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| Product | Description | |
|---|---|---|
| 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. |  |
| 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 | ≥95%. Group: Electronic materials. CAS No. 13826-86-3. Mole weight: NO2BF4. O=[N+]=O.F[B-](F)(F)F. | |
| Nitronium tetrafluoroborate | Nitronium tetrafluoroborate. CAS No. 13826-86-3. |  Pennsylvania PA |
| Nitronium tetrafluoroborate solution | 0.5 M in sulfolane. Group: Electronic chemicals. | |
| Nitro-Phip-[d3] | Nitro-Phip-[d3]. Uses: Labelled nitro-phip. shows potent mutagenic activity in the reversion assay of salmonella typhimurium. Synonyms: 1-Methyl-d3-2-nitro-6-phenylimidazo[4,5-B]pyridine. Grade: 95% atom D. CAS No. 303173-40-2. Molecular formula: C13H7D3N4O2. Mole weight: 257.26. |  |
| 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 |
| Nitrosobiotin | Nitrosobiotin is a N-nitrosamine derivative of biotin. Nitrosobiotin has high affinity for avidin and streptavidin, making it an ideal tool for affinity labeling experiments. Synonyms: 1'-Nitrosobiotin. CAS No. 56859-26-8. Molecular formula: C10H15N3O4S. Mole weight: 273.31. | |
| 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. | |
| Nitroso-sertraline-[d3] (cis racemic mixture) | Nitroso-sertraline-[d3] (cis racemic mixture) is a labelled analogue of nitroso-sertraline. Nitroso-sertraline is undergoing extensive first-pass metabolism by cytochrome P450 and selectively inhibits the reuptake of serotonin at the presynaptic neuronal membrane that is used to treat the major depressive disorder, a social anxiety disorder. Synonyms: N-((1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl)-N-(methyl-d3)nitrous amide; Nitroso-sertraline-d3 (cis racemic mixture). Molecular formula: C17H13D3Cl2N2O. Mole weight: 338.25. | |
| 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. |  |
| Nitroterephthalic acid | Nitroterephthalic acid. Group: Metal organic frameworks (mofs). Alternative Names: 2-NitroterephthalicAcid. CAS No. 610-29-7. Product ID: 2-nitroterephthalic acid. Molecular formula: 211.13. Mole weight: C8H5NO6. C1=CC (=C (C=C1C (=O)O)[N+] (=O)[O-])C (=O)O. InChI=1S/C8H5NO6/c10-7 (11)4-1-2-5 (8 (12)13)6 (3-4)9 (14)15/h1-3H, (H, 10, 11) (H, 12, 13). QUMITRDILMWWBC-UHFFFAOYSA-N. 99%. | |
| Nitrotetrazolium blue chloride 98+% (HPLC) | Nitrotetrazolium blue chloride 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Nitrotyrosine, Positive Control (NT, 3-Nitro-L-Tyrosine, 3-Nitrotyrosine) | Nitrotyrosine, Positive Control (NT, 3-Nitro-L-Tyrosine, 3-Nitrotyrosine). Group: Molecular Biology. Pack Sizes: 15ul. US Biological Life Sciences. | Worldwide |
| nitrous-oxide reductase | The reaction is observed only in the direction of nitrous oxide reduction. Contains the mixed-valent dinuclear CuA species at the electron entry site of the enzyme, and the tetranuclear Cu-Z centre in the active site.In Paracoccus pantotrophus, the electron donor is cytochrome c552. Group: Enzymes. Synonyms: nitrous oxide reductase; N2O reductase; nitrogen:(acceptor) oxidoreductase (N2O-forming). Enzyme Commission Number: EC 1.7.2.4. CAS No. 55576-44-8. 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-1619; nitrous-oxide reductase; EC 1.7.2.4; 55576-44-8; nitrous oxide reductase; N2O reductase; nitrogen:(acceptor) oxidoreductase (N2O-forming). Cat No: EXWM-1619. | |
