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A805

Sigma-Aldrich

Acenaphthylene

75%

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About This Item

Empirical Formula (Hill Notation):
C12H8
CAS Number:
208-96-8
Molecular Weight:
152.19
Beilstein:
774092
EC Number:
205-917-1
MDL number:
MFCD00003806
UNSPSC Code:
12352100
PubChem Substance ID:
24891309
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
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

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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Zhiru Ma et al.
The journal of physical chemistry. A, 111(10), 2020-2027 (2007-03-29)
13C chemical shift tensor data from 2D FIREMAT spectra are reported for 4,7-di-t-butylacenaphthene and 4,7-di-t-butylacenaphthylene. In addition, calculations of the chemical shielding tensors were completed at the B3LYP/6-311G** level of theory. While the experimental tensor data on 4,7-di-t-butylacenaphthylene are in
N D Marsh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(8), 1499-1511 (2000-07-25)
We have examined the UV spectra of six newly-synthesized ethynyl-PAH (1-ethynylnaphthalene, 5-ethynylacenaphthylene, 1-ethynylanthracene, 9-ethynylphenanthrene, 3-ethynylfluoranthene, and 1-ethynylpyrene) and five corresponding CP-PAH (acenaphthylene, aceanthrylene, acephenanthrylene, cyclopenta[cd]fluoranthene, and cyclopenta[cd]pyrene) and have found the following systematic behavior: ethynyl-substitution results in average bathochromic shifts
Onruthai Pinyakong et al.
FEMS microbiology letters, 238(2), 297-305 (2004-09-11)
Sphingomonas sp. strain A4 is capable of utilizing acenaphthene and acenaphthylene as sole carbon and energy sources, but it is unable to grow on other polycyclic aromatic hydrocarbons (PAHs). The genes encoding terminal oxygenase components of ring-hydroxylating dioxygenase (arhA1 and
Xiuhua Zhu et al.
Environmental pollution (Barking, Essex : 1987), 156(2), 461-466 (2008-03-04)
Gaseous emissions of combusted electronic scrap, PVC, carpet and wood were monitored for polycyclic aromatic hydrocarbons (PAHs) by simultaneous use of semipermeable membrane devices (SPMDs) and shoots of spruce needles (Picea abies). It was found that phenanthrene, acenaphthylene and fluorene
Ling Zi Sang et al.
Talanta, 78(4-5), 1339-1344 (2009-04-14)
A fluorimetric method for simultaneous determination of dissolved acenaphthylene (Ace) phenanthrene (Ph) and pyrene (Py), mixed in an aqueous mineral salts medium (MSM), was developed. The linear ranges for determination of Ace, Ph and Py dissolved in the mixture were
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