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5-Nitro-1,10-phenanthroline, 98%, Thermo Scientific Chemicals
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Catalog number A11428.14
also known as A11428-14
Price (USD)/ Each
1,582.00
-
Quantity:
25 g
Price (USD)/ Each
1,582.00
5-Nitro-1,10-phenanthroline, 98%, Thermo Scientific Chemicals
Catalog numberA11428.14
Price (USD)/ Each
1,582.00
-
Chemical Identifiers
CAS4199-88-6
IUPAC Name5-nitro-1,10-phenanthroline
Molecular FormulaC12H7N3O2
InChI KeyPDDBTWXLNJNICS-UHFFFAOYSA-N
SMILES[O-][N+](=O)C1=CC2=CC=CN=C2C2=NC=CC=C12
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Pale yellow to yellow or cream to pale brown
FormPowder
Assay (Non-aqueous acid-base Titration)≥97.5 to ≤102.5%
Water Content (Karl Fischer Titration)≤2.5%
5-Nitro-1,10-phenanthroline complexes of iron find wide applications in redox titrations. It is used as a precursor for the synthesis of 5-amino-1,10-phenanthroline, 5-isothiocyanato-1,10-phenanthroline.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
5-Nitro-1,10-phenanthroline complexes of iron find wide applications in redox titrations. It is used as a precursor for the synthesis of 5-amino-1,10-phenanthroline, 5-isothiocyanato-1,10-phenanthroline.
Solubility
Soluble in ethanol. Insoluble in water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents.
5-Nitro-1,10-phenanthroline complexes of iron find wide applications in redox titrations. It is used as a precursor for the synthesis of 5-amino-1,10-phenanthroline, 5-isothiocyanato-1,10-phenanthroline.
Solubility
Soluble in ethanol. Insoluble in water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Redox indicator; reagent for rare earth metals.
- Ramanavicius, A.; Minkstimiene, A. K.; Vilkonciene, I. M.; Genys, P.; Mikhailova, R.; Semashko, T.; Voronovic, J.; Ramanaviciene, A. Biofuel cell based on glucose oxidase from Penicillium funiculosum 46.1 and horseradish peroxidase. Chem. Eng. J. 2015, 264, 165-173.
- Ramos, P. M.; Silva, P. S. P.; Lavin, V.; Martin, I. R.; Lahoz, F.; Posada, P. C.; Silva, M. R.; Gil, J. M. Structure and NIR-luminescence of ytterbium(III) beta-diketonate complexes with 5-nitro-1,10-phenanthroline ancillary ligand: assessment of chain length and fluorination impact. Dalton Trans. 2013, 42 (37), 13516-13526.