The structure of phenothiazine is rigid, being tricyclic. It is known to alter dopamine (3,4-dihydroxyphenethylamine). Its use as an electron donor is based on its unique hole transporting ability, electron releasing nitrogen and sulfur heteroatoms and its non-planar structure leading to lower molecular aggregation.
less than 1 mg/mL at 68° F (NTP, 1992);7.98e-06 M;FREELY SOL IN BENZENE; SOL IN ETHER & IN HOT ACETIC ACID; SLIGHTLY SOL IN ALCOHOL & IN MINERAL OILS; PRACTICALLY INSOL IN PETROLEUM ETHER, CHLOROFORM;VERY SOL IN ACETONE;Water solubilty = 1.59 mg/l at 25 °C;Solubility in water: none;Insoluble
Appearance
Solid
Application
Phenothiazine finds uses in metal free organic dye sensitizers, dyes and antioxidants.
Storage
room temp
Autoignition Temperature
471 °C
Complexity
187
Covalently-Bonded Unit Count
1
Defined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Exact Mass
199.04557046
Formal Charge
0
Heavy Atom Count
14
Hydrogen Bond Acceptor Count
2
Hydrogen Bond Donor Count
1
Isotope Atom Count
0
Monoisotopic Mass
199.04557046
Physical State
Yellow prills or beads
Rotatable Bond Count
0
Topological Polar Surface Area
37.3 Ų
Undefined Atom Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Vapor Pressure
0 mm Hg (approx) (NIOSH, 2016);0 mmHg (approx);0 mmHg (approx)