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301841

Sigma-Aldrich

1,7-Phenanthroline

99%

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About This Item

Formule empirique (notation de Hill):
C12H8N2
Numéro CAS:
230-46-6
Poids moléculaire :
180.21
Numéro MDL:
MFCD00004971
Code UNSPSC :
12352100
ID de substance PubChem :
24858213
Nomenclature NACRES :
NA.22

Pureté

99%

Forme

solid

Pf

79-81 °C (lit.)

Chaîne SMILES 

c1cnc2c(c1)ccc3ncccc23

InChI

1S/C12H8N2/c1-3-9-5-6-11-10(4-2-7-13-11)12(9)14-8-1/h1-8H

Clé InChI

OZKOMUDCMCEDTM-UHFFFAOYSA-N

Description générale

1,7-Phenanthroline has inhibitory effect on germination and growth of plants. 1,7-Phenanthroline is an aza-analog of phenanthrene, was found to be mutagenic in the Ames test using Salmonella typhimurium TA100 in the presence of a rat liver S9 fraction. Supramolecular assemblies of 1,2,4,5-benzenetetracarboxylic acid with 1,7-phenanthroline (aza donor molecule) were investigated.

Pictogrammes

Skull and crossbonesCorrosionEnvironment
GHS06,GHS05,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301,H318,H410

Classification des risques

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Certificats d'analyse (COA)

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2-Phenylpyridine 98%

Sigma-Aldrich

P33402

2-Phenylpyridine

Neocuproine ≥98%

Sigma-Aldrich

N1501

Neocuproine

2,2′-Bipyridyl ReagentPlus®, ≥99%

Sigma-Aldrich

D216305

2,2′-Bipyridyl

Kapildev K Arora et al.
The Journal of organic chemistry, 68(24), 9177-9185 (2003-11-25)
Supramolecular assemblies of 1,2,4,5-benzenetetracarboxylic acid, 1, with aza donor molecules such as 1,10-phenanthroline, 2, 1,7-phenanthroline, 3, phenazine, 4, 4-(N,N-dimethylamino)pyridine, 5, 1,2-bis(4-pyridyl)ethene, 6, and 1,2-bis(4-pyridyl)ethane, 7, have been synthesized and characterized by single-crystal X-ray diffraction methods. All the complexes crystallize in
Martin Saurer et al.
Science (New York, N.Y.), 365(6458), 1144-1149 (2019-09-14)
Mitochondrial ribosomes (mitoribosomes) are large ribonucleoprotein complexes that synthesize proteins encoded by the mitochondrial genome. An extensive cellular machinery responsible for ribosome assembly has been described only for eukaryotic cytosolic ribosomes. Here we report that the assembly of the small
Wei Xiao et al.
Environmental science & technology, 52(1), 114-123 (2017-12-06)
Iron (oxyhydr)oxides are widespread in natural and engineered systems, potent adsorbents of contaminants and a source of energy for iron-reducing bacteria. Microbial reduction of iron (oxyhydr)oxides results in the formation of Fe(II) which can induce the transformation of these iron
Veronika Paková et al.
Environmental toxicology and chemistry, 25(12), 3238-3245 (2007-01-16)
N-heterocyclic derivatives of polycyclic aromatic hydrocarbons (NPAHs) are widespread concomitantly with their parent analogues and have been detected in air, water, sediments, and soil. Although they were shown to be highly toxic to some organisms, our understanding of their occurrence
Katsuya Yamada et al.
Mutation research, 559(1-2), 83-95 (2004-04-07)
Phenanthrene, a simplest angular polycyclic aromatic hydrocarbon with a bay-region in its molecule, is reported to be non-mutagenic, although most angular (non-linear) polycyclic aromatic hydrocarbons, such as benzo[a]pyrene and chrysene, are known to show genotoxicity after metabolic transformation into a
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