Phenanthrene

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Catalog Number
ACM85018
Product Name
Phenanthrene
Structure
Structure
CAS
85-01-8
Category
Organic & Printed Electronics
Description
Phenanthrene is a polycyclic aromatic hydrocarbon (PAH) which consists of three benzene rings that are prepared by Bardhan-Sengupta phenanthrene synthesis. Its properties include low volatility, high toxicity and resistance to microbial biodegradation.
Synonyms
Phenanthren
IUPAC Name
phenanthrene
Molecular Weight
178.23
Molecular Formula
C14H10
Canonical SMILES
c1ccc2c(c1)ccc3ccccc23
InChI
1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H,YNPNZTXNASCQKK-UHFFFAOYSA-N
InChI Key
YNPNZTXNASCQKK-UHFFFAOYSA-N
Boiling Point
642 °F at 760 mm Hg (NTP, 1992)
Melting Point
98-100 °C (lit.)
Flash Point
340 °F (NTP, 1992);171 °C (340 °F) open cup;340°F
Density
1.025 (NTP, 1992);1.179 at 25 °C;1.025
Solubility
less than 1 mg/mL at 79° F (NTP, 1992);6.45e-06 M;In water, 1.10 mg/L at 25 deg (average of 14 measured values);In water, 1.15 mg/L at 25 °C;In water, 1.6 mg/L at 15 °C; 0.42 mg/L at 8.5 °C; 0.82 mg/L at 21 °C; 1.3 mg/L at 30 °C; In seawater: 0.6 mg/L at 22 °C;Soluble in organic solvents, especially in aromatic hydrocarbons. One gram dissolves in 60 mL cold, 10 mL boiling 95% alcohol, 25 mL absolute alcohol, 2.4 mL toluene or carbon tetrachloride, 2 mL benzene, 1 mL carbon disulfide, 3.3 mL anhydr ether. Soluble in glacial acetic acid.;Soluble in ethanol, diethyl ether, acetone, benzene, and carbon disulfide.
Storage
room temp
Assay
≥99.5%
Color/Form
Monoclinic plates from alcohol;Colorless, shining crystals;Leaves (sublimes)
Complexity
174
Covalently-Bonded Unit Count
1
Decomposition
Hazardous decomposition products formed under fire conditions - Carbon oxides.;When heated to decomposition it emits acrid smoke & fumes.
Defined Atom Stereocenter Count
0
EC Number
201-581-5
Exact Mass
178.0782
Form
crystals
Formal Charge
0
Grade
sublimed grade
H-Bond Acceptor
0
H-Bond Donor
0
Heat of Vaporization
75.50 kJ/mol at 25 °C
Heavy Atom Count
14
Hydrogen Bond Acceptor Count
0
Hydrogen Bond Donor Count
0
Isotope Atom Count
0
LogP
4.46 (LogP);log Kow = 4.46
MDL Number
MFCD00001168
Monoisotopic Mass
178.0782
NSC Number
26256
Odor
Faint aromatic odor
Other Experimental
Isomeric with anthracene; sublimes in high vacuum;Can be hydrogenated, nitrated, sulfonated, and halogenated at various positions; Forms a 9,10-ozonide from which a 2,2'-diformyl diphenyl can be obtained; Lithium, sodium, and potassium add at the 9,10- position; reacts with Nitrogen oxide and Nitrogen dioxide to form nitro derivatives.;Heat of formation: 116.2 kJ/mol (solid); 207.5 kJ/mol (gas). Molar entropy: 215.1 J/mol-K. Heat capacity: 220.6 J/mol-K;Heat of fusion: 16.46 kJ/mol;Sublimation pressure = 0.025 Pa at 300 K;Solutions exhibit a blue fluorescence;/Phenanthrene/ does not contain a group amenable to hydrolysis.;Henry's Law constant = 4.23X10-5 atm-cu m/mol at 25 °C;Hydroxyl radical reaction rate constant = 2.71X10-11 cu cm/molec-sec at 25 °C
Packaging
1, 5 g in glass bottle
Quality Level
100
Refractive Index
Max absorption (heptane): 187.5 nm (log e = 4.48); 211.5 nm (log e= 4.57); Index of refraction: 1.59427; sadtler reference number: 810 (IR, prism); 8035 (IR, grating);Index of refraction: 1.5943
Rotatable Bond Count
0
Stability
Stable under recommended storage conditions.
Topological Polar Surface Area
0 Ų
UNII
448J8E5BST
UN Number
1137
Vapor Density
6.14 (NTP, 1992) (Relative to Air);6.15 (Air = 1) at boiling point of phenanthrene;6.14
Vapor Pressure
1 mm Hg at 68 °F (NTP, 1992);1.21e-04 mmHg;1.21X10-4 mm Hg at 25 °C;1 mmHg
XLogP3
4.5
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