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Dicyclohexyldichlorotin, with the chemical formula C12H22Cl2Sn, is a white solid organotin compound. It is primarily recognized for its catalytic properties in organic synthesis, particularly in the production of polyurethanes and polyesters. Additionally, it serves as a stabilizer in PVC (polyvinyl chloride) products, preventing degradation caused by heat and light exposure. Despite being part of a family of organotin compounds that have raised environmental and health concerns, dicyclohexyldichlorotin is considered to have low toxicity and is not believed to pose a significant risk when used as directed.

3342-69-6

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3342-69-6 Usage

Uses

Used in Chemical Synthesis Industry:
Dicyclohexyldichlorotin is used as a catalyst in the production of polyurethanes and polyesters, facilitating the synthesis of these polymers for various applications, including flexible and rigid foams, coatings, adhesives, and elastomers.
Used in Plastics and Polymer Industry:
As a stabilizer in PVC products, dicyclohexyldichlorotin is used to prevent the degradation of polyvinyl chloride caused by exposure to heat and light, thereby enhancing the durability and longevity of PVC-based materials in construction, automotive, and consumer goods applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3342-69-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,4 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3342-69:
(6*3)+(5*3)+(4*4)+(3*2)+(2*6)+(1*9)=76
76 % 10 = 6
So 3342-69-6 is a valid CAS Registry Number.
InChI:InChI=1/2C6H11.2ClH.Sn/c2*1-2-4-6-5-3-1;;;/h2*1H,2-6H2;2*1H;/q;;;;+2/p-2/rC12H22Cl2Sn/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-12H,1-10H2

3342-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dichloro(dicyclohexyl)stannane

1.2 Other means of identification

Product number -
Other names Dichlorodicyclohexylstannane

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:3342-69-6 SDS

3342-69-6Relevant articles and documents

ORGANOTIN BIOCIDES. V. THE STRUCTURE OF DICYCLOHEXYLTIN DICHLORIDE

Molloy, K. C.,Quill, K.,Nowell, I. W.

, p. 271 - 280 (1985)

The crystal and molecular structure of dicyclohexyltin dichloride has been solved by heavy atom methods in conjunction with least-squares data collected on a two-circle automatic diffractometer.Crystals are orthorhombic, space group Pbcm, cell dimensions a 6.671(5), b 9.445(6), c 24.203(12) Angstroem, U 1525.0 Angstroem3 and Z=4.The structure was refined using 1527 reflections to final discrepancy factors of R=0.047 and R'=0.058.The local geometry at tin is a severely distorted trans-R2SnCl4 octahedron.Chlorine atoms serve as bridging groups to link sub-units into a one dimensional polymer along b.

Electrophilic cleavage of tin-alicyclic and tin-aryl bonds involving the synthesis of cyclohexyl-tin, -tellurium and -antimony compounds - Part I

Singhal, Kiran

, p. 542 - 544 (2007/10/02)

Cyclohexyl-tin, -tellurium and -antimony halides have been obtained in good yields by the electrophilic cleavage of Sn-C bond(s) from symmetrical and unsymmetrical cyclohexyl tins, CynPnPh4-n (n = 1, 2, 4) employing Br2, I2, ICl, IBr, TeCl4 and SbCl5 in CCl4 under mild conditions.

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