2,9-Dimethyl-1,10-phenanthroline hemihydrate, 98+%
2,9-Dimethyl-1,10-phenanthroline hemihydrate, 98+%
2,9-Dimethyl-1,10-phenanthroline hemihydrate, 98+%
Thermo Scientific Chemicals

2,9-Dimethyl-1,10-phenanthroline hemihydrate, 98+%

CAS: 34302-69-7 | C28H26N4O | 434.54 g/mol
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5 g
25 g
100 g
Catalog number A11398.14
also known as A11398-14
Price (EUR)
222,00
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Quantity:
25 g
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Price (EUR)
222,00
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Chemical Identifiers
CAS34302-69-7
IUPAC Namebis(2,9-dimethyl-1,10-phenanthroline) hydrate
Molecular FormulaC28H26N4O
InChI KeyIEBXFSLFDFHSRD-UHFFFAOYSA-N
SMILESO.CC1=CC=C2C=CC3=CC=C(C)N=C3C2=N1.CC1=CC=C2C=CC3=CC=C(C)N=C3C2=N1
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SpecificationsSpecification SheetSpecification Sheet
FormPowder
Appearance (Color)White to cream
Assay (Non-aqueous acid-base Titration)≥98.0 to ≤102.0%
Identification (FTIR)Conforms
Water Content (Karl Fischer Titration)1.95-6.09% (0.23-0.75 waters)
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2,9-Dimethyl-1,10-phenanthroline hemihydrate, is used as a reagent for the spectrophotometric determination of copper. It is used as an intermediate in medicine and chemical research.

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
2,9-Dimethyl-1,10-phenanthroline hemihydrate, is used as a reagent for the spectrophotometric determination of copper. It is used as an intermediate in medicine and chemical research.

Solubility
It is soluble in methanol: 0.1 g/mL.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible to Strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Reagent for copper: Anal. Chem., 46, 692 (1974).
  2. Complexing agent for Cu(I) in the formation of aryl-sulfur bonds by reaction of aryl iodides with aryl and alkyl thiols: Org. Lett., 4, 2803 (2002). Co-catalyst in the Pd-catalyzed oxidation of alcohols: Adv. Synth. Catal., 345, 1341 (2003).