176125
Trichloroisocyanuric acid
Synonym(s):
1,3,5-Trichloro-2,4,6-triazinetrione, Symclosene, TCICA, Trichlorocyanuric acid
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About This Item
Empirical Formula (Hill Notation):
C3Cl3N3O3
CAS Number:
Molecular Weight:
232.41
Beilstein:
202022
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39160318
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
form
powder
mp
249-251 °C (lit.)
SMILES string
ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O
InChI
1S/C3Cl3N3O3/c4-7-1(10)8(5)3(12)9(6)2(7)11
InChI key
YRIZYWQGELRKNT-UHFFFAOYSA-N
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Application
Trichloroisocyanuric acid is used in the synthesis of 2-halomethylene-3-oxoketoximes.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Ox. Sol. 2 - STOT SE 3
Target Organs
Respiratory system
Supplementary Hazards
Storage Class Code
5.1B - Oxidizing hazardous materials
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Rensheng Zhuang et al.
Acta chimica Slovenica, 60(4), 826-832 (2013-12-24)
In our study, the transformation of two most widely used UV filters, benzophenone-3 (BP3) and benzophenone-4 (BP4), in chlorinated water with disinfection reagents sodium hypochlorite (NaClO) and trichloroisocyanuric acid (TCCA) was studied. Based on the HPLC/MS and UV-Vis analysis the
Mustafa J Raihan et al.
The Journal of organic chemistry, 78(17), 8872-8879 (2013-08-16)
A protocol for the N-bromosuccinimide (NBS)- and trichloroisocyanuric acid (TCCA)-mediated synthesis of novel 2-halomethylene-3-oxoketoximes via one-pot halogenation/oxidation of isoxazoline N-oxide derivatives is described here. The keto functionality of 3-ketoximes was selectively reduced by lithiumaluminum hydride to synthesize an unprecedented type
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