Determine the necessary mass, volume, or concentration for preparing a solution.
≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
1,10-Phenanthroline Maleimide is used in the synthesis of hybrid transition-metalloproteins via thiol-selective covalent anchoring of Rh-phosphine and Ru-phenanthroline complexes.
| Pubchem Sid | 504765158 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504765158 |
| Sonrisas canónicas | C1=CC2=CC(=C3C=CC=NC3=C2N=C1)N4C(=O)C=CC4=O |
| IUPAC Name | 1-(1,10-phenanthrolin-5-yl)pyrrole-2,5-dione |
| InChIKey | IXIRFFCTTLSORQ-UHFFFAOYSA-N |
| INCHI | 1S/C16H9N3O2/c20-13-5-6-14(21)19(13)12-9-10-3-1-7-17-15(10)16-11(12)4-2-8-18-16/h1-9H |
| Isómeros SMILES | C1=CC2=CC(=C3C=CC=NC3=C2N=C1)N4C(=O)C=CC4=O |
| PubChem CID | 9961599 |
| Peso molecular | 275.26 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Phenanthrolines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenanthrolines |
| Alternative Parents | Quinolines and derivatives Maleimides Pyridines and derivatives N-substituted carboxylic acid imides Benzenoids Pyrrolines Heteroaromatic compounds Dicarboximides Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | 1,10-phenanthroline - Quinoline - Maleimide - Carboxylic acid imide, n-substituted - Pyridine - Benzenoid - Carboxylic acid imide - Dicarboximide - Pyrroline - Heteroaromatic compound - Carboxylic acid derivative - Azacycle - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | May 20, 2026 | P345281 | |
| Certificate of Analysis | Feb 09, 2026 | P345281 | |
| Certificate of Analysis | Feb 09, 2026 | P345281 | |
| Certificate of Analysis | Jul 28, 2023 | P345281 |
| Sensibilidad | Light sensitive |
|---|---|
| Punto de fusión (°C) | >213° C |
| Peso molecular | 275.260 g/mol |
| XLogP3 | 1.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 275.069 Da |
| Monoisotopic Mass | 275.069 Da |
| Topological Polar Surface Area | 63.200 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 472.000 |
| 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 |