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Peroxides - Isolation & purification
Research News and Information
Definition of 'Peroxides'A group of compounds that contain a bivalent O-O group, i.e., the oxygen atoms are univalent. They can either be inorganic or organic in nature. Such compounds release atomic (nascent) oxygen readily. Thus they are strong oxidizing agents and fire hazards when in contact with combustible materials, especially under high-temperature conditions. The chief industrial uses of peroxides are as oxidizing agents, bleaching agents, and initiators of polymerization. (From Hawley's Condensed Chemical Dictionary, 11th ed) |
Monday, November 23, 2009
30 Jul 2009
Six unreported aromatic compounds, 1-6, were isolated, along with the known compounds dehydrocurcuphenol and manoalide, from a sample of Plakortis sp., which was the main component of a Pacific sponge consortium. The new molecules were chemically ... Read more...
Mycangimycin, a polyene peroxide from a mutualist Streptomyces sp.
3 Feb 2009
A mutualist actinomycete of the southern pine beetle, Dendroctonus frontalis, produces a polyene peroxide with pronounced antifungal activity. Its structure, absolute configuration, and biological activity were determined by spectral analysis, ... Read more...
Larvicidal and nematicidal activities of the leaf essential oil of Croton regelianus.
29 Nov 2008
The chemical composition of the leaf essential oil of Croton regelianus collected from wild plants growing in two different sites at Ceará State (Brazil) was analyzed by GC/MS and GC-FID. Twenty monoterpenoids, representing more than 96% of the ... Read more...
Latest indexed articles for 'Peroxides - Isolation & purification'
These are the very latest articles for this heading:
- Aromatic cyclic peroxides and related keto-compounds from the Plakortis sp. component of a sponge consortium.
30 Jul 2009 - Mycangimycin, a polyene peroxide from a mutualist Streptomyces sp.
3 Feb 2009 - Larvicidal and nematicidal activities of the leaf essential oil of Croton regelianus.
29 Nov 2008 - New butyrylcholinesterase inhibitory steroid and peroxy acid from Leucas urticifolia.
10 Sep 2008 - Diacarperoxides, norterpene cyclic peroxides from the sponge Diacarnus megaspinorhabdosa.
31 Jul 2008 - Speciosaperoxide, a new triterpene acid, and other terpenoids from Chaenomeles speciosa.
28 Feb 2008 - The first limonoid peroxide in the Meliaceae family: walsuronoid A from Walsura robusta.
14 May 2007 - Antifungal agent and other constituents from Cynanchum otophyllum.
27 Feb 2007 - Cytotoxic terpene hydroperoxides from the aerial parts of Aster spathulifolius.
29 Sep 2006 - Removal of peroxides in polyethylene glycols by vacuum drying: implications in the stability of biotech and pharmaceutical formulations.
26 Jul 2006 - Cyclic peroxides derived from the marine sponge Plakortis simplex.
29 Apr 2005 - Antineoplastic agents. 535. Isolation and structure of plakorstatins 1 and 2 from the Indo-Pacific sponge Plakortis nigra.
30 Aug 2004 - Tasnemoxides A-C, new cytotoxic cyclic norsesterterpene peroxides from the Red Sea sponge Diacarnus erythraenus.
30 Dec 2003 - A short synthesis of antimalarial peroxides.
13 Aug 2003 - Three new cyclic peroxides from the marine sponge Plakortis aff simplex.
29 Apr 2003 - A new alpha,beta,gamma,delta-unsaturated carboxylic acid and three new cyclic peroxides from the marine sponge, Monotria japonica, which selectively lyse starfish oocytes without affecting nuclear morphology.
15 Apr 2003 - Mycaperoxide H, a new cytotoxic norsesterterpene peroxide from a Thai marine sponge Mycale sp.
30 Jan 2003 - Activity of ascaridol from the anthelmintic herb Chenopodium anthelminticum L. against sensitive and multidrug-resistant tumor cells.
30 Oct 2002 - New bioactive peroxides from marine sponges of the family plakiniidae.
29 Sep 2002 - Constituents of Clerodendrum bungei.
30 Aug 2002
See a longer list of these articles.
Technical information about 'Peroxides'
Definition: A group of compounds that contain a bivalent O-O group, i.e., the oxygen atoms are univalent. They can either be inorganic or organic in nature. Such compounds release atomic (nascent) oxygen readily. Thus they are strong oxidizing agents and fire hazards when in contact with combustible materials, especially under high-temperature conditions. The chief industrial uses of peroxides are as oxidizing agents, bleaching agents, and initiators of polymerization. (From Hawley's Condensed Chemical Dictionary, 11th ed)
Registry Number: 0
Descriptor UI: D010545
Alternative terms: Peroxides;
Related Mesh Headings: Benzoyl Peroxide; Lipid Peroxides; Reactive Oxygen Species;
Allowable Qualifiers: administration & dosage; adverse effects; analysis; antagonists & inhibitors; blood; cerebrospinal fluid; chemical synthesis; classification; diagnostic use; economics; history; immunology; isolation & purification; metabolism; pharmacokinetics; pharmacology; poisoning; radiation effects; standards; supply & distribution; therapeutic use; toxicity; urine; chemistry; contraindications; agonists;
Pharmacological Action: Oxidants;
Tree Number: D01.248.497.158.685.750; D01.339.431.374; D01.650.550.750; D02.389.338; D02.737;