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Details

Stereochemistry ACHIRAL
Molecular Formula C3Cl2N3O3.K
Molecular Weight 236.055
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TROCLOSENE POTASSIUM

SMILES

[K+].ClN1C(=O)[N-]C(=O)N(Cl)C1=O

InChI

InChIKey=IFIDXBCRSWOUSB-UHFFFAOYSA-M
InChI=1S/C3HCl2N3O3.K/c4-7-1(9)6-2(10)8(5)3(7)11;/h(H,6,9,10);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula K
Molecular Weight 39.0983
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C3HCl2N3O3
Molecular Weight 197.964
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: http://www.preciseformulation.com/nadcc-tablets-general-applications.html | http://akvopedia.org/wiki/Chlorine_(NaDCC) | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b345ae6a-0b36-45c7-b31e-2a15508a2ef5 | https://www.ncbi.nlm.nih.gov/pubmed/20064989

Troclosene is chlorinated hydroxytriazine and it is used as a source of free available chlorine, in the form of hypochlorous acid, for the disinfection of water. It kills bacteria, bacterial spores, cysts, algae, fungi, protozoa and virus and are especially lethal to Entamoeba histolytica. Troclosene kills mastitis-causing organisms. It is now widely available for household water treatment. It does not prevent diarrhea but improved water quality.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Flow-injection chemiluminescence determination of chlorinated isocyanuric acids.
2003 Feb
Sanichlor-induced atopic dermatitis and asthma in ophthalmologists.
2003 Jan
The effect of sterilization methods on the light transmission characteristics and structure of light-curing tips.
2004 Sep
Comparative sporicidal effects of disinfectants after release of a biological agent.
2007 Jun
Analytical method for the quantitative determination of cyanuric acid as the degradation product of sodium dichloroisocyanurate in urine by liquid chromatography mass spectrometry.
2007 Jun 15
Tonometer disinfection practice in the United Kingdom: a national survey.
2008 Aug
Sporicidal activity of two disinfectants against Clostridium difficile spores.
2008 Mar 13-26
Advantages of sodium hypochlorite or sodium dichloroisocyanurate disinfection for teats and bottles in newborn infants' feeding.
2008 Mar-Apr
A comparative study assaying commonly used sanitizers for antimicrobial activity against indicator bacteria and a Salmonella Typhimurium strain on fresh produce.
2009 Nov
Collection of indonaphthol blue on a membrane filter for the spectrophotometric determination of ammonia with 1-naphthol and dichloroisocyanurate.
2010
Improvements to water purification and sanitation infrastructure may reduce the diarrheal burden in a marginalized and flood prone population in remote Nicaragua.
2010 Dec 8
Sodium dichloroisocyanurate tablets for routine treatment of household drinking water in periurban Ghana: a randomized controlled trial.
2010 Jan
Root canal irrigants.
2010 Oct
Field assessment of a novel household-based water filtration device: a randomised, placebo-controlled trial in the Democratic Republic of Congo.
2010 Sep 10
1,1'-Azobis-1,2,3-triazole: a high-nitrogen compound with stable N8 structure and photochromism.
2010 Sep 8
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Viral suspensions were prepared containing 10(4)-10(5) syncitial forming units ml-1 in 0.9% saline or 0.9% saline containing 10% v/v plasma to simulate clean and dirty conditions. A syncitial inhibition assay on C8166 lymphoblastoid line was used to determine viral titre. Results indicate that satisfactory disinfection (3-4 log reduction in 2 min) can be achieved using Troclosene and NaOCl at concentrations of 50 ppm and 2500 ppm available chlorine (AvCl2) for clean and soiled conditions respectively. For treatment of blood spillages, the addition of Troclosene and NaOCl solutions (10,000 ppm) to equal volumes of contaminated blood (giving a final AvCl2 concentration of 5000 ppm of blood) was sufficient to produce total kill within 2 min.
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:52:23 UTC 2023
Edited
by admin
on Sat Dec 16 17:52:23 UTC 2023
Record UNII
8A85D111P0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TROCLOSENE POTASSIUM
HSDB   INN   MART.   MI   USAN  
USAN   INN  
Official Name English
POTASSIUM DICHLOROISOCYANURATE
Common Name English
POTASSIUM DICHLOROCYANURATE
Common Name English
1,3,5-TRIAZINE-2,4,6(1H,3H,5H)-TRIONE, 1,3-DICHLORO-, POTASSIUM SALT
Common Name English
TROCLOSENE POTASSIUM [MART.]
Common Name English
POTASSIUM TROCLOSENE [INCI]
Common Name English
troclosene potassium [INN]
Common Name English
1,3-DICHLORO-S-TRIAZINE-2,4,6(1H,3H,5H)TRIONE POTASSIUM SALT
Common Name English
POTASSIUM TROCLOSENE
INCI  
INCI  
Official Name English
TROCLOSENE POTASSIUM [USAN]
Common Name English
NSC-251767
Code English
TROCLOSENE POTASSIUM [MI]
Common Name English
TROCLOSENE POTASSIUM [HSDB]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 81403
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
NCI_THESAURUS C28394
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
Code System Code Type Description
PUBCHEM
517106
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
ChEMBL
CHEMBL2111065
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
HSDB
5871
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
EVMPD
SUB11330MIG
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
ECHA (EC/EINECS)
218-828-8
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
NSC
251767
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
MERCK INDEX
m11216
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY Merck Index
CAS
2244-21-5
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
INN
1772
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
NCI_THESAURUS
C152756
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
EPA CompTox
DTXSID5026178
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
SMS_ID
100000076973
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
FDA UNII
8A85D111P0
Created by admin on Sat Dec 16 17:52:23 UTC 2023 , Edited by admin on Sat Dec 16 17:52:23 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY