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BCR081R

5-Methyl-chrysen

BCR®, certified reference material

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About This Item

Empirische Formel (Hill-System):
C19H14
CAS-Nummer:
3697-24-3
Molekulargewicht:
242.31
Beilstein:
2048519
MDL-Nummer:
MFCD00215919
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329774213

Qualität

certified reference material

Agentur

BCR®

Hersteller/Markenname

JRC

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

environmental
pharmaceutical (small molecule)

Format

neat

Lagertemp.

2-8°C

SMILES String

Cc1cc2ccccc2c3ccc4ccccc4c13

InChI

1S/C19H14/c1-13-12-15-7-3-4-8-16(15)18-11-10-14-6-2-5-9-17(14)19(13)18/h2-12H,1H3

InChIKey

GOHBXWHNJHENRX-UHFFFAOYSA-N

Hinweis zur Analyse

For more information please see:
BCR080R

Rechtliche Hinweise

BCR is a registered trademark of European Commission

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

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Toshiaki Yoshioka et al.
Journal of bioscience and bioengineering, 126(1), 126-130 (2018-03-04)
Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic substances that are mainly generated during heating in food; therefore, the European Union (EU) has regulated the amount of benzo[a]pyrene and PAH4 in various types of food. In addition, the Scientific Committee on Food
K Peltonen et al.
Chemical research in toxicology, 4(3), 305-310 (1991-05-01)
Eight deoxyribonucleoside adducts formed from reactions of syn-5-methylchrysene 1,2-dihydrodiol 3,4-epoxide with DNA or with nucleotides were characterized spectroscopically. The adducts arose from both cis and trans opening of the epoxide ring at C4 by the amino group of either deoxyadenosine
C E Afshar et al.
Carcinogenesis, 17(11), 2507-2511 (1996-11-01)
The three-dimensional structure of the product of the reaction of a diol epoxide of the carcinogen 5-methylchrysene with methanol has been determined by an X-ray diffraction analysis. The diol epoxide used to obtain this compound contains a stereochemically hindered bay
T Kuljukka-Rabb et al.
Mutagenesis, 16(4), 353-358 (2001-06-23)
Cultures of a human mammary carcinoma cell line (MCF-7) were exposed to the soluble organic fraction of diesel particle emissions, benzo[a]pyrene (B[a]P) and 5-methylchrysene (5-MeCHR) to study time- and dose-related PAH-DNA binding. The concentrations of 14 PAHs in three extracts
S Amin et al.
Chemical research in toxicology, 5(2), 237-241 (1992-03-01)
In previous studies, we have observed unexpected structure-tumorigenicity relationships among the dimethylchrysenes. Thus, 5,6-dimethylchrysene and 5,7-dimethylchrysene were only weakly tumorigenic and were significantly less active than 5-methylchrysene. These results were surprising in view of the known route of metabolic activation
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