| Nitroxinil | analytical standard. Group: Application areas. | |
| Nitroxinil | Nitroxynil is an anthelmintic used in the treatment of liver fluke. Nitroxynil is used for the treatment of fascioliasis in cattle and sheep. Group: Biochemicals. Alternative Names: 4-Hydroxy-3-iodo-5-nitrobenzonitrile; 2-Iodo-4-cyano-6-nitrophenol; 3-Iodo-5-nitro-4-hydroxybenzonitrile; 3-Nitro-4-hydroxy-5-iodobenzonitrile; 3-Nitro-5-iodo-4-hydroxybenzonitrile; 4-Cyano-2-iodo-6-nitrophenol; M and B 10755; Nitroxynil. Grades: Highly Purified. CAS No. 1689-89-0. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Nitroxoline | Nitroxoline. Alternative Names: 5-NITRO-8-HYDROXYQUINOLINE;5-NITRO-8-QUINOLINE;5-NITRO-8-QUINOLINOL;8-HYDROXY-5-NITROQUINOLINE;NOTROXOLINE;NITROXOLINE;5-Nitro-8-oxychinoline;5-Nitro-8-oxyquinoline. CAS No. 4008-48-4. Product ID: INT4008484. Molecular formula: C9H6N2O3. Mole weight: 190.16. EINECS: 223-662-4. SMILES: C1=CC2=C(C=CC(=C2N=C1)O)[N+](=O)[O-]. Appearance: powder to Crystal. Category: Intermediates. |  |
| Nitroxoline | Nitroxoline (8-Hydroxy-5-nitroquinoline), an antibiotic , is an orally active antibiofilm agent. Nitroxoline reduces the formation and induces the dispersal of Pseudomonas aeruginosa biofilms by chelation of iron and zinc. Nitroxoline can be used for the urinary tract infections and cancer research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 8-Hydroxy-5-nitroquinoline; 5-Nitro-8-quinolinol. CAS No. 4008-48-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1159. | |
| Nitroxoline | Nitroxoline. Group: Biochemicals. Grades: Highly Purified. CAS No. 4008-48-4. Pack Sizes: 25g, 50g, 100g. Molecular Formula: C?H?N?O?, Melting Point: 177-183°C. US Biological Life Sciences. | Worldwide |
| Nitroxylene | Nitroxylene. Uses: Designed for use in research and industrial production. Additional or Alternative Names: nitroxylene;Dimethylnitrobenzene;NA-1665;Nitroxylen. Product Category: Heterocyclic Organic Compound. CAS No. 25168-04-1. Molecular formula: C8H9NO2. Mole weight: 151.164. Purity: 0.96. IUPACName: 1,2-dimethyl-3-nitrobenzene. Canonical SMILES: CC1=C(C(=CC=C1)[N+](=O)[O-])C. Density: 1.129g/cm³. ECNumber: 201-474-3. Product ID: ACM25168041. Alfa Chemistry ISO 9001:2015 Certified. Categories: 3-Nitro-o-xylene. | |
| Nitroxynil | Nitroxynil, anthelmintic agent, is active against parasites in both adult and immature stages. Nitroxynil is widely used for the research of infection of Fasciola hepatica [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1689-89-0. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-W049875. | |
| Nitroxynil-[13C6] | Nitroxynil-[13C6] is the labelled analogue of Nitroxynil, which is an anthelmintic used in the treatment of liver fluke such as fascioliasis in cattle and sheep. Synonyms: Nitroxynil-13C6; 4-Hydroxy-3-iodo-5-nitrobenzonitrile-13C6; Nitroxynil-(phenyl-13C6); Nitroxinil-13C6; Dovenix-13C6; Trodax-13C6; 4-cyano-2-iodo-6-nitrophenol-13C6. Grade: 95% by HPLC; 98% atom 13C. CAS No. 1325559-31-6. Molecular formula: C[13C]6H3IN2O3. Mole weight: 295.97. | |
| Nitroxynil-(phenyl13C6) | analytical standard. Group: Application areas. | |
