Chlorine Dioxide Suppliers USA
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Product | Description | |
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ADOX Inline Generator Quick inquiry Where to buy Suppliers range | International Dioxcides patent pending design integrates the highest levels of safety, functionality, and industrial robustness in a self-contained modular design that is easy to install. Uses: Chlorine dioxide generation systems. Group: Chlorine dioxide systems. Categories: Chlorine Dioxide Generators. | International Dioxcide |
ADOX MG II Generator Quick inquiry Where to buy Suppliers range | The ADOX MG II uses chlorine gas to react with the precursor sodium chlorite to generate chlorine dioxide and is certified by NSF for standard 61. Uses: Chlorine dioxide generation systems. Group: Chlorine dioxide systems. Categories: Chlorine Dioxide Generators. | International Dioxcide |
ADOX MG III Generator Quick inquiry Where to buy Suppliers range | The ADOX MG III uses sodium hypochlorite (bleach) and hydrochloric acid to react with the precursor sodium chlorite to generate chlorine dioxide and is certified by NSF under standard 61. Uses: Chlorine dioxide generation systems. Group: Chlorine dioxide systems. Categories: Chlorine Dioxide Generators. | International Dioxcide |
ADOX Mini-AC Generator Quick inquiry Where to buy Suppliers range | The highly popular acid/chlorite reaction chemistry utilized in the MiniAC generator efficiently generates 7 lbs. to 30 lbs. of chlorine dioxide daily without the need for any electrical hookups. Uses: Chlorine dioxide generation systems. Group: Chlorine dioxide systems. Categories: Chlorine Dioxide Generators. | International Dioxcide |
Lead Quick inquiry Where to buy Suppliers range | Lead. Uses: The metal is not attacked by hot water. But in the presence of free oxygen, lead(II) hydroxide is formed. The overall reaction is: 2Pb + 2H2O + O2 ? 2Pb(OH)2 In hard water, however, the presence of small amounts of carbonate, sulfate, or silicate ions form a protective film on the metal surface, and prevent the occurrence of the above reaction and thus, corrosion of the metal. Lead does not evolve hydrogen readily with acids. Nitric acid attacks the metal readily, forming lead nitrate and oxides of nitrogen: 3Pb + 8HNO3 ? 3Pb(NO3)2 + 2NO + 4H2O This reaction is faster in dilute nitric acid than strong acid. Hydrochloric acid has little effect on the metal. At ordinary temperatures, lead dissolves slowly in hydrochloric acid, forming a coating of lead(II) chloride, PbCl2 over the metal, which prevents further attack. At ordinary temperatures, lead is not readily attacked by sulfuric acid. A coating of insoluble lead sulfate formed on the metal surface prevents any further reaction of the metal with the acid. The acid is, therefore, stored in specially designed lead containers. Also, the action of hot concentrated sulfuric acid is very low up to about 200°C. However, at temperatures near 260°C, both the concentrated sulfuric and hydrochloric acids dissolve lead completely. At ordinary temperatures, hydrofluoric acid also has little action on the metal. Formation of insoluble PbF2 prevents dissolution of lead in the acid. Organic acids in the presence of oxygen react slowly with lead, forming their soluble salts. Thus, acetic acid in the presence of oxygen forms lead(II) acetate: 2Pb + 4CH3COOH + O2 ? 2Pb(CH3COO)2 + 2H2O Lead dissolves in alkalies forming plumbite ion, Pb(OH)42¯ with the evolution of hydrogen: Pb + 2OH¯ + 2H2O ? Pb(OH)42¯ + H2 Lead combines with fluorine, chlorine, and bromine, forming bivalent lead halides: Pb + Cl2 ? PbCl2 Fusion with sulfur at elevated temperatures yields lead sulfide, PbS. The metal is oxidized to PbO when heated with sodium nitrate at elevated temperatures. Pb + NaNO3 ? PbO + NaNO2 Lead is widely used in storage batteries. Each cell consists of a spongy lead plate as cathode and lead dioxide as anode immersed in the electrolyte sulfuric acid. The overall chemical reaction in the cell during discharge is as follow | |
Lindlar Catalyst Quick inquiry Where to buy Suppliers range | Lindlar Catalyst. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. | |
