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| Product | Description | |
|---|---|---|
| Nitrofurazone - [13C, 15N2] | Cas No. 1217220-85-3. |  |
| Nitrofurazone-13C,15N2 | analytical standard. Group: Application areas. |  |
| Nitrofurazone Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Nitrofurazone solution | 100 ?g/mL in acetonitrile, analytical standard. Group: Application areas. | |
| Nitrofurfural diacetate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsbritish pharmacopoeiapharmacopoeial standards. Alternative Names: (5-Nitrofuran-2-yl)methylidene Diacetate, Nitrofurfural Diacetate, Nitrofural Imp. B (EP),Nifuroxazide Imp. C (EP). | |
| Nitrogen-15N2 | 98 atom % 15N. Group: Compressed and liquefied gases. | |
| Nitrogen and sulfur doping modification Nb2CTx MXene | N-Nb2CTx has an accordion-like layered structure, and N successfully enters and is evenly distributed on the Ti3C2 matrix. Uses: N-nb2ctx nanomaterials were prepared by a simple one-step hydrothermal method and applied to electrochemical capacitors. Group: Mxenes materials. 0.99. |  |
| Nitrogen and sulfur doping modification Ti2CTx MXene | Ti2CTx has an accordion-like layered structure, and N successfully enters and is evenly distributed on the Ti3C2 matrix. Uses: N-ti2ctx nanomaterials were prepared by a simple one-step hydrothermal method and applied to electrochemical capacitors. Group: Mxenes materials. CAS No. 12316-56-2. 0.99. | |
| Nitrogen and sulfur doping modification Ti3C2Tx MXene | N-Ti3C2 nanomaterials were prepared by a simple one-step hydrothermal method and applied to electrochemical capacitors. The experimental results show that: N-Ti3C2 has an accordion-like layered structure, and N successfully enters and is evenly distributed on the Ti3C2 matrix. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12363-89-2. 0.999. | |
| Nitrogen and sulfur doping modification Ti3C2Tx Solution | N-Ti3C2 nanomaterials were prepared by a simple one-step hydrothermal method and applied to electrochemical capacitors. The experimental results show that: N-Ti3C2 has an accordion-like layered structure, and N successfully enters and is evenly distributed on the Ti3C2 matrix. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12363-89-2. 0.999. | |
| Nitrogen and sulfur doping modification V2CTx MXene | N-V2CTx has an accordion-like layered structure, and N successfully enters and is evenly distributed on the Ti3C2 matrix. Uses: V2ctx nanomaterials were prepared by a simple one-step hydrothermal method and applied to electrochemical capacitors. Group: Mxenes materials. 0.99. | |
| nitrogenase | Requires Mg2+. It is composed of two proteins that can be separated but are both required for nitrogenase activity. Dinitrogen reductase is a [4Fe-4S] protein, which, with two molecules of ATP and ferredoxin, generates an electron. The electron is transferred to the other protein, dinitrogenase (molybdoferredoxin). Dinitrogenase is a molybdenum-iron protein that reduces dinitrogen in three succesive two-electron reductions from nitrogen to diimine to hydrazine to two molecules of ammonia. The molybdenum may be replaced by vanadium or iron. The reduction is initiated by formation of hydrogen in stoichiometric amounts. Acetylene is reduced to ethylene (but only very slowly to ethane), azide to nitrogen and ammonia, and cyanide to methane and ammonia. In the absence of a suitable substrate, hydrogen is slowly formed. Ferredoxin may be replaced by flavodoxin [see EC 1.19.6.1 nitrogenase (flavodoxin)]. Group: Enzymes. Enzyme Commission Number: EC 1.18.6.1. CAS No. 9013-4-1. 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-1114; nitrogenase; EC 1.18.6.1; 9013-04-1. Cat No: EXWM-1114. |  |
