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Tris (hexafluoroacetylacetonato)iron (III)
Tris (hexafluoroacetylacetonato)iron (III). Group: Magnetic metal complexes. CAS No. 17786-67-3. Product ID: 1,1,1,5,5,5-hexafluoro-4-oxopent-2-en-2-olate; iron(3+). Molecular formula: 677g/mol. Mole weight: C15H3F18FeO6. C(=C(C(F)(F)F)[O-])C(=O)C(F)(F)F. C(=C(C(F)(F)F)[O-])C(=O)C(F)(F)F. C(=C(C(F)(F)F)[O-])C(=O)C(F)(F)F. [Fe+3]. InChI=1S/3C5H2F6O2.Fe/c3*6-4(7, 8)2(12)1-3(13)5(9, 10)11;/h3*1, 12H;/q;;;+3/p-3. NBPRJLXRDBDIFS-UHFFFAOYSA-K.
Tungsten carbide is a gray powder. (NTP, 1992);GREY-TO-BLACK POWDER.;A mixture of tungsten carbide, nickel, and sometimes other metals & metal oxides or carbides.;A mixture of tungsten carbide, cobalt, and sometimes other metals & metal oxides or carbides. Group: Nanopowders. CAS No. 12070-12-1. Product ID: methanidylidynetungsten(1+). Molecular formula: 195.85 g/mol. Mole weight: WC. [C-]#[W+]. InChI=1S/C.W/q-1;+1. UONOETXJSWQNOL-UHFFFAOYSA-N. 99.9 %.
Vanadium trioxide appears as a black crystalline solid. Density 4.87 g / cm³. Slightly soluble in water. Irritating to skin and eyes. May be toxic by ingestion. Used to make other chemicals. Used as a catalyst.;DryPowder;BLACK POWDER. Group: Electrode materials solid oxide fuel cell materials. CAS No. 1314-34-7. Product ID: oxo(oxovanadiooxy)vanadium. Molecular formula: 149.881g/mol. Mole weight: V2O3;V2O3;O3V2. O=[V]O[V]=O. InChI=1S/3O.2V. KFAFTZQGYMGWLU-UHFFFAOYSA-N.
Vanadyl sulfate appears as a blue crystalline solid. Very soluble in water. Denser than water. Contact may irritate skin, eyes, and mucous membranes. May be toxic by ingestion, inhalation and skin absorption. Group: Glass additives. Product ID: oxovanadium(2+); sulfate. Molecular formula: 163.01g/mol. Mole weight: VOSO4;O5SV. [O-]S(=O)(=O)[O-].O=[V+2]. InChI=1S/H2O4S.O.V/c1-5(2, 3)4;;/h(H2, 1, 2, 3, 4);;/q;;+2/p-2. UUUGYDOQQLOJQA-UHFFFAOYSA-L.
Vinylene Carbonate (stabilized with BHT)
Liquid. Group: Battery materials monomers. Alternative Names: 1,3-Dioxol-2-one (stabilized with BHT). CAS No. 872-36-6. Product ID: 1,3-dioxol-2-one. Molecular formula: 86.05. Mole weight: C3H2O3. C1=COC(=O)O1. InChI=1S/C3H2O3/c4-3-5-1-2-6-3/h1-2H. VAYTZRYEBVHVLE-UHFFFAOYSA-N. >98.0%(GC).
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Vinylsulfone-PEG-Vinylsulfone, VS-PEG-VS. Molecular formula: average Mn 5000.
Vinyltris(2-Methoxyethoxy)Silane
It is a vinyl functional silane coupling agent which can improve adhesion on various organic polymers. Uses: It can be used to improve adhesion between various organic polymers and inorganic materials such as silica, silicates and fiber glass. Group: Silane coupling agentsself assembly and contact printing materials. Alternative Names: Vinyltris(2-methoxyethoxy)silane. CAS No. 1067-53-4. Pack Sizes: 10 g; 100 g. Product ID: ethenyl-tris(2-methoxyethoxy)silane. Molecular formula: 280.39. Mole weight: C11H24O6Si. COCCO[Si](C=C)(OCCOC)OCCOC. InChI=1S/C11H24O6Si/c1-5-18 (15-9-6-12-2, 16-10-7-13-3)17-11-8-14-4/h5H, 1, 6-11H2, 2-4H3. WOXXJEVNDJOOLV-UHFFFAOYSA-N. 95%.
Wheat germ Untreated
Wheat germ Untreated. Group: Polysaccharide.
