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Acenaphthene

ALDRICH/215376 - 99%

Synonym: 1,8-Ethylenenaphthalene

CAS Number: 83-32-9
Empirical Formula (Hill Notation): C12H10
Molecular Weight: 154.21
EC Number: 201-469-6
MDL Number: MFCD00003807
Linear Formula: C12H10
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-215376-1G 1 g
$41.60
1/EA
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45-215376-5G 5 g
$57.60
1/EA
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45-215376-100G 100 g
$165.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 215376-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 215376-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 215376-5G

 

assay 99%
bp 279 °C (lit.)
form solid
InChI 1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2
InChI key CWRYPZZKDGJXCA-UHFFFAOYSA-N
mp 90-94 °C (lit.)
Quality Level 100 
SMILES string C1Cc2cccc3cccc1c23
solubility chloroform: soluble 5%, clear, colorless to faintly yellow
vapor density 5.32 (vs air)
vapor pressure 10 mmHg ( 131 °C)
Application:

  • Optimization of Acenaphthene Production: A research article demonstrated the use of high-efficiency HILIC capillary columns for slurry packing at 2100 bar, showcasing an advanced technique that could optimize the synthesis and purification of complex polycyclic aromatic hydrocarbons like acenaphthene, essential for enhancing productivity and purity in chemical processes (Anderson et al., 2024 ).

  • Environmental Impact Assessment: A study investigated the relationship between polycyclic aromatic hydrocarbons (PAHs) and reactive oxygen species in PM2.5 emissions, providing a critical evaluation of the environmental impacts of compounds like acenaphthene in industrial regions, thus informing pollution control and environmental safety strategies (Xu et al., 2024 ).

  • Advances in Organic Semiconductor Materials: Research focused on the synthesis and properties of pyrene-bridged acenaphthenes, contributing to the development of novel organic semiconductor materials, which are crucial for electronic and photonic applications, thus broadening the utility of acenaphthene in high-tech industries (Polkaehn et al., 2023 ).

  • Bioassays for Organic Pollutants: Researchers developed bioassays for organic pollutants, including acenaphthene, using chemical activity-based loading of artificial sediments. This approach offers a new method to assess ecological risks associated with organic contaminants, while also optimizing the derivation of predicted no-effect concentrations (PNECs) for polycyclic aromatic hydrocarbons, critical for regulatory compliance and environmental health. (Abel et al., 2024 ), (Sun et al., 2023 ).

General description: Acenaphthene is a polycyclic aromatic hydrocarbon used as a building block in the synthesis of polymers and resins.
Bacterial oxidation of acenaphthene by Beijerinckia sp. and Beijerinckia sp. strain B8/36 has been reported. Acenapthene forms 1:1:1 inclusion compound by complexing with inclusion compound of β-cyclodextrin and alcohol. Kinetics of the atmospherically important gas-phase reactions of acenaphthene with OH and NO3 radicals, O3 and N2O5 has been investigated at 296 ± 2K.
Packaging: 1, 5, 100 g in poly bottle
Purity 99%
bp 279 °C (lit.)
mp 90-94 °C (lit.)
UNSPSC 12352100

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