Canadian Medical Guide > Chemicals and Drugs > Organic Chemicals > Aldehydes Terms and Definitions




Aldehydes

Medical Definition: Organic compounds containing a carbonyl group in the form -CHO.
Aldehydes Categories.
Canadian Medical Guide Definition Acetaldehyde - A colorless, flammable liquid used in the manufacture of acetic acid, perfumes, and flavors. It is also an intermediate in the metabolism of alcohol. It has a general narcotic action and also causes irritation of mucous membranes. Large doses may cause death from respiratory paralysis.
Canadian Medical Guide Definition Acrolein
Canadian Medical Guide Definition Benzaldehydes
Canadian Medical Guide Definition Formaldehyde - A highly reactive aldehyde gas formed by oxidation or incomplete combustion of hydrocarbons. In solution, it has a wide range of uses: in the manufacture of resins and textiles, as a disinfectant, and as a laboratory fixative or preservative. Formaldehyde solution (formalin) is considered a hazardous compound, and its vapor toxic. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p717)
Canadian Medical Guide Definition Furaldehyde
Canadian Medical Guide Definition Glutaral - One of the protein CROSS-LINKING REAGENTS that is used as a disinfectant for sterilization of heat-sensitive equipment and as a laboratory reagent, especially as a fixative.
Canadian Medical Guide Definition Glyceraldehyde
Canadian Medical Guide Definition Glyoxal
Canadian Medical Guide Definition Malondialdehyde - The dialdehyde of malonic acid.
Canadian Medical Guide Definition o-Phthalaldehyde - A reagent that forms fluorescent conjugation products with primary amines. It is used for the detection of many biogenic amines, peptides, and proteins in nanogram quantities in body fluids.
Canadian Medical Guide Definition Retinaldehyde - A carotenoid constituent of visual pigments. It is the oxidized form of retinol which functions as the active component of the visual cycle. It is bound to the protein opsin forming the complex rhodopsin. When stimulated by visible light, the retinal component of the rhodopsin complex undergoes isomerization at the 11-position of the double bond to the cis-form; this is reversed in "dark" reactions to return to the native trans-configuration.

Aldehydes Medical Definitions and Terms

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