Names | |
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IUPAC name Arsenic pentasulfide | |
Other names Arsenic(V) sulfide Diarsenic pentasulfide | |
Identifiers | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.154.195 |
EC Number |
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PubChem CID | |
UNII | |
UN number | 1557 |
CompTox Dashboard (EPA) | |
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Properties | |
As2S5 | |
Molar mass | 310.14 g·mol−1 |
Appearance | Vivid, dark orange, opaque crystals |
Melting point | 300 °C (572 °F; 573 K)(minimum) |
Boiling point | 500 °C (932 °F; 773 K)(decomposes) |
0.014 g dm−3 (at 0 °C) | |
Hazards | |
GHS labelling: | |
Danger | |
H301, H331, H410 | |
P261, P264, P270, P271, P273, P301+P310, P304+P340, P311, P321, P330, P391, P403+P233, P405, P501 | |
Related compounds | |
Related compounds | Arsenic pentoxide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Arsenic pentasulfide is an inorganic compound containing arsenic and sulfur. [1]
Solids of the approximate formula As2 S5 have been used as pigments and chemical intermediates but are generally only of interest in academic laboratories. [2]
Arsenic pentasulfide is prepared by precipitation from an acidic solution of soluble As(V) salts by treatment with hydrogen sulfide. [3] It may be also prepared by heating a mixture of arsenic and sulfur, extracting the fused mass with an ammonia solution and reprecipitating arsenic pentasulfide at low temperature by addition of hydrochloric acid.
Phosphorus pentasulfide with the formula P4S10, is a molecular compound featuring tetrahedral phosphorus(V) centres. Trends in arsenic redox potentials suggest that As2S5 adopts a similar structure, a plausible alternative being an arsenic polysulfide.
Arsenic pentasulfide hydrolyzes in boiling water, giving arsenous acid and sulfur:
It oxidizes in air at elevated temperatures producing arsenic oxides, the products and yields of which are variable. In alkali metal sulfide solutions arsenic pentasulfide forms a thioarsenate anion, [AsS4]3−, which contain As(V) centres.
Sulfide (British English also sulphide) is an inorganic anion of sulfur with the chemical formula S2− or a compound containing one or more S2− ions. Solutions of sulfide salts are corrosive. Sulfide also refers to chemical compounds large families of inorganic and organic compounds, e.g. lead sulfide and dimethyl sulfide. Hydrogen sulfide (H2S) and bisulfide (SH−) are the conjugate acids of sulfide.
Arsenic trioxide, sold under the brand name Trisenox among others, is an inorganic compound with the formula As
2O
3. As an industrial chemical, its major uses include the manufacture of wood preservatives, pesticides, and glass. It is also used as a medication to treat a type of cancer known as acute promyelocytic leukemia. For this use it is given by injection into a vein.
Ammonium hydrosulfide is the chemical compound with the formula [NH4]SH.
Arsenic acid or trihydrogen arsenate is the chemical compound with the formula H3AsO4. More descriptively written as AsO(OH)3, this colorless acid is the arsenic analogue of phosphoric acid. Arsenate and phosphate salts behave very similarly. Arsenic acid as such has not been isolated, but is only found in solution, where it is largely ionized. Its hemihydrate form (2H3AsO4·H2O) does form stable crystals. Crystalline samples dehydrate with condensation at 100 °C.
Phosphorus sulfides comprise a family of inorganic compounds containing only phosphorus and sulfur. These compounds have the formula P4Sn with n ≤ 10. Two are of commercial significance, phosphorus pentasulfide, which is made on a kiloton scale for the production of other organosulfur compounds, and phosphorus sesquisulfide, used in the production of "strike anywhere matches".
Phosphorus pentasulfide is the inorganic compound with the formula P2S5 (empirical) or P4S10 (molecular). This yellow solid is the one of two phosphorus sulfides of commercial value. Samples often appear greenish-gray due to impurities. It is soluble in carbon disulfide but reacts with many other solvents such as alcohols, DMSO, and DMF.
Phosphorus sesquisulfide is the inorganic compound with the formula P4S3. It was developed by Henri Sevene and Emile David Cahen in 1898 as part of their invention of friction matches that did not pose the health hazards of white phosphorus. This yellow solid is one of two commercially produced phosphorus sulfides. It is a component of "strike anywhere" matches.
