Examples of 'aminoalkyl' in a sentence
Meaning of "aminoalkyl"
Aminoalkyl refers to a chemical compound containing both amino and alkyl functional groups
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- Any amino derivative of an alkyl radical
How to use "aminoalkyl" in a sentence
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aminoalkyl
A preferred class of aminoalkyl silicone are the amodimethicones.
Aminoalkyl means alkyl having an amine group.
Is preferably hydroxyl or an unsubstituted alkyl or aminoalkyl group.
The preparation of cyclic aminoalkyl halides is known to the art.
These polymers are polydimethylsiloxanes with aminoalkyl groups.
The aminoalkyl polysiloxanes of the invention may be end capped.
They also include substituted aminoalkyl piperazines.
The aminoalkyl can be optionally substituted as described herein elsewhere.
Preferably the aminosilane is an aminoalkyl alkoxy silane.
Certain aminoalkyl glucosaminide phosphate compounds and their use.
Amodimethicones are polydimethylsiloxane polymers containing aminoalkyl groups.
The linker arms include an aminoalkyl or carboxyalkyl linker arm.
Amodimethicones are polydimethyl siloxane polymers containing aminoalkyl groups.
Aminoalkyl represents an alkyl radical substituted with an amino group.
Is preferably an unsubstituted alkyl or aminoalkyl group.
See also
Aminoalkyl silicones do not adversely affect the antiplaque activity of chlorhexidine.
Hydroxy aliphatic substituted phenyl aminoalkyl ether derivatives.
The aminoalkyl radical is typically located in an ortho position to the hydroxygroup.
The same applies to the radicals hydroxyalkyl and aminoalkyl.
Particular examples include bis or tris aminoalkyl piperazines or morpholines.
Preferred lubricants are polydialkylsiloxanes terminated with a carboxyalkyl or aminoalkyl group.
The amino proton couplings in the aminoalkyl radicals were not resolved.
The aminoalkyl silicones form a hydrophobic layer on the surface of teeth.
R can be an aminoalkyl group.
A lower aminoalkyl comprises an aminoalkyl having one to four carbon atoms.
Preferred polyamino silanes are amino alkyl substituted aminoalkyl trialkoxy silanes.
The aminoalkyl silicone forms a residual film on the surface of teeth.
As in a primary or secondary aminoalkyl.
The aminoalkyl silicone did not interfere with the colorimetric reaction.
Useful amino functional monomers include aminoalkyl acrylates and methacrylates.
The aminoalkyl can be optionally substituted with one or more halo.
Similar comments apply in respect of the radicals hydroxyalkyl and aminoalkyl.
These polymers comprise aminoalkyl groups affixed to a predominantly polydimethylsiloxane structure.
The desired amount of a lipophilic compound is added to the aminoalkyl silicone.
The aminoalkyl radical is typically located in an ortho position to the hydroxy group.
The polar lubricants are noncuring polysiloxanes terminated with an aminoalkyl group.
These polymers comprise aminoalkyl groups affixed to a predominently polydimethyl siloxane structure.
Other spacer lengths are possible by straightforward variation of the starting aminoalkyl heterocycle.
Examples of such aminoalkyl substituents are as given above in relation to the alicyclic diamines.
Characterized in that the polysiloxane lubricant is a noncuring aminoalkyl terminated polysiloxane lubricant.
With aminoalkyl groups as substituent the active compounds can be prepared in one stage.
The compounds ofthe subject invention are aminoalkyl glucosamine compounds which are phosphorylated.
This process makes it possible to produce bead polymers containing aminoalkyl groups.
Usually the aminoalkyl substituents are substituted on a nitrogen atom forming part of the heterocycle.
The reaction is complete in several hours with the formation of the aminoalkyl compound.
Usually the aminoalkyl substituents are substituted on a nitrogen atom forming part of the hetero ring.
Particular examples include but are not limited to bis or tris aminoalkyl piperazines or morpholines.
Increasing the number of aminoalkyl groups per molecule enhances the substantivity of the silicone.
Deprotection of synthetic oligonucleotides with ammonia in the presence of aminoalkyl resins as acrylonitrile scavengers.
Most preferred are aminoalkyl radicals having lower alkyl radicals having one to eight carbon atoms.