Xanthan from Xanthomonas campestris
Xanthan gum is a monospore polysaccharide produced by the fermentation of Pseudomonas sp. It is made of carbohydrates as the main raw material from the cabbage black rot Xanthomonas spp. through aerobic fermentation bioengineering technology to cut 1,6 - Glycosidic bond, after opening the branched chain, an acidic extracellular polysaccharide composed of straight chains is synthesized by 1,4-bond. The structure and conformation of xanthan gum determine the functional properties of its solution: the complex aggregated structure and intermolecular forces of xanthan gum determine that its solution has high viscosity at low shear and low concentration, and is more viscous than other polysaccharide solutions. High modulus, as well as pseudoplastic behavior; Xanthan gum has hydrogen bonds, anions, and side chains entangled in the rigid and straight molecular chains of the molecular chain to protect the main chain, so that the solution has good heat and salt resistance. It also has good stability to acid-base and enzymatic hydrolysis. Due to its excellent physical and chemical properties, including high viscosity, thixotropy, and stability of dispersions, xanthan gum has been widely used in the food industry, oil extraction, coatings, and many other fields. Uses: ·useful matrix components for drug delivery systems: functional components in microencapsulated drug capsules ·used as food additives such as emulsi
Xanthan gum from Xanthomonas campestris
Xanthan gum is a monospore polysaccharide produced by the fermentation of Pseudomonas sp. It is made of carbohydrates as the main raw material from the cabbage black rot Xanthomonas spp. through aerobic fermentation bioengineering technology to cut 1,6 - Glycosidic bond, after opening the branched chain, an acidic extracellular polysaccharide composed of straight chains is synthesized by 1,4-bond. The structure and conformation of xanthan gum determine the functional properties of its solution: the complex aggregated structure and intermolecular forces of xanthan gum determine that its solution has high viscosity at low shear and low concentration, and is more viscous than other polysaccharide solutions. High modulus, as well as pseudoplastic behavior; Xanthan gum has hydrogen bonds, anions, and side chains entangled in the rigid and straight molecular chains of the molecular chain to protect the main chain, so that the solution has good heat and salt resistance. It also has good stability to acid-base and enzymatic hydrolysis. Due to its excellent physical and chemical properties, including high viscosity, thixotropy, and stability of dispersions, xanthan gum has been widely used in the food industry, oil extraction, coatings, and many other fields. Uses: ·useful matrix components for drug delivery systems: functional components in microencapsulated drug capsules ·used as food additives such as em
YD2
Alfa Chemistry offers YD2 products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Dye-sensitized solar cell (dssc) materials phthalocyanine dyes, porphyrin dyes. Alternative Names: [5-[Bis(4-hexylphenyl)amino]-15-[2-(4-carboxyphenyl)ethynyl]-10,20-bis(3,5-di-tert-butylphenyl)porphyrinato]zinc(II). CAS No. 1201915-91-4. Product ID: zinc; 4-[2-[10,20-bis(3,5-ditert-butylphenyl)-15-(4-hexyl-N-(4-hexylphenyl)anilino)porphyrin-22,24-diid-5-yl]ethynyl]benzoic acid. Molecular formula: 1230.02. Mole weight: C81H89N5O2Zn. CCCCCCC1=CC=C (C=C1)N (C2=CC=C (C=C2)CCCCCC)C3=C4C=CC (=N4)C (=C5C=CC (=C (C6=NC (=C (C7=CC=C3[N-]7)C8=CC (=CC (=C8)C (C) (C)C)C (C) (C)C)C=C6)C#CC9=CC=C (C=C9)C (=O)O)[N-]5)C1=CC (=CC (=C1)C (C) (C)C)C (C) (C)C. [Zn+2]. InChI=1S/C81H90N5O2. Zn/c1-15-17-19-21-23-53-27-34-63 (35-28-53) 86 (64-36-29-54 (30-37-64) 24-22-20-18-16-2) 76-72-45-43-70 (84-72) 74 (57-47-59 (78 (3, 4) 5) 51-60 (48-57) 79 (6, 7) 8) 68-41-39-66 (82-68) 65 (38-31-55-25-32-56 (33-26-55) 7
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 40000.
Y-PEG40K-Acetaldehyde
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-Acetaldehyde. Molecular formula: average Mn 40000.
Y-PEG40K-Alkyne
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide).
Y-PEG40K-COOH
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-COOH. Molecular formula: average Mn 40000.
Y-PEG40K-Fluorescein
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 40000. ≥95%.
Y-PEG40K-MAL
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-MAL. Molecular formula: average Mn 40000.
Y-PEG40K-NH2
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-shape PEG Amine, Y-PEG-NH2. Molecular formula: average Mn 40000.
