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Safety Information

131377

Sigma-Aldrich

1,10-Phenanthroline

≥99%

Synonym(s):

o-phenanthroline

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About This Item

Empirical Formula (Hill Notation):
C12H8N2
CAS Number:
66-71-7
Molecular Weight:
180.21
EC Number:
200-629-2
MDL number:
MFCD00011678
UNSPSC Code:
12352100
eCl@ss:
39210124
PubChem Substance ID:
24848008
NACRES:
NA.22

Quality Level

200

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)

Related Categories

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.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301,H410

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

131377-25G:
131377-2.5G:
131377-5G:
131377-100G:
131377-VAR:
131377-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBK8623
STBK4451
MKCP6984
STBJ8906
MKCM1913

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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
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
Aswan Sci. Technol. Bull., 13, 3-3 (1992)
Chunming Sun et al.
ACS applied materials & interfaces, 6(2), 739-744 (2014-01-07)
We reported a significant improvement in the efficiency of organic solar cells by introducing hybrid TiO2:1,10-phenanthroline as a cathode buffer layer. The devices based on polymer thieno[3,4-b]thiophene/benzodithiophene:[6,6]-phenyl C71-butyric acid methyl ester (PTB7:PC71BM) with hybrid buffer layer exhibited an average power
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Global Trade Item Number

SKUGTIN
131377-100G4061835554157
131377-2.5G4061835531653
131377-25G4061835508532
131377-5G4061835505197

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