Molybdenum Quick inquiry Where to buy Suppliers range | Molybdenum. Uses: Molybdenum is very stable to oxygen at ambient temperatures. However, when heated in air or oxygen to red heat the metal readily converts to its trioxide, MoO3: 2Mo + 3O2 ? 2MoO3 Heating the finely divided metal with its trioxide at 750°C makes molybdenum pentoxide, Mo2O5: Mo + MoO3 + O2 ? Mo2O5 When heated in steam at 800°C, the metal is converted to its dioxide, MoO2: Mo + 2H2O ? MoO2 + 2H2 Molybdenum combines with fluorine gas at ordinary temperatures forming colorless hexafluoride, MoF6: Mo + 3F2 ? MoF6 In the presence of oxygen, an oxyfluoride MoOF4 is obtained: 2Mo + O2 + 4F2 ? 2MoOF4 Reactions with chlorine and bromine occur only at elevated temperatures. With chlorine the product is molybdenum pentachloride: 2Mo + 5Cl2 ? 2MoCl5 When bromine vapor is passed over molybdenum metal at 600 to 700°C in an atmosphere of nitrogen, the product is trimeric molybdenum dibromide (trimolybdenum hexabromide) (Mo3Br6): 3Mo + 3Br2 ? Mo3Br6 Two other bromides are also obtained from the elements. These are molybdenum tribromide, MoBr3, and molybdenum tetrabromide, MoBr4. MoBr3, a black solid, is obtained by heating the elements at 350 to 400°C. Group: Nanoparticles & Nanopowders. Alternative Names: Molybdenum, foil, 250x300mm, thickness 0.1mm, annealed, 99.9%; Molybdenum, foil, 4mm disks, thickness 0.30mm, annealed, 99.9%; Molybdenum, foil, light tested, 50x50mm, thickness 0.008mm, 99.9%; Molybdenum sheet; Molybdenum, foil, light tested, 25x25mm, thickness 0.008mm, 99.9%; Molybdenum slug, 6.35mm (0.25in) dia x 12.7mm (0.50in) length; Molybdenum, Oil based standard solution, Specpure, Mo 1000 g/g; Molybdenum, foil, thickness 0.025 mm, purity 99.9%, size 25 x 25 mm; Molybdenum, foil, 50x50mm, thickness 0.15mm, annealed, 99.9%; Molybdenum, foil, 25mm disks, thickness 0.01mm, annealed, 99.9%. CAS No. 7439-98-7. Molecular formula: Mo. Mole weight: 95.95g/mol. IUPAC Name: molybdenum. Exact Mass: 97.905g/mol. EC Number: 231-107-2. Melting Point: 4752 ° F (NIOSH, 2016);2622 deg C;2617 °C;4752°F;4752°F;4752°F. Solubility: Insoluble (NIOSH, 2016);Practically insoluble in alkali hydroxides or fused alkalis; reacts with nitric acid, hot concentrated sulfuric acid, fused potassium chlorate or nitrate;Insoluble in water; soluble in nitric acid, sulfuric acid; slight | |
Palladium Quick inquiry Where to buy Suppliers range | Palladium and its alloys are used for hydrogen purification in fuel cells. Energy dispersive x-ray diffraction during electrochemical loading of palladium foils with hydrogen and deuterium was studied. Palladium foil was tested as a catalyst for Suzuki-Miyaura cross coupling reaction. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Group: Electrode Materials; Evaporation Slugs; High-Purity Metal Foils. Alternative Names: Palladium (powder),Palladium black,Palladium element. CAS No. 7440-5-3. IUPAC Name: palladium. Molecular Weight: Pd. Molecular Formula: 106.42. SMILES: [Pd]. Density: 12.02 g/cu cm. | |
Palladium Quick inquiry Where to buy Suppliers range | Palladium and its alloys are used for hydrogen purification in fuel cells. Energy dispersive x-ray diffraction during electrochemical loading of palladium foils with hydrogen and deuterium was studied. Palladium foil was tested as a catalyst for Suzuki-Miyaura cross coupling reaction. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Group: Electrode Materials; Evaporation Slugs; High-Purity Metal Foils. Alternative Names: Palladium (powder),Palladium black,Palladium element. CAS No. 7440-5-3. IUPAC Name: palladium. Molecular Weight: 106.42. Molecular Formula: Pd. SMILES: [Pd]. | |
Palladium Quick inquiry Where to buy Suppliers range | Palladium and its alloys are used for hydrogen purification in fuel cells. Energy dispersive x-ray diffraction during electrochemical loading of palladium foils with hydrogen and deuterium was studied. Palladium foil was tested as a catalyst for Suzuki-Miyaura cross coupling reaction. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Group: Oil & Gas. Alternative Names: Palladium (powder),Palladium black,Palladium element. CAS No. 7440-5-3. IUPAC Name: palladium. Molecular Weight: 106.42. Molecular Formula: Pd. SMILES: [Pd]. | |
Palladium on calcium carbonate Quick inquiry Where to buy Suppliers range | Palladium on calcium carbonate. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Molecular formula: Pd. | |
