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| Product | Description | |
|---|---|---|
| Nitrided Multilayer Ti3C2Tx | Nitrided Multilayer Ti3C2Tx. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors. Group: Mxene materials. CAS No. 12363-89-2. 99%. |  |
| Nitriding multilayer Ti3C2 MXene | Nitriding multilayer Ti3C2 MXene. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12363-89-2. 0.99. | |
| nitrilase | Acts on a wide range of aromatic nitriles including (indol-3-yl)acetonitrile, and also on some aliphatic nitriles, and on the corresponding acid amides. cf. EC 4.2.1.84 nitrile hydratase. Group: Enzymes. Synonyms: acetonitrilase; benzonitrilase. Enzyme Commission Number: EC 3.5.5.1. CAS No. 9024-90-2. Nitrilase. 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-4578; nitrilase; EC 3.5.5.1; 9024-90-2; acetonitrilase; benzonitrilase. Cat No: EXWM-4578. |  |
| Nitrilase | recombinant, expressed in E. coli, ?2.0 U/mg. Group: Fluorescence/luminescence spectroscopy. |  |
| Nitrilase (Crude Enzyme) | Nitrilase enzymes catalyse the hydrolysis of nitriles to carboxylic acids and ammonia, without the formation of "free" amide intermediates. Nitrilases are involved in natural product biosynthesis and post translational modifications in plants, animals, fungi and certain prokaryotes. Nitrilases can also be used as catalysts in preparative organic chemistry. Among others, nitrilases have been used for the resolution of racemic mixtures. Nitrilase should not be confused with nitrile hydratase (nitrile hydro-lyase; EC 4. 2. 1. 84) which hydrolyses nitriles to amides. Nitrile hydratases are almost invariably co-expressed with an amidase, which converts the amide to the carboxylic acid, consequently it can sometimes be difficult to distinguish nitrilase activity from nitrile hydratase plus amidase activity. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; industry. Group: Enzymes. Synonyms: acetonitrilase; benzonitrilase. Enzyme Commission Number: EC 3.5.5.1. CAS No. 9024-90-2. Nitrilase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. acetonitrilase; benzonitrilase. Pack: 100ml. Cat No: NATE-1842. | |
| Nitrilase, Recombinant | Nitrilase enzymes catalyse the hydrolysis of nitriles to carboxylic acids and ammonia, without the formation of "free" amide intermediates. Nitrilases are involved in natural product biosynthesis and post translational modifications in plants, animals, fungi and certain prokaryotes. Nitrilases can also be used as catalysts in preparative organic chemistry. Among others, nitrilases have been used for the resolution of racemic mixtures. The isoelectric point (pi) of this protein is 8.1. native page analysis indicates that the active complex of this enzyme consists of 14 identical subunits. Group: Enzymes. Synonyms: nitrilase; acetonitrilase; benzonitrilase; EC 3.5.5.1; 9024-90-2. Enzyme Commission Number: EC 3.5.5.1. CAS No. 9024-90-2. Nitrilase. Mole weight: mol wt 41 kDa. Activity: > 2.0 units/mg. Storage: 2-8°C. Source: E. coli. nitrilase; acetonitrilase; benzonitrilase; EC 3.5.5.1; 9024-90-2. Pack: Bottomless glass bottle. Contents are inside inserted fused cone. Cat No: NATE-0487. | |
| Nitrilases | synthesis of chiral carboxylic acids from nitriles. Group: Enzymes. Synonyms: Nitrilases; NIT. Form: 1. Enzyme Powder: 40 items*50mg / item, or other quantity2. Screening Kit: 40 items*1mg / item. Nitrilases; NIT; Screening Kit; library of enzyme; enzyme library. Cat No: ENLC-005. | |
| nitrile hydratase | Acts on short-chain aliphatic nitriles, converting them into the corresponding amides. Does not act on these amides or on aromatic nitriles. cf. EC 3.5.5.1 nitrilase. Group: Enzymes. Synonyms: nitrilase (ambiguous); 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase. Enzyme Commission Number: EC 4.2.1.84. CAS No. 82391-37-5. Nhase. 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-5069; nitrile hydratase; EC 4.2.1.84; 82391-37-5; nitrilase (ambiguous); 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase. Cat No: EXWM-5069. | |