| Nivalenol | Nivalenol, classified as type B trichotecenes toxins produced by Fusarium graminearum , is a fungal metabolite present in agricultural product [1]. Nivalenol induces cell death through caspase -dependent mechanisms and via the intrinsic apoptotic pathway. Nivalenol affects the immune system, causes emesis, growth retardation, reproductive disorders and has a haematotoxic/myelotoxic effect [2]. Uses: Scientific research. Group: Natural products. CAS No. 23282-20-4. Pack Sizes: 1 mg. Product ID: HY-N6801. | |
| Nivasorexant | Nivasorexant is a potent orexin receptor antagonist [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ACT-539313. CAS No. 1435480-40-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147294. | |
| Nivatrotamab | Nivatrotamab (Hu3F8-BsAb) is a humanized anti- GD2/CD3 bispecific antibody. Nivatrotamab is a CD3- and GD2-specific bsAb-based T-cell engager. Nivatrotamab can be used in research of neuroblastoma [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Hu3F8-BsAb. CAS No. 2278244-14-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99757. | |
| Nivolumab | Nivolumab Inhibitor. Uses: Scientific use. Product Category: T9907. CAS No. 946414-94-4. |  |
| Nivolumab | Nivolumab is a programmed death receptor-1 ( PD-1 ) blocking human IgG4 antibody to treat advanced (metastatic) non-small cell lung cancer. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BMS-936558; ONO-4538; MDX-1106. CAS No. 946414-94-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P9903. | |
| niyq22a-Hydroxy cholesterol | niyq22a-Hydroxy cholesterol. Group: Biochemicals. Alternative Names: (3b,22R)-Cholest-5-ene-3,22-diol; (20S,22R)-Cholest-5-ene-3b,22-diol; (22R)-22-Hydroxycholesterol. Grades: Highly Purified. CAS No. 17954-98-2. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C27H46O2. US Biological Life Sciences. | Worldwide |
| Nizatidine | Nizatidine. Group: Biochemicals. Alternative Names: N- [2- [ [ [2- [ (Dimethylamino) methyl] -4-thiazolyl] methyl] thio] ethyl] -N'-methyl-2-nitro-1, 1-ethenediamine; LY-139037; ZE-101. Grades: Highly Purified. CAS No. 76963-41-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C12H21N5O2S2. US Biological Life Sciences. | Worldwide |
| Nizatidine | analytical standard. Group: Stomach acid inhibitor standards. | |
| Nizatidine | Nizatidine is a potent and orally active histamine H 2 receptor antagonist, can be used for the research of stomach and intestines ulcers. Nizatidine works by decreasing the secretion of gastric acid the stomach makes and prevent ulcers from coming back after they have healed in animal models [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 76963-41-2. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-B0310. | |
| Nizatidine | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Acinon, LY 139037, Gastrax, N-[2-[[[2-[(Dimethylamino)methyl]-4-thiazolyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine, Axid,Nizatidine, Naxidine, Distaxid, Tazac, Cronizat, N'-[2-[[[2-[(Dimethylamino)methyl]-4-thiazolyl]methyl]thio]ethyl]-N-methyl-2-nitro-1,1-ethenediamine, Nizax, Zanizal, Bonacid, Calmaxid, Nizaxid, ZL 101. | |
| Nizatidine-d3 | Nizatidine-d3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1246833-99-7. Molecular formula: C12H18D3N5O2S2. Mole weight: 334.47. Catalog: APB1246833997. | |
