15719-34-3

Usage

Uses

Used in Polyurethane Production:
DIBUTYLTIN DIISOTHIOCYANATE, 97% is used as a catalyst for the urethane reaction in the production of polyurethane foam and elastomers, enabling fast curing times and high crosslinking density for improved product quality and performance.
Used in Coatings Industry:
DIBUTYLTIN DIISOTHIOCYANATE, 97% is used as a catalyst in the production of coatings, enhancing the curing process and contributing to the final product's durability and resistance properties.
Used in Adhesives and Sealants Industry:
DIBUTYLTIN DIISOTHIOCYANATE, 97% is used as a catalyst in the formulation of adhesives and sealants, promoting rapid curing and ensuring strong bonding and sealing capabilities.

InChI:InChI=1/2C4H9.2CNS.Sn/c2*1-3-4-2;2*2-1-3;/h2*1,3-4H2,2H3;;;/q;;2*-1;+2/rC8H18Sn.2CNS/c1-3-5-7-9-8-6-4-2;2*2-1-3/h3-8H2,1-2H3;;/q+2;2*-1

Upstream product

• 818-08-6 di(n-butyl)tin oxide 
• 683-18-1 dibutyltin chloride 

Downstream Products

• 683-18-1 dibutyltin chloride 
• 90040-25-8 (thiocyanato)(dibutyl) tin N-phenyl-p-chlorobenzohydroxamate 
• 674798-81-3 ([Sn(n-Bu)2(NCS)(H2-3-MeOsalen)]2(μ-H2-3-MeOsalen))[Sn(n-Bu)2(NCS)4] 

Relevant academic research and scientific papers

THE SYNTHESIS AND TIN-119m MOESSBAUER SPECTRA OF SOME DIORGANOTIN DIHALIDE AND DIPSEUDOHALIDE COMPLEXES WITH NITROGEN AND OXYGEN-DONOR LIGANDS

The synthesis and 119mSn Moessbauer spectra of 114 complexes of the type R2SnX2, L2 (R = Me, Et, n-Pr, n-Bu, n-Oct, Ph, Bz; X = F, Cl, Br, I, NCS; L2 = 2 monodentate or 1 bidentate O- or N-donor ligand(s)), 74 of which are new, are reported.The majority of the complexes are isostructural, having an octahedral trans-R2SnX4 geometry about tin, whilst five of the diphenyltin complexes (R = Ph; X = Cl; L2 = AMP, Nphen; X = NCS; L2 = bipy, phen, TMphen) adopt a cis-R2SnX4 octahedral structure.A convenient method for the synthesis of a number of novel 1:1 diorganotin difluoride complexes using hot acetonitrile is reported and a structure for the unusual adduct, Ph2SnF2 * 0.5 phen, is proposed.

Azolobenzazepine derivatives as neurologically active agents

PCT No. PCT/GB97/00592 Sec. 371 Date Sep. 3, 1998 Sec. 102(e) Date Sep. 3, 1998 PCT Filed Mar. 4, 1997 PCT Pub. No. WO97/32883 PCT Pub. Date Sep. 12, 1997The invention relates to azolobenzazepine derivatives of formula (I), wherein: X is O or S; R1, R2, R3 and R4 are independently hydrogen, perfluorolower-alkyl, halogen, nitro or cyano; and C together with the carbon atoms to which it is attached forms a 5-membered aromatic heterocycle selected from the group consisting of a pyrazol and triazole, to pharmaceutical compositions containing them and to methods for the treatment of neurological disorders utilizing them.