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15231-44-4

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15231-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15231-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,3 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15231-44:
(7*1)+(6*5)+(5*2)+(4*3)+(3*1)+(2*4)+(1*4)=74
74 % 10 = 4
So 15231-44-4 is a valid CAS Registry Number.
InChI:InChI=1/2C8H17.Sn/c2*1-3-5-7-8-6-4-2;/h2*1,3-8H2,2H3;/rC16H34Sn/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3-16H2,1-2H3

15231-44-4SDS

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 DIOCTYLTIN

1.2 Other means of identification

Product number -
Other names dioctylstannane

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:15231-44-4 SDS

15231-44-4Downstream Products

15231-44-4Related news

A detailed analysis of the pyrolysis products from DIOCTYLTIN (cas 15231-44-4) maleate and its mixture with PVC08/04/2019

The thermal decomposition of dioctyltin maleate (DOTM) and a blend of PVC and DOTM has been studied in air, nitrogen and under vacuum. TG was used to examine the effect of different amounts of DOTM on stability. The PVC/DOTM mixture shows delayed dehydrochlorination in both the air and inert env...detailed

Acute toxic effects of DIOCTYLTIN (cas 15231-44-4) on immune system of rats08/03/2019

In the present study, dioctyltin chloride (DOTC: 100 mg/kg, BW) was orally administered to immature (30-day-old) male rats, and the acute toxic effects were studied. Di- and monooctyltin (its metabolite) accumulations were mainly detected in the liver, and peaked 48 h later. A similar pattern wa...detailed

“Simulated gastric hydrolysis and developmental toxicity of DIOCTYLTIN (cas 15231-44-4) bis(2-Ethylhexylthioglycolate) [DOTE] in rabbits and mice”08/02/2019

Based on previous studies, dioctyltin dichloride [DOTC] was a putative toxophore for dioctyltin thioesters. Our results, generated with the use of 119Sn-NMR spectroscopy demonstrated that dioctyltin bis(2-ethylhexyl thioglycolate) [DOTE] hydrolyzed to form dioctyltin chloro-(2-ethylhexyl thiogly...detailed

Preparation of tin oxide particles using tin-contained organic substance of DIOCTYLTIN (cas 15231-44-4) oxide as the starting material by a calcination method08/01/2019

For the first time, erect and flaky particles of tin oxides (SnO2), as anode materials for lithium ion batteries (LIBs), were prepared by a calcination method using dioctyltin oxide as the starting material. The samples calcined at 300, 500 and 700 °C under the air conditions were nominated as ...detailed

15231-44-4Relevant articles and documents

Une methode simple et efficace de preparation des dihydrures organostanniques

Deleuze, H.,Maillard, B.

, p. C14 - C17 (2007/10/02)

A new and efficient method of preparation of R2SnH2 is proposed.Organodioxastannolanes were used as starting materials, these compounds being easily obtained by azeotropic distillation of water from a solution of diorganotin oxides and 1,2 diols in cyclohexane.Their reduction by commercial BH3/THF complex gave raw dialkyltin dihydrides with excellent yields and high purity degrees. Keywords: Borane; Reduction; Dialkylstannanes; 1,3-dioxa-2-stannolanes; Synthesis

Novel tin (IV) compounds

-

, (2008/06/13)

Novel tetracoordinated tin (IV) compounds, well suited as latent catalysts for the preparation of polyurethanes or for the crosslinking of curable diorganopolysiloxanes (upon thermal decomposition thereof into diorganotin dicarboxylates or dialcoholates), have the general formula (1): STR1 in which the radicals R, which may be the same or different, are each a linear or branched chain C1 -C20 alkyl radical, a mononuclear aryl radical, or an aralkyl or alkaryl radical, the alkyl moieties of which having from 1 to 6 carbon atoms; the radicals R1 and R2, which may be the same or different, are each a hydrogen atom, a cyano radical, a C1 -C6 alkyl radical, or an alkoxycarbonyl radical, the alkyl moiety of which having from 1 to 6 carbon atoms, with the proviso that R1 and R2 may together form a saturated hydrocarbon ring member having from 5 to 8 carbon atoms; the radical R3 is a hydrogen atom, a linear or branched chain C1 -C20 alkyl radical, a linear or branched chain C1 -C20 alkoxy radical, a mononuclear aryl radical or a mononuclear aryloxy radical; and a is 0 or 1.

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