Arsenic pentoxide is the inorganic compound with the formula As2O5. This glassy, white, deliquescent solid is relatively unstable, consistent with the rarity of the As(V) oxidation state. More common, and far more important commercially, is arsenic(III) oxide (As2O3). All inorganic arsenic compounds are highly toxic and thus find only limited commercial applications.
Arsenic trichloride is an inorganic compound with the formula AsCl3, also known as arsenous chloride or butter of arsenic. This poisonous oil is colourless, although impure samples may appear yellow. It is an intermediate in the manufacture of organoarsenic compounds.
Thiophosphoryl chloride is an inorganic compound with the formula PSCl3. It is a colorless pungent smelling liquid that fumes in air. It is synthesized from phosphorus chloride and used to thiophosphorylate organic compounds, such as to produce insecticides.
Antimony pentasulfide is an inorganic compound of antimony and sulfur, also known as antimony red. It is a nonstoichiometric compound with a variable composition. Its structure is unknown. Commercial samples are contaminated with sulfur, which may be removed by washing with carbon disulfide in a Soxhlet extractor.
Thiosulfuric acid is the inorganic compound with the formula H2S2O3. It has attracted academic interest as a simple, easily accessed compound that is labile. It has few practical uses.
Thiophosphates (or phosphorothioates, PS) are chemical compounds and anions with the general chemical formula PS
4−xO3−
x (x = 0, 1, 2, or 3) and related derivatives where organic groups are attached to one or more O or S. Thiophosphates feature tetrahedral phosphorus(V) centers.
Iron(III) sulfide, also known as ferric sulfide or sesquisulfide, is one of the several binary iron sulfides. It is a solid, black powder that degrades at ambient temperature.
Berkelium forms a number of chemical compounds, where it normally exists in an oxidation state of +3 or +4, and behaves similarly to its lanthanide analogue, terbium. Like all actinides, berkelium easily dissolves in various aqueous inorganic acids, liberating gaseous hydrogen and converting into the trivalent oxidation state. This trivalent state is the most stable, especially in aqueous solutions, but tetravalent berkelium compounds are also known. The existence of divalent berkelium salts is uncertain and has only been reported in mixed lanthanum chloride-strontium chloride melts. Aqueous solutions of Bk3+ ions are green in most acids. The color of the Bk4+ ions is yellow in hydrochloric acid and orange-yellow in sulfuric acid. Berkelium does not react rapidly with oxygen at room temperature, possibly due to the formation of a protective oxide surface layer; however, it reacts with molten metals, hydrogen, halogens, chalcogens and pnictogens to form various binary compounds. Berkelium can also form several organometallic compounds.
Thiophosphoryl fluoride is an inorganic molecular gas with formula PSF3 containing phosphorus, sulfur and fluorine. It spontaneously ignites in air and burns with a cool flame. The discoverers were able to have flames around their hands without discomfort, and called it "probably one of the coldest flames known". The gas was discovered in 1888.
Compounds of lead exist with lead in two main oxidation states: +2 and +4. The former is more common. Inorganic lead(IV) compounds are typically strong oxidants or exist only in highly acidic solutions.
Thiophosphoric acid is a chemical compound. Structurally, it is the acid derived from phosphoric acid with one extra sulfur atom, although it cannot be prepared from phosphoric acid. It is a colorless compound that is rarely isolated in pure form, but rather as a solution. The structure of the compound has not been reported, but two tautomers are reasonable: SP(OH)3 and OP(OH)2SH.
Gallium compounds are compounds containing the element gallium. These compounds are found primarily in the +3 oxidation state. The +1 oxidation state is also found in some compounds, although it is less common than it is for gallium's heavier congeners indium and thallium. For example, the very stable GaCl2 contains both gallium(I) and gallium(III) and can be formulated as GaIGaIIICl4; in contrast, the monochloride is unstable above 0 °C, disproportionating into elemental gallium and gallium(III) chloride. Compounds containing Ga–Ga bonds are true gallium(II) compounds, such as GaS (which can be formulated as Ga24+(S2−)2) and the dioxan complex Ga2Cl4(C4H8O2)2. There are also compounds of gallium with negative oxidation states, ranging from -5 to -1, most of these compounds being magnesium gallides (MgxGay).
Thiophosphoryl bromide is an inorganic compound with the formula PSBr3.
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