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05426

Supelco

Acenafteno

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Sinónimos:

1,8-etilenonaftaleno

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About This Item

Fórmula empírica (notación de Hill):
C12H10
Número de CAS:
83-32-9
Peso molecular:
154.21
Beilstein/REAXYS Number:
386081
EC Number:
201-469-6
MDL number:
MFCD00003807
UNSPSC Code:
41116107
PubChem Substance ID:
329748062
NACRES:
NA.24

grade

certified reference material
TraceCERT®

Quality Level

300

vapor density

5.32 (vs air)

vapor pressure

10 mmHg ( 131 °C)

product line

TraceCERT®

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

279 °C (lit.)

mp

90-94 °C (lit.)

application(s)

environmental

format

neat

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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General description

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

257.0 °F - closed cup

flash_point_c

125.0 °C - closed cup

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCB9572
BCBR5531V
BCBJ5852V
BCBD1028V
BCBD1028

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Aurore Vergnoux et al.
Environmental research, 111(2), 193-198 (2010-02-13)
Surface (0-5 cm) and subsurface (-5 to 15 cm) soils from burned forest areas in South of France were analyzed to determine contents of 14 priority polycyclic aromatic hydrocarbons (PAHs) and their distribution profile. The sampling procedure allowed us to
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
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
F Mermillod-Blondin et al.
Chemosphere, 72(2), 213-223 (2008-03-11)
In urban area, the accumulation of polluted stormwater sediments (SWS) in retention ponds may be a source of dissolved pollutants and nutrients for the aquatic ecosystems. Our objective was to quantify the influence of the thickness of SWS layer and
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)
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