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Nitrendipine (1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid Ethyl Methyl Ester, Bay e 5009, Bayotensin, Baypress, Bylotensin, Deiten, Nidrel)
Antihypertensive. Group: Biochemicals. Alternative Names: 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid Ethyl Methyl Ester; Bay e 5009; Bayotensin; Baypress; Bylotensin; Deiten; Nidrel. Grades: Highly Purified. CAS No. 39562-70-4. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
Nitrendipine-d5
Nitrendipine-d5. Group: Biochemicals. Alternative Names: 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid Ethyl Methyl Ester-d5; Bay e 5009-d5; Bayotensin-d5; Baypress-d5; Bylotensin-d5; Deiten-d5; Nidrel. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: C18H15D5N2O6, Molecular Weight: 365.39. US Biological Life Sciences.
Worldwide
Nitrendipine EP Impurity A
Nitrendipine EP Impurity A. Uses: For analytical and research use. CAS No. 89267-41-4. Molecular formula: C18H18N2O6. Mole weight: 358.35. Catalog: APB89267414.
Nitrendipine EP Impurity C (M-Nifedipine)
Nitrendipine EP Impurity C (M-Nifedipine). Uses: For analytical and research use. CAS No. 21829-28-7. Molecular formula: C19H22N2O6. Mole weight: 374.39. Catalog: APB21829287.
Nitrendipine Impurity1219
Nitrendipine Impurity1219. Uses: For analytical and research use. CAS No. 80890-07-9. Molecular formula: C18H20N2O6. Mole weight: 360.37. Catalog: APB80890079.
Nitrendipine Impurity1220
Nitrendipine Impurity1220. Uses: For analytical and research use. CAS No. 80873-62-7. Molecular formula: C18H20N2O6. Mole weight: 360.37. Catalog: APB80873627.
Nitrendipine Impurity1221
Nitrendipine Impurity1221. Uses: For analytical and research use. CAS No. 4408-96-2. Molecular formula: C19H20N2O6. Mole weight: 372.38. Catalog: APB4408962.
Nitrendipine Impurity 2
Nitrendipine Impurity 2. Uses: For analytical and research use. Molecular formula: C38H46ClN3O6. Mole weight: 676.25. Catalog: APB08829.
Nitrendipine Impurity 3
Nitrendipine Impurity 3. Uses: For analytical and research use. Molecular formula: C35H40ClN3O6. Mole weight: 634.17. Catalog: APB08830.
Nitrendipine Impurity 41
Nitrendipine Impurity 41. Uses: For analytical and research use. CAS No. 23510-18-1. Molecular formula: C10H15Cl2N. Mole weight: 220.14. Catalog: APB23510181.
Nitrendipine Impurity D
Nitrendipine Impurity D. Uses: For analytical and research use. CAS No. 89267-43-6. Molecular formula: C17H16N2O7. Mole weight: 360.32. Catalog: APB89267436.
Nitrendipine Impurity E
Nitrendipine Impurity E. Uses: For analytical and research use. CAS No. 74936-73-5. Molecular formula: C17H18N2O6. Mole weight: 346.34. Catalog: APB74936735.
Nitrendipine Impurity J
Nitrendipine Impurity J. Uses: For analytical and research use. CAS No. 14205-46-0. Molecular formula: C7H13NO2. Mole weight: 143.19. Catalog: APB14205460.
Nitrendipine Impurity R
Nitrendipine Impurity R. Uses: For analytical and research use. CAS No. 22502-03-0. Molecular formula: C7H12O4. Mole weight: 160.17. Catalog: APB22502030.
Nitrendipine Propyl Ester (Lercanidipine Impurity 7). Uses: For analytical and research use. CAS No. 225785-54-6. Molecular formula: C19H22N2O6. Mole weight: 374.39. Catalog: APB225785546.
Nitrendipine (Standard)
Nitrendipine (Standard) is the analytical standard of Nitrendipine (HY-B0424). This product is intended for research and analytical applications. Nitrendipine (BAY-E-5009) is an orally active analog of Nifedipine (HY-B0284) and dihydropyridine calcium channel blocker. Nitrendipine induces Apoptosis. Nitrendipine has antihypertensive effects. Nitrendipine blocks alcohol and Morphine withdrawal symptoms. Nitrendipine reduces right ventricular hypertrophy and pulmonary vascular changes induced by intermittent hypoxia. Nitrendipine has anticancer effects on neuroblastoma[1][2][3][4][5][6][7][8][9][10][11]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BAY-E-5009 (Standard). CAS No. 39562-70-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0424R.
