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88158-33-2

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88158-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88158-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,5 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88158-33:
(7*8)+(6*8)+(5*1)+(4*5)+(3*8)+(2*3)+(1*3)=162
162 % 10 = 2
So 88158-33-2 is a valid CAS Registry Number.

88158-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name butyltin tris(dibutyl phosphate)

1.2 Other means of identification

Product number -
Other names -

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:88158-33-2 SDS

88158-33-2Downstream Products

88158-33-2Relevant articles and documents

119Sn NMR spectroscopic studies of organotin phosphates as catalysts for the polymerization of epoxides

Otera, Junzo,Yano, Toru,Kunimoto, Etsuko,Nakata, Tetsuya

, p. 426 - 431 (2008/10/08)

Various organotin phosphates and pyrophosphates were prepared as model compounds for organotin phosphate catalysts effective for polymerization of epoxides. Pyrolysis of the butyltin compounds thus obtained was conducted with the pure compounds or in the presence of dibutyl phosphate (DBP). 119Sn NMR spectra allowed the characterization of these compounds. It was found that phosphate ligands are easily condensed to give P-O-P linkages and that DBP cleaves Sn-C bonds. Quite interestingly, however, the last butyl group attached to the tin resisted cleavage, and thus monobutyltin compounds resulted as final products in all cases. When an excess of DBP was present, condensation of this compound with pyrophosphato ligands took place. Condensates prepared from di- or tributyltin chlorides and oxides with tributyl phosphate under various reaction conditions also were characterized on the basis of 119Sn NMR spectra. In every case, it was found that the final products are analogous to those derived from model compounds. Polymerization studies of epichlorohydrin by various organotin phosphates and pyrophosphates as model compounds led to the conclusion that the monobutyltin pyrophosphate 11 is associated with an actual active species. On the basis of these results, the nature of organotin phosphate catalysts is discussed.

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