Examples of 'glycidol' in a sentence
Meaning of "glycidol"
'Glycidol' is a noun that refers to a chemical compound used in various industrial processes, such as the production of resins, plastics, and other materials. It is also known for its potential health risks and is a subject of research and regulation in occupational and environmental health
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- The epoxide derived from glycerol; it has a number of industrial uses
How to use "glycidol" in a sentence
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glycidol
Glycidol itself is categorised as probably carcinogenic to humans.
Glycidyl fatty acid esters expressed as glycidol.
Preparation of glycidol in the presence of different catalysts.
Examples of epoxide monomers are epichlorhydrine and glycidol.
Methanol and glycidol are very particularly preferred.
Examples of epoxide monomers are epichlorohydrine and glycidol.
Glycidol is then added to the mixture obtained.
Essentially quantitative conversion of glycidol to glycidyl acetoacetate was confirmed.
Glycidol and acrolein were primarily produced by glycerin degradation.
As the epoxy compound is preferably mentioned glycidol or epoxypropane.
Use of glycidol gives also polyols with increased functionalities.
They may be prepared by reacting a fluoroalcohol with glycidol.
Glycidol is added under nitrogen to a cooled stirring solution of neat ethanolamine.
Synthesis of a protected form of glycidol.
The reaction of an alcohol with glycidol using an acidic or basic catalyst.
See also
Complete hydrolysis of the racemic ester mixture leads to racemic glycidol.
The polymerization of the glycidol was monitored by measuring epoxy equivalent weight.
Glycidol ethers can also be prepared by following the procedures described below.
Glycidyl fatty acid esters are hydrolysed into glycidol in the gastrointestinal tract.
The glycidol is thereafter recovered from its azeotrope by extraction with water.
Some seed monomers may comprise epoxy groups such as glycidol methacrylate.
A small fraction of glycidol may react with the secondary alcohol grouping.
It is also possible to use esters of dibasic acids or multibasic acids with glycidol.
Glycidol is used as a stabilizer for natural oils and vinyl polymers and as a demulsifier.
The enantiomeric excess in the glycidol formed in hydrolysis decreases as the conversion proceeds.
Glycidol is an organic compound that contains both epoxide and alcohol functional groups.
Carrying out ring opening polymerization of glycidol on the aromatic hydrophobic polymeric segment.
This process comprises storing refined diphenylmethane diisocyanate in intimate admixture with glycidol.
The glycidol addition was then continued while maintaining the reaction temperature at a mild reflux.
Several consecutive extractions may be run to recover a maximum amount of the glycidol product.
The extraction of the glycidol product from the organic mixture is effected with water.
Examples of such base compounds that may be mentioned include glycidol and trimethylolpropane oxetane.
Glycidol in THF is slowly added using a stainless steel capillary.
Another component has been to compare the results of glycidol with results for ionizing radiation.
A GC of the reaction mixture showed no residual glycidol.
The Authority concluded that glycidol is a genotoxic and carcinogenic compound.
Glycidol is expensive, and also has carcinogenic properties.
The copolymers of the invention may be prepared from glycidol and ethylene oxide monomers.
Preparation of glycidol in the presence of different co-reagents.
Hopes to reduce people 's exposure to glycidol.
Molar yield in glycidol isolated, based on glycerol carbonate.
Cyanoethylated polyamines adducted with glycidol and their salts ;.
Preparation of glycidol in the thoroughly stirred semi-continuous reactor.
Example 1 shows a random copolymer of glycidol and ethylene oxide.
During the reaction, glycidol condensed by the condenser was recovered in the flask 6.
In the third batch, the mole ratio of glycidol to dextran was varied.
Suitable methods for the production of polyglycerol include polymerization of glycidol e . g.
At higher temperatures, the amount of glycidol compounds is significantly increased.
Where the biocatalyst is an immobilized dehalogenase, the product of the reaction is glycidol.
Of course, this results in glycidol with an excess of the other enantiomer.