| nitrogenase (flavodoxin) | Requires Mg2+. It is composed of two components, dinitrogen reductase and dinitrogenase, that can be separated but are both required for nitrogenase activity. Dinitrogen reductase is a [4Fe-4S] protein, which, at the expense of ATP, transfers electrons from a dedicated flavodoxin to dinitrogenase. Dinitrogenase is a protein complex that contains either a molybdenum-iron cofactor, a vanadium-iron cofactor, or an iron-iron cofactor, that reduces dinitrogen in three succesive two-electron reductions from nitrogen to diimine to hydrazine to two molecules of ammonia. The reduction is initiated by formation of hydrogen. The enzyme can also reduce acetylene to ethylene (but only very slowly to ethane), azide to nitrogen and ammonia, and cyanide to methane and ammonia. In the absence of a suitable substrate, hydrogen is slowly formed. Some enzymes utilize ferredoxin rather than flavodoxin as the electron donor (see EC 1.18.6.1, nitrogenase). Group: Enzymes. Enzyme Commission Number: EC 1.19.6.1. CAS No. 9013-4-1. 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-1115; nitrogenase (flavodoxin); EC 1.19.6.1; 9013-04-1. Cat No: EXWM-1115. | |
| Nitrogen doped CMK-3 | Nitrogen doped CMK-3. Uses: Designed for use in research and industrial production. Product Category: Mesoporous Carbon and Carbon Nanomaterials. CAS No. 7440-44-0. Product ID: ACM7440440-109. Alfa Chemistry ISO 9001:2015 Certified. Categories: methane. |  |
| Nitrogen-doped graphene | This highly exfoliated nitrogen-doped graphene exhibits high electrochemical activity towards oxygen reduction in alkali medium providing an affordable industrial alternative to currently used noble metal-based catalysts (i.e. Pt, Pd). This nitrogen-doped graphene shows high onset potential (ca. 940 mV vs. RHE) carrying out the electrochemical oxygen reduction reaction (ORR) towards a 4 electron pathway avoiding the production of H2O2. Furthermore, this material is reported to be more stable (to MeOH) and durable (CO tolerance) than Pt-based catalysts.This highly exfoliated nitrogen-doped graphene exhibits high electrochemical activity towards oxygen reduction in alkali medium providing an affordable industrial alternative to currently used noble metal-based catalysts (i.e. Pt, Pd). This nitrogen-doped graphene shows high onset potential (ca. 940 mV vs. RHE) carrying out the electrochemical oxygen reduction reaction (ORR) towards a 4 electron pathway avoiding the production of H2O2. Furthermore, this material is reported to be more stable (to MeOH) and durable (CO tolerance) than Pt-based catalysts. Uses: Electrocatalyst. field-effect transistors. sensors. lithium ion batteries. supercapacitors. Group: Graphene series. Molecular formula: 12.01. | |
