230847
5-Methyl-1,10-phenanthroline
≥99%
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About This Item
Empirical Formula (Hill Notation):
C13H10N2
CAS Number:
Molecular Weight:
194.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
221-099-9
MDL number:
Product Name
5-Methyl-1,10-phenanthroline, ≥99%
InChI key
UJAQYOZROIFQHO-UHFFFAOYSA-N
InChI
1S/C13H10N2/c1-9-8-10-4-2-6-14-12(10)13-11(9)5-3-7-15-13/h2-8H,1H3
SMILES string
Cc1cc2cccnc2c3ncccc13
assay
≥99%
form
powder
mp
113-114 °C (lit.)
solubility
methanol: soluble 50 mg/mL, clear to slightly hazy, colorless to yellow
Quality Level
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Application
5-Methyl-1,10-phenanthroline was used in the determination of Cu(II) in duralmin alloy by capillary zone electrophoresis.
General description
5-Methyl-1,10-phenanthroline forms iron(II)-phenanthroline complexes and their gas-phase stabilities has been investigated in an electrospray ionization mass spectrometer.
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Sandor Keki et al.
Journal of the American Society for Mass Spectrometry, 17(7), 962-966 (2006-05-23)
The gas-phase stabilities of Fe(Phi)3(2+) complexes, where Phi represents the 1,10-phenanthroline, 5-chloro-1,10-phenanthroline, 5-methyl-1,10-phenanthroline, 3,4,7,8-tetramethyl-1,10-phenanthroline, and 4,7-diphenyl-1,10-phenanthroline ligands were investigated by collision-induced dissociation (CID) in the capillary-first skimmer region upon changing the voltage difference between the capillary and the skimmer. The
Zdeněk Trávníček et al.
Chemistry Central journal, 6(1), 160-160 (2012-12-22)
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Capillary electrophoretic separation of several transition-metal ions as their complexes with 1, 10-phenanthroline derivatives and its application to the determination of copper in duralmin alloys.
Yokoyama T, et al.
Analytica Chimica Acta, 364(1), 75-81 (1998)
K Benjamin Garbutcheon-Singh et al.
Dalton transactions (Cambridge, England : 2003), 42(4), 918-926 (2012-09-29)
Twelve metallointercalators of the type [Pt(I(L))(A(L))](2+), where A(L) is either the R,R or S,S enantiomer of 1,2-diaminocyclopentane (DACP) and I(L) is either 1,10-phenathroline, 4-methyl-1,10-phenanthroline, 5-methyl-1,10-phenanthroline, 4,7-dimethyl-1,10-phenanthroline, 5,6-dimethyl-1,10-phenanthroline or 3,4,7,8-tetramethyl-1,10-phenanthroline, were synthesised, characterised and the cytotoxicity to the L1210 cell line
Tiffany K Rundstadler et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-06)
Cancer stem cells (CSCs) are thought of as a clinically pertinent subpopulation of tumors, partly responsible for cancer relapse and metastasis. Research programs aimed at discovering anti-CSC agents have largely focused on biologics and purely organic molecules. Recently, we showed
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