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9-Phenanthrol

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Identification
Molecular formula
C14H10O
CAS number
484-17-3
IUPAC name
phenanthren-9-ol
State
State

At room temperature, 9-Phenanthrol is in a solid state. It maintains its integrity as a crystalline substance, reflecting its stable aromatic hydrocarbon nature.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.15
General information
Molecular weight
194.22g/mol
Molar mass
194.2230g/mol
Density
1.1910g/cm3
Appearence

9-Phenanthrol appears as a pale yellow solid with crystalline characteristics. It may also present as powdery, depending on its handling and processing. The compound is known for the distinct planar, aromatic configuration common to polycyclic aromatic hydrocarbons.

Comment on solubility

Solubility of Phenanthren-9-ol

Phenanthren-9-ol, with the chemical formula C14H10O, is an organic compound containing an alcohol functional group. The solubility characteristics of this compound can be understood through several key factors:

  • Polar vs. Nonpolar: As a hydroxyl (-OH) functional group is present, the compound exhibits some degree of polarity. This allows for potential interactions with polar solvents like water.
  • Solvent Compatibility: Phenanthren-9-ol is likely to be more soluble in organic solvents such as ethanol, methanol, and acetone due to its hydrophobic aromatic ring structure. However, its solubility in water is limited.
  • Temperature Influence: Generally, the solubility of organic compounds can increase with temperature. If heated, the solubility of phenanthren-9-ol in organic solvents would increase, making it easier to dissolve.
  • Concentration Factors: At higher concentrations, the solubility of phenanthren-9-ol in nonpolar solvents may outperform its solubility in polar environments, indicating that it aligns more with nonpolar characteristics at elevated concentrations.

In conclusion, while the presence of the hydroxyl group offers some polar characteristics, the overall solubility of phenanthren-9-ol is largely dictated by its hydrophobic nature, favoring organic solvents over water. As with many organic compounds, considerations of temperature and solvent compatibility remain crucial for understanding solubility behavior.

Interesting facts

Interesting Facts About Phenanthren-9-ol

Phenanthren-9-ol, a fascinating organic compound, belongs to the family of polycyclic aromatic hydrocarbons (PAHs). This compound is particularly noteworthy for several reasons:

  • Chemical Structure: Phenanthren-9-ol features a distinctive tri-cyclic structure, which is composed of three fused benzene rings. This arrangement not only contributes to its unique chemical properties but also influences its reactivity.
  • Biological Implications: As a member of the PAH group, Phenanthren-9-ol can be involved in biological systems. Some studies suggest it may play a role in various biological processes, including those related to disease mechanisms.
  • Environmental Concerns: Compounds like Phenanthren-9-ol can arise from the incomplete combustion of organic matter, raising concern due to potential toxicity and the impact on environmental health. They are often studied in the context of pollution and remediation.
  • Applications: Beyond its theoretical interest, Phenanthren-9-ol has potential applications in organic synthesis and materials science. It can serve as a precursor for creating more complex chemical compounds.

In the words of a prominent chemist, “Understanding the properties of aromatic compounds like Phenanthren-9-ol is crucial for advancing both organic chemistry and environmental sciences.” This compound exemplifies the importance of intricate molecular structures and their implications in both nature and industry.

Overall, Phenanthren-9-ol not only enriches the field of chemistry but also highlights the interconnectedness of chemical substances with biological and ecological systems.

Synonyms
Phenanthren-9-ol
9-PHENANTHROL
9-Hydroxyphenanthrene
NSC 50554
CCRIS 1840
CHEBI:28820
UNII-9FYU45OV9H
EINECS 207-602-4
9FYU45OV9H
BRN 2047057
DTXSID9047592
NSC-50554
DTXCID7027592
DZKIUEHLEXLYKM-UHFFFAOYSA-
4-06-00-04937 (Beilstein Handbook Reference)
9phenanthrol
9Phenanthrenol
Phenanthren9ol
9Hydroxyphenanthrene
dzkiuehlexlykm-uhfffaoysa-n
inchi=1/c14h10o/c15-14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9,15h
484-17-3
9-Phenanthrenol
MFCD00082298
CHEMBL2407182
9-Hydroxyphenanthrene; NSC 50554
9-Phenanthrol-D8
9-Phenanthrenol; 9-Hydroxyphenanthrene; NSC 50554;
phenanthrene-9-ol
YSZC378
SCHEMBL508755
9-Phenanthrol, technical grade
GTPL4114
NSC50554
Tox21_300618
BDBM50526033
AKOS015856392
NCGC00248109-01
NCGC00254471-01
BS-16893
CAS-484-17-3
SY113803
DB-022746
HY-108457
CS-0028825
E0028
NS00015630
Q24063303