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Stannane, dibutylbis(butylthio)-, also known as dibutyltin bis(butylthioglycolate), is a chemical compound with the formula (C4H9)2Sn(SC2H4OC2H5)2. It is a derivative of dibutyltin, where two butylthio groups are attached to the central tin atom. This organotin compound is primarily used as a catalyst in various industrial processes, such as the production of polyurethane foams and the vulcanization of rubber. It is known for its effectiveness in promoting cross-linking and improving the mechanical properties of the final products. However, due to concerns over the environmental impact and potential health risks associated with organotin compounds, its use has been restricted or banned in some applications and regions.

3065-53-0

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3065-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3065-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3065-53:
(6*3)+(5*0)+(4*6)+(3*5)+(2*5)+(1*3)=70
70 % 10 = 0
So 3065-53-0 is a valid CAS Registry Number.

3065-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutyl-bis(butylsulfanyl)stannane

1.2 Other means of identification

Product number -
Other names dibutyltin dibutanethiolate

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:3065-53-0 SDS

3065-53-0Upstream product

3065-53-0Relevant academic research and scientific papers

Mechanism of tin(IV) -catalysed urethane formation

Houghton, Roy P.,Mulvaney, Andrew W.

, p. 21 - 27 (1996)

It has been found that dibutyltin dilaurate and dibutyltin dibutanethiolate are almost equally effective as catalysts in the formation of a urethane from phenyl isocyanate and butanol, and that the catalytic activity of both compounds is inhibited by thiols. These results are consistent with a mechanism which involves the N-coordination of the isocyanate with a tin alkoxide that is formed by alcoholysis of the starting tin compound.

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