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Chemical elements
Sulphur
Isotopes
Energy
Extraction
Refining
Applications
Allotropy
Crystalline
Amorphous Sulphur
Colloidal Sulphur
Physical Properties
Chemical Properties
Detection
Estimation
Compounds
Hydrogen Sulphide
Metal Polysulphides
Hydrogen Polysulphides
Hydrogen Pentasulphide
Hydrogen Trisulphide
Hydrogen Disulphide
Sulphur Monofluoride
Sulphur Tetrafluoride
Sulphur Hexafluoride
Sulphur Monochloride
Sulphur Dichloride
Sulphur Tetrachloride
Sulphur Monobromide
Thionyl Fluoride
Sulphuryl Fluoride
Fluorosulphonic Acid
Thionyl Chloride
Sulphuryl Chloride
Sulphur Oxytetrachloride
Pyrosulphuryl Chloride
Chlorosulphonic Acid
Thionyl Bromide
Sodium Sulphoxylate
Sulphur Dioxide
Sulphurous Acid
Sulphites
Sulphur Trioxide
Pyrosulphuric Acid
Pyrosulphates
Sulphuric Acid
Persulphuric Anhydride
Persulphuric Acid or Perdisulphuric Acid
Perdisulphates
Permonosulphuric Acid
Amidopermonosulphuric Acid
Thiosulphuric Acid
Thiosulphates
Polythionic Acids
Dithionic Acid
Trithionic Acid
Trithionates
Tetrathionic Acid
Tetrathionates
Pentathionic Acid
Pentathionates
Wackenroders Solution
Hexathionic Acid
Polythionic Acids
Sulphur Sesquioxide
Hydrosulphurous Acid
Hydrosulphites
Nitrogen Sulphide
Nitrogen Persulphide
Nitrogen Pentasulphide
Sulphammonium
Hexasulphamide
Nitrogen Chlorosulphide
Trithiazyl Chloride
Thiotrithiazyl Chloride
Dithiotetrathiazyl Chloride
Nitrogen Bromosulphide
Thiotrithiazyl Bromide
Thiotrithiazyl Iodide
Thiotrithiazyl Nitrate
Thiotrithiazyl Hydrogen Sulphate
Thiotrithiazyl Thiocyanate
Thionylamide
Sulphamide
Imidodisulphamide
Sulphimide
Sulphonic Acids
Amidosulphonic Acid
Imidosulphonic Acid
Nitrilosulphonic Acid
Hydroxylamine-monosulphonic Acid
Nitrososulphonic Acid
Hydroxylamine-disulphonic Acid
Hydroxylamine-isodisulphonic Acid
Hydroxylamine-trisulphonic Acid
Dihydroxylamidosulphonic Acid
Sulphazinic Acid
Sulphazotinic Acid
Dehydrosulphazotinic Acid
Nitrosulphonic Acid
Nitrosulphonyl Chloride
Nitrosulphonic Anhydride
Nitrosulphuric Acid
Nitrosodisulphonic Acid
Sulphonitronic Acid
Sulphates of Hydroxylamine
Hydroxylamine Dithionate
Hydrazine Dithionate
Hydrazine Amidosulphonate
Carbon Subsulphide
Carbon Monosulphide
Carbon Disulphide
Thioformaldehyde
Thiocarbonic Acid
Ammonium thiocarbonate
Thiolcarbonic Acid
Xanthic Acid
Perthiocarbonic Acid
Sodium perthiocarbonate
Carbonyl Sulphide
Thiocarbonyl Chloride
Thiocarbonyl Tetrachloride or
Carbon Hexachlorosulphide
Trichloromethyl Disulphide
Thiocarbonyl Sulphochloride
Carbon Bromosulphide
Amino-derivatives of Thiocarbonic Acid
Dithiocarbamic Acid
Thiocarbamide
Azidodithiocarbonic Acid
Thiocyanogen
Cyanogen Monosulphide
Cyanogen Trisulphide
Sulphur Thiocyanate
Disulphur Dithiocyanate
Thiocyanic Acid
Thiocyanates
Dithiocyanic Acid
Trithiocyanuric Acid
Perthiocyanic Acid
Perthiocyanogen
Sulphates
Trithiocyanuric Acid, (
H
C
N
S
)
3
Follow @Atomistry
Trithiocyanuric Acid, (
H
C
N
S
)
3
, may be obtained by treating cyanuric chloride with sodium sulphide. It forms yellow needles, stable up to 200° C., soluble in water. At 200° C. hydrochloric acid transforms it into cyanuric acid.
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