| Nitrile Hydratase (Crude Enzyme) | In enzymology, nitrile hydratases are mononuclear iron or non-corrinoid cobalt enzymes that catalyse the hydration of diverse nitriles to their corresponding amides. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; degradation; environmental protection. Group: Enzymes. Synonyms: nitrilase (ambiguous); 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase. Enzyme Commission Number: EC 4.2.1.84. CAS No. 82391-37-5. Nhase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. nitrilase (ambiguous); 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase. Pack: 100ml. Cat No: NATE-1852. | |
| Nitrile hydratase from Recombinant microoganism | In enzymology, nitrile hydratases (NHases; EC 4.2.1.84) are mononuclear iron or non-corrinoid cobalt enzymes that catalyse the hydration of diverse nitriles to their corresponding amides: R-C?N + H2O ? R-C(O)NH2. Group: Enzymes. Synonyms: Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming). Enzyme Commission Number: EC 4.2.1.84. CAS No. 82391-37-5. Nhase. Storage: 4°C or lower. Form: Liquid in 70% (NH4)2SO4 precipitate. Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming); nitrile hydratases; EC 4.2.1.84. Cat No: NATE-1626. | |
| Nitrile hydratase from Rhodococcus erythropolis, Recombinant | In enzymology, nitrile hydratases (NHases; EC 4.2.1.84) are mononuclear iron or non-corrinoid cobalt enzymes that catalyse the hydration of diverse nitriles to their corresponding amides: R-C?N + H2O ? R-C(O)NH2. Group: Enzymes. Synonyms: Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming). Enzyme Commission Number: EC 4.2.1.84. CAS No. 82391-37-5. Purity: > 95 % as judged by SDS-PAGE. Nhase. Mole weight: 23487.3 Da (α-subunit), 25159.4 Da (β-subunit). Activity: > 4 U/mg (freeze-dried CFE). Storage: Store at -20°C (shipped at ambient temperature). Form: Supplied as a freeze-dried CFE powder. Source: Rhodococcus erythropolis AJ270. Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming). Cat No: NATE-1217. | |
| Nitrile hydratase from Rhodopseudomonas palustris, Recombinant | In enzymology, nitrile hydratases (NHases; EC 4.2.1.84) are mononuclear iron or non-corrinoid cobalt enzymes that catalyse the hydration of diverse nitriles to their corresponding amides: R-C?N + H2O ? R-C(O)NH2. Group: Enzymes. Synonyms: Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming). Enzyme Commission Number: EC 4.2.1.84. CAS No. 82391-37-5. Purity: > 95 % as judged by SDS-PAGE. Nhase. Mole weight: 25878.9 Da (α-subunit), 24204.3 Da (β-subunit). Activity: 21.97 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Rhodopseudomonas palustris CGA009. Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming). Cat No: NATE-1218. | |
| Nitrile hydratase from Sinorhizobium meliloti, Recombinant | In enzymology, nitrile hydratases (NHases; EC 4.2.1.84) are mononuclear iron or non-corrinoid cobalt enzymes that catalyse the hydration of diverse nitriles to their corresponding amides: R-C?N + H2O ? R-C(O)NH2. Group: Enzymes. Synonyms: Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming). Enzyme Commission Number: EC 4.2.1.84. CAS No. 82391-37-5. Purity: > 95 % as judged by SDS-PAGE. Nhase. Mole weight: 16126.0 Da (α-subunit), 24098.0 Da (β-subunit). Activity: 33.82 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Sinorhizobium meliloti 1021. Nitrilase; 3-cyanopyridine hydratase; NHase; L-NHase; H-NHase; acrylonitrile hydratase; aliphatic nitrile hydratase; nitrile hydro-lyase; aliphatic-amide hydro-lyase (nitrile-forming). Cat No: NATE-1219. | |
| Nitrile Hydratases | synthesis of chiral amides from nitriles. Group: Enzymes. Synonyms: Nitrile Hydratases; NHT. Form: 1. Enzyme Powder: 24 items*50mg / item, or other quantity2. Screening Kit: 24 items*1mg / item. Nitrile Hydratases; NHT; Screening Kit; library of enzyme; enzyme library. Cat No: ENLC-004. | |
| Nitriloriacetic acid trisodium salt | Nitriloriacetic acid trisodium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 5064-31-3. Pack Sizes: 500g, 1kg, 2kg, 5kg, 10kg. US Biological Life Sciences. |  Worldwide |
