Examples of 'dibutyltin' in a sentence
Meaning of "dibutyltin"
Dibutyltin is an adjective that refers to a compound containing tin and two butyl groups, commonly used in chemical reactions or as a catalyst
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- A metabolite byproduct of tributyltin.
How to use "dibutyltin" in a sentence
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dibutyltin
Monobutyltin and dibutyltin were not detected detection.
Dibutyltin dimethoxide is reported as a particularly effective catalyst.
Organotin compounds such as dibutyltin dilaurate are preferred.
Dibutyltin diacetate and dibutyltin dilaurate are preferred.
An example that may be mentioned is dibutyltin dilaurate.
Examples are dibutyltin dilaurate and dibutyltin oxide.
An exemplary organotin compound comprises dibutyltin dilaurate.
Dibutyltin dilaurate is a preferred metalorganic catalyst.
Particularly preferred is stannous dioctoate or dibutyltin dilaurate.
Triethylene diamine and dibutyltin dilaurate are preferred catalysts.
This resulted in stable emulsion of dibutyltin dioleate.
Catalysts such as dibutyltin dilaurate may accelerate the reaction.
A very particularly preferred dialkyltin dicarboxylate is dibutyltin dilaurate.
Dibutyltin dilaurate was employed as catalyst.
An example of the catalyst is dibutyltin dilaurate.
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A drop of dibutyltin dilaurate catalyst is added to the reaction mixture.
One suitable example of the catalyst is dibutyltin dilaurate.
Dibutyltin diacetate was obtained pure.
An exemplary organotin compound is dibutyltin dilaurate.
Dibutyltin dilaurate is used in high concentrations to catalyze the reaction.
Usually butyl stannoic acid or dibutyltin oxide are used.
Dibutyltin dilaurate and stannous octoate are used most routinely.
The catalyst used was dibutyltin dilaurate.
The dibutyltin dilaurate was then added and the solution mixed.
The catalyst used in the examples is dibutyltin laurate.
Some examples include dibutyltin dilaurate and dibutyltin oxide.
Suitable catalysts include dioctyltin oxide and dibutyltin oxide.
Catalysts employed are preferably dibutyltin dilaurates or triethylenediamine in dipropylene glycol.
Most preferred according to the present invention is dibutyltin dilaurate.
It is preferred to use dibutyltin dilaurate in the preparation of the stabiliser.
The reaction is carried out in the presence of dibutyltin dilaurate.
Dibutyltin dilaurate is preferred.
Particularly suitable is dibutyltin diacetylacetonate.
Dibutyltin dilaurate may be used to significantly improve the reaction rate.
A preferred catalyst is dibutyltin diacetate.
Catalysts such as dibutyltin dilaurate may be used to assist uralkyd formation.
Tetrabutyltin is the starting material of the tributyltin and dibutyltin compounds.
The reaction is carried out using dibutyltin oxide as transesterification catalyst.
Then dibutyltin dilaurate was gradually added to the solution with stirring.
Examples include materials such as dibutyltin dilaurate and dibutyltin diacetate.
Dibutyltin dilaurate and dibutyltin diacetate may be mentioned as illustrations of organometallic compounds.
Of these stannous octoate and dibutyltin dilaureate are most frequently applied.
The catalyst can be an organotin compound for example dibutyltin dilaurate.
The use of dibutyltin oxide in a reaction with carbohydrates is also disclosed in the article.
The preferred catalyst used in the present invention is dibutyltin dilaurate.
Dibutyltin dilaurate is used as a catalyst in the step of forming the functionalised isocyanate product.
The activity of the novel catalysts is compared with that of dibutyltin dilaurate.
The patentees describe the use of a dibutyltin diacetyl acetonate catalyst to avoid these problems.
This is emphatically not the case with the corresponding dibutyltin compounds.
This confirmed that activation by dibutyltin oxide was necessary for the observed regioselectivity of sulfation.