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Merck

ERI-001

Supelco

Indeno[1,2,3-cd]pyren

vial of 25 mg, analytical standard, Cerilliant®

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About This Item

Empirische Formel (Hill-System):
C22H12
CAS-Nummer:
Molekulargewicht:
276.33
Beilstein:
1879312
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
Preise und Verfügbarkeit sind derzeit nicht verfügbar.

Qualität

analytical standard

Verpackung

vial of 25 mg

Hersteller/Markenname

Cerilliant®

Anwendung(en)

environmental
forensics and toxicology

Format

neat

Lagertemp.

room temp

SMILES String

c1ccc-2c(c1)-c3ccc4ccc5cccc6cc-2c3c4c56

InChI

1S/C22H12/c1-2-7-17-16(6-1)18-11-10-14-9-8-13-4-3-5-15-12-19(17)22(18)21(14)20(13)15/h1-12H

InChIKey

SXQBHARYMNFBPS-UHFFFAOYSA-N

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Rechtliche Hinweise

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

Piktogramme

Health hazard

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Carc. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Analysenzertifikate (COA)

Lot/Batch Number

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Luke Chandler Short et al.
Journal of the American Society for Mass Spectrometry, 18(4), 589-599 (2006-12-26)
The technique of atmospheric pressure photoionization (APPI) has several advantages over electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI), including efficient ionization of nonpolar or low charge affinity compounds, reduced susceptibility to ion suppression, high sensitivity, and large linear
J E Rice et al.
Carcinogenesis, 11(11), 1971-1974 (1990-11-01)
Indeno[1,2,3-cd]pyrene (IP) is a non-alternant polycyclic aromatic hydrocarbon that has tumor-initiating activity on mouse skin and is carcinogenic in newborn mice and in rat lungs. Previous studies have shown that 8- and 9-hydroxyIP and IP-1,2-diol are major metabolites formed in
J E Rice et al.
Carcinogenesis, 7(10), 1761-1764 (1986-10-01)
Indeno[1,2,3-cd]pyrene is a ubiquitous environmental pollutant which is active as a tumor initiator and complete carcinogen on mouse skin and is carcinogenic in rat lung. The major metabolites of indeno[1,2,3-cd]pyrene as formed in vivo in mouse skin have been identified.
B Muel et al.
International journal of environmental analytical chemistry, 19(2), 111-131 (1985-01-01)
Twenty-three polycyclic aromatic hydrocarbons (PAH) were determined in atmospheric particulate matter in 4 places of the Paris area at several times of the year. Fractionation was performed by reversed-phase high-pressure liquid chromatography. Determination was done by recording emission or excitation
E J Lavoie et al.
Cancer letters, 34(1), 15-20 (1987-01-01)
The tumorigenic activity of benzo[b]fluoranthene, benