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Details

Stereochemistry ACHIRAL
Molecular Formula C3N3S3.3Na
Molecular Weight 243.217
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM TRITHIOCYANURATE

SMILES

[Na+].[Na+].[Na+].[S-]C1=NC([S-])=NC([S-])=N1

InChI

InChIKey=NYVOYAFUSJONHU-UHFFFAOYSA-K
InChI=1S/C3H3N3S3.3Na/c7-1-4-2(8)6-3(9)5-1;;;/h(H3,4,5,6,7,8,9);;;/q;3*+1/p-3

HIDE SMILES / InChI

Molecular Formula C3H3N3S3
Molecular Weight 177.271
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Approval Year

PubMed

PubMed

TitleDatePubMed
Tris(methylammonium thiocyanurate) monohydrate.
2010-12-08
Tripropyl-ammonium trithio-cyanurate.
2010-10-13
Design and synthesis of a stable supramolecular trigonal prism formed by the self-assembly of a linear tetrakis(Zn2+-cyclen) complex and trianionic trithiocyanuric acid in aqueous solution and its complexation with DNA (cyclen = 1,4,7,10-tetraazacyclododecane).
2009-10-05
A hydrogen-bonded channel structure formed by a complex of uracil and melamine.
2007-05-23
Heavy metal removal from winery wastewater in the case of restrictive discharge regulation.
2007
Coordination polymers of copper(I) halides and neutral heterocyclic thiones with new coordination modes.
2005-05-30
Structural rationalisation of co-crystals formed between trithiocyanuric acid and molecules containing hydrogen bonding functionality.
2005-04-08
UV-Induced trithione --> trithiol triple proton transfer in trithiocyanuric acid isolated in low-temperature matrixes.
2005-03-17
Synthesis, structure, redox, NLO and DNA interaction aspects of [((L'-'")2RuII)3(mu3-L)]3+ and [(L')2RuII(NC5H4S-)]+[L3- = 1,3,5-triazine-2,4,6-trithiolato, L'-'" = arylazopyridine].
2004-06-07
[Supramolecular chemistry of multinuclear zinc(II) complexes in aqueous solution].
2002-12
[Creation of new supramolecular chemistry based on multiple interaction in aqueous solution].
2002-10
Effectiveness of commercial reagents for heavy metal removal from water with new insights for future chelate designs.
2002-05-27
A cuboctahedral supramolecular capsule by 4:4 self-assembly of Tris(Zn(II)-cyclen) and trianionic trithiocyanurate in aqueous solution at neutral pH (cyclen=1,4,7,10-tetraazacyclododecane).
2002-02-15
Aqueous leaching properties and environmental implications of cadmium, lead and zinc trimercaptotriazine (TMT) compounds.
2001-10
Chemistry of 2,4,6-trimercapto-1,3,5-triazine (TMT): acid dissociation constants and group 2 complexes.
2001-08-13
Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.
1994-08-17
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:20:25 GMT 2025
Edited
by admin
on Mon Mar 31 22:20:25 GMT 2025
Record UNII
EW8XOU36QW
Record Status Validated (UNII)
Record Version
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Name Type Language
SODIUM TRITHIOCYANURATE
Common Name English
TMT 18
Preferred Name English
2,4,6-TRIMERCAPTO-S-TRIAZINE TRISODIUM SALT
Systematic Name English
TRISODIUM TRITHIOCYANURIC ACID
Systematic Name English
1,3,5-TRIAZINE-2,4,6(1H,3H,5H)-TRITHIONE, TRISODIUM SALT
Systematic Name English
TRISODIUM 2,4,6-TRITHIOXO-1,3,5-TRIAZINANE-1,3,5-TRIIDE
Systematic Name English
1,3,5-TRIAZINE-2,4,6(1H,3H,5H)-TRITHIONE, SODIUM SALT (1:3)
Systematic Name English
1,3,5-TRIAZINE-2,4,6-TRITHIOL TRISODIUM
Systematic Name English
TRIMERCAPTO-S-TRIAZINE TRISODIUM SALT
Systematic Name English
TRITHIOCYANURIC ACID TRISODIUM SALT
Systematic Name English
TRISODIUM 1,3,5-TRIAZINE-2,4,6-TRITHIOLATE
Systematic Name English
TRISODIUM TRITHIOCYANURATE
Systematic Name English
S-TRIAZINE-2,4,6-TRITHIOL, TRISODIUM SALT
Systematic Name English
Code System Code Type Description
CAS
17766-26-6
Created by admin on Mon Mar 31 22:20:25 GMT 2025 , Edited by admin on Mon Mar 31 22:20:25 GMT 2025
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FDA UNII
EW8XOU36QW
Created by admin on Mon Mar 31 22:20:25 GMT 2025 , Edited by admin on Mon Mar 31 22:20:25 GMT 2025
PRIMARY
PUBCHEM
3647359
Created by admin on Mon Mar 31 22:20:25 GMT 2025 , Edited by admin on Mon Mar 31 22:20:25 GMT 2025
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ECHA (EC/EINECS)
241-749-5
Created by admin on Mon Mar 31 22:20:25 GMT 2025 , Edited by admin on Mon Mar 31 22:20:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID1044853
Created by admin on Mon Mar 31 22:20:25 GMT 2025 , Edited by admin on Mon Mar 31 22:20:25 GMT 2025
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