Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3Cl3N3O3 |
| Molecular Weight | 232.409 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O
InChI
InChIKey=YRIZYWQGELRKNT-UHFFFAOYSA-N
InChI=1S/C3Cl3N3O3/c4-7-1(10)8(5)3(12)9(6)2(7)11
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 |
|---|---|---|
| Consumer exposure to biocides--identification of relevant sources and evaluation of possible health effects. | 2010-02-03 |
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| Characterization of the products formed by the reaction of trichlorocyanuric acid with 2-propanol. | 2009-11 |
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| Iridium/monodentate phosphoramidite catalyzed asymmetric hydrogenation of N-aryl imines. | 2009-06-24 |
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| Impregnated silica nanoparticles for the reactive removal of sulphur mustard from solutions. | 2009-01-30 |
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| Cytotoxic and genotoxic effect in RTG-2 cell line exposed to selected biocides used in the disinfection of cooling towers. | 2008-05 |
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| Response of the freshwater Alga chlorella vulgaris to trichloroisocyanuric acid and ciprofloxacin. | 2008-01 |
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| Synthesis of paromomycin derivatives modified at C(5'') to selectively target bacterial rRNA. | 2007-02-26 |
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| [Sodium dichlorinated isocyanuric acid and trichloroisocyanuric acid for removing cells of Phaeochystis globosa]. | 2006-05 |
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| Effects of selected biocides used in the disinfection of cooling towers on toxicity and bioaccumulation in Artemia larvae. | 2005-12 |
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| N,N-dichlorotaurine: chemical and bactericidal properties. | 2005-10 |
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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. | 2005-03-15 |
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| Flow-injection determination of isoniazid using sodium dichloroisocyanurate- and trichloroisocyanuric acid-luminol chemiluminescence systems. | 2004-06 |
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| A highly enantioselective phase-transfer catalyzed epoxidation of enones with a mild oxidant, trichloroisocyanuric acid. | 2003-11-07 |
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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. | 2003-09 |
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| Trichloroisocyanuric/TEMPO oxidation of alcohols under mild conditions: a close investigation. | 2003-06-13 |
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| Flow-injection chemiluminescence determination of chlorinated isocyanuric acids. | 2003-02 |
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| Flow injection chemiluminescence determination of hydrazine by oxidation with chlorinated isocyanurates. | 2002-10-16 |
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| A very mild and chemoselective oxidation of alcohols to carbonyl compounds. | 2001-09-20 |
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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EPA PESTICIDE CODE |
81405
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NCI_THESAURUS |
C28394
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DTXSID2026523
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2375531
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C72647
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201-782-8
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TRICHLOROISOCYANURIC ACID
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SUB10790MIG
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6909
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RL3HK1I66B
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100000082971
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3629
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C051718
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885
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CHEMBL1698868
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405124
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33015
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m11076
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87-90-1
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ACTIVE MOIETY