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Merck

46434

3-Methylcholanthrene solution

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

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About This Item

Empirical Formula (Hill Notation):
C21H16
CAS Number:
56-49-5
Molecular Weight:
268.35
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757181
EC Number:
200-835-2
Beilstein/REAXYS Number:
1913890
MDL number:
MFCD00003704

Product Name

3-Methylcholanthrene solution, 100 μg/mL in acetonitrile, PESTANAL®, analytical standard

InChI key

PPQNQXQZIWHJRB-UHFFFAOYSA-N

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

SMILES string

Cc1ccc2cc3c(ccc4ccccc34)c5CCc1c25

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-8°C

Quality Level

100

Related Categories

Application

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

General description

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

Legal Information

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

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM3756
BCCL7216
BCCC7514
BCBW9628

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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
Benjamin Lemaire et al.
Environmental science & technology, 46(18), 10310-10316 (2012-08-21)
While deep-sea fish accumulate high levels of persistent organic pollutants (POPs), the toxicity associated with this contamination remains unknown. Indeed, the recurrent collection of moribund individuals precludes experimental studies to investigate POP effects in this fauna. We show that precision-cut
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