Y-PEG40K-NHS
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-NHS. Molecular formula: average Mn 40000.
Y-PEG40K-Propionaldehyde
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-Propionaldehyde. Molecular formula: average Mn 40000.
Ytterbium Aluminum Garnet
Ytterbium Aluminum Garnet. Uses: Ytterbium aluminum garnet (ybag) is a promising optical crystal with solid-state laser and scintillation applications. Group: Nanoparticles. CAS No. 12005-22-0. Molecular formula: 846.02g/mol. Mole weight: Yb3Al5O12.
Ytterbium Oxide
Ytterbium Oxide, also called Ytterbia, is being applied to numerous fiber amplifier and fiber optic technologies, HHigh purity Ytterbium Oxide are widely applied as a doping agent for garnet crystals in lasers a important colourant in glasses and porcelain enamel glazes. As Ytterbium Oxide has a significantly hHigher emissivity in the infrared range than Magnesium Oxide, a hHigher radiant intensity is obtained with Ytterbium-based payloads in comparison to those commonly based on Magnesium/Teflon/Viton (MTV). Uses: Also called ytterbia, is being applied to numerous fiber amplifier and fiber optic technologies, high purity ytterbium oxide are widely applied as a doping agent for garnet crystals in lasers a important colourant in glasses and porcelain enamel glazes. Group: Ceramic materials. CAS No. 1314-37-0. Product ID: oxygen(2-); ytterbium(3+). Molecular formula: 394g/mol. Mole weight: Yb2O3. [O-2].[O-2].[O-2].[Yb+3].[Yb+3]. InChI=1S/3O.2Yb/q3*-2;2*+3. UZLYXNNZYFBAQO-UHFFFAOYSA-N.
Yttria Stabilized Zirconia (12 Mol. %)
Yttria Stabilized Zirconia is available both partially and fully stabilized. Grades are available for applications include structural ceramics for turbine blades and anti-ballistic and armour ceramics and ionically conductive uses. A variety of surface areas can be produced. Forms include tape casting powder, screen printable ink and plasma spray/thermal spray powder. Proprietary formulations can be produced under non-disclosure arrangements. Group: Ceramic materials. Alternative Names: YSZ-12. Mole weight: Y2O3 ·ZrO2. YttriaStabilizedZirconia(12Mol.%).
Yttria Stabilized Zirconia (5 Mol. %)
Yttria Stabilized Zirconia is available both partially and fully stabilized. Grades are available for applications include structural ceramics for turbine blades and anti-ballistic and armour ceramics and ionically conductive uses. A variety of surface areas can be produced. Group: Ceramic materials. Alternative Names: YSZ-5. Mole weight: Y2O3 ·ZrO2. YttriaStabilizedZirconia(5Mol.%).
Yttria Stabilized Zirconia (6 Mol. %)
Yttria Stabilized Zirconia is available both partially and fully stabilized. Grades are available for applications include structural ceramics for turbine blades and anti-ballistic and armour ceramics and ionically conductive uses. A variety of surface areas can be produced. Forms include tape casting powder, screen printable ink and plasma spray/thermal spray powder. Group: Ceramic materials. Alternative Names: YSZ-6. Mole weight: Y2O3 ·ZrO2. YttriaStabilizedZirconia(6Mol.%).
Yttrium Aluminum Borate. Uses: Yttrium aluminum borate is a ceramic phosphor host material and, with dopants, can act as a laser, uv, and non-linear optical crystal. Group: Phosphors - phosphor materials. CAS No. 13813-76-8. Molecular formula: 405g/mol. Mole weight: YAl3(BO3)4.
Transparent to gray, odorless powder. Irritating to the skin and eyes on contact. Inhalation will cause irritation in the respiratory tract. [Note: Amorphous silica is the non-crystalline form of SiO2.];PelletsLargeCrystals, OtherSolid, Liquid;DryPowder; Liquid;DryPowder; OtherSolid;DryPowder; DryPowder, Liquid; DryPowder, OtherSolid; Liquid; OtherSolid; PelletsLargeCrystals; WetSolid; WetSolid, Liquid;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals;DryPowder; OtherSolid;DryPowder; DryPowder, Liquid; DryPowder, OtherSolid; DryPowder, OtherSolid, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, Liquid; DryPowder, PelletsLargeCrystals, OtherSolid; DryPowder, PelletsLargeCrystals, WetSolid; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid; WetSolid, Liquid;PelletsLargeCrystals;White, fluffy powder or granules. Hygroscopic;Solid;FINE WHITE POWDER.;COLOURLESS OR WHITE CRYSTALS.;COLOURLESS WHITE CRYSTALS.;COLOURLESS OR WHITE CRYSTALS.;Solid;Transparent to gray, odorless powder. [Note: Amorphous silica is the non-crystalline form of SiO2.]. Group: Zeolites. CAS No. 7631-86-9. Product ID: dioxosilane. Molecular formula: 60.084g/mol. Mole weight: (SiO2)n; SiO2; SiO2; SiO2; SiO2; SiO2; O2Si. O=[Si]=O. InChI=1S/O2Si/c1-3-2. VYPSYNLAJGMNEJ-UHFFFAOYSA-N.
