382922
Trithiocyanuric acid trisodium salt hydrate
98%
Synonym(s):
1,3,5-Triazine-2,4,6-trithiol trisodium salt hydrate
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About This Item
Empirical Formula (Hill Notation):
C3N3Na3S3 · xH2O
CAS Number:
Molecular Weight:
243.22 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
form
powder
mp
82-84 °C (lit.)
SMILES string
O.[Na]Sc1nc(S[Na])nc(S[Na])n1
InChI
1S/C3H3N3S3.3Na.H2O/c7-1-4-2(8)6-3(9)5-1;;;;/h(H3,4,5,6,7,8,9);;;;1H2/q;3*+1;/p-3
InChI key
TZJODYRMPMPAMB-UHFFFAOYSA-K
General description
Trithiocyanuric acid trisodium salt hydrate is the hydrated trisodium salt of trithiocyanuric acid (1,3,5-triazine-2,4,6(1H,3H,5H)-trithione). 2,4,6-trimercapto-s-triazine, trisodium salt commonly referred as TMT-55, is employed for the removal of heavy metals from polluted waters.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Crystal packing in tetraphenylphosphonium salts of trithiocyanuric acid and its methanol solvate.
Dean PAW, et al.
CrystEngComm, 6(88), 543-548 (2004)
Structure and powder diffraction pattern of 2, 4, 6-Trimercapto-s-triazine, trisodium salt (Na3S3C3N3? 9H2O).
Henke KR, et al.
Powder Diffraction, 12(1), 7-12 (1997)
Shin Aoki
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 122(12), 1095-1108 (2003-01-04)
We report novel supramolecular polyhedrons formed by three-dimensional self-assembly of multinuclear zinc(II)-12-membered tetraamine (= cyclen = 1,4,7,10-tetraazacyclododecane) complexes with potentially multidentate ligands such as cyanuric acid (CA) and trithiocyanuric acid (TCA) in aqueous solution. Two new supermolecular frameworks were isolated
F J Koschier et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 21(4), 495-498 (1983-08-01)
Trithiocyanuric acid (TCY) is a rubber curative of low oral and dermal toxicity and with a low potential for eye and skin irritation. This study determined the effects of TCY on Sprague-Dawley rats at levels of 0.0, 625, 2500 and
Mohd Zulkefeli et al.
Inorganic chemistry, 48(19), 9567-9578 (2009-09-12)
A new supramolecular complex, {(Zn(4)L(4))(3)-(TCA(3-))(4)}(12+), was designed and synthesized by the 3:4 self-assembly of a linear tetrakis(Zn(2+)-cyclen) complex (Zn(4)L(4))(8+) and trianionic trithiocyanurate (TCA(3-)) in aqueous solution (cyclen = 1,4,7,10-tetraazacyclododecane). The {(Zn(4)L(4))(3)-(TCA(3-))(4)}(12+) complex, which should have a trigonal prism configuration, was
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