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48574

Supelco

Dibenz[a,h]anthracen

analytical standard

Synonym(e):

1,2:5,6-Dibenzanthracen

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About This Item

Empirische Formel (Hill-System):
C22H14
CAS-Nummer:
53-70-3
Molekulargewicht:
278.35
Beilstein:
1912416
EG-Nummer:
200-181-8
MDL-Nummer:
MFCD00003708
UNSPSC-Code:
12000000
PubChem Substanz-ID:
24872126

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
GHS08,GHS09

Signalwort

Danger

H-Sätze

H350,H410

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
LRAD6114
LRAC4043
LRAC8481
LRAC6026
LRAB7733

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Suche nach COA

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Dibenzo[a,h]pyren BCR®, certified reference material

BCR159

Dibenzo[a,h]pyren

Benzo[k]fluoranthen certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

03323

Benzo[k]fluoranthen

Benzo[e]pyren 98%

Sigma-Aldrich

B10102

Benzo[e]pyren

Benzo[a]pyren ≥96% (HPLC)

Sigma-Aldrich

B1760

Benzo[a]pyren

P Sartorelli et al.
Toxicology and industrial health, 17(1), 17-21 (2002-05-15)
To understand the dermal uptake of chemicals bound to soil and dust, information on the neat substance is helpful but does not seem sufficient. Because of its content of polycyclic aromatic hydrocarbons (PAHs) coal is suspected to be carcinogenic. However
Heinz Frank et al.
Chemical research in toxicology, 24(12), 2258-2268 (2011-11-18)
The synthesis of the 8 possible stereoisomeric diol epoxides (DEs) at the terminal benzo ring of carcinogenic dibenz[a,h]anthracene (DBA) is reported. trans-3,4-Dihydroxy-3,4-dihydro-DBA (1) afforded the 4 bay region DEs: the enantiomeric pairs of the anti diastereomers (+)-3/(-)-3 and of the
K B Okona-Mensah et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 43(7), 1103-1116 (2005-04-19)
Evidence suggests that people living in urban areas have an increased risk of lung cancer due to higher levels of air pollution in these areas. Benzo[a]pyrene (B[a]P) is currently used as the main indicator of carcinogenic polycyclic aromatic hydrocarbons (PAHs)
S Nesnow et al.
Carcinogenesis, 15(10), 2225-2231 (1994-10-01)
The major routes of metabolic activation of dibenz[a,h]-anthracene (DBA) have been studied in transformable C3H10T1/2CL8 (C3H10T1/2) mouse embryo fibroblasts in culture. The morphological transforming activities of three potential intermediates formed by metabolism of DBA by C3H10T1/2 cells, trans-3,4-dihydroxy-3,4-dihydro-DBA-(DBA-3,4-diol), trans-dihydroxy-3,4-dihydro-DBA-anti-1,2-oxide (DBA-3,4-diol-1,2-oxide)
Zhi-Xin Yuan et al.
Chemical research in toxicology, 16(12), 1581-1588 (2003-12-19)
Benzo[b]phenanthro[2,3-d]thiophene (BPT), a thia analogue of dibenz[a,h]anthracene (DBA), is a carcinogenic environmental pollutant. We have examined the metabolism of BPT by rodent liver microsomes to investigate the mechanism by which BPT produces mutagenic and carcinogenic effects. Both rat and mouse
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