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Merck

291234

Sigma-Aldrich

Dibutyltin dilaurate

95%

Sinónimos:

DBTDL

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About This Item

Fórmula lineal:
(CH3CH2CH2CH2)2Sn[OCO(CH2)10CH3]2
Número de CAS:
Peso molecular:
631.56
Beilstein/REAXYS Number:
4156980
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

0.2 mmHg ( 160 °C)

Quality Level

assay

95%

refractive index

n20/D 1.471 (lit.)

density

1.066 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC

InChI

1S/2C12H24O2.2C4H9.Sn/c2*1-2-3-4-5-6-7-8-9-10-11-12(13)14;2*1-3-4-2;/h2*2-11H2,1H3,(H,13,14);2*1,3-4H2,2H3;/q;;;;+2/p-2

InChI key

UKLDJPRMSDWDSL-UHFFFAOYSA-L

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General description

Dibutyltin dilaurate, also known as dibutyltin didodecanoate, is a dibutyltin laurate hydroxide intermediate that is commonly used as a catalyst. It is also used in the transesterification reaction.

Application

Dibutyltin dilaurate is used as a catalyst in:
  • The synthesis of polyurethane (PU) and polyhydroxyurethane (PHU) prepolymers and lignin urethane.
  • A protocol for the covalent attachment of poly(ethylene glycol) (PEG) to silicon oxide to form a hydrophilic non-fouling surface.
  • Preparation of polymers by reacting hydroxyl-terminated macromonomers and aliphatic diisocyanates.

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Muta. 2 - Repr. 1B - Skin Sens. 1 - STOT RE 1 - STOT SE 1

target_organs

thymus, thymus,Immune system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

372.2 - 379.4 °F - closed cup

flash_point_c

189 - 193 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Derivatization of pillared silicon substrates using poly (ethylene glycol) and 1-dodecanethiol.
White A
Journal of undergraduate neuroscience education : JUNE : a publication of FUN, Faculty for Undergraduate Neuroscience, 7(1), 91-98 (2007)
High bio-content polyurethane composites with urethane modified lignin as filler
Chaoqun Z,et al.
Polymer, 69, 52-57 (2015)
Preparation of polyurethane/acrylic hybrid nanoparticles via a miniemulsion polymerization process.
Li M
Macromolecules, 38(10), 4183-4192 (2005)
Mei Li et al.
ACS omega, 5(1), 529-536 (2020-01-21)
A tung-oil-based polyphenol (ATOM), containing the phenolic hydroxyl group, was synthesized from tung oil and 4-maleimidophenol by the Diels-Alder addition reaction. Then self-healing thermosetting polyurethanes were prepared from ATOM and the polyurethane prepolymer. The chemical structure and cross-link network were
Self-assembled supramolecular hydrogels formed by biodegradable PEO?PHB?PEO triblock copolymers and ?-cyclodextrin for controlled drug delivery.
Li J
Biomaterials, 27(22), 4132-4140 (2006)

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