| Nizatidine-d3 | Labeled Nizatidine. Histamine H2-receptor antagonist related to Ranitidine. Antiulcerative. Group: Biochemicals. Alternative Names: N- [2- [ [ [2- [ (Dimethylamino) methyl] -4-thiazolyl] methyl] thio] ethyl] -N- (methyl-d3) -2-nitro-1, 1-ethenediamine; LY-139037-d3; ZE-101-d3; ZL-101-d3; Axid-d3; Calmaxid-d3; Cronizat-d3; Distaxid-d3; Gastrax-d3; Nizax-d3; Nizaxid-d3. Grades: Highly Purified. CAS No. 1246833-99-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Nizatidine-d3 | Nizatidine-d 3 is the deuterium labeled Nizatidine. Nizatidine is a potent and orally active histamine H2 receptor antagonist, can be used for the research of stomach and intestines ulcers. Nizatidine works by decreasing the secretion of gastric acid the stomach makes and prevent ulcers from coming back after they have healed in animal models[1]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1246833-99-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0310S. | |
| Nizatidine-[d3] | Nizatidine-[d3] is the labelled analogue of Nizatidine, which is a histamine H2 receptor antagonist with IC50 of 0. 9 nM, also inhibits AChE with IC50 of 6. 7 μM. Synonyms: Nizatidine D3; N-[2-[[[2-[(Dimethylamino)methyl]-4-thiazolyl]methyl]thio]ethyl]-N'-(methyl-d3)-2-nitro-1,1-ethenediamine. Grade: 95% by HPLC; 95% atom D. CAS No. 1246833-99-7. Molecular formula: C12H18D3N5O2S2. Mole weight: 334.48. | |
| Nizatidine (N- [2- [ [ [2- [ (Dimethylamino) methyl] -4-thiazolyl] methyl] thio] ethyl] -N-methyl-2-nitro-1, 1-ethenediamine, LY-139037, ZE-101, ZL-101, Axid, Calmaxid, Cronizat, Distaxid, Gastrax, Nizax, Nizaxid) | Histamine H2-receptor antagonist related to ranitidine. Group: Biochemicals. Alternative Names: N- [2- [ [ [2- [ (Dimethylamino) methyl] -4-thiazolyl] methyl] thio] ethyl] -N-methyl-2-nitro-1, 1-ethenediamine; LY-139037; ZE-101; ZL-101; Axid; Calmaxid; Cronizat; Distaxid; Gastrax; Nizax; Nizaxid. Grades: Highly Purified. CAS No. 76963-41-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Nizatidine Sulfoxide | Nizatidine Sulfoxide. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Nizatidine Imp. C (EP),(EZ)-N-[2-[[[2-[(Dimethylamino)methyl]thiazol-4-yl]methyl]sulphinyl]ethyl]-N'-methyl-2-nitroethene-1,1-diamine. CAS No. 102273-13-2. Pack Sizes: 10MG. IUPAC Name: 1-N'-[2-[[2-[(dimethylamino)methyl]-1,3-thiazol-4-yl]methylsulfinyl]ethyl]-1-N-methyl-2-nitroethene-1,1-diamine. Molecular formula: C12H21N5O3S2. Mole weight: 347.46. Catalog: APS102273132A. SMILES: CNC(=C[N+](=O)[O-])NCCS(=O)Cc1csc(CN(C)C)n1. Format: Neat. Shipping: Room Temperature. | |
| Nizatidine Sulfoxide-[d3] | Nizatidine Sulfoxide-[d3] is the labelled analogue of Nizatidine Sulfoxide, which is an impurity of Nizatidine. Nizatidine is a histamine H2 receptor antagonist. Synonyms: Nizatidine-d3 Sulfoxide; N-[2-[[[2-[(Dimethylamino)methyl]-4-thiazolyl]methyl]sulfinyl]ethyl]-N'-(methyl-d3)-2-nitro-1,1-ethenediamine; Nizatidine EP Impurity C-d3. CAS No. 1795136-43-4. Molecular formula: C12H18D3N5O3S2. Mole weight: 350.48. | |
| Nizofenone fumarate | Nizofenone fumarate. Group: Biochemicals. Grades: Highly Purified. CAS No. 54533-86-7. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| N-[(+)-Jasmonoyl]-(L)-isoleucine | N-[(+)-Jasmonoyl]-(L)-isoleucine has been used in synthetic preparation of isoleucine conjugate of epi-jasmonic acid. Synonyms: JA-L-Ile; N-[(1S,2S)-3-oxo-2-(2-(Z)-pentenyl)cyclopentane-1-acetyl]-isoleucine. CAS No. 120330-92-9. Molecular formula: C18H29NO4. Mole weight: 323.43. | |
