oxime


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Related to oxime: Semicarbazone, Phenylhydrazone

oxime

[′äk‚sēm]
(organic chemistry)
Compound containing the CH(:NOH) radical; condensation product of hydroxylamine with aldehydes or ketones.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
References in periodicals archive ?
Furthermore, the timeous use of oximes may have aided in reversing any nicotinic effects such as respiratory muscle weakness, but because of the ongoing controversy surrounding their role in acute OPP [8,9] and their expense, they are rarely available or used in our setting.
Osman et al., "Clinical experience with [sup.99m]Tc-hexamethylpropyleneamine oxime for labeling leucocytes and imaging inflammation," The Lancet, vol.
Apak, "Novel oxime based flavanone, naringin-oxime: Synthesis, characterization and screening for antioxidant activity," Chemico-Biological Interactions, vol.
The bond lengths of N1-C1 and N1-O1 are 1.298(3) [Angstrom] and 1.382(3) [Angstrom], respectively, which confirms that the bond between N1 and O1 atoms is oxime bond.
The carbonyl group in the acetoxy group has a higher activation effect on the Si-OC hydrolysis, compared to the C=N double bond in the oxime group.
The protonated molecule of the oxime (m/z 502) was observed
Water quality--determination of manganese--formaldehyde oxime spectrophotometry (HJ/T 344-2007) [Article in Chinese].
"Assessing the therapeutic efficacy of oxime therapies against percutaneous organophosphorus pesticide and nerve agent challenges in the Hartley guinea pig." The Journal of Toxicological Sciences 40, no.
It details conditions of typical syntheses, limitations of their applicability, and the possibility of vinyl chloride or dichloroethane application instead of acetylene; chemical engineering aspects of the first synthesis of tetrahydroindole and indole from commercially available oxime of cyclohexanone and acetylene; new facets of pyrroles and N-vinyl pyrroles reactivity in the reactions with the participation of the pyrrole ring and N-vinyl groups; and about 1,000 structures of novel pyrrole compounds and their yields and physical-chemical characteristics.
Pralidoxime mesylate (P2S) is less effective in producing sustained oxime concentrations and requires 4-hourly dosing, the balance between ageing and reactivation reaction rates for the inhibited acetylcholinesterase is altered in favour of the latter.