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46434

Supelco

3-Methylcholanthrene solution

100 μg/mL in acetonitrile, PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C21H16
Numero CAS:
Peso molecolare:
268.35
Beilstein:
1913890
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

Concentrazione

100 μg/mL in acetonitrile

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

environmental

Formato

single component solution

Temperatura di conservazione

2-8°C

Stringa SMILE

Cc1ccc2cc3c(ccc4ccccc34)c5CCc1c25

InChI

1S/C21H16/c1-13-6-7-15-12-20-17-5-3-2-4-14(17)8-9-18(20)19-11-10-16(13)21(15)19/h2-9,12H,10-11H2,1H3
PPQNQXQZIWHJRB-UHFFFAOYSA-N

Descrizione generale

3-Methylcholanthrene is a potent carcinogenic polycyclic aromatic hydrocarbon. It plays a role in the pathogenesis of human colon cancer.

Applicazioni

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

Note legali

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

Pittogrammi

FlameExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

35.6 °F - closed cup

Punto d’infiammabilità (°C)

2.0 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificati d'analisi (COA)

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Advances in Applied Microbiology, Volume 30, 258-258 (1984)
A method for measurement of nanogram quantities of 3-methylcholanthrene in stool samples.
Duane W C, et al.
Journal of Lipid Research, 25(5), 523-526 (1984)
Elin Swedenborg et al.
Molecular and cellular endocrinology, 362(1-2), 39-47 (2012-05-29)
The two estrogen receptor isoforms ERα and ERβ mediate biological effects of estrogens, but are also targets for endocrine disruptive chemicals (EDCs), compounds that interfere with hormonal signaling. 3-Methylcholanthrene (3-MC) and dioxin (TCDD) are EDCs and prototypical aryl hydrocarbon receptor
Tarquin Dorrington et al.
Aquatic toxicology (Amsterdam, Netherlands), 124-125, 106-113 (2012-09-04)
In fish there are four cytochrome P450 (CYP1) subfamilies: CYP1A, CYP1B, CYP1C, and CYP1D. Here we cloned Poecilia vivipara CYP1A, with an inferred amino acid sequence 91% identical to CYP1A from the killifish Fundulus heteroclitus, another member of the Cypriniformes
Feiyan Liu et al.
The Journal of biological chemistry, 287(30), 25530-25540 (2012-06-07)
Fas is a member of the death receptor family. Stimulation of Fas leads to induction of apoptotic signals, such as caspase 8 activation, as well as "non-apoptotic" cellular responses, notably NF-κB activation. Convincing experimental data have identified NF-κB as a

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