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Sigma-Aldrich

Dibutyltin dilaurate

95%

Synonym(s):

DBTDL

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About This Item

Linear Formula:
(CH3CH2CH2CH2)2Sn[OCO(CH2)10CH3]2
CAS Number:
Molecular Weight:
631.56
Beilstein:
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.

Signal Word

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 Code

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

WGK

WGK 3

Flash Point(F)

372.2 - 379.4 °F - closed cup

Flash Point(C)

189 - 193 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Controlled tin catalyzed hydrolysis of 3-acryloxypropyltrimethoxysilane with mono-and multi-functional mercaptans
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Journal of Organometallic Chemistry, 724, 213-224 (2013)
Polyurethane/polyhydroxyurethane hybrid polymers and their applications as adhesive bonding agents
Emily LK,et al.
International Journal of Adhesion and Adhesives, 64, 1-8 (2016)
Catalytic mechanisms of triphenyl bismuth, dibutyltin dilaurate, and their combination in polyurethane?forming reaction.
Luo S
Journal of Applied Polymer Science, 65(6), 1217-1225 (1997)

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