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05426

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Acénaphtène

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

Synonyme(s) :

1,8-éthylènenaphthalène

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About This Item

Formule empirique (notation de Hill):
C12H10
Numéro CAS:
83-32-9
Poids moléculaire :
154.21
Numéro Beilstein :
386081
Numéro CE :
201-469-6
Numéro MDL:
MFCD00003807
Code UNSPSC :
41116107
ID de substance PubChem :
329748062
Nomenclature NACRES :
NA.24

Qualité

certified reference material
TraceCERT®

Niveau de qualité

300

Densité de vapeur

5.32 (vs air)

Pression de vapeur

10 mmHg ( 131 °C)

Gamme de produits

TraceCERT®

Durée de conservation

limited shelf life, expiry date on the label

Fabricant/nom de marque

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Point d'ébullition

279 °C (lit.)

Pf

90-94 °C (lit.)

Application(s)

environmental

Format

neat

Chaîne SMILES 

C1Cc2cccc3cccc1c23

InChI

1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2

Clé InChI

CWRYPZZKDGJXCA-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Produits recommandés

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.

Informations légales

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

Pictogrammes

Environment
GHS09

Mention d'avertissement

Warning

Mentions de danger

H410

Conseils de prudence

P273 - P391 - P501

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

257.0 °F - closed cup

Point d'éclair (°C)

125.0 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
BCCK5492
BCCB9572
BCBR5531V
BCBJ5852V
BCBD1028V

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Polynuclear aromatic hydrocarbons 16 solution

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
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)
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
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
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
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