Description
1,10-Phenanthroline-5-carboxylic Acid (CAS No. 630067-06-0) is a high-purity heterocyclic organic compound with the molecular formula C13H8N2O2. This derivative of 1,10-phenanthroline features a carboxylic acid functional group at the 5-position, enhancing its chelating and coordination properties. Ideal for research applications, it serves as a versatile building block in coordination chemistry, catalysis, and material science. The compound is characterized by its excellent stability, solubility in polar organic solvents, and ability to form stable complexes with transition metals. Available in ≥95% purity (HPLC), it is supplied as a fine powder with rigorous QC testing to ensure batch-to-batch consistency. Store in a cool, dry place, protected from light.
Properties
- CAS Number: 630067-06-0
- Complexity: 308
- IUPAC Name: 1,10-phenanthroline-5-carboxylic acid
- InChI: InChI=1S/C13H8N2O2/c16-13(17)10-7-8-3-1-5-14-11(8)12-9(10)4-2-6-15-12/h1-7H,(H,16,17)
- InChI Key: UCJSMIWAXWPDOJ-UHFFFAOYSA-N
- Exact Mass: 224.058577502
- Molecular Formula: C13H8N2O2
- Molecular Weight: 224.21
- SMILES: C1=CC2=CC(=C3C=CC=NC3=C2N=C1)C(=O)O
- Topological: 63.1
- Monoisotopic Mass: 224.058577502
- Synonyms: 1,10-phenanthroline-5-carboxylic Acid, 630067-06-0, DTXSID90392542, DTXCID40343403, 1,10-Phenanthroline-5-carboxylicacid, MFCD06255104, YSWG031, SCHEMBL679992, SBB044940, STL490573, AKOS000275014, CS-W004571, AS-63023, DB-027076, pyridino[3,2-h]quinoline-5-carboxylic acid, C16119
Application
1,10-Phenanthroline-5-carboxylic Acid is widely used as a chelating ligand in the synthesis of metal-organic frameworks (MOFs) and coordination polymers. Its carboxylic acid group enables covalent attachment to surfaces or other molecules, making it valuable for functionalizing nanomaterials. Researchers also employ it in catalytic systems for oxidation reactions and as a fluorescent probe due to its strong metal-binding affinity. Additionally, it serves as a precursor for designing advanced sensors and optoelectronic materials.
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