| Nitrilotri-2,1-ethanediyl tris[(2,4-dichlorophenoxy)acetate] | Nitrilotri-2,1-ethanediyl tris[(2,4-dichlorophenoxy)acetate]. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nitrilotri-2,1-ethanediyl tris((2,4-dichlorophenoxy)acetate), 93858-74-3, CTK5H3609, EINECS 299-308-8, AG-H-84355. Product Category: Heterocyclic Organic Compound. CAS No. 93858-74-3. Molecular formula: C30H27Cl6NO9. Mole weight: 758.254680 [g/mol]. Purity: 0.96. IUPACName: 2-[bis[2-[2-(2,4-dichlorophenoxy)acetyl]oxyethyl]amino]ethyl 2-(2,4-dichlorophenoxy)acetate. Canonical SMILES: C1=CC(=C(C=C1Cl)Cl)OCC(=O)OCCN(CCOC(=O)COC2=C(C=C(C=C2)Cl)Cl)CCOC(=O)COC3=C(C=C(C=C3)Cl)Cl. ECNumber: 299-308-8. Product ID: ACM93858743. Alfa Chemistry ISO 9001:2015 Certified. |  |
| nitrilotriacetate monooxygenase | Requires Mg2+. The enzyme from Aminobacter aminovorans (previously Chelatobacter heintzII) is part of a two component system that also includes EC 1.5.1.42 (FMN reductase), which provides reduced flavin mononucleotide for this enzyme. Group: Enzymes. Enzyme Commission Number: EC 1.14.14.10. 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-0907; nitrilotriacetate monooxygenase; EC 1.14.14.10. Cat No: EXWM-0907. | |
| Nitrilotriacetic acid | Nitrilotriacetic acid is an aminotricarboxylic acid. Nitrilotriacetic acid can be used as a chelating agent, forming coordination compounds with metal ions [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Triglycollamic acid. CAS No. 139-13-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-W030778. |  |
| Nitrilotriacetic acid | Nitrilotriacetic acid (NTA) is the aminopolycarboxylic acid with the formula N(CH2CO2H)3. It is a colourless solid that is used as a chelating agent, which forms coordination compounds with metal ions (chelates) such as Ca2+, Cu2+, and Fe3+. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Triglycollamic Acid;Nitrilotriacetic Acid;N,N-Bis(carb;Glycine, N,N-bis(carboxymethyl)-;combretastatin A2. Product Category: Heterocyclic Organic Compound. Appearance: White powder. CAS No. 139-13-9. Molecular formula: C6H9NO6. Mole weight: 191.14. Density: 1.61 g/cm³. ECNumber: 205-355-7. Product ID: ACM139139. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitrilotriacetic acid | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Nitrilotriacetic acid | 500g Pack Size. Group: Building Blocks, Ligands, Organics. Formula: C6H9NO6. CAS No. 139-13-9. Prepack ID 31172055-500g. Molecular Weight 191.14. See USA prepack pricing. |  |
| Nitrilotriacetic Acid | Nitrilotriacetic acid is a chelating agent which forms coordination compounds with metal ions. Nitrilotriacetic acid is used in complexometric titrations and as well as for protein isolation and purification in the His-tag method. This compound is a contaminant of emerging concern (CECs). Group: Biochemicals. Alternative Names: N, N-bis (carboxymethyl) glycine; 412: Chel 300; Chelest NT; Complexon I; Dissolvine A; Hampshire NTA Acid; N, N-Bis (carboxymethyl) glycine; N, N-Bis (carboxymethyl) glycine; NSC 2121; NTA; Nitrilo-2,2',2''-triacetic Acid; Nitrilo-N,N,N-triacetic Acid; Nitrilotriacetic Acid; Nitrilotris (methylenecarboxylic Acid); Titriplex I; Triglycine; Triglycollamic Acid; Trilon AS; Tris (carboxymethyl)amine; Tris (hydroxycarbonyl methyl ) amine; Versene NTA Acid; α , α ', α ''-Tri methyl aminetricarboxylic Acid. Grades: Highly Purified. CAS No. 139-13-9. Pack Sizes: 1g. Molecular Formula: C6H9NO6. US Biological Life Sciences. | Worldwide |
| Nitrilotriacetic acid 99+% | Nitrilotriacetic acid 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences. | Worldwide |
| Nitrilotriacetic acid-[d9] | Nitrilotriacetic acid-[d9]. Grade: 98% by CP; 98% atom D. CAS No. 807630-34-8. Molecular formula: C6D9NO6. Mole weight: 200.19. |  |
