131377
1,10-Phenanthroline
≥99%
Synonym(s):
o-phenanthroline
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About This Item
Empirical Formula (Hill Notation):
C12H8N2
CAS Number:
Molecular Weight:
180.21
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39210124
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
≥99%
form
powder
mp
114-117 °C (lit.)
SMILES string
c1cnc2c(c1)ccc3cccnc23
InChI
1S/C12H8N2/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1/h1-8H
InChI key
DGEZNRSVGBDHLK-UHFFFAOYSA-N
Gene Information
human ... FNTA(2339)
Application
1,10-Phenanthroline can be used as:
- A cathode buffer layer to improve the efficiency of organic solar cells.
- A conventional chelator to study its efficacy in Fenton′s reaction-luminol chemiluminescence system.
- A ligand in mild, copper (II)-catalyzed cross-coupling of organoboronic acids and sulfinate salts, leading to aryl- and alkenylsulfones.
- A versatile ligand employed in the spectrophotometric determination of metals and photocatalytic reduction of carbon dioxide.
- A building block for metallomacrocycles.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Catalysis by Metal Complexes, 14, 217-217 (1993)
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Copper(II) (1(Cu)-21(Cu)) and previously established experimental anticancer platinum(II) metallointercalator complexes (1(Pt)-16(Pt)) have been prepared and investigated for their antimicrobial properties. These complexes are of the general structure [M(I(L))(A(L))](2+) where I(L) represents functionalised 1,10-phenanthrolines (1(IL)-10(IL)), and A(L) represents 1,2-diaminoethane, 1S,2S- or
Aswan Sci. Technol. Bull., 13, 3-3 (1992)
In vitro screening of Fe2+-chelating effect by a Fenton's reaction-luminol chemiluminescence system.
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Luminescence : the journal of biological and chemical luminescence, 29(7), 955-958 (2014-01-10)
In vitro screening of a Fe(2+) -chelating effect using a Fenton's reaction-luminol chemiluminescence (CL) system is described. The luminescence between the reactive oxygen species generated by the Fenton's reaction and luminol was decreased on capturing Fe(2+) using a chelator. The
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