| NK 1001 | NK 1001 is produced by the strain of Streptomyces kanamyceticus var. NK 1001 has weak activity against gram-positive, gram-negative and mycobacterium bacteria. Synonyms: Antibiotic NK 1001; 4,6-Diamino-3-(hexopyranosyloxy)-2-hydroxycyclohexyl 6-amino-6-deoxyhexopyranoside. CAS No. 53025-93-7. Molecular formula: C18H35N3O12. Mole weight: 485.48. | |
| NK-1013-1 | NK-1013-1 is an aminoglycoside antibiotic isolated from Streptomyces kanamyceticus var.21-16. It is active against gram-positive bacteria. Synonyms: Streptamine, O-2-amino-2-deoxy-alpha-D-glucopyranosyl-(1-4)-O-3-amino-3-deoxy-alpha-D-glucopyranosyl-(1-6)-N(sup 3)-acetyl-, D-. CAS No. 102612-61-3. Molecular formula: C20H38N4O13. Mole weight: 542.5. | |
| NK-1013-2 | NK-1013-2 is an aminoglycoside antibiotic isolated from Streptomyces kanamyceticus var.21-16. It is active against gram-positive and gram-negative bacteria. Molecular formula: C22H40N4O14. Mole weight: 584.6. | |
| NK10958P | NK10958P is a plant growth regulator produced by Streptomyces sp. NK10958. Synonyms: NK-10958P. Molecular formula: C18H30O4. Mole weight: 310.4. | |
| NK 154183A | NK 154183A is a 24-membered macrolide antibiotic isolated from the fermentation broth of Streptomyces sp. NK154183. It exhibits antifungal and antitumor activity against the human colon adenocarcinoma. Synonyms: NK154183A; (4E,18E)-11,12,13,14,16,17,27a-Heptahydroxy-6'-(2-hydroxybutyl)-2,2,11,15,17,28-hexamethyl-2,3,3',3a,4',5',6,6',7,8,9,10,11,12,13,14,15,16,17,22,23,26,27,27a-tetracosahydro-20H-spiro[22,26-methanofuro[2,3-h][1,5]dioxacyclohexacosine-24,2'-pyran]-20-one. CAS No. 152986-47-5. Molecular formula: C41H70O13. Mole weight: 771. | |
| NK 154183B | NK 154183B is a 24-membered macrolide antibiotic isolated from the fermentation broth of Streptomyces sp. NK154183. It exhibits antifungal and antitumor activity against the human colon adenocarcinoma. Synonyms: NK154183B; (4E,18E)-13-{[5-(Dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy}-11,12,14,16,17,27a-hexahydroxy-6'-(2-hydroxybutyl)-2,2,11,15,17,28-hexamethyl-2,3,3',3a,4',5',6,6',7,8,9,10,11,12,13,14,15,16,17,22,23,26,27,27a-tetracosahydro-20H-spiro[22,26-methanofuro[2,3-h][1,5]dioxacyclohexacosine-24,2'-pyran]-20-one. CAS No. 152986-49-7. Molecular formula: C49H85NO14. Mole weight: 912.2. | |
| NK1 receptor antagonist 2 | NK1 receptor antagonist 2 is a NK1 receptor antagonist. NK1 receptor antagonist 2 can be used for the research of tinnitus and hearing loss [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 579475-17-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145250. | |
| NK 252 | NK 252. Group: Biochemicals. Grades: Purified. CAS No. 1414963-82-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| NK-252 | NK-252 is a potential Nrf2 activator, which exhibits a great Nrf2 -activating potential. Uses: Scientific research. Group: Signaling pathways. CAS No. 1414963-82-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19734. | |
| NK-252 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| NK30424A | NK30424A is an inhibitor of lipopolysaccharide-induced tumour necrosis factor alpha production with IC50 value of 1 μmol/L. It is produced by Streptomyces sp. NA30424. Molecular formula: C30H46N2O10S. Mole weight: 626.8. | |
| NK30424B | NK30424B is an inhibitor of lipopolysaccharide-induced tumour necrosis factor alpha production with IC50 value of 0.9 μmol/L. It is produced by Streptomyces sp. NA30424. Molecular formula: C30H46N2O10S. Mole weight: 626.8. | |
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