| Nitrilotriacetic acid trisodium salt | Nitrilotriacetic acid trisodium salt. Synonyms: N,N-Bis(carboxymethyl)glycine, NTA, Triglycollamic acid. CAS No. 5064-31-3. Pack Sizes: 250 g in glass bottle. Product ID: CDC10-0117. Molecular formula: C6H6NO6Na3. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Nitrilotriacetic acid trisodium salt; CDC10-0117; 5064-31-3; C6H6NO6Na3; N,N-Bis(carboxymethyl)glycine, NTA, Triglycollamic; 225-768-6; MFCD00064231; 5064-31-3. Purity: ≥98%. EC Number: 225-768-6. Physical State: Powder. Quality Level: 200. Application: An excellent chelating agent. |  |
| Nitrilotris (methylene) triphosphonic Acid | A powerful complexing agent. A potent acid sphingomyelinase inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 6419-19-8. Pack Sizes: 1g, 10g, 50g. Molecular Formula: C?H??NO?P?. US Biological Life Sciences. | Worldwide |
| nitrite dismutase | Contains ferriheme b. The enzyme is one of the nitrophorins from the salivary gland of the blood-feeding insect Rhodnius prolixus. Nitric oxide produced induces vasodilation after injection. Nitrophorins 2 and 4 can also catalyse this reaction. Group: Enzymes. Synonyms: Prolixin S; Nitrophorin 7. Enzyme Commission Number: EC 1.7.6.1. 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-1631; nitrite dismutase; EC 1.7.6.1; Prolixin S; Nitrophorin 7. Cat No: EXWM-1631. | |
| Nitrite ionophore I | function tested. Group: Ionophores potentiometric for ise. | |
| Nitrite ionophore VI | function tested. Group: Ionophores potentiometric for ise. | |
| nitrite reductase (cytochrome; ammonia-forming) | Found as a multiheme cytochrome in many bacteria. The enzyme from Escherichia coli contains five hemes c and requires Ca2+. It also reduces nitric oxide and hydroxylamine to ammonia, and sulfite to sulfide. Group: Enzymes. Synonyms: cytochrome c nitrite reductase; multiheme nitrite reductase. Enzyme Commission Number: EC 1.7.2.2. 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-1617; nitrite reductase (cytochrome; ammonia-forming); EC 1.7.2.2; cytochrome c nitrite reductase; multiheme nitrite reductase. Cat No: EXWM-1617. | |
| nitrite reductase (NADH) | An iron-sulfur flavoprotein (FAD) containing siroheme. This prokaryotic enzyme is specific for NADH. In addition to catalysing the 6-electron reduction of nitrite to ammonia, the enzyme from Escherichia coli can also catalyse the 2-electron reduction of hydroxylamine to ammonia. cf. EC 1.7.1.4, nitrite reductase [NAD(P)H]. Group: Enzymes. Synonyms: nitrite reductase (reduced nicotinamide adenine dinucleotide); NADH-nitrite oxidoreductase; assimilatory nitrite reductase (ambiguous); nirB (gene name); nirD (gene name). Enzyme Commission Number: EC 1.7.1.15. CAS No. 9029-29-2. 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-1608; nitrite reductase (NADH); EC 1.7.1.15; 9029-29-2; nitrite reductase (reduced nicotinamide adenine dinucleotide); NADH-nitrite oxidoreductase; assimilatory nitrite reductase (ambiguous); nirB (gene name); nirD (gene name). Cat No: EXWM-1608. | |
| nitrite reductase [NAD(P)H] | An iron-sulfur flavoprotein (FAD) containing siroheme. The enzymes from the fungi Neurospora crassa, Emericella nidulans and Candida nitratophila and the bacterium Aliivibrio fischeri can use either NADPH or NADH as electron donor. cf. EC 1.7.1.15, nitrite reductase (NADH). Group: Enzymes. Synonyms: nitrite reductase (reduced nicotinamide adenine dinucleotide (phosphate)); assimilatory nitrite reductase (ambiguous); nitrite reductase [NAD(P)H2]; NAD(P)H2:nitrite oxidoreductase; nit-6 (gene name). Enzyme Commission Number: EC 1.7.1.4. CAS No. 9029-29-2. 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-1611; nitrite reductase [NAD(P)H]; EC 1.7.1.4; 9029-29-2; nitrite reductase (reduced nicotinamide adenine dinucleotide (phosphate)); assimilatory nitrite reductase (ambiguous); nitrite reductase [NAD(P)H2]; NAD(P)H2:nitrite oxidoreductase; nit-6 (gene name). Cat No: EXWM-1611. | |