| Nitrogen-doped graphene | This highly exfoliated nitrogen-doped graphene exhibits high electrochemical activity towards oxygen reduction in alkali medium providing an affordable industrial alternative to currently used noble metal-based catalysts (i.e. Pt, Pd). This nitrogen-doped graphene shows high onset potential (ca. 940 mV vs. RHE) carrying out the electrochemical oxygen reduction reaction (ORR) towards a 4 electron pathway avoiding the production of H2O2. Furthermore, this material is reported to be more stable (to MeOH) and durable (CO tolerance) than Pt-based catalysts.This highly exfoliated nitrogen-doped graphene exhibits high electrochemical activity towards oxygen reduction in alkali medium providing an affordable industrial alternative to currently used noble metal-based catalysts (i.e. Pt, Pd). This nitrogen-doped graphene shows high onset potential (ca. 940 mV vs. RHE) carrying out the electrochemical oxygen reduction reaction (ORR) towards a 4 electron pathway avoiding the production of H2O2. Furthermore, this material is reported to be more stable (to MeOH) and durable (CO tolerance) than Pt-based catalysts. Uses: Electrocatalyst. field-effect transistors. sensors. lithium ion batteries. supercapacitors. Group: Carbon nano materials. Molecular formula: 12.01. | |
| Nitrogen-doped Graphene | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;Bl | |
| Nitrogen-Doped Graphene Aerogel | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; Wet | |
| Nitrogen doped graphene oxide | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSo | |
| Nitrogen-doped Graphene Oxide | Nitrogen-doped Graphene Oxide. Uses: Electrocatalyst. field-effect transistors. sensors. lithium ion batteries. supercapacitors. Group: other nano materials. Molecular formula: 14.5. | |
| Nitrogen-doped Graphene Powder | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetS | |
| Nitrogen-doped Graphene Powder | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetS | |
| Nitrogen-Doped Graphene Powder | Nitrogen-Doped Graphene Powder. Group: Graphene nanopowders. CAS No. 1034343-98-0. 99.9 %. | |
| Nitrogen doped graphene quantum dots | Nitrogen doped graphene quantum dots. Group: Graphene quantum dots. | |
| Nitrogen doped ordered mesoporous carbon | Nitrogen doped ordered mesoporous carbon. Group: Carbon compounds. | |
| Nitrogen doped TiO2 Nanotubes | Nitrogen doped TiO2 Nanotubes. Group: Graphene nanopowdersdoped nanoparticles. CAS No. 13463-67-7. Molecular formula: 79.8658 g/mol. 99.9%. | |
| Nitrogenistein | Nitrogenistein. Group: Biochemicals. Alternative Names: 4'-Nitro-6-hydroxyflavone; 6-Hydroxy-2-(4-nitrophenyl)-4H-1-benzopyran-4-one. Grades: Highly Purified. CAS No. 39679-60-2. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C15H9NO5. US Biological Life Sciences. |  Worldwide |
| Nitrogenistein (4'-Nitro-6-hydroxyflavone) | Nitrogenistein (4'-Nitro-6-hydroxyflavone). Group: Biochemicals. Alternative Names: 4'-Nitro-6-hydroxyflavone. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Nitrogen Oxide in Impinger Solution | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| Nitrogen Oxide Ion Selective Electrode Solutions | We offer the products in four grades: ISA; Fill Solution; 0.1 M Standard; 1000ppm Standard. Group: Ion selective electrode solutions. Alternative Names: Nitric oxide ion electrode solution. | |
| Nitrogen Oxide Ion Selective Electrode Solutions | Nitrogen Oxide Ion Selective Electrode Solutions. Group: Electrolytes. | |
| Nitrogen Pesticides | certified reference material. Group: Certified reference materials (crms). | |
| Nitrogen/Phosphorus co-doped graphene | Typical thickness: 1-5 layers.Typical size : 0.5-5 μm. Uses: Electrocatalyst. field-effect transistors. sensors. lithium ion batteries. supercapacitors. Group: other nano materials. Molecular formula: 12.01. | |
