Examples of 'dialdehyde' in a sentence
Meaning of "dialdehyde"
Dialdehyde (noun): A dialdehyde is a chemical compound containing two aldehyde groups
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- Any compound containing two aldehyde groups
How to use "dialdehyde" in a sentence
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dialdehyde
The cellulose reactive agent is preferably a dialdehyde.
Glyoxal is the smallest dialdehyde two aldehyde groups.
The dialdehyde used can for example be glutaraldehyde.
One interesting application concerns coupling with a dialdehyde.
Such a dialdehyde is not therefore preferred.
Other references disclose the use of dialdehyde crosslinking agents.
Dialdehyde is added in excess to incorporated diamines.
The preferred dialdehyde is glutaraldehyde.
The significant product of the oxidation step was dialdehyde oxycellulose.
It is the smallest dialdehyde a compound with two aldehyde groups.
Alternate binding agents may include dialdehyde starch itself.
Aromatic dialdehyde solutions have bacteriostatic and fungistatic activity.
The aldehyde may be a dialdehyde.
The dialdehyde is then purified by recrystallisation in an alcohol such as ethanol or isopropanol.
Measurement of a rate of modification of an alcoholic hydroxyl group with a dialdehyde.
See also
Dialdehyde starch is preferred.
The preferred agent of the present invention is dialdehyde starch.
This modified dialdehyde will advantageously be used mixed with terephthalic aldehyde.
Glutaraldehyde is an important dialdehyde.
Chemical stability of the aromatic dialdehyde is determined by high performance liquid chromatography.
Conversion to glutacon dialdehyde.
Water soluble dialdehyde was added to the web as indicated in each individual example.
Reaction of disulfur dichloride with isobutyraldehyde yields the corresponding dialdehyde disulfide.
Aromatic dialdehyde disinfecting and sterilizing solutions are well known in the art.
The diol is then cleaved to the corresponding dialdehyde using sodium metaperiodate.
The use of the dialdehyde purportedly affords a more stabilized heparin coating.
Disinfecting and sterilizing concentrate containing an aromatic dialdehyde and a neutral ph buffering system.
The germicidal aromatic dialdehyde may often be included as either a solution or as a dry solid.
Unfunctionalized polyvinylamine is polyvinylamine which has not been treated with a dialdehyde to form an adduct.
Dialdehyde starch is a polysaccharide derived by chemical modification from natural starch from wheat or corn.
The cellulose reactive agent will comprise a compound having at least dialdehyde functionality.
The dialdehyde content in the resulting oxidized dextran was determined using the following procedure.
The binder composition is crosslinked with both aziridine compounds and dialdehyde compounds.
A dialdehyde compound having high reactivity generally has small carbon atoms such as malondialdehyde.
This is directly related to the lower production of panose in the glutaric dialdehyde conjugate.
Kits including only the germicidal aromatic dialdehyde compound and the acetal are contemplated.
The component that reflects NADPH oxidase activity can be malonic dialdehyde.
A disinfecting and sterilizing concentrate containing an aromatic dialdehyde and a neutral pH buffering system is provided.
This example demonstrates that various acetals may be converted to the germicidal aromatic dialdehyde OPA.
Prior Art Saturated dialdehyde sterilizing and disinfecting compositions are well known.
MFC was modified by oxidation to lead to reactive dialdehyde functions.
Then, the dialdehyde starch was allowed to precipitate.
An effective amount of an antimicrobial dialdehyde compound ; and.
Next, the aromatic dialdehyde is admixed to the solution.
Accordingly, it is desirable to avoid hydration of the aromatic dialdehyde.
The dialdehyde starch was subsequently converted to dicarboxy starch as described in example 5.
The composition of claim 1 in which the aromatic dialdehyde is phthalaldehyde.
Suitable dialdehydes include glyoxal, malonic dialdehyde, succinic dialdehyde and glutaraldehyde.
A formulation according to claim 3 wherein the aldehyde is glutaric dialdehyde.
Therefore, acetalization with the dialdehyde is inefficient and poor in yields.