| nitrite reductase (NO-forming) | The reaction is catalysed by two types of enzymes, found in the perimplasm of denitrifying bacteria. One type comprises proteins containing multiple copper centres, the other a heme protein, cytochrome cd1. Acceptors include c-type cytochromes such as cytochrome c-550 or cytochrome c-551 from Paracoccus denitrificans or Pseudomonas aeruginosa, and small blue copper proteins such as azurin and pseudoazurin. Cytochrome cd1 also has oxidase and hydroxylamine reductase activities. May also catalyse the reaction of hydroxylamine reductase (EC 1.7.99.1) since this is a well-known activity of cytochrome cd1. Group: Enzymes. Synonyms: cd-cytochrome nitrite reductase; [nitrite reductase (cytochrome)] [misleading, see comments.]; cytochrome c-551:O2, NO2+ oxidoreductase; cytochrome cd; cytochrome cd1; hydroxylamine. Enzyme Commission Number: EC 1.7.2.1. CAS No. 9080-3-9. 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-1616; nitrite reductase (NO-forming); EC 1.7.2.1; 9080-03-9; cd-cytochrome nitrite reductase; [nitrite reductase (cytochrome)] [misleading, see comments.]; cytochrome c-551:O2, NO2+ oxidoreductase; cytochrome cd; cytochrome cd1; hydroxylamine (acceptor) reductase; methyl viologen-nitrite reductase; nitrite reductase (cytochrome; NO-forming). Cat No: EXWM-1616. | |
| Nitrite - WP | Proficiency Testing Material, Concentrate for dilution to 1 L. Group: Waste water. | |
| Nitritocobalamin | Nitritocobalamin is a useful synthetic intermediate in the synthesis of Hydroxocobalamin Acetate; a physiological analog of vitamin B12 where the CN group is replaced with OH. Exists in aqueous solution as an equilibrium mixture of the hydroxy isomer and the ionic aqua isomer (aquacobalamin). Precursor of the coenzymes methylcobalamin and cobamamide. Coordination Compound. Vitamin (hematopoietic). Group: Biochemicals. Alternative Names: Co-(nitrito-κO)-cobinamide Dihydrogen Phosphate (Ester) Inner Salt 3-Ester with (5,6-Dimethyl-1-alpha-D-ribofuranosyl-1H-benzimidazole-κN3), Nitrocobalamin; Vitamin B12c; Cobinamide, hydroxide nitrite (salt), dihydrogen phosphate (ester), inner salt, 3-ester with 5, 6-di methyl -1-alpha-D-ribofuranosyl benzimidazole, Cobinamide, nitrite (salt), dihydrogen phosphate (ester), inner salt, 3-ester with 5,6-dimethyl-1-alpha-D-ribofuranosyl-1H-benzimidazole, Cobinamide, nitrite phosphate, 3-ester with 5, 6-di methyl -1-apha-D-ribofuranosyl benzimidazole, inner salt. Grades: Highly Purified. CAS No. 20623-13-6. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C62H88CoN14O16P. US Biological Life Sciences. | Worldwide |
| Nitroacetaldehyde dimethyl acetal | Nitroacetaldehyde dimethyl acetal. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nitroacetaldehydedimethylacetal;NITROACETALDEHYDE DIMETHYL;1,1-Dimethoxy-2-nitroethane;2-Nitroacetaldehyde dimethyl acetal. Product Category: Heterocyclic Organic Compound. CAS No. 69425-53-2. Molecular formula: C4H9NO4. Mole weight: 135.12. Purity: 0.96. IUPACName: 1,1-dimethoxy-2-nitroethane. Canonical SMILES: COC(C[N+](=O)[O-])OC. Density: 1.12. Product ID: ACM69425532. Alfa Chemistry ISO 9001:2015 Certified. | |
| nitroalkane oxidase | Has an absolute requirement for FAD. While nitroethane may be the physiological substrate, the enzyme also acts on several other nitroalkanes, including 1-nitropropane, 2-nitropropane, 1-nitrobutane, 1-nitropentane, 1-nitrohexane, nitrocyclohexane and some nitroalkanols. Differs from EC 1.13.11.16, nitronate monooxygenase, in that the preferred substrates are neutral nitroalkanes rather than anionic nitronates. Group: Enzymes. Synonyms: nitroethane oxidase; NAO; nitroethane:oxygen oxidoreductase. Enzyme Commission Number: EC 1.7.3.1. CAS No. 9029-36-1, 65802-82-6. 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-1624; nitroalkane oxidase; EC 1.7.3.1; 9029-36-1, 65802-82-6; nitroethane oxidase; NAO; nitroethane:oxygen oxidoreductase. Cat No: EXWM-1624. | |