| Nitrogen/Phosphorus co-doped graphene | Typical thickness: 1-5 layers.Typical size : 0.5-5 μm. Uses: Electrocatalyst. field-effect transistors. sensors. lithium ion batteries. supercapacitors. Group: Carbon nano materials. Molecular formula: 12.01. | |
| Nitrogen/Sulfur co-doped graphene | Typical thickness: 1-5 layers.Typical size : 0.5-5 μm. Uses: Bioimaging photocatalysis led energy conversion sensing. Group: Carbon nano materials. | |
| Nitrogen/Sulfur co-doped graphene | Typical thickness: 1-5 layers.Typical size : 0.5-5 μm. Uses: Bioimaging photocatalysis led energy conversion sensing. Group: other nano materials. | |
| Nitro-grela | Nitro-grela. Uses: This catalyst is used for an efficient synthesis of hcv protease inhibitor, biln 2061. the nitro-grela catalyst is a stable olefin metathesis initiator active in various ring-closing, cross, and enyne metathesis reactions. its efficiency has been proven in numerous total syntheses of natural and biologically active compounds, and in material science. Group: Polymerization catalystspolymerization reagents. Alternative Names: [1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro[(2-isopropoxy-5-nitrobenzylidene)]ruthenium(II). CAS No. 502964-52-5. Product ID: [1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-dichloro-[(5-nitro-2-propan-2-yloxyphenyl)methylidene]ruthenium. Molecular formula: 671.63. Mole weight: C31H37Cl2N3O3Ru. CC1=CC (=C (C (=C1)C)N2CCN (C2=[Ru] (=CC3=C (C=CC (=C3)[N+] (=O)[O-])OC (C)C) (Cl)Cl)C4=C (C=C (C=C4C)C)C)C. InChI=1S/C21H26N2. C10H11NO3. 2ClH. Ru/c1-14-9-16 (3)20 (17 (4)10-14)22-7-8-23 (13-22)21-18 (5)11-15 (2)12-19 (21)6; 1-7 (2)14-10-5-4-9 (11 (12)13)6-8 (10)3; /h9-12H, 7-8H2, 1-6H3; 3-7H, 1-2H3; 2*1H; /q; +2/p-2. RQQSRSPQJIAORC-UHFFFAOYSA-L. 97%+. | |
| Nitro-L-arginine methyl ester hydrochloride | 5g Pack Size. Group: Amino Acids. Formula: C7H16ClN5O4. CAS No. 51298-62-5. Prepack ID 10827891-5g. Molecular Weight 269.69. See USA prepack pricing. |  |
| Nitromethane | Nitromethane is used in the preparation of Thermobaric explosives (TBX's). Group: Biochemicals. Grades: Highly Purified. CAS No. 75-52-5. Pack Sizes: 100g, 250g. Molecular Formula: CH3NO2. US Biological Life Sciences. | Worldwide |
| Nitromethane | 100g Pack Size. Group: Solvents. Formula: CH NO . CAS No. 75-52-5. Prepack ID 53899410-100g. Molecular Weight 61.04. See USA prepack pricing. | |
| NITROMETHANE-13C | NITROMETHANE-13C. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nitromethane-13C, 292141_ALDRICH, AKOS015913373, I14-45386, 32480-00-5. Product Category: Heterocyclic Organic Compound. CAS No. 32480-00-5. Molecular formula: CH3NO2. Mole weight: 62.05. Purity: 0.96. IUPACName: nitromethane. Density: 1.145 g/mL at 25ºC. Product ID: ACM32480005. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitromethane-d3 | Nitromethane-d3 is a useful reagent in deuteration of stable carbene perdeuterio-?1,?3,?4,?5-?tetramethylimidazol-?2-?ylidene (2). Group: Biochemicals. Grades: Highly Purified. CAS No. 13031-32-8. Pack Sizes: 250mg, 1g. Molecular Formula: CD3NO2, Molecular Weight: 64.06. US Biological Life Sciences. | Worldwide |
