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A805

Sigma-Aldrich

Acenaphthylene

75%

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About This Item

Empirical Formula (Hill Notation):
C12H8
CAS Number:
Molecular Weight:
152.19
Beilstein:
774092
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

75%

form

solid

impurities

20% acenaphthene

bp

280 °C (lit.)

mp

78-82 °C (lit.)

density

0.899 g/mL at 25 °C (lit.)

SMILES string

c1cc2C=Cc3cccc(c1)c23

InChI

1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H

InChI key

HXGDTGSAIMULJN-UHFFFAOYSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

251.6 °F - closed cup

Flash Point(C)

122.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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K Schirmer et al.
Toxicology, 127(1-3), 129-141 (1998-08-12)
Sixteen polycyclic aromatic hydrocarbons (PAHs) were screened for their ability to be directly cytotoxic to a cell line from the rainbow trout gill, RTgill-W1. Exposure times of 2 h or less were sufficient for direct cytotoxicity to be detected, which
Eldra Delannay et al.
Journal of chromatography. A, 1127(1-2), 45-51 (2006-06-30)
Nowadays, centrifugal partition chromatography (CPC) separations can be routinely achieved at the laboratory scale. The solvent system selection has been made easy, as generic sets of solvent systems are described in publications and books. This approach, however, generally reduces the
F J Rivas et al.
Journal of hazardous materials, 75(1), 89-98 (2000-06-01)
Removal of acenaphthylene from water has been carried out by means of different treatments combining UV radiation, ozone and hydrogen peroxide. Ozonation alone or in conjunction with hydrogen peroxide (10(-3) M) resulted in the highest elimination rates. Thus, conversions as
Fabienne Reisen et al.
Environmental science & technology, 36(20), 4302-4311 (2002-10-22)
Acenaphthene and acenaphthylene are polycyclic aromatic hydrocarbons (PAHs) emitted into the atmosphere from a variety of incomplete combustion sources such as diesel exhaust. Both PAHs are present in the gas phase under typical atmospheric conditions and therefore can undergo atmospheric
Siriwat Poonthrigpun et al.
Applied and environmental microbiology, 72(9), 6034-6039 (2006-09-08)
The acenaphthylene-degrading bacterium Rhizobium sp. strain CU-A1 was isolated from petroleum-contaminated soil in Thailand. This strain was able to degrade 600 mg/liter acenaphthylene completely within three days. To elucidate the pathway for degradation of acenaphthylene, strain CU-A1 was mutagenized by

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