| nitroarene dioxygenase | This enzyme is a member of the naphthalene family of bacterial Rieske non-heme iron dioxygenases. It comprises a multicomponent system, containing a Rieske [2Fe-2S] ferredoxin, an NADH-dependent flavoprotein reductase (EC 1.18.1.3, ferredoxin-NAD+ reductase), and an α3β3 oxygenase. The enzyme forms of a cis-dihydroxylated product that spontaneously rearranges to form a catechol with accompanying release of nitrite. It can typically act on many different nitroaromatic compounds, including chlorinated species. Enzymes found in different strains may have different substrate preferences. Requires Fe2+. Group: Enzymes. Synonyms: cnbA (gene name). Enzyme Commission Number: EC 1.14.12.23. 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-0690; nitroarene dioxygenase; EC 1.14.12.23; cnbA (gene name). Cat No: EXWM-0690. | |
| Nitroarginine | Nitroarginine, or Nω-nitro-L-arginine, is a nitro derivative of the amino acid arginine. It is an inhibitor of nitric oxide synthase and hence a vaso-constrictor and coronary constrictor. As such, it finds widespread use as a biochemical tool in the study of nitric oxide and its biological effects. Nitroarginine has been used in research studying coronary constriction, in the presence of midazolam vasodilatation was unaffected by nitroarginine. Nitroarginine is currently in clinical trials for treating patients with advanced solid tumors. Uses: Enzyme inhibitors. Synonyms: Nitroarginine; N5-(nitroamidino)-L-Ornithine; (+)-NG-Nitroarginine; NG-nitro-L-Arginine, L-NG-Nitroarginine; L-NNA; L-NOARG; NG-Nitro-L-arginine; NG-Nitroarginine; NOLA; NSC 53662; NSC-53662; NSC53662; Nitro-L-arginine; Nω-Nitro-L-arginine; Nω-Nitro-L-arginine; ω-Nitro-L-arginine; ω-Nitroarginine. Grade: >98%. CAS No. 2149-70-4. Molecular formula: C6H13N5O4. Mole weight: 219.20. | |
| Nitroarginine Methyl Ester Hydrochloride | Nitroarginine Methyl Ester Hydrochloride. Group: Biochemicals. Alternative Names: N5-[Imino (nitroamino)methyl]-, L-ornithine Methyl Ester Monohydrochloride; L-NAME Hydrochloride; NG-Nitroarginine Methyl Ester Hydrochloride. Grades: Highly Purified. CAS No. 51298-62-5. Pack Sizes: 1g. Molecular Formula: C7H16ClN5O4, Molecular Weight: 269.69. US Biological Life Sciences. | Worldwide |
| Nitroaromatics/Nitrosamine - Loamy Sand 1 | certified reference material, pkg of 10 g. Group: Certified reference materials (crms). | |
| Nitrobenzene | Nitrobenzene. Group: Biochemicals. Grades: Highly Purified. CAS No. 98-95-3. Pack Sizes: 5kg. US Biological Life Sciences. | Worldwide |
| Nitrobenzene(13c6) | Nitrobenzene(13c6). Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nitrobenzene-13C6, SureCN1330714, 490369_ALDRICH, 89059-37-0. Product Category: Heterocyclic Organic Compound. CAS No. 89059-37-0. Molecular formula: C6H5NO2. Mole weight: 129.16. Purity: 0.96. IUPACName: nitrobenzene. Canonical SMILES: C1=CC=C(C=C1)[N+](=O)[O-]. Density: 1.253 g/mL at 25ºC. Product ID: ACM89059370. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitrobenzene-13C6 | Nitrobenzene-13C6. Group: Biochemicals. Alternative Names: 1-Nitrobenzene-1,2,3,4,5,6-13C6. Grades: Highly Purified. CAS No. 89059-37-0. Pack Sizes: 10mg. Molecular Formula: 13C6H5NO2, Molecular Weight: 129.07. US Biological Life Sciences. | Worldwide |
| Nitrobenzene-d5 | Nitrobenzene-d5. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nitrobenzene-d5, Oil of mirbane, Nitro(2H5)benzene, Benzene-D5-, nitro-, Benzene-d5, nitro-, Pentadeuteronitrobenzene, 151955_ALDRICH, 269751_ALDRICH, 442718_SUPELCO, MolPort-003-926-702, EINECS 224-014-3, CID123210, 4165-60-0. Product Category: Heterocyclic Organic Compound. CAS No. 4165-60-0. Molecular formula: C6D5NO2. Mole weight: 128.14. Purity: 99 atom % D. IUPACName: 1,2,3,4,5-pentadeuterio-6-nitrobenzene. Canonical SMILES: C1=CC=C(C=C1)[N+](=O)[O-]. Density: 1.25. ECNumber: 224-014-3. Product ID: ACM4165600. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitrobenzene-d5 | Nitrobenzene-d5. Group: Biochemicals. Alternative Names: Essence of Mirbane-d5; Essence of Myrbane-d5; Mirbane Oil-d5; NSC 9573-d5; Nitrobenzene-d5; Nitrobenzol-d5; Oil of Mirbane-d5; Oil of Myrbane-d5. Grades: Highly Purified. CAS No. 4165-60-0. Pack Sizes: 250mg. Molecular Formula: C6D5NO2, Molecular Weight: 128.139999999999. US Biological Life Sciences. | Worldwide |
