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
PubChem Substance ID:
eCl@ss:
39210124
UNSPSC Code:
12352100
NACRES:
NA.22
EC Number:
200-629-2
MDL number:
Assay:
≥99%
Form:
powder
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.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
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
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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In vitro screening of Fe2+-chelating effect by a Fenton's reaction-luminol chemiluminescence system.
Mitsuhiro Wada et al.
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
Daisuke Nishimiya et al.
Scientific reports, 9(1), 11436-11436 (2019-08-09)
Proteases are one of attractive therapeutic targets to play key roles in pharmacological action. There are many protease inhibitors in nature, and most of them structurally have cystine knot motifs. Their structures are favorable for recognition of active pockets of
Novel Osmium-based Coordination Complexes as Photosensitizers for Panchromatic Photodynamic Therapy.
Savo Lazic et al.
Photochemistry and photobiology, 93(5), 1248-1258 (2017-04-04)
Cancer remains a major global malaise requiring the advent of new, efficient and low-cost treatments. Photodynamic therapy, which combines a photosensitizer and photons to produce cytotoxic reactive oxygen species, has been established as an effective cancer treatment but has yet
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 131377-100G | 04061835554157 |
| 131377-2.5G | 04061835531653 |
| 131377-25G | 04061835508532 |
| 131377-5G | 04061835505197 |