PurDOX Generator ,"λ","λ" Quick inquiry Where to buy Suppliers range | The PurDOX 700 VB is a complete chlorine dioxide generator in a self-contained modular design that is easy to install and requires a small footprint. Uses: Chlorine dioxide generation systems. Group: Chlorine dioxide systems. Categories: Chlorine Dioxide Generators. | International Dioxcide |
Ruthenium 5% on Carbon (wetted with ca. 50% Water) Quick inquiry Where to buy Suppliers range | Ruthenium 5% on Carbon (wetted with ca. 50% Water). Uses: When heated in air at 500 to 700°C, ruthenium converts to its dioxide, RuO2, a black crystalline solid of rutile structure. A trioxide of ruthenium, RuO3, also is known; formed when the metal is heated above 1,000°C. Above 1,100°C the metal loses weight because trioxide partially volatilizes. Ruthenium also forms a tetroxide, RuO4, which, unlike osmium, is not produced by direct union of the elements. Halogens react with the metal at elevated temperatures. Fluorine reacts with ruthenium at 300°C forming colorless vapors of pentafluoride, RuF5, which at ordinary temperatures converts to a green solid. Chlorine combines with the metal at 450°C to form black trichloride, RuCl3, which is insoluble in water. Ru metal at ambient temperature is attacked by chlorine water, bromine water, or alcoholic solution of iodine. Ruthenium is stable in practically all acids including aqua regia. Fusion with an alkali in the presence of an oxidizing agent forms ruthenate, RuO42- and perruthenate, RuO4¯. When finely-divided Ru metal is heated with carbon monoxide under 200 atm pressure, ruthenium converts to pentacarbonyl, Ru(CO)5, a colorless liquid that decomposes on heating to diruthenium nonacarbonyl, Ru2(CO)9, a yellow crystalline solid. Ruthenium reacts with cyclopentadiene in ether to form a sandwich complex, a yellow crystalline compound, bis(cyclopentadiene) ruthenium(0), also known as ruthenocene. Group: Pure Element Single Crystals. Alternative Names: Ruthenium, powder; Ru on carbon; Ruthenium nanoparticle (<20nm) in water at 100mg/L (stabilized with < 0.01 mmol/l of citrate); 44Ru; Ruthenium, Ruthenium, pellets, 2.5g, max. size 10mm, 99.9%; Ruthenium on alumina, extent of labeling: 5 wt. % loading, powder, Degussa type H213 R/D; 7440-18-8; rutenio; AN-19416; Ruthenium powder, -200 mesh, Premion(R). CAS No. 7440-18-8. Molecular formula: Ru. Mole weight: 101.07g/mol. IUPAC Name: ruthenium. Exact Mass: 101.904g/mol. EC Number: 231-127-1. Melting Point: 2334°C. SMILES: [Ru]. InChI: InChI=1S/Ru. InChIKey: KJTLSVCANCCWHF-UHFFFAOYSA-N. Monoisotopic Mass: 101.904g/mol. | |
Ruthenium dioxide Quick inquiry Where to buy Suppliers range | Ruthenium dioxide. Uses: Ruthenium dioxide is one of the primary oxygen catalysts used in a majority of chemical reactions such as the production of chlorine oxides. Ruthenium (IV) oxide is applied as an electrochemical supercapacitor agent as it has a high potential to store charge. Ruthenium dioxide is applied as a catalyst in the Deacon process where chlorine is produced through oxidation of hydrogen chloride. The high charge potential makes Ruthenium dioxide appropriate for use as an active agent in supercapacitors. The dispersion aspect of Ruthenium dioxide enhances the capacitance of nanocomposite electrode substances for supercapacitors. Ruthenium dioxide is widely used as a doping agent, as a catalyst, and as a coating material for titanium anodes, for the elimination of hydrogen sulfide from oil refineries. Hydrogen sulfide can be divided by light in the presence of a photocatalyst-containing CdS crystals doped with Ruthenium (IV) oxide. The hydrogen obtained could be essential in the synthesis of methanol, ammonia and potentially fuel an economy driven by hydrogen. Group: Nanoparticles & Nanopowders. Alternative Names: Ruthenium(IV) oxide, anhydrous, Premion(R); RuO2; ruthenium(iv) dioxide; 740R797; ruthenium(iv) oxide anhydrous, 99.9%; Ruthenium oxide (RuO2); AC1L348B; MFCD00011210; 12036-10-1; EINECS 234-840-6. CAS No. 12036-10-1. Molecular formula: O2Ru. Mole weight: 133.068g/mol. IUPAC Name: dioxoruthenium. Exact Mass: 133.894g/mol. EC Number: 234-840-6. SMILES: O=[Ru]=O. InChI: InChI=1S/2O.Ru. InChIKey: WOCIAKWEIIZHES-UHFFFAOYSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 133.894g/mol. | |
