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Merck

48574

Supelco

Dibenz[a,h]anthracen

analytical standard

Synonym(e):

1,2:5,6-Dibenzanthracen

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

Empirische Formel (Hill-System):
C22H14
CAS-Nummer:
Molekulargewicht:
278.35
Beilstein:
1912416
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12000000
PubChem Substanz-ID:

Qualität

analytical standard

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

vial of 100 mg

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

524 °C (lit.)

mp (Schmelzpunkt)

262-265 °C (lit.)

Anwendung(en)

cleaning products
cosmetics
environmental
food and beverages
personal care

Format

neat

Lagertemp.

2-30°C

SMILES String

c1ccc2c(c1)ccc3cc4c(ccc5ccccc45)cc23

InChI

1S/C22H14/c1-3-7-19-15(5-1)9-11-17-14-22-18(13-21(17)19)12-10-16-6-2-4-8-20(16)22/h1-14H

InChIKey

LHRCREOYAASXPZ-UHFFFAOYSA-N

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Anwendung

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

Piktogramme

Health hazardEnvironment

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

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Kunden haben sich ebenfalls angesehen

M F Kirby et al.
Aquatic toxicology (Amsterdam, Netherlands), 81(3), 233-244 (2007-01-24)
The extent to which biological systems interact in fish from multi-contaminant areas needs to be understood for full interpretation of monitoring data. This study investigates the interaction between two biomarkers, ethoxyresorufin-O-deethylase (EROD) activity and plasma vitellogenin (VTG) in the European
Katarzyna Skupinska et al.
Toxicology in vitro : an international journal published in association with BIBRA, 23(5), 763-771 (2009-04-14)
Polycyclic aromatic hydrocarbons (PAHs)--environmental carcinogens--are metabolized by CYP1A1 and CYP1A2 enzymes to oxy-derivatives, which are able to bind to DNA and initiate carcinogenesis. PAHs induce CYP1A1 and CYP1A2 activity, which increases the risk of development of carcinogenesis. Isothiocyanates (ITCs), naturally
Sander Delahaye et al.
Journal of chromatography. A, 1258, 152-160 (2012-09-04)
Supercritical fluid chromatography (SFC) is attributed many advantages over high performance liquid chromatography (HPLC). Next to the fact that SFC is greener than HPLC, which is especially important for preparative separations, SFC is claimed to be able to deliver faster
Santiago A Bortolato et al.
Analytical chemistry, 80(21), 8276-8286 (2008-10-02)
This work presents a novel approach for the simultaneous ultratrace determination of benzo[ a]pyrene and dibenzo[ a,h]anthracene, the two most carcinogenic polycyclic aromatic hydrocarbons (PAHs), in a very interfering environment, combining the recently discovered ability of the nylon membrane to
A Perico et al.
Archives of environmental health, 56(6), 506-512 (2002-04-18)
In this study, the authors evaluated exposure to airborne polycyclic aromatic hydrocarbons (PAHs) in workers exposed to exhaust gas from cars, and they assessed the efficiency of urinary 1-hydroxypyrene as an indicator of exposure to pyrene and PAHs. The authors

Artikel

This application note describes the fast and efficient separation of the EU’s list of 15 + 1 polynuclear aromatic hydrocarbons (PAHs) using Ascentis® Express PAH HPLC column.

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

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