631507
1,10-Phenanthrolin-5-amine
97%
Synonym(s):
(1,10)-Phenanthrolin-5-ylamine
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About This Item
Empirical Formula (Hill Notation):
C12H9N3
CAS Number:
Molecular Weight:
195.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
mp
254-258 °C (lit.)
SMILES string
Nc1cc2cccnc2c3ncccc13
InChI
1S/C12H9N3/c13-10-7-8-3-1-5-14-11(8)12-9(10)4-2-6-15-12/h1-7H,13H2
InChI key
DKPSSMOJHLISJI-UHFFFAOYSA-N
Application
1,10-Phenanthrolin-5-amine can be used in the synthesis of bis-[1,10]phenanthrolin-5-yl-pyromellitic diimide (Bphen-PMD), which can find applications in organic light-emitting devices.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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"Phenanthroline diimide as an organic electron-injecting material for organic light-emitting devices"
Lee H, et al.
Royal Society of Chemistry Advances, 2(23), 8762-8767 (2012)
Barbara Feist et al.
Mikrochimica acta, 186(2), 91-91 (2019-01-12)
Graphene oxide (GO) was chemically functionalized with 5-amino-1,10-phenanthroline. The resulting conjugate (phen-GO) was characterized by scanning electron microscopy and X-ray photoelectron spectroscopy. The experiments show that phen-GO has a high affinity for extraction of Pb(II) ions. Isotherms and kinetics fit
Mona Amiri et al.
Dalton transactions (Cambridge, England : 2003), 49(29), 10173-10184 (2020-07-16)
1,10-Phenanthroline (phen) was grafted to either indium tin oxide (ITO), fluorine-doped tin oxide (FTO), or titanium dioxide (TiO2) semiconductors (SC's) by electrochemical reduction of 5-diazo-phen. The phen ligand is bonded to the semiconductor at C5, and it can be handled
Siew San Tan et al.
Physical chemistry chemical physics : PCCP, 19(37), 25734-25745 (2017-09-16)
An absorbance-based sensor employing ruthenium bipyridyl with a phenanthroline-fused benzoylthiourea moiety formulated as [Ru(ii)(bpy)
Jacek E Nycz et al.
Molecules (Basel, Switzerland), 24(22) (2019-11-27)
New approaches to the synthesis of 4,7-dichloro-1,10-phenanthrolines and their corresponding 9H-carbazol-9-yl-, 10H-phenothiazin-10-yl- and pyrrolidin-1-yl derivatives were developed. Their properties have been characterized by a combination of several techniques: MS, HRMS, GC-MS, electronic absorption spectroscopy and multinuclear NMR in both solution
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