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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
Structure of SODIUM TRICHLOROCYANURATE

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

HIDE SMILES / InChI
Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C3Cl3N3O3
Molecular Weight 232.409
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
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

Unknown
149124
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Consumer exposure to biocides--identification of relevant sources and evaluation of possible health effects.
2010-02-03
Characterization of the products formed by the reaction of trichlorocyanuric acid with 2-propanol.
2009-11
Iridium/monodentate phosphoramidite catalyzed asymmetric hydrogenation of N-aryl imines.
2009-06-24
Impregnated silica nanoparticles for the reactive removal of sulphur mustard from solutions.
2009-01-30
Cytotoxic and genotoxic effect in RTG-2 cell line exposed to selected biocides used in the disinfection of cooling towers.
2008-05
Response of the freshwater Alga chlorella vulgaris to trichloroisocyanuric acid and ciprofloxacin.
2008-01
Synthesis of paromomycin derivatives modified at C(5'') to selectively target bacterial rRNA.
2007-02-26
[Sodium dichlorinated isocyanuric acid and trichloroisocyanuric acid for removing cells of Phaeochystis globosa].
2006-05
Effects of selected biocides used in the disinfection of cooling towers on toxicity and bioaccumulation in Artemia larvae.
2005-12
N,N-dichlorotaurine: chemical and bactericidal properties.
2005-10
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
Flow-injection determination of isoniazid using sodium dichloroisocyanurate- and trichloroisocyanuric acid-luminol chemiluminescence systems.
2004-06
A highly enantioselective phase-transfer catalyzed epoxidation of enones with a mild oxidant, trichloroisocyanuric acid.
2003-11-07
Comparison of the disinfection efficacy of chlorine-based products for inactivation of viral indicators and pathogenic bacteria in produce wash water.
2003-09
Trichloroisocyanuric/TEMPO oxidation of alcohols under mild conditions: a close investigation.
2003-06-13
Flow-injection chemiluminescence determination of chlorinated isocyanuric acids.
2003-02
Flow injection chemiluminescence determination of hydrazine by oxidation with chlorinated isocyanurates.
2002-10-16
A very mild and chemoselective oxidation of alcohols to carbonyl compounds.
2001-09-20
Patents

Patents

04324892
4
04380501
2
05260261
2
05411966
3
05491239
3
06723719
2
06900200
4
06903091
2
07067537
5
07528136
2
07790747
8
08158634
3
08278282
2
08487108
8
JP2000351752A
7
JP2008189560A
2
JPH01128905A
2
JPH02147697A
2
JPH0291172A
2
JPH08231314A
2
JPH0826917A
3
JPS5663432A
3
JPS57183742A
2
JPS60136549A
2
JPS6019773A
2
JPS61179203A
3
JPS6185483A
2
JPS62141037A
2
JPS6388108A
2
JPS6431703A
3

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
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))
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:29 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:29 GMT 2025
Record UNII
U6R2TZ2K3A
Record Status Validated (UNII)
Record Version
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Name Type Language
SODIUM TRICHLOROCYANURATE
Common Name English
JIAN ZHI SU
Preferred Name English
1,3,5-TRIAZINE-2,4,6(1H,3H,5H)-TRIONE, 1,3,5-TRICHLORO-, SODIUM SALT
Systematic Name English
S-TRIAZINE-2,4,6(1H,3H,5H)-TRIONE, 1,3,5-TRICHLORO-, SODIUM SALT
Systematic Name English
TRICHLOROISOCYANURIC ACID SODIUM SALT
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
249-771-7
Created by admin on Mon Mar 31 19:56:29 GMT 2025 , Edited by admin on Mon Mar 31 19:56:29 GMT 2025
PRIMARY
PUBCHEM
169072
Created by admin on Mon Mar 31 19:56:29 GMT 2025 , Edited by admin on Mon Mar 31 19:56:29 GMT 2025
PRIMARY
CAS
29680-41-9
Created by admin on Mon Mar 31 19:56:29 GMT 2025 , Edited by admin on Mon Mar 31 19:56:29 GMT 2025
PRIMARY
FDA UNII
U6R2TZ2K3A
Created by admin on Mon Mar 31 19:56:29 GMT 2025 , Edited by admin on Mon Mar 31 19:56:29 GMT 2025
PRIMARY
Related Record Type Details
Structure of SODIUM TRICHLOROCYANURATE
IONIC MOIETY
NIH
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