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48574

Supelco

Dibenz[a,h]anthracene

analytical standard

Synonym(s):

1,2:5,6-Dibenzanthracene

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About This Item

Empirical Formula (Hill Notation):
C22H14
CAS Number:
53-70-3
Molecular Weight:
278.35
Beilstein:
1912416
EC Number:
200-181-8
MDL number:
MFCD00003708
UNSPSC Code:
12000000
PubChem Substance ID:
24872126

grade

analytical standard

CofA

current certificate can be downloaded

packaging

vial of 100 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

524 °C (lit.)

mp

262-265 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

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

InChI key

LHRCREOYAASXPZ-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.

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Danger

Hazard Statements

H350,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
LC26902V
LC17792V
LC08119V
LB98826V
LB95471V

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B Z Zhong et al.
Mutation research, 326(2), 147-153 (1995-02-01)
Benz[a]anthracene (BA), dibenz[a,h]anthracene (DBA) and dibenzo[a,i]pyrene (DBP) are polycyclic aromatic hydrocarbons (PAHs) found in incomplete combustion products of fossil fuels, coal tar, and other organic materials. Workers in related industries may be exposed to these chemicals by inhalation. The information
M Shou et al.
Archives of biochemistry and biophysics, 328(1), 201-207 (1996-04-01)
The metabolic activation of the potent carcinogen dibenzo[a,h]anthracene (DB[a,h]A) was investigated with recombinant human cytochrome P450 enzymes 1A2, 2B6, 2C8, 2C9, 2E1, 3A3, 3A4, and 3A5 expressed in hepatoma G2 cells and with 14 different human liver microsomes. Three dihydrodiols
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
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
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)
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