Ruthenium on alumina Quick inquiry Where to buy Suppliers range | Ruthenium on alumina. Uses: When heated in air at 500 to 700°C, ruthenium converts to its dioxide, RuO2, a black crystalline solid of rutile structure. A trioxide of ruthenium, RuO3, also is known; formed when the metal is heated above 1,000°C. Above 1,100°C the metal loses weight because trioxide partially volatilizes. Ruthenium also forms a tetroxide, RuO4, which, unlike osmium, is not produced by direct union of the elements. Halogens react with the metal at elevated temperatures. Fluorine reacts with ruthenium at 300°C forming colorless vapors of pentafluoride, RuF5, which at ordinary temperatures converts to a green solid. Chlorine combines with the metal at 450°C to form black trichloride, RuCl3, which is insoluble in water. Ru metal at ambient temperature is attacked by chlorine water, bromine water, or alcoholic solution of iodine. Ruthenium is stable in practically all acids including aqua regia. Fusion with an alkali in the presence of an oxidizing agent forms ruthenate, RuO42- and perruthenate, RuO4¯. When finely-divided Ru metal is heated with carbon monoxide under 200 atm pressure, ruthenium converts to pentacarbonyl, Ru(CO)5, a colorless liquid that decomposes on heating to diruthenium nonacarbonyl, Ru2(CO)9, a yellow crystalline solid. Ruthenium reacts with cyclopentadiene in ether to form a sandwich complex, a yellow crystalline compound, bis(cyclopentadiene) ruthenium(0), also known as ruthenocene. | |
Sodium Chlorate Quick inquiry Where to buy Suppliers range | Sodium Chlorate is used in the preparation of chlorine dioxide solution use in water treatment, as a food preservative agent, an antiseptic and also as a deodorant. Group: Biochemicals. Grades: Highly Purified. CAS No. 7775-9-9. Pack Sizes: 5g, 25g. Molecular Formula: ClNaO3. US Biological Life Sciences. | Worldwide |
Sodium Chlorate Quick inquiry Where to buy Suppliers range | International Dioxcide manufactures a proprietary mixture of sodium chlorate and hydrogen peroxide, which is used to produce chlorine dioxide for biocidal and oxidative water treatment applications. Uses: Chemical precursors. Group: sodium chlorate. Categories: NaClO3. | International Dioxcide |
Tin Quick inquiry Where to buy Suppliers range | Tin. Uses: At ordinary temperatures tin is stable in air. It actually forms a very thin protective oxide film. In powder form, and especially in the presence of moisture, it oxidizes. When heated with oxygen it forms tin(IV) oxide, SnO2.Tin reacts with all halogens forming their halides. Reaction with fluorine is slow at ordinary temperatures; however, chlorine, bromine and iodine readily react with the metal. Tin is attacked by concentrated acids. With dilute acids the reaction may be slow or very slow. The metal readily reacts with hot concentrated hydrochloric acid and aqua regia but slowly with cold dilute hydrochloric acid. The reaction also is slow with hot dilute sulfuric acid, which dissolves the metal, particularly in the presence of an oxidizing agent. The reaction with nitric acid is generally slow. Hot concentrated acid converts the metal to an insoluble hydrated tin(IV) oxide. The reaction is rapid with moist sulfur dioxide or sulfurous acid, chlorosulfonic, and pyrosulfuric acids. Organic acids such as, acetic, oxalic, and citric acids react slowly with the metal, particularly in the presence of air or an oxidizing agent. Strong alkaline solutions of caustic soda or caustic potash dissolve tin forming the stannate, Na2SnO3, or K2SnO3. The metal is stable in dilute solutions of ammonia or sodium carbonate. Tin dissolves in solutions of oxidizing salts such as potassium chlorate or potassium persulfate. The metal does not react with neutral salts in aqueous solutions. In air, tin reacts slowly with neutral salts. The metal does not combine directly with hydrogen, nitrogen or ammonia gas. Group: Nanoparticles & Nanopowders. Alternative Names: Tin, wire reel, 5m, diameter 1.0mm, as drawn, 99.99+%; Tin, foil, 300x300mm, thickness 0.5mm, as rolled, 98.8%; Tin, wire, diam. 0.25 mm, 99.99%; Tin, foil, 0.5m coil, thickness 0.15mm, as rolled, 98.8%; Tin, foil, light tested, 100x100mm, thickness 0.0125mm, 97.4%; Tin, foil, 2m coil, thickness 0.05mm, as rolled, 98.8%; Tin, rod, 100mm, diameter 2.0mm, 99.999+%; Tin, foil, 25mm disks, thickness 0.006mm, 97.4%; Tin, foil, 10mm disks, thickness 0.20mm, as rolled, 98.8%; Tin, foil, 50mm disks, thickness 0.006mm, 97.4%. CAS No. 7440-31-5. Molecular formula: Sn. Mole weight: 118.71g/mol. IUPAC Name: tin. Exact Mass |