Details
Stereochemistry | ACHIRAL |
Molecular Formula | C3Cl3N3O3.Na |
Molecular Weight | 255.399 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 1 |
SHOW SMILES / InChI
SMILES
[Na+].ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O
InChI
InChIKey=XSXSKSKONCDOMZ-UHFFFAOYSA-N
InChI=1S/C3Cl3N3O3.Na/c4-7-1(10)8(5)3(12)9(6)2(7)11;/q;+1
DescriptionSources: DOI: 10.1002/047084289X.rt209Curator's Comment: description was created based on several sources, including
http://www.doiserbia.nb.rs/img/doi/0352-5139/2012/0352-51391200028H.pdf
Sources: DOI: 10.1002/047084289X.rt209
Curator's Comment: description was created based on several sources, including
http://www.doiserbia.nb.rs/img/doi/0352-5139/2012/0352-51391200028H.pdf
Trichloroisocyanuric acid (1,3,5-trichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-tri-one or TCCA) is an N-halo compound which has been known since 1902. It has been used primarily as a disinfectant in swimming pools and water treatment as bleaching agent and bactericide. Recently, TCCA has become attractive candidate as a homogeneous catalyst in organic transformations due to its lack of volatility, commercial availability, low cost and ease of handling. And is also used as a bleaching agent in the textile industry
Approval Year
PubMed
Title | Date | PubMed |
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A very mild and chemoselective oxidation of alcohols to carbonyl compounds. | 2001 Sep 20 |
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Flow injection chemiluminescence determination of hydrazine by oxidation with chlorinated isocyanurates. | 2002 Oct 16 |
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Flow-injection chemiluminescence determination of chlorinated isocyanuric acids. | 2003 Feb |
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Trichloroisocyanuric/TEMPO oxidation of alcohols under mild conditions: a close investigation. | 2003 Jun 13 |
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A highly enantioselective phase-transfer catalyzed epoxidation of enones with a mild oxidant, trichloroisocyanuric acid. | 2003 Nov 7 |
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Comparison of the disinfection efficacy of chlorine-based products for inactivation of viral indicators and pathogenic bacteria in produce wash water. | 2003 Sep |
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Flow-injection determination of isoniazid using sodium dichloroisocyanurate- and trichloroisocyanuric acid-luminol chemiluminescence systems. | 2004 Jun |
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Flow-injection potentiometric determination of triiodide by plasticized poly(vinyl chloride) membrane electrodes and its application to the determination of chlorine-containing disinfectants. | 2005 Mar 15 |
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N,N-dichlorotaurine: chemical and bactericidal properties. | 2005 Oct |
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Response of the freshwater Alga chlorella vulgaris to trichloroisocyanuric acid and ciprofloxacin. | 2008 Jan |
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Impregnated silica nanoparticles for the reactive removal of sulphur mustard from solutions. | 2009 Jan 30 |
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Iridium/monodentate phosphoramidite catalyzed asymmetric hydrogenation of N-aryl imines. | 2009 Jun 24 |
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Characterization of the products formed by the reaction of trichlorocyanuric acid with 2-propanol. | 2009 Nov |
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Consumer exposure to biocides--identification of relevant sources and evaluation of possible health effects. | 2010 Feb 3 |
Patents
Sample Use Guides
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/18274895
DNA damage has been evaluated on RTG-2 cultures by means of an in vitro assay based on the ability of PicoGreen fluorochrome to interact preferentially with dsDNA, and the results indicated that trichloroisocyanuric acid (Symclosene) induced DNA strand breaks at concentrations above 1.2 mg/l, equivalent to 1/50-EC(50(48))
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249-771-7
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169072
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29680-41-9
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U6R2TZ2K3A
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SUBSTANCE RECORD