Examples of 'amino alcohols' in a sentence
Meaning of "amino alcohols"
Amino alcohols are organic compounds that contain both an amine group and an alcohol group. They are commonly used in the synthesis of pharmaceuticals, chiral catalysts, and surfactants
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- plural of amino alcohol
How to use "amino alcohols" in a sentence
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amino alcohols
Amino alcohols are useful hydroxy containing compounds.
The ethanolamines comprise a group of amino alcohols.
Examples of amino alcohols are ethanolamine and diethanolamine.
Production method of optically active amino alcohols.
The amino alcohols are applied in liquid form.
Polyalkoxy ether containing amino alcohols are also useful.
Amino alcohols from amino acids.
This invention relates to a mixture of tertiary amino alcohols.
A process for producing amino alcohols by electrosynthesis of nitro alcohols.
Certain examples of amino acid variants are amino alcohols.
Examples of the amino alcohols include ethanolamine and hydroxyethylaniline.
Oxazolidines are produced when aldehydes are reacted with primary amino alcohols.
This buffering effect of the amino alcohols is significant.
Useful amino alcohols include monoamino and polyamino compounds.
Synthesis of amino alcohols.
See also
Amino alcohols are particularly useful.
Common amino alcohols.
Amino alcohols are able to undergo the reactions of both amines and alcohols.
These compounds are the reaction product of formaldehyde and certain amino alcohols.
Process for making amino alcohols by electrochemical reduction of nitro alcohols.
A preferred means for the preparation of beta amino alcohols uses amino acids.
Alkylation to yield amino alcohols can also be accomplished vÃa an epoxide opening reaction.
By correctly balancing the stoichiometry the polyesteramide may be prepared using amino alcohols.
This method affords amino alcohols of sufficient purity for most purposes.
Certain Mannich bases were reduced to diastereoisomeric allylic amino alcohols.
The amino alcohols contain both an amino group and an alcohol group.
Compounds Ics can be prepared from amino alcohols IIci by ring closure with cyanogen bromide.
The amino alcohols described herein have been found to be useful in preserving ophthalmic compositions.
The publications cited above also illustrate the preparation of the amino alcohols of formula XIV.
Several amines and amino alcohols are also useful in practicing the present invention.
According to some embodiments, the targeting elements are amino alcohols.
The protected amino alcohols may be used as intermediates to further elaborate the side chain.
Currently, processes exist for the preparation of amino alcohols.
Amino alcohols reduce pigmentation of those tissues very effectively by eluting the hem from hemoglobin.
Is a hydrophilic biodistribution ligand advantageously chosen from amino alcohols or PEGs ;.
Amino alcohols 8 can be prepared as described in the experimental section.
Furthermore, a second dispersant selected from the group of amino alcohols is added.
For example, amino alcohols and alkyl amines are thus suitable.
Compounds useful for element a, are selected from polyols, amino alcohols and diamines.
Illustrative of such amino alcohols are propanolamine, isopropanolamine, ethanolamine, butanolamine and isobutanolamine.
By procedures analogous to that described above, the following amino alcohols can be prepared,.
Amino alcohols 19 are commercially available or can be synthesised as outlined in the experimental section.
Suitable organic dispersants include amino alcohols and amino acids, such as arginine.
The amino alcohols of formula ( II ) are known compounds described in the prior art.
Illustrative initiators include alcohols, amines, mercaptans, phenols, amino alcohols and mercapto alcohols.
Table 1 shows representative amino alcohols prepared according to the above general procedures.
There are many commercial diacid dichlorides and amino alcohols ( Table 3 ).
Specific examples of the amino alcohols ( B3 ) include ethanol amine and hydroxyethyl aniline.
The amino alcohols ( B3 ) include, but are not limited to, ethanolamine, and hydroxyethylaniline.
Non-limiting examples of chiral amino alcohols of formula ( III ) include and.
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