Nitric Acid
42° Baumé IndustrialGrade / 67%. Nitric Acid CAS Number: 7697-37-2. Pack Sizes: 1 lb or 5 lb.
Los Angeles, CA 90023
Nitric Acid
Minimum Quantity 25 kgs. Nitric Acid - Agriculture Chemicals. SUPPLIERS TO BUSINESS CUSTOMERS ONLY.
Nitric Acid is a highly corrosive mineral acid used in organic nitration reactions. Also used in fertilizers. Group: Biochemicals. Grades: Highly Purified. CAS No. 7697-37-2. Pack Sizes: 25ml, 100ml. Molecular Formula: HNO3, Molecular Weight: 63.01. US Biological Life Sciences.
Nitric Acid-d is an isotopic analog of Nitric Acid (7697-37-2), the primary reagent used for nitration. It is a highly corrosive mineral acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 13587-52-5. Pack Sizes: 1g, 2.5g. Molecular Formula: DNO3, Molecular Weight: 64.02. US Biological Life Sciences.
Nitric acid,praseodymium(3+) salt, pentahydrate (8CI,9CI). Alternative Names: Praseodymium trinitrate pentahydrate, CID3084199, Nitric acid, praseodymium(3+) salt, pentahydrate, 14483-17-1. CAS No. 14483-17-1. Purity: 96%. Product ID: ACM14483171. Molecular formula: H2O. 3/5 H N O3. 1/5 Pr. Mole weight: 417. IUPAC Name: praseodymium(3+) trinitrate pentahydrate. Alfa Chemistry - ISO 9001:32057 Certified.
Nitric acid,zirconium(4+) salt (4:1)
Nitric acid,zirconium(4+) salt (4:1). CAS No. 13773-58-5. Product ID: ACM13773585. Molecular formula: HN O3. 1/4 Zr. Alfa Chemistry - ISO 9001:32057 Certified.
Nitric acid, zirconium salt
Nitric acid, zirconium salt. CAS No. 16092-48-1. Product ID: ACM16092481. Molecular formula: HN O3. x Zr. Mole weight: 339.2436. Alfa Chemistry - ISO 9001:32057 Certified.
nitric oxide dioxygenase
A flavohemoglobin (FAD). It has been proposed that FAD functions as the electron carrier from NADPH to the ferric heme prosthetic group. Group: Enzymes. Enzyme Commission Number: EC 1.14.12.17. CAS No. 214466-78-1. 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-0686; nitric oxide dioxygenase; EC 1.14.12.17; 214466-78-1. Cat No: EXWM-0686.
nitric oxide reductase (cytochrome c)
The enzyme from Pseudomonas aeruginosa contains a dinuclear centre comprising a non-heme iron centre and heme b3, plus heme c, heme b and calcium; the acceptor is cytochrome c551. Group: Enzymes. Enzyme Commission Number: EC 1.7.2.5. 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-1620; nitric oxide reductase (cytochrome c); EC 1.7.2.5. Cat No: EXWM-1620.
nitric oxide reductase (menaquinol)
Contains copper. Group: Enzymes. Enzyme Commission Number: EC 1.7.5.2. 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-1630; nitric oxide reductase (menaquinol); EC 1.7.5.2. Cat No: EXWM-1630.
A heme-thiolate protein (P-450). The enzyme from Fusarium oxysporum utilizes only NADH, but the isozyme from Trichosporon cutaneum utilizes both NADH and NADPH. The electron transfer from NAD(P)H to heme occurs directly, not requiring flavin or other redox cofactors. Group: Enzymes. Synonyms: fungal nitric oxide reductase; cytochrome P450nor; NOR (ambiguous). Enzyme Commission Number: EC 1.7.1.14. 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-1607; nitric oxide reductase [NAD(P)+, nitrous oxide-forming]; EC 1.7.1.14; fungal nitric oxide reductase; cytochrome P450nor; NOR (ambiguous). Cat No: EXWM-1607.
