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| Product | Description | |
|---|---|---|
| Nickel carbonate, basic hydrate | Nickel carbonate, basic hydrate. Group: Electrolytes. CAS No. 958638-02-3. Product ID: nickel; carbonate; hydroxide; hydrate. Molecular formula: 153.72g/mol. Mole weight: CH3NiO5-3. C(=O)([O-])[O-].O.[OH-].[Ni]. InChI=1S/CH2O3.Ni.2H2O/c2-1(3)4; ; ; /h(H2, 2, 3, 4); ; 2*1H2/p-3. VLVVKKSBFDPDOX-UHFFFAOYSA-K. |  |
| Nickel (II) Carbonate | NICKEL (II) CARBONATE, 99.9% pure, -100 mesh, (Synonym: Nickelous Carbonate), Formula: NiCO3. CAS No. 3333-67-3. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Nickel(II) carbonate basic tetrahydrate 98+% (48-50% ex Ni). | Nickel(II) carbonate basic tetrahydrate 98+% (48-50% ex Ni). Group: Biochemicals. Grades: Highly Purified. CAS No. 12607-70-4. Pack Sizes: 100g, 250g, 25g, 1Kg, 2.5Kg. US Biological Life Sciences. |  Worldwide |
| 1,1'-Bis(dicyclohexylphosphino)ferrocene | 1,1'-Bis(dicyclohexylphosphino)ferrocene. Uses: Ligand for palladium-catalyzed synthesis of oxindoles by amide ?-arylation. ligand for palladium-catalyzed alkoxycarbonylation of aryl chlorides. ligand for ruthenium-catalyzed alcohol-allene c-c coupling reaction via hydrohydroxyalkylation of 1,1-disubstituted allenes employing alcohols. ligand for nickel-catalyzed cross-coupling reaction of arylboronic acids with aryl carbonates. ligand for palladium-catalyzed regiodivergent hydroesterification of aryl olefins with phenyl formate to form linear structured phenyl arylpropanoates. ligand for palladium-catalyzed direct borylation of benzyl alcohol and its analogues in the absence of bases. Additional or Alternative Names: 1,1-Bis(dicyclohexylphosphino)ferrocene; 1,1-Bis(Dicyclohexylphosphino)Ferrocene; 1,1-BIS(DICYCLOHEXYLPHOSPHINO)FERROCENE. Product Category: Organic Phosphine Compounds. Appearance: Orange-red powder. CAS No. 146960-90-9. Molecular formula: C34H52FeP2. Mole weight: 578.57. Purity: 0.98. IUPACName: dicyclohexyl(cyclopentyl)phosphane;iron. Canonical SMILES: C1CCC(CC1)P(C2CCCCC2)[C]3[CH][CH][CH][CH]3.C1CCC(CC1)P(C2CCCCC2)[C]3[CH][CH][CH][CH]3.[Fe]. Product ID: ACM146960909. Alfa Chemistry ISO 9001:2015 Certified. Categories: AKOS026674396. |  |
| 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl | 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl. Uses: Phosphine ligand kit component. useful ligand for palladium-catalyzed carbon-nitrogen bond formation. useful ligand for rhodium-catalyzed c-c bond formation. useful ligand for palladium-catalyzed intramolecular acylation of aryl bromides via c-h activation. used in the preparation of buchwald third generation precatalyst. used in methoxy directed rhodium migration. used in nickel catalyzed c-n cross-coupling reactions. Additional or Alternative Names: F0001-2326; DB-009478; AC1LCPMX; (S)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL; AN-10356; SC-19338; (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene, puriss.; PubChem8136; TL8005203; (S)-(-)-2,2 inverted exclamation mark -Bis(diphenylphosphino)-1,1 inverted exclamation mark -binaphthalene. Product Category: Organic Phosphine Compounds. CAS No. 98327-87-8. Molecular formula: C44H32P2. Mole weight: 622.688g/mol. IUPACName: [1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=CC=C7)C8=CC=CC=C8. ECNumber: 616-304-7. Product ID: ACM98327878. