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Fluoranthen-8-amine

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Identification
Molecular formula
C16H11N
CAS number
33512-74-0
IUPAC name
fluoranthen-8-amine
State
State

Fluoranthen-8-amine is typically found in a solid state at room temperature. It is relatively stable and does not sublimate readily under normal conditions.

Melting point (Celsius)
100.50
Melting point (Kelvin)
373.65
Boiling point (Celsius)
286.00
Boiling point (Kelvin)
559.15
General information
Molecular weight
229.29g/mol
Molar mass
229.2910g/mol
Density
1.2010g/cm3
Appearence

Fluoranthen-8-amine typically appears as a pale yellow solid. It may also be found as a powder form and is not highly reflective.

Comment on solubility

Solubility of Fluoranthen-8-amine (C16H11N)

Fluoranthen-8-amine is a compound that showcases a moderate degree of solubility, which can be attributed to its molecular structure. Here are some important aspects of its solubility:

  • Polarity: The presence of the amine group (-NH2) imparts some degree of polarity, aiding its solubility in polar solvents to an extent.
  • Solvent Compatibility: Fluoranthen-8-amine is generally more soluble in organic solvents, such as:
    • Ethyl acetate
    • Dichloromethane
    • Dimethyl sulfoxide (DMSO)
    • Acetone
  • Water Solubility: Its solubility in water is quite limited, primarily due to its larger hydrophobic fluoranthene portion overshadowing the hydrophilic amine group.

In summary, while fluoranthen-8-amine shows some solubility in organic solvents, its ability to dissolve in water is significantly restricted, aligning with the typical behavior observed in polycyclic aromatic amines. Understanding these solubility characteristics is essential for applications involving the compound in synthetic chemistry and biochemical studies.

Interesting facts

Interesting Facts about Fluoranthen-8-amine

Fluoranthen-8-amine is a fascinating organic compound that serves as an excellent example of the intricate chemistry associated with aromatic amines. This compound, belonging to the polycyclic aromatic hydrocarbons (PAHs) family, is primarily studied for its unique properties and potential applications. Here are some engaging highlights:

  • Polycyclic Aromatic Hydrocarbon: As a member of the PAH family, fluoranthen-8-amine consists of multiple fused aromatic rings, which contribute to its interesting electronic properties and chemical reactivity.
  • Industrial Applications: This compound plays a role in the synthesis of dyes, pigments, and pharmaceuticals. Its ability to influence electronic characteristics makes it useful in developing organic semiconductors and optoelectronic devices.
  • Environmental Concerns: Like many PAHs, fluoranthen-8-amine can be generated through the incomplete combustion of organic material. Understanding its mechanisms and effects is crucial for addressing environmental pollution and health risks.
  • Research Interest: Scientists are keenly investigating fluoranthen-8-amine for its potential biological activities, particularly its interactions with enzymes and proteins, which could lead to new therapeutic avenues.
  • Molecular Structure: The structure of fluoranthen-8-amine features an amino group attached to a fluoranthene skeleton, which enhances its stability and reactivity, making it a target of interest in organic synthesis.

As we continue to unravel the mysteries of compounds like fluoranthen-8-amine, it becomes evident that the interplay of structure and function may unlock new pathways in materials science and medicinal chemistry. Scientists often remark, "In the world of aromatic compounds, the complexities are both a challenge and a treasure trove of possibilities."

Fluoranthen-8-amine exemplifies how diving deeper into chemical properties can pave the way for innovations with practical implications in various fields.

Synonyms
8-Aminofluoranthene
8-FLUORANTHENAMINE
WFZ9PN4QH6
DTXSID10207386
DTXCID10129877
9-Fluoranthenamine
5869-25-0
fluoranthen-8-amine
CCRIS 7013
BRN 2103609
UNII-WFZ9PN4QH6
3-12-00-03368 (Beilstein Handbook Reference)
SCHEMBL23022682
DB-229682