Transparent to gray, odorless powder. Irritating to the skin and eyes on contact. Inhalation will cause irritation in the respiratory tract. [Note: Amorphous silica is the non-crystalline form of SiO2.];PelletsLargeCrystals, OtherSolid, Liquid;DryPowder; Liquid;DryPowder; OtherSolid;DryPowder; DryPowder, Liquid; DryPowder, OtherSolid; Liquid; OtherSolid; PelletsLargeCrystals; WetSolid; WetSolid, Liquid;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals;DryPowder; OtherSolid;DryPowder; DryPowder, Liquid; DryPowder, OtherSolid; DryPowder, OtherSolid, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, Liquid; DryPowder, PelletsLargeCrystals, OtherSolid; DryPowder, PelletsLargeCrystals, WetSolid; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid; WetSolid, Liquid;PelletsLargeCrystals;White, fluffy powder or granules. Hygroscopic;Solid;FINE WHITE POWDER.;COLOURLESS OR WHITE CRYSTALS.;COLOURLESS WHITE CRYSTALS.;COLOURLESS OR WHITE CRYSTALS.;Solid;Transparent to gray, odorless powder. [Note: Amorphous silica is the non-crystalline form of SiO2.]. Group: Zeolites. CAS No. 7631-86-9. Product ID: dioxosilane. Molecular formula: 60.084g/mol. Mole weight: (SiO2)n; SiO2; SiO2; SiO2; SiO2; SiO2; O2Si. O=[Si]=O. InChI=1S/O2Si/c1-3-2. VYPSYNLAJGMNEJ-UHFFFAOYSA-N.
Transparent to gray, odorless powder. Irritating to the skin and eyes on contact. Inhalation will cause irritation in the respiratory tract. [Note: Amorphous silica is the non-crystalline form of SiO2.];PelletsLargeCrystals, OtherSolid, Liquid;DryPowder; Liquid;DryPowder; OtherSolid;DryPowder; DryPowder, Liquid; DryPowder, OtherSolid; Liquid; OtherSolid; PelletsLargeCrystals; WetSolid; WetSolid, Liquid;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals;DryPowder; OtherSolid;DryPowder; DryPowder, Liquid; DryPowder, OtherSolid; DryPowder, OtherSolid, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, Liquid; DryPowder, PelletsLargeCrystals, OtherSolid; DryPowder, PelletsLargeCrystals, WetSolid; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid; WetSolid, Liquid;PelletsLargeCrystals;White, fluffy powder or granules. Hygroscopic;Solid;FINE WHITE POWDER.;COLOURLESS OR WHITE CRYSTALS.;COLOURLESS WHITE CRYSTALS.;COLOURLESS OR WHITE CRYSTALS.;Solid;Transparent to gray, odorless powder. [Note: Amorphous silica is the non-crystalline form of SiO2.]. Group: Zeolites. CAS No. 7631-86-9. Product ID: dioxosilane. Molecular formula: 60.084g/mol. Mole weight: (SiO2)n; SiO2; SiO2; SiO2; SiO2; SiO2; O2Si. O=[Si]=O. InChI=1S/O2Si/c1-3-2. VYPSYNLAJGMNEJ-UHFFFAOYSA-N.
Zinc carbonate appears as a white crystalline solid or powder that is insoluble in water. The primary hazard is the threat posed to the environment. Immediate steps should be taken to limit its spread to the environment. Used in pharmaceuticals, to make other zinc compounds, as a feed additive.;DryPowder; OtherSolid. Group: Glass additives. Product ID: zinc; carbonate. Molecular formula: 125.4g/mol. Mole weight: ZnCO3;CO3Zn. C(=O)([O-])[O-].[Zn+2]. InChI=1S/CH2O3.Zn/c2-1(3)4;/h(H2, 2, 3, 4);/q;+2/p-2. FMRLDPWIRHBCCC-UHFFFAOYSA-L.