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4,4'-Di-tert-butyl-2,2'-bipyridine | 4,4'-Di-tert-butyl-2,2'-bipyridine. Uses: Ligand for the iridium-catalyzed borylation of arenes ligand for the iridium-catalyzed synthesis of arylboronic acids and aryl trifluoroborates ligand for the nickel-catalyzed hydroxycarboxylation of 1,2-dienes by reaction carbon dioxide and oxygen ligand for the iridium-catalyzed meta borylation followed by halogenation of 1,3-disubstituted arenes ligand for the iridium-catalyzed silyl-directed ortho-borylation of arenes ligand for the iridium-catalyzed silane borylation followed by aryl borylation ligand for the iridium-catalyzed microwave-accelerated borylation of aromatic c-h bonds ligand for the iridium-catalyzed silyl-directed borylation of indoles ligand for the nickel-catalyzed synthesis of functionalized dialkyl ketones from carboxylic acids and alkyl halides ligand for the iron-catalyzed arylation of heterocycles. Additional or Alternative Names: BBBPY; 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine. Product Category: Polymer/Macromolecule. Appearance: White solid. CAS No. 72914-19-3. Molecular formula: C18H24N2. Mole weight: 268.4. Purity: 0.98. IUPACName: 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine. Canonical SMILES: CC(C)(C)C1=CC(=NC=C1)C2=NC=CC(=C2)C(C)(C)C. Product ID: ACM72914193-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| anaerobic carbon-monoxide dehydrogenase | This prokaryotic enzyme catalyses the reversible reduction of CO2 to CO. The electrons are transferred to redox proteins such as ferredoxin. In purple sulfur bacteria and methanogenic archaea it catalyses the oxidation of CO to CO2, which is incorporated by the Calvin-Benson-Basham cycle or released, respectively. In acetogenic and sulfate-reducing microbes it catalyses the reduction of CO2 to CO, which is incorporated into acetyl CoA by EC 2.3.1.169, CO-methylating acetyl CoA synthase, with which the enzyme forms a tight complex in those organisms. The enzyme contains five metal clusters per homodimeric enzyme: two nickel-iron-sulfur clusters called the C-Clusters, one [...-4S] clusters exist, presumably as part of the electron transfer chain. In purple sulfur bacteria the enzyme forms complexes with the Ni-Fe-S protein EC 1.12.7.2, ferredoxin hydrogenase, which catalyse the overall reaction: CO + H2O = CO2 + H2. cf. EC 1.2.5.3, aerobic carbon monoxide dehydrogenase. Group: Enzymes. Synonyms: Ni-CODH; carbon-monoxide dehydrogenase (ferredoxin). Enzyme Commission Number: EC 1.2.7.4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1227; anaerobic carbon-monoxide dehydrogenase; EC 1.2.7.4; Ni-CODH; carbon-monoxide dehydrogenase (ferredoxin). Cat No: EXWM-1227. |  |
| Carbon Nanotube Nickel | Carbon Nanotube Nickel. Group: Single wall cnt. CAS No. 308068-56-6. >99% (SWCNT). | |
| Carbonyl Nickel Coated Aluminum Powder (Ni Shell, Al Core) | Carbonyl Nickel Coated Aluminum Powder (Ni Shell, Al Core). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. | |
| Carbonyl Nickel Iron Alloy Powder | Carbonyl Nickel Iron Alloy Powder. Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Alloys nanopowders. | |
| Carbonyl Nickel Powder (2-3 μm) | Carbonyl Nickel Powder (2-3 μm). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. | |
| Carbonyl Nickel Powder (4-7 μm) | Carbonyl Nickel Powder (4-7 μm). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. | |
| CO-methylating acetyl-CoA synthase | Contains nickel, copper and iron-sulfur clusters. Involved, together with EC 1.2.7.4, carbon-monoxide dehydrogenase (ferredoxin), in the synthesis of acetyl-CoA from CO2 and H2. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.169. CAS No. 176591-19-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2109; CO-methylating acetyl-CoA synthase; EC 2.3.1.169; 176591-19-8. Cat No: EXWM-2109. | |