| Nitrobenzylthioinosine | Nitrobenzylthioinosine is an ENT1 transporter inhibitor that binds to ENT1 transporter with high affinity. Nitrobenzylthioinosine is a photoaffinity probe for adenosine uptake sites in brain. Nitrobenzylthioinosine can cross the blood-brain barrier[1][2][3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NBMPR. CAS No. 38048-32-7. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W010936. | |
| Nitro blue tetrazolium chloride | Nitro blue tetrazolium chloride (NBT) is a substrate for dehydrogenases; is used with the alkaline phosphatase substrate 5-Bromo-4-Chloro-3-Indolyl Phosphate (BCIP) in western blotting and immunohistological staining procedures [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: NBT. CAS No. 298-83-9. Pack Sizes: 10 mM * 1 mL; 250 mg; 500 mg. Product ID: HY-15925. | |
| Nitro Blue Tetrazolium Chloride (NBT) | Chromogenic substrate; competitive inhibitor of NOS. Group: Biochemicals. Alternative Names: 3, 3'- (3, 3'-dimethoxy-4, 4'-biphenylylene) bis[2- (p-nitrophenyl) -5-phenyl-2H-chloride]2, 2'-Bis (p-nitrophenyl) -5, 5'-diphenyl-3, 3'- (3, 3'-dimethoxy-4, 4'-biphenylylene) ditetrazolium chloride; 2, 2'-Bis (p-nitrophenyl) -5, 5'-diphenyl-3, 3'- (3, 3'-dimethoxy-4, 4'-diphenylene) ditetrazolium chloride; 2, 2'-Di-p-nitrophenyl-5, 5'-diphenyl-3, 3'-bis (3, 3'-dimethoxy-4, 4'-biphenylene) ditetrazolium chloride; 2, 2'-Dinitrophenyl-5, 5'-diphenyl-3, 3'-dimethoxy-4, 4'-diphenylene) ditetrazolium chloride; 3,3'-(3,3'-Dimethoxy-4,4'-biphenylylene)bis[2-(p-nitrophenyl)-5-phenyl-2H-tetrazolium chloride; [3,3'-(3,3'-Dimethoxy-4,4'-diphenylene)bis[2-(p-nitrophenyl)-5-phenyltetrazolium chloride]; NSC 27622. Grades: Molecular Biology Grade. CAS No. 298-83-9. Pack Sizes: 1g, 5g. Molecular Formula: C??H??N??O? 2(Cl), Molecular Weight: 817.65. US Biological Life Sciences. | Worldwide |
| Nitrocaramiphen HCl | Nitrocaramiphen is a muscarinic antagonist with 71-fold selectivity for M1 over M2. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nitrocaramiphen HCl; Nitrocaramiphen hydrochloride; Nitrocaramiphen. Product Category: Antagonists. Appearance: Solid powder. CAS No. 98636-73-8. Molecular formula: C18H27ClN2O4. Mole weight: 370.87. Purity: >98%. IUPACName: 2-Diethylaminoethyl 1-(4-nitrophenyl)cyclopentanecarboxylate hydrochloride. Canonical SMILES: O=C(C1(C2=CC=C([N+]([O-])=O)C=C2)CCCC1)OCCN(CC)CC.[H]Cl. Product ID: ACM98636738. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nitrocaramiphen hydrochloride | Nitrocaramiphen hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 98636-73-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Nitrocefin | Nitrocefin Inhibitor. Uses: Scientific use. Product Category: T19709. CAS No. 41906-86-9. |  |
| Nitrocefin | 5mg Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C21H16N4O8S2. CAS No. 41906-86-9. Prepack ID 90005324-5mg. Molecular Weight 516.51. See USA prepack pricing. | |
| Nitrocefin | Nitrocefin is a highly activated, chromogenic cephalosporin derivative. Nitrocefin is a chromogenic ?-lactamase substrate. Nitrocefin undergoes a distinctive color change from yellow to red as the amide bond in the ?-lactam ring is hydrolyzed by ?-lactamase. Nitrocefin is used in competitive inhibition studies in developmental work on ?-lactamase-resistant antibiotics[1][2][3][4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 41906-86-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108913. | |
| Nitrocefin | Nitrocefin is a chromogenic cephalosporin substrate routinely used to detect the presence of beta-lactamase enzymes produced by various microbes. Synonyms: 3-(2,4-Dinitrostyryl)-(6R,7R)-7-(2-thienylacetamido)-ceph-3-em-4-carboxylic acid; UNII-EWP54G0J8F; EWP54G0J8F. Grade: 90%. CAS No. 41906-86-9. Molecular formula: C21H16N4O8S2. Mole weight: 516.50. | |
| Nitrocellulose | Nitrocellulose. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  California |
| Nitrocellulose 9004-70-0 | Nitrocellulose - Surface Coatings. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| NITROCELLULOSE suppliers wanted | Nitrocellulose suppliers wanted with local stock available in the UK | Suppliers Needed |
