EDT)2Sn(IV)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:176-56-7 SDS

176-56-7Downstream Products

176-56-7Relevant academic research and scientific papers

The structures of 2,2-dialkyl-1,3,2-dithiastannolanes

Davies, Alwyn G.,Slater, Sean D.,Povey, David C.,Smith, Gallienus W.

, p. 283 - 294 (1988)

The structure of 2,2-dibutyl-1,3,2-dithiastannolane in the solid state has been determined by single crystal X-ray diffraction.Individual molecules interact weakly with two neighbouring molecules to form two long (3.688 Angstroem) Sn-S coordinate bonds.The tin atoms can therefore be regarded as being weakly 6-coordinate.In contrast, in the crystal, 2,2-dimethyl-1,3,2-dithiastannolane forms one short coordinate bond (3.18 Angstroem) to a neighbouring molecule, and the tin can be regarded as being strongly 5-coordinate.The (13)C and (117/119)Sn NMR spectra of the dimethyl-, diethyl-, diisopropyl-, and dibutyl-stannolanes, and of spirobis(ethane-l,2-dithiolato)tin have been recorded in solution and the solid state, and correlated with the evidence from X-ray crystallography.It is argued that the diethyl- and diisopropyl-stannolanes have structures similar to that of the dibutyl derivative.

Dissolution of Sn, SnO, and SnS in a Thiol-Amine Solvent Mixture: Insights into the Identity of the Molecular Solutes for Solution-Processed SnS

Buckley, Jannise J.,McCarthy, Carrie L.,Del Pilar-Albaladejo, Joselyn,Rasul, Golam,Brutchey, Richard L.

, p. 3175 - 3180 (2016)

Binary solvent mixtures of alkanethiols and 1,2-ethylenediamine have the ability to readily dissolve metals, metal chalcogenides, and metal oxides under ambient conditions to enable the facile solution processing of semiconductor inks; however, there is little information regarding the chemical identity of the resulting solutes. Herein, we examine the molecular solute formed after dissolution of Sn, SnO, and SnS in a binary solvent mixture comprised of 1,2-ethanedithiol (EDT) and 1,2-ethylenediamine (en). Using a combination of solution 119Sn NMR and Raman spectroscopies, bis(1,2-ethanedithiolate)tin(II) was identified as the likely molecular solute present after the dissolution of Sn, SnO, and SnS in EDT-en, despite the different bulk material compositions and oxidation states (Sn0 and Sn2+). All three semiconductor inks can be converted to phase-pure, orthorhombic SnS after a mild annealing step (~350 °C). This highlights the ability of the EDT-en solvent mixture to dissolve and convert a variety of low-cost precursors to SnS semiconductor material.

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