Examples of 'monocarboxylic acids' in a sentence
Meaning of "monocarboxylic acids"
Monocarboxylic acids are organic compounds that contain a single carboxyl group (-COOH) attached to a carbon atom. They are characterized by their acidic properties, which arise from the dissociation of the carboxyl group into a hydrogen ion (H+) and a carboxylate ion. Monocarboxylic acids have various applications in industries such as pharmaceuticals, food production, and chemical synthesis
How to use "monocarboxylic acids" in a sentence
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monocarboxylic acids
If desired also monocarboxylic acids can be applied.
Monocarboxylic acids may also be used if desired.
Examples of suitable monocarboxylic acids are fatty acids.
Particularly preferred carboxylic acids are monocarboxylic acids.
The monocarboxylic acids include isoaliphatic acids.
The fatty acids are usually monocarboxylic acids.
Unsaturated monocarboxylic acids and compounds.
The most preferred linear acids are monocarboxylic acids.
Saturated acyclic monocarboxylic acids and their derivatives.
Monocarboxylic acids and their salts.
Preferred are saturated monocarboxylic acids and derivatives thereof.
Monocarboxylic acids of the general formula.
Examples of capping agents are monocarboxylic acids and phenols.
Useful monocarboxylic acids are discussed above.
Preferred aliphatic carboxylic acids are aliphatic monocarboxylic acids.
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One or more of these monocarboxylic acids can be used.
Monocarboxylic acids are preferred as the monovalent organic acid.
One or more of the monocarboxylic acids may be used.
Monocarboxylic acids may be present in the condensation reaction.
Saturated acyclic monocarboxylic acids.
Monocarboxylic acids may be added to control molecular weight.
Mixture of such aromatic monocarboxylic acids may obviously be used.
It is of course possible to use a mixture of said aromatic monocarboxylic acids.
Suitable acids include monocarboxylic acids and dicarboxylic acids.
It is obviously possible to use a mixture of such aromatic monocarboxylic acids.
Acyclic monocarboxylic acids are preferred.
Also useful are unsaturated monoolefinic straight chain monocarboxylic acids.
Examples of monocarboxylic acids are glycolic acid and lactic acid.
The fatty acids as referred to herein are aliphatic monocarboxylic acids.
Such materials include monocarboxylic acids and polycarboxylic acids.
Suitable viscosity reducing agents are the aliphatic monocarboxylic acids.
The monocarboxylic acids according to the invention may be linear or branched.
Advantageously trimethylolpropane is transesterified with methyl esters of monocarboxylic acids.
Typical examples of monocarboxylic acids are lactic acid and ascorbic acids.
Preference is given to salts of the polymer with organic monocarboxylic acids.
Exemplary monocarboxylic acids include acrylic acid and methacrylic acid.
Preference is given to salts of the polvmer with organic monocarboxylic acids.
The ester may derive from monocarboxylic acids or polycarboxylic acids.
The reaction is preferably carried out in the presence of monocarboxylic acids.
Salts with organic monocarboxylic acids and sulfonic acids are preferred.
Examples of the terminal blocking agent include monocarboxylic acids and monoamines.
The monocarboxylic acids may be used singly or in combination of two or more thereof.
Rosin is mainly a mixture of fused ring monocarboxylic acids known as resin acids.
Monocarboxylic acids function to terminate a polyester chain and are chosen for that purpose.
It was desired to retain the advantages and positive effects of the monocarboxylic acids.
Specific examples of organic monocarboxylic acids suitably usable in this invention are as follows.
Other suitable polyalcohols are partial esters from polyalcohols with monocarboxylic acids.
Monocarboxylic acids are more preferred due to their generally better solubility in the copolymer.
Saturated short or medium branched chain monocarboxylic acids are preferred in the present invention.
Said organic acids were chosen because of the reported positive effects of monocarboxylic acids.
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