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  2. Antimicrobial - Wikipedia

    en.wikipedia.org/wiki/Antimicrobial

    An antimicrobial is an agent that kills microorganisms (microbicide) or stops their growth ... Aldehydes are highly effective against bacteria, fungi, and viruses.

  3. Reuterin - Wikipedia

    en.wikipedia.org/wiki/Reuterin

    It is a bifunctional molecule, containing both a hydroxy and aldehyde functional groups. The name reuterin is derived from Lactobacillus reuteri , which produces the compound biosynthetically from glycerol as a broad-spectrum antibiotic ( bacteriocin ). [ 1 ]

  4. Fluorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzaldehyde

    Due to the aldehyde group, the fluorobenzaldehydes can be used to make a variety of schiff base compounds through a condensation reaction, some of which have antimicrobial properties. [ 2 ] [ 3 ] References

  5. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.

  6. Disinfectant - Wikipedia

    en.wikipedia.org/wiki/Disinfectant

    The antimicrobial action of hydrogen peroxide can be enhanced by surfactants and organic acids. The resulting chemistry is known as Accelerated hydrogen peroxide . A 2% solution, stabilized for extended use, achieves high-level disinfection in 5 minutes, and is suitable for disinfecting medical equipment made from hard plastic, such as in ...

  7. Alkaloid - Wikipedia

    en.wikipedia.org/wiki/Alkaloid

    Schiff bases can be obtained by reacting amines with ketones or aldehydes. [189] These reactions are a common method of producing C=N bonds. [190] In the biosynthesis of alkaloids, such reactions may take place within a molecule, [188] such as in the synthesis of piperidine: [41]

  8. Schiff base - Wikipedia

    en.wikipedia.org/wiki/Schiff_base

    Schiff bases are common enzymatic intermediates where an amine, such as the terminal group of a lysine residue, reversibly reacts with an aldehyde or ketone of a cofactor or substrate. The common enzyme cofactor pyridoxal phosphate (PLP) forms a Schiff base with a lysine residue and is transaldiminated to the substrate(s). [7]

  9. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Pigment Yellow 97, a popular yellow colorant, is a hydrazone. [6]Hydrazones are the basis for various analyses of ketones and aldehydes. For example, dinitrophenylhydrazine coated onto a silica sorbent is the basis of an adsorption cartridge.