Nitric Oxide Synthase, Inducible from mouse, Recombinant
Nitric oxide synthases (NOSs) are a family of enzymes catalyzing the production of nitric oxide (NO) from L-arginine. NO is an important cellular signaling molecule. It helps modulate vascular tone, insulin secretion, airway tone, and peristalsis, and is involved in angiogenesis and neural development. It may function as a retrograde neurotransmitter. Nitric oxide is mediated in mammals by the calcium-calmodulin controlled isoenzymes eNOS (endothelial NOS) and nNOS (neuronal NOS). The inducible isoform, iNOS, is involved in immune response, binds calmodulin at physiologically relevant concentrations, and produces NO as an immune defense mechanism, as NO is a free.DPH); Inducible Nitric Oxide Synthase; NOS II; iNOS; macNOS; EC 1.14.13.39; NOSs. Enzyme Commission Number: EC 1.14.13.39. CAS No. 125978-95-2. NOSs. Mole weight: mol wt 130 kDa (homodimer); mol wt 130 kDa (subunit, homodimer). Storage: -70°C. Form: buffered aqueous solution; Solution in 50 mM HEPES, pH 7.4, with 10% glycerol, 8 μM tetrahydrobiopterin. Source: E. coli. Species: Mouse. nitric oxide synthetase; endothelium-derived relaxation factor-forming enzyme; endothelium-derived relaxing factor synthase; NO synthase; NADPH-diaphorase; nitric-oxide synthase (NADPH); Inducible Nitric Oxide Synthase; NOS II; iNOS; macNOS; EC 1.14.13.39; NOSs. Cat No: NATE-0489.
nitric-oxide synthase (NADPH)
Binds FAD, FMN, heme (iron protoporphyrin IX) and tetrahydrobiopterin. This eukaryotic enzyme, which is found in plants and animals, consists of oxygenase and reductase domains that are linked via a regulatory calmodulin-binding domain. Upon calcium-induced calmodulin binding, the reductase and oxygenase domains form a complex, allowing electrons to flow from NADPH via FAD and FMN to the active center. May produce superoxide under certain conditions. cf. EC 1.14.13.165, nitric-oxide synthase [NAD(P)H dependent]. Group: Enzymes. Synonyms: nitric oxide synthetase; endothelium-derived relaxation factor-forming enzyme; endothelium-derived relaxing factor synthase; NO synthase; NADPH-diaphorase. Enzyme Commission Number: EC 1.14.13.39. CAS No. 125978-95-2. NOSs. 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-0846; nitric-oxide synthase (NADPH); EC 1.14.13.39; 125978-95-2; nitric oxide synthetase; endothelium-derived relaxation factor-forming enzyme; endothelium-derived relaxing factor synthase; NO synthase; NADPH-diaphorase. Cat No: EXWM-0846.
nitric-oxide synthase [NAD(P)H]
Binds heme (iron protoporphyrin IX) and tetrahydrobiopterin. Most of the bacterial and archaeal enzymes consist of only an oxidase domain and function together with bacterial ferredoxins. The enzyme from the Δ-proteobacterium Sorangium cellulosum also includes a reductase domain that binds FAD, FMN and a [2Fe-2S] cluster. The similar enzymes from plants and animals use only NADPH as acceptor (cf. EC 1.14.13.39). Group: Enzymes. Synonyms: nitric oxide synthetase; NO synthase. Enzyme Commission Number: EC 1.14.13.165. 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-0764; nitric-oxide synthase [NAD(P)H]; EC 1.14.13.165; nitric oxide synthetase; NO synthase. Cat No: EXWM-0764.
Nitrided Multilayer Ti3C2Tx
Nitrided Multilayer Ti3C2Tx. CAS No. 12363-89-2. Purity: 99%.
Nitriding multilayer Ti3C2 MXene
Nitriding multilayer Ti3C2 MXene. CAS No. 12363-89-2. Purity: 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
Nitrilase is able to hydrolyze nitriles into their corresponding carboxylic acids and ammonia. Nitrilase is a green biocatalyst for the production of high value-added products[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9024-90-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P3188.
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
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 (CAS# 139-13-9) 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). Alternative Names: 2-[bis(carboxymethyl)amino]acetic acid. CAS No. 139-13-9. Molecular formula: C6H9NO6. Mole weight: 191.14.
Nitrilotriacetic acid
Nitrilotriacetic acid. Alternative Names: Triglycollamic Acid;Nitrilotriacetic Acid;N,N-Bis(carb;Glycine, N,N-bis(carboxymethyl)-;combretastatin A2. CAS No. 139-13-9. Product ID: ACM139139. Molecular formula: C6H9NO6. Mole weight: 191.14. ECNumber: 205-355-7. Alfa Chemistry - ISO 9001:32057 Certified.
Nitrilotriacetic acid
Nitrilotriacetic acid is an orally active chelating agent for metal ions. Nitrilotriacetic acid is an aminotricarboxylic acid that can sequester metal ions as water soluble complexes. Nitrilotriacetic acid reacts with strong oxidizing agents such as hypochlorite, chlorine, ozone, or oxygen in the presence of palladium/carbon catalyst. Nitrilotriacetic acid interacts with solid phases such as cell membranes and bone matrices in the mammalian system. Nitrilotriacetic acid is classified as an epigenetic rodent carcinogen[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Triglycollamic acid. CAS No. 139-13-9. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-W030778.
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.