| Nitromethanetrispropanol | Nitromethanetrispropanol. Uses: This product is suitable for scientific research. Additional or Alternative Names: 4-(3-Hydroxypropyl)-4-nitro-1,7-heptanediol. Product Category: Heterocyclic Organic CompoundAlcohol-Multifunctional. CAS No. 116747-80-9. Molecular formula: C10H21NO5. Mole weight: 235.28 g/mol. Purity: 0.95. IUPACName: 4-(3-hydroxypropyl)-4-nitroheptane-1,7-diol. Canonical SMILES: OCCCC(CCCO)(CCCO)[N+]([O-])=O. Density: 1.182g/cm³. Product ID: ACM-MO-116747809. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitromethanetrispropionic acid | Nitromethanetrispropionic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,1,1-Tris(2-carboxyethyl)nitromethane. Product Category: Carboxylic Acid Monomers. CAS No. 59085-15-3. Molecular formula: C10H15NO8. Mole weight: 277.23 g/mol. Purity: 0.97. Product ID: ACM-MO-59085153. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitromide | analytical standard. Group: Application areas. | |
| Nitromifene citrate | Nitromifene citrate is a non-steroidal estrogen antagonist. It is structurally similar to Tamoxifen, which is a selective estrogen response modifier. It is most commonly used as a research tool in animal studies. Uses: Nitromifene citrate is most commonly used as a research tool in animal studies. Synonyms: CI-628 citrate; CI 628 citrate; CI628 citrate; 1- (2- (p- (alpha- (p-Methoxyphenyl) -beta-nitrostyryl) phenoxy) ethyl) pyrrolidine citrate (1:1); NSC 110407. Grades: 98%. CAS No. 5863-35-4. Molecular formula: C33H36N2O11. Mole weight: 636.65. | |
| nitronate monooxygenase | Previously classified as 2-nitropropane dioxygenase (EC 1.13.11.32), but it is now recognized that this was the result of the slow ionization of nitroalkanes to their nitronate (anionic) forms. The enzymes from the fungus Neurospora crassa and the yeast Williopsis saturnus var. mrakii (formerly classified as Hansenula mrakII) contain non-covalently bound FMN as the cofactor. Neither hydrogen peroxide nor superoxide were detected during enzyme turnover. Active towards linear alkyl nitronates of lengths between 2 and 6 carbon atoms and, with lower activity, towards propyl-2-nitronate. The enzyme from N. crassa can also utilize neutral nitroalkanes, but with lower activity. Group: Enzymes. Synonyms: NMO; 2-nitropropane dioxygenase (incorrect). Enzyme Commission Number: EC 1.13.12.16. 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-0608; nitronate monooxygenase; EC 1.13.12.16; NMO; 2-nitropropane dioxygenase (incorrect). Cat No: EXWM-0608. | |
| Nitron(bicyclic compd.) | Nitron(bicyclic compd.). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-(4-chlorophenyl)-5-(trifluoromethyl)-1h-pyrazole-4-carboxylic acid, 98534-80-6, 1-(4-chlorophenyl)-5-(trifluoromethyl)pyrazole-4-carboxylic acid, SBB001190, 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid, 2-(4-chlorophenyl)-3-(trifluoromethyl)-2h-pyrazole-4-carboxylic acid, 99994-22-6, Maybridge1_004008, AC1LEML0, AC1Q4JYT, AC1Q72CP, AC1Q72CQ, SureCN2064195, CTK5H9954, HMS552O04, MolPort-000-144-390, KST-1B9590, AR-1B1928, AKOS000200540, AG-H-99875. Product Category: Heterocyclic Organic Compound. CAS No. 99994-22-6. Molecular formula: C20H16N4. Mole weight: 312.3678. Purity: 0.96. IUPACName: 1-(4-chlorophenyl)-5-(trifluoromethyl)pyrazole-4-carboxylic acid. Canonical SMILES: C1=CC(=CC=C1N2C(=C(C=N2)C(=O)O)C(F)(F)F)Cl. Product ID: ACM99994226. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitronium hexafluoroantimonate | Nitronium hexafluoroantimonate. Group: Electrolytes. Alternative Names: Dioxoammonium hexafluoroantimonate(1-). CAS No. 17856-92-7. Product ID: Nitronium; hexafluoroantimony(1-). Molecular formula: 281.76. Mole weight: F6NO2Sb. [N+](=O)=O.F[Sb-](F)(F)(F)(F)F. InChI=1S/6FH.NO2.Sb/c; 2-1-3; /h6*1H; /q; +1; +5/p-6. OFNJLTRMKNMFSW-UHFFFAOYSA-H. 99%+. | |
