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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 5-Nitro-1,10-phenanthroline - ≥98% , CAS No.4199-88-6
Synonyms
NSC 4263 | 5-Nitro-1,10-diazaphenanthrene | MFCD00004981 | 5-NP | AKOS003368622 | DTXSID7063346 | Octachloro-hexahydro-methanoisobenzofuran | PD158530 | Zynophos | 10.14272/PDDBTWXLNJNICS-UHFFFAOYSA-N.1 | AMY23551 | 1,10-Phenanthroline, 5-nitro- | NSC4263
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
NSC 4263 | 5-Nitro-1, 10-diazaphenanthrene | MFCD00004981 | 5-NP | AKOS003368622 | DTXSID7063346 | Octachloro-hexahydro-methanoisobenzofuran | PD158530 | Zynophos | 10.14272/PDDBTWXLNJNICS-UHFFFAOYSA-N.1 | AMY23551 | 1, 10-Phenanthroline, 5-nitro- | NSC4263
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Platinum chelates of a variety of 5-substituted phenanthrolines, including this compound, were tested for cytotoxicity against L1210 murine leukemia cells. Though all tested compounds had very similar DNA-binding affinities, they exhibited a wide range of
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 488184712 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488184712 Sonrisas canónicas C1=CC2=CC(=C3C=CC=NC3=C2N=C1)[N+](=O)[O-] IUPAC Name 5-nitro-1,10-phenanthroline InChIKey PDDBTWXLNJNICS-UHFFFAOYSA-N INCHI 1S/C12H7N3O2/c16-15(17)10-7-8-3-1-5-13-11(8)12-9(10)4-2-6-14-12/h1-7H Isómeros SMILES C1=CC2=CC(=C3C=CC=NC3=C2N=C1)[N+](=O)[O-] WGK Alemania 3 Peso molecular 225.21 Beilstein 196245 Reaxy-Rn 196245 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=196245&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Clase Phenanthrolines Subclass Not available Intermediate Tree Nodes Not available Direct Parent Phenanthrolines Alternative Parents Nitroquinolines and derivatives Nitroaromatic compounds Pyridines and derivatives Benzenoids Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 1,10-phenanthroline - Nitroquinoline - Quinoline - Nitroaromatic compound - Pyridine - Benzenoid - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Organic oxoazanium - Azacycle - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxide - Organopnictogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Insoluble in water Punto de fusión (°C) 202°C Peso molecular 225.200 g/mol XLogP3 2.300 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 0 Exact Mass 225.054 Da Monoisotopic Mass 225.054 Da Topological Polar Surface Area 71.600 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 305.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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