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1,10-Phenanthroline monohydrate, 99%

Catalog Number
ACM5144898-2
Product Name
1,10-Phenanthroline monohydrate, 99%
CAS
5144-89-8
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Synonyms
ZX-AT006983; SCHEMBL3790396; KSC269G7H; UNII-KSX215X00E; 1,10-phenanthroline-hydrate; TL8003406; 1,10-Phenanthroline hydrate; AX8021147; 1,10-Phenanthroline monohydrate, ACS reagent, 99%; TR-018323;
IUPAC Name
1,10-phenanthroline;hydrate;
Molecular Weight
198.225g/mol
Molecular Formula
C12H10N2O;
Canonical SMILES
C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1.O;
InChI
InChI=1S/C12H8N2.H₂O/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;/h1-8H;1H2;
InChI Key
PPQJCISYYXZCAE-UHFFFAOYSA-N;
Melting Point
212 to 219 ° F (NTP, 1992);
Solubility
less than 0.1 mg/mL at 70° F (NTP, 1992);
Storage
Store at RT.
Complexity
183
Covalently-Bonded Unit Count
2
Exact Mass
198.079g/mol
H-Bond Acceptor
3
H-Bond Donor
1
Heavy Atom Count
15
Monoisotopic Mass
198.079g/mol
Topological Polar Surface Area
26.8A^2
UNII
KSX215X00E
UN Number
2811
Application
1,10-Phenanthroline monohydrate, 99%, serves multiple purposes due to its unique properties as a white crystalline powder. It is primarily employed in studying DNA-protein interactions attributed to its nuclease activity, enhanced when complexed with copper. As a versatile chemical, it functions as a redox indicator and is instrumental in spectrophotometric assays, particularly for silver. Its capability as a chelating ligand is essential in the determination of metals such as iron, palladium, and vanadium. Additionally, it acts as a matrix metalloproteinase inhibitor and as a photometric reagent for iron by forming a red chelate with ferrous ions. Despite having a slight odor and being insoluble in water, 1,10-Phenanthroline hydrate forms complex compounds with ferrous ions but remains incompatible with strong oxidizers and acids, making it an indispensable tool in various chemical analyses and preparations of metal-chelate complexes.
February 4, 2025

Reliable Reagent for Advanced Research

1,10-Phenanthroline monohydrate from Alfa Chemistry has proven invaluable in studying DNA-protein interactions, particularly due to its effective nuclease activity when complexed with copper. Great for precise spectrophotometric assays and redox indicators.

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