| Nitronium tetrafluoroborate | Nitronium tetrafluoroborate. CAS No. 13826-86-3. |  Pennsylvania PA |
| Nitronium tetrafluoroborate | corrosive moisture sensitive. CAS No. 13826-86-3. Product ID: 8-01380. Molecular formula: NO2BF4. Mole weight: 132.81. |  |
| Nitronium tetrafluoroborate | ≥95%. Group: Electronic materials. CAS No. 13826-86-3. Mole weight: NO2BF4. O=[N+]=O.F[B-](F)(F)F. | |
| Nitronium tetrafluoroborate solution | 0.5 M in sulfolane. Group: Electronic chemicals. | |
| nitroquinoline-N-oxide reductase | This enzyme belongs to the family of oxidoreductases, specifically those acting on other nitrogenous compounds as donors with NAD+ or NADP+ as acceptor. Group: Enzymes. Synonyms: 4-nitroquinoline 1-oxide reductase; 4NQO reductase; NAD(P)H2:4-nitroquinoline-N-oxide oxidoreductase. Enzyme Commission Number: EC 1.7.1.9. CAS No. 37256-35-2. 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-1615; nitroquinoline-N-oxide reductase; EC 1.7.1.9; 37256-35-2; 4-nitroquinoline 1-oxide reductase; 4NQO reductase; NAD(P)H2:4-nitroquinoline-N-oxide oxidoreductase. Cat No: EXWM-1615. | |
| Nitroreductase from Escherichia coli | ?90% (SDS-PAGE), recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Nitroreductase from Escherichia coli, Recombinant | Nitroreductase increases the sensitivity of organisms to nitro-containing drugs such as metronidazole by converting the nitro group to a cytotoxic nitro radical. Shows ability to reduce quinines. Enzyme for activating prodrugs in antibody directed enzyme prodrug therapy. Applications: Nitroreductase has been used in a study that used a set of pcr primers to clone a gene encoding a hypothetical nitroreductases (named as ssap-ntrb) from uropathogenic staphyl oc occus. it has also been used to improve prodrug activation. nitroreductase from escherichia coli has been used in a study to assess anaerobic bacteria as a gene delivery system for cancer treatment. it has also been used in a study to investigate its applications in antibody-directed enzyme prodrug therapy. Group: Enzymes. Synonyms: Nitroreductase. Purity: > 90% (SDS-PAGE). Nitroreductase. Mole weight: monomer mol wt 24 kDa. Storage: -20°C. Source: E. coli. Species: Escherichia coli. Nitroreductase. Cat No: NATE-0488. | |
| Nitro Reductases | synthesis of amines from nitro compounds. Group: Enzymes. Synonyms: Nitro Reductases; NTR. Form: 1. Enzyme Powder: 12 items*50mg / item, or other quantity2. Screening Kit: 12 items*1mg / item. Nitro Reductases; NTR; Screening Kit; library of enzyme; enzyme library. Cat No: ENLC-008. | |
| NITROSALICYLALDEHYDE, SPL | NITROSALICYLALDEHYDE, SPL. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-Nitrosalicylaldehyde, 2-Hydroxy-3-nitrobenzaldehyde, 5274-70-4, Salicylaldehyde, 3-nitro-, Benzaldehyde, 2-hydroxy-3-nitro-, 3-Nitro-2-hydroxybenzaldehyde, SBB023884, NSC38026, PubChem7773, AC1Q1GXB, ACMC-209l1g, AC1L2WA4, Benzaldehyde, 2-hydroxynitro-, 527424_ALDRICH, AC1Q788W, CTK1G5039, NUGOTBXFVWXVTE-UHFFFAOYSA-, MolPort-000-894-395, EINECS 226-098-7, ANW-31538. Product Category: Heterocyclic Organic Compound. CAS No. 51294-09-8. Molecular formula: C7H5NO4. Mole weight: 167.118900 [g/mol]. Purity: 0.96. IUPACName: 2-hydroxy-3-nitrobenzaldehyde. Canonical SMILES: C1=CC(=C(C(=C1)[N+](=O)[O-])O)C=O. ECNumber: 226-098-7. Product ID: ACM51294098. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitrosamines/Nitroaromatics | certified reference material. Group: Certified reference materials (crms). | |
