203-12-3

Basic information

• Product Name: BENZO(G,H,I)FLUORANTHENE
• Synonyms: BENZO(G,H,I)FLUORANTHENE;1,10-Benzofluoranthrene;2,13-benzofluoranthene;7,10-benzofluoranthene;b(ghi)f;benz(m,n,o)fluoranthene;benzo(fhi)fluoranthene;benzo(mno)fluoranthene
• CAS NO: 203-12-3
• Molecular Formula: C₁₈H₁₀
• Molecular Weight: 226.27
• EINECS: 205-903-5
• Product Categories: Alphabetic;B;BA - BH
• Mol File: 203-12-3.mol
• Article Data: 22

Chemical Properties

• Melting Point: 149 °C
• Boiling Point: 302.89°C (rough estimate)
• Flash Point: 189.9°C
• Appearance: /
• Density: 1.1624 (estimate)
• Vapor Pressure: 1.97E-06mmHg at 25°C
• Refractive Index: 1.5500 (estimate)
• Storage Temp.: 2-8°C
• BRN: 2047005
• CAS DataBase Reference: BENZO(G,H,I)FLUORANTHENE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZO(G,H,I)FLUORANTHENE(203-12-3)
• EPA Substance Registry System: BENZO(G,H,I)FLUORANTHENE(203-12-3)

Safety Data

• RIDADR: 2811
• HazardClass: 6.1(b)
• PackingGroup: III
• Hazardous Substances Data: 203-12-3(Hazardous Substances Data)

Usage

Description

BENZO(G,H,I)FLUORANTHENE, also known as a polycyclic aromatic hydrocarbon, is a chemical compound characterized by its unique molecular structure consisting of multiple interconnected rings. It exhibits distinctive physical properties, such as yellow needles with greenish-yellow fluorescence when recrystallized from petroleum ether and blue fluorescence in solution.

Uses

Used in Analytical Chemistry:
BENZO(G,H,I)FLUORANTHENE is used as a chemical marker for the detection of carbon black mutagenicity. Its presence in samples can indicate the potential mutagenicity of carbon black, which is crucial for understanding the health and environmental implications of exposure to this substance.
Used in Research and Development:
Due to its unique chemical properties, BENZO(G,H,I)FLUORANTHENE is employed as a research compound in various scientific studies. It aids in the investigation of the properties and behavior of polycyclic aromatic hydrocarbons, which can contribute to the development of new materials and technologies.
Used in Industrial Applications:
BENZO(G,H,I)FLUORANTHENE may also find use in specific industrial applications where its chemical properties are advantageous. For instance, its fluorescence characteristics could be utilized in the development of certain types of sensors or imaging technologies.

Safety Profile

Mutation data reported.Questionable carcinogen. When heated to decompositionit emits acrid smoke and irritating vapors.

Carcinogenicity

Available data are inadequate to evaluate the carcinogenicity of benzo[ghi]fluoranthene in experimental animals.

InChI:InChI=1/C18H10/c1-3-11-7-9-13-10-8-12-4-2-6-15-14(5-1)16(11)18(13)17(12)15/h1-10H

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Downstream Products

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Relevant articles and documents

High-Temperature Behavior of 1,8-Diethynylanthracene. Benzaceanthrylene, a Transient Intermediate for Cyclopentapyrene

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From phenylenes to acenes: Flash vacuum pyrolytic isomerization of angular [3]phenylene to benzo[ghi]fluoranthene

The flash vacuum pyrolysis of angular [3]phenylene and bis(2-ethynylphenyl)ethyne produces benzo[ghi]fluoranthene and chrysene, respectively.

Use of external radical sources in flash vacuum pyrolysis to facilitate cyclodehydrogenation reactions in polycyclic aromatic hydrocarbons

A new process to facilitate the cyclodehydrogenation of polycyclic aromatic hydrocarbons (PAHs) in flash vacuum pyrolysis (FVP) using an external radical source is described. Using hexanes as an external radical source the conversion of various PAHs to their cyclodehydrogenated products is vastly increased. Various other volatile organic compounds were also examined to determine their ability to act as external radical sources in FVP.

Facile bucky-bowl synthesis by regiospecific cove-region closure by Hf elimination

Building bowls: An effective intramolecular aryl-aryl coupling is the key step in rational fullerene synthesis and in synthesis of extended buckybowl structures. Such a process can be embodied very efficiently through quantitative HF elimination on active Al2O3. The process is characterized by an unprecedentedly high chemoselectivity and regiospecificity. Copyright

Aryl-aryl bond formation by flash vacuum pyrolysis of benzannulated thiopyrans

(Chemical Equation Presented) In contrast to fully unsaturated 7-membered ring sulfur heterocycles (thiepines), some of which extrude sulfur and give the ring-contracted hydrocarbon even at room temperature in solution, benzannulated thiopyrans (6-membere