esterification

The synthesis of aspirin is classified as an esterification reaction.

Chemical modification by esterification is also used to control solubility.

Could someone confirm whether it should be 'estrification' or 'esterification'.

It has a minor use as an esterification catalyst.

Esterification can also be done using waste to energy technologies, and the result of this process is biodiesel.

It can be prepared by the esterification of creatine with methanol.

Esterification and lipolysis are, in essence, reversals of one another.

Some are manufactured by esterification or soaping of organic compounds.

A generic mechanism for an acid Fischer esterification is shown below.

It is also known to function in the esterification of Chlide and transesterification.

The manufacturing process of lactylates is an esterification reaction.

Triflic acid is mainly used in research as a catalyst for esterification.

It is produced from the esterification of isobutanol with acetic acid.

However, gelling reactions with calcium increase as the degree of esterification falls.

They are the product of esterification between a carboxylic acid and a thiol.

Glycerolysis is a special case of esterification or transesterification.

Some of the third generation drugs can be absorbed orally without the need of esterification.

The ethyl ester is formed through an acid-catalyzed esterification reaction.

This was overcome by the esterification of enalaprilat with ethanol to produce enalapril.

Water, a by-product of esterification reactions, is continuously removed, driving the reaction to completion.

Esterification entails the attachment of organic groups to phosphorus through oxygen linkers.

Esterification of the hydroxyl groups yields stronger compounds.

Under acidic conditions, the reaction is the reverse reaction of the Fischer esterification.

It is not known whether this occurs before or after the esterification of monic acid to 9-hydroxy-nonanoic acid.

This value is a useful measure of the degree of esterification in ester synthesis.