| Nitrosamines/Nitroaromatics - PT | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| Nitroscanate | Nitroscanate. Group: Biochemicals. Grades: Highly Purified. CAS No. 19881-18-6. Pack Sizes: 250g, 500g, 1kg. Molecular Formula: C13H8N2O3S. US Biological Life Sciences. | Worldwide |
| Nitrosoantipyrine | Nitrosoantipyrine is a derivative of antipyrine (A697500), an analgesic agent. Group: Biochemicals. Alternative Names: 1-Phenyl-2,3-dimethyl-4-nitroso-5-pyrazolone; 2,3-Dimethyl-4-nitroso-1-phenyl-5-pyrazolone; 4-Nitrosoantipyrin; 4-Nitrosoantipyrine; NSC163932; NSC75060;1,2-Dihydro-1,5-dimethyl-4-nitroso-2-phenyl-3H-pyrazol-3-one. Grades: Highly Purified. CAS No. 885-11-0. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Nitrosobis(2-hydroxyethyl)amine | A potent liver carcinogen in several species of animals, is one of the most widespread N-nitroso compounds in the human environment. Group: Biochemicals. Alternative Names: 2, 2- (Nitrosoimino) bisethanol; Diethanolnitrosamine; N,N-Diethanolnitrosamine; N-Nitrosodiethanolamine; NDELA. Grades: Highly Purified. CAS No. 1116-54-7. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Nitrosobis(2-hydroxyethyl)amine-d8 | A potent liver carcinogen in several species of animals, is one of the most widespread N-nitroso compounds in the human environment. Group: Biochemicals. Alternative Names: 2, 2- (Nitrosoimino) bisethanol-d8; Diethanolnitrosamine-d8; N,N-Diethanolnitrosamine-d8; N-Nitrosodiethanolamine-d8; NDELA-d8. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Nitrosoglutathione | Nitrosoglutathione (GSNO), a exogenous NO donor and a substrate for rat alcohol dehydrogenase class III isoenzyme, inhibits cerebrovascular angiotensin II-dependent and -independent AT1 receptor responses [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GSNO; RVC-588; S-Nitroso-L-glutathione. CAS No. 57564-91-7. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-D0845. |  |
| Nitrosonium hexafluoroantimonate | Nitrosonium hexafluoroantimonate. Group: Electrolytes. Alternative Names: Nitrosonium (nitrosyl) hexafluoroantimonate. CAS No. 16941-06-3. Product ID: Azanylidyneoxidanium; hexafluoroantimony(1-). Molecular formula: 265.76. Mole weight: F6NOSb. N#[O+].F[Sb-](F)(F)(F)(F)F. InChI=1S/6FH.NO.Sb/c; 1-2; /h6*1H; /q; +1; +5/p-6. AMGJCGWYCZRXHS-UHFFFAOYSA-H. 99%+. | |
| Nitrosonium hexafluoroantimonate | 99.9% trace metals basis. Group: Biosensing and bioimaging. | |
| Nitrosonium (nitrosyl) tetrafluoroborate | Nitrosonium (nitrosyl) tetrafluoroborate. CAS No. 14635-75-7. Product ID: 8-01381. Molecular formula: NOBF4. Mole weight: 116.81. Reference: P.N. Rylander, 'Catalytic Hydrogenation over Platinum Metals', Academic Press, New York, NY, 1976, p 464. | |
| Nitroso-prodenafil | Cas No. 1266755-08-1. | |
| Nitrosylsulfuric acid 40% in sulfuric acid | 100ml Pack Size. Group: Analytical Reagents, Building Blocks, Inorganic Chemicals. Formula: HNO5S. CAS No. 7782-78-7. Prepack ID 90028530-100ml. Molecular Weight 127.08. See USA prepack pricing. | |
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