| Nitrochin | Nitrochin (4-NQO) is a chemical carcinogen. Nitrochin induces oncostatin-M (OSM) in esophageal cells. Nitrochin induces DNA damage, and induces apoptosis via a p53-dependent mitochondrial signaling pathway[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 4-NQO. CAS No. 56-57-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-33354. | |
| Nitrochloroform | Nitrochloroform. Group: Biochemicals. Alternative Names: Acquinite; Chloropicrin; Chlorpicrin; G 25; Larvacide; Microlysin; NSC 8743; Nitrotrichloromethane; PS; Picfume; Trichloronitromethane. Grades: Highly Purified. CAS No. 76-06-2. Pack Sizes: 1g. Molecular Formula: CCl3NO2, Molecular Weight: 164.38. US Biological Life Sciences. | Worldwide |
| Nitrocyclohexane | Nitrocyclohexane. Group: Biochemicals. Grades: Highly Purified. CAS No. 1122-60-7. Pack Sizes: 5g, 10g, 25g. Molecular Formula: C6H11NO2. US Biological Life Sciences. | Worldwide |
| Nitrodenafil | Nitrodenafil is a related compound of Sildenafil as phosphodiesterase inhibitor. Group: Biochemicals. Alternative Names: 5-(2-Ethoxy-5-nitrophenyl)-1,6-dihydro-1-methyl-3-propyl-7H-pyrazolo[4,3-d]pyrimidin-7-one. Grades: Highly Purified. CAS No. 147676-99-1. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Nitrofen | Nitrofen is a selective contact herbicide. Nitrofen is a retinal dehydrogenase (belongs to the ALDH family) and protoporphyrinogen oxidase inhibitor [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1836-75-5. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1877. | |
| Nitrofen-(nitrophenyl-d4) | analytical standard. Group: Pesticides & metabolites standards. | |
| Nitroferroin | Nitroferroin is a high potential oxidation-reduction indicator. Synonyms: 5-Nitro-1,10-Phenanthroline. CAS No. 4199-88-6. Molecular formula: C12H7N3O2. Mole weight: 225.20. | |
| Nitrofluorescein, isomer 1 | Nitrofluorescein, isomer 1. Group: Biochemicals. Alternative Names: 3',6'-Dihydroxy-5-nitro-spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one; 5-Nitrofluorescein. Grades: Highly Purified. CAS No. 3326-35-0. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C20H11NO7. US Biological Life Sciences. | Worldwide |
| Nitrofluorescein, isomer 2 | Nitrofluorescein, isomer 2. Group: Biochemicals. Alternative Names: 6-Nitrofluorescein. Grades: Highly Purified. CAS No. 27402-68-2. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C20H11NO7. US Biological Life Sciences. | Worldwide |
| Nitroflurbiprofen | Nitroflurbiprofen is a cyclooxygenase ( COX ) inhibitor with nitric oxide (NO)-donating properties, modulates the increased intrahepatic vascular tone in portal hypertensive cirrhotic rats. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HCT 1206; NO-flurbiprofen; Nitroxybutyl flurbiprofen. CAS No. 158836-71-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-U00013. | |
| Nitrofurantoin | Nitrofurantoin is a potent and orally active broad-spectrum beta-lactamase antimicrobial agent. Nitrofurantoin acts as an antibiotic and can be used for the study of urinary tract infections (UTIs), including cystitis and kidney infections [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 67-20-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-A0090. | |
| Nitrofurantoin | Nitrofurantoin is a nitrofuran antibiotic that is used as a substrate of bacterial nitrofuran reductase to study the interactions of active metabolites with DNA, ribosomal proteins and metabolic and pro-oxidant processes. It is used to treat urinary tract infections. It is active against both Gram-positive and Gram-negative bacteria. Synonyms: N-(5-Nitro-2-furfurylidene)-1-aminohydantoin; Furadoxyl; 1-(((5-nitro-2-furanyl)methylene)amino)-2,4-imidazolidinedione; 1-(5-Nitro-2-furfurylideneamino)hydantoin; 5-Nitrofurantoin; Berkfurin; Chemiofuran; Cyantin; Cystit; Furadantoin; Furadoine; Nifuranti. Grade: ≥98.0%. CAS No. 67-20-9. Molecular formula: C8H6N4O5. Mole weight: 238.16. | |
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