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Safety Information

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

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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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
Fergus R Knight et al.
Dalton transactions (Cambridge, England : 2003), 41(11), 3154-3165 (2012-02-01)
Sterically crowded peri-substituted selenium and tellurium acenaphthene donors D1-D7 [Acenap(EPh)(Br) E = Se, Te; Acenap(SePh)(EPh) E = Se, S; Acenap(TePh)(EPh) E = S, Se, Te] react with dibromine and diiodine acceptors to afford a group of structurally diverse addition products
Zhipei Qin et al.
Journal of chromatography. A, 1196-1197, 89-95 (2008-04-22)
The characterization of a poly(dimethylsiloxane) (PDMS) thin film for active extraction of some polycyclic aromatic hydrocarbons was investigated in both a 1-L aqueous solution and a flow-through system. The thin film was attached to an electric bench-drill at a constant
A Arun et al.
Applied biochemistry and biotechnology, 151(2-3), 132-142 (2008-11-01)
The polycyclic aromatic hydrocarbons (PAHs) biodegradation potential of the five basidiomycetes' fungal monocultures and their cocultures was compared with that of a Pseudomonas isolate recovered from oil-spilled soil. As utilization of hydrocarbons by the microorganisms is associated with biosurfactant production
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