| Fluopsin N | Fluopsin N is an antibiotic containing metallic nickel produced by Pseudomonas fluorescent KY 4032 cultured with n-alkane as a carbon source. It has strong anti-Gram-positive and negative bacteria activity and anti-tumor activity. CAS No. 31541-90-9. Molecular formula: C4H8O2N2S2Ni. Mole weight: 238.94. |  |
| MWCNT-Ni Type 1 Carbon Nanotubes Multi Walled, Nickel coated | MWCNT-Ni Type 1 Carbon Nanotubes Multi Walled, Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| MWCNT-Ni Type 2 Carbon Nanotubes Multi Walled , Nickel coated | MWCNT-Ni Type 2 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| MWCNT-Ni Type 3 Carbon Nanotubes Multi Walled , Nickel coated | MWCNT-Ni Type 3 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| MWCNT-Ni Type 4 Carbon Nanotubes Multi Walled , Nickel coated | MWCNT-Ni Type 4 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| N6-Carbobenzyloxy-N2,N2-bis(carboxymethyl)-L-lysine | It is used in the synthesis of nickel-chelating fluorinated lipids for protein monolayer crystallizations. Group: Biochemicals. Alternative Names: N2, N2-Bis (carboxymethyl) -N6-[ (phenylmethoxy) carbonyl]-. Grades: Highly Purified. CAS No. 113231-04-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Nickel Carbon-Coated nanoparticles | Nickel Carbon-Coated nanoparticles. Group: Compounds nanoparticles. | |
| Nickel Carbon Core Shell Nanoparticles | Nickel Carbon Core Shell Nanoparticles. Group: Core shell nanoparticles. 99.9%. | |
| Nickel Carbon Nanotubes | Nickel Carbon Nanotubes. Group: Nanotubes. Mole weight: SiC. | |
| Nickel Nanoparticles, Carbon Coated | Nickel Nanoparticles, Carbon Coated. Group: Elements nanoparticles. 99.9 %. | |
| oxalate oxidoreductase | Contains thiamine diphosphate and [4Fe-4S] clusters. Acceptors include ferredoxin and the nickel-dependent carbon monoxide dehydrogenase (EC 1.2.7.4). Group: Enzymes. Enzyme Commission Number: EC 1.2.7.10. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1224; oxalate oxidoreductase; EC 1.2.7.10. Cat No: EXWM-1224. | |
| Titanium Carbon Nanotubes | Titanium Carbon Nanotubes are generally immediately available in most volumes. Additional technical, research and safety (MSDS) information is available. Carbon Nanotubes are Single-Walled, Double Walled and Multi-Walled black nano scale cylindrical tubes of graphitic carbon with numerous applications. Carbon Nanotubes are the stiffest and strongest known fibers and have unique electrical properties. When used as reinforcement fibers, carbon nanotubes can improve the quality and properties of metal, polymer and ceramics. Carbon nanotubes can behave like a conductive metallic or semiconductor depending on their structure, which is useful for nanoscale electronic devices and in electrically conductive films in coatings, plastics, nanowire, nanofiber and in certain bioscience applications. Recently, carbon nanotubes have been demonstrated to create the "darkest" known material absorbing all wavelengths or "colors" of light which will prove useful in solar and electronic applications. When combined with Aluminum, Copper, Magnesium, Nickel, Titanium, and Tin, Single-Walled Carbon Nanotube materials reveal enhanced tensile strength, hardness and elastic modulus characteristics. Titanium/Carbon Nanotube composites, research shows, demonstrate a considerable increase in tensile stress, hardness and yield stress. In an additional study, when compared to pure Titanium, Titanium/Carbon Nanotube composites displayed increas | |
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