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48643

Supelco

Acenaphthene solution

certified reference material, 200 μg/mL in methanol

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About This Item

Empirical Formula (Hill Notation):
C12H10
CAS Number:
83-32-9
Molecular Weight:
154.21
Beilstein:
386081
EC Number:
200-659-6
MDL number:
MFCD00003807
UNSPSC Code:
12000000
PubChem Substance ID:
24872166

grade

certified reference material
TraceCERT®

Quality Level

100

product line

TraceCERT®

packaging

ampule of 1 mL

concentration

200 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

SMILES string

C1Cc2cccc3cccc1c23

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

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

Regulatory Information

危险化学品

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Javier Rivas et al.
Journal of hazardous materials, 169(1-3), 509-515 (2009-05-05)
A three-level full factorial design has been conducted to assess the influence of gas flow-rate, ozone concentration and reaction time on the remediation of soil contaminated with four PAHs (namely acenaphthene, phenanthrene, anthracene and fluoranthene). Under the operating conditions investigated
Yanzheng Gao et al.
Journal of environmental quality, 40(2), 653-656 (2011-04-28)
The subcellular process and distribution of polycyclic aromatic hydrocarbons (PAHs) in arbuscular mycorrhizal plants remains to be elucidated. This work used a greenhouse experiment to show that, accompanied by the apoplastic and symplastic water movement through the root, acenaphthene (ACE)
Ningjing Hu et al.
Environmental science and pollution research international, 18(2), 163-172 (2010-06-26)
The levels and possible sources of 16 polycyclic aromatic hydrocarbons (PAHs) were investigated in the surface sediments of Liaodong Bay, Bohai Sea, China. The sum of 16 PAHs (∑PAH(16)) concentrations varied from 144.5 to 291.7 ng/g, with a mean value
Lili Wang et al.
Chemosphere, 82(6), 895-900 (2010-11-13)
In aqueous environment temperature is considered to play a significant role in the sorption process of polycyclic aromatic hydrocarbons (PAHs) and its influence on the sorption equilibrium is indicative of sorption energies and mechanisms. In this study, sorptions of five
Debajyoti Ghosal et al.
Research in microbiology, 164(2), 155-163 (2012-11-28)
Utilization of an enrichment technique led to isolation of a bacterium from municipal waste-contaminated soil in which acenaphthene was used as the sole source of carbon and energy. The isolate was identified as Acinetobacter sp. strain AGAT-W based on morphological
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