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Key Documents

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Sigma-Aldrich

Dibutyltin dilaurate

95%

Sinonimo/i:

DBTDL

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About This Item

Formula condensata:
(CH3CH2CH2CH2)2Sn[OCO(CH2)10CH3]2
Numero CAS:
Peso molecolare:
631.56
Beilstein:
4156980
Numero CE:
Numero MDL:
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.22

Tensione di vapore

0.2 mmHg ( 160 °C)

Livello qualitativo

Saggio

95%

Indice di rifrazione

n20/D 1.471 (lit.)

Densità

1.066 g/mL at 25 °C (lit.)

Stringa SMILE

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
UKLDJPRMSDWDSL-UHFFFAOYSA-L

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Descrizione generale

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.

Applicazioni

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.

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

thymus, thymus,Immune system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

372.2 - 379.4 °F - closed cup

Punto d’infiammabilità (°C)

189 - 193 °C - closed cup

Dispositivi di protezione individuale

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


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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
Preparation of polyurethane/acrylic hybrid nanoparticles via a miniemulsion polymerization process.
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Macromolecules, 38(10), 4183-4192 (2005)
Catalytic mechanisms of triphenyl bismuth, dibutyltin dilaurate, and their combination in polyurethane?forming reaction.
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Journal of Applied Polymer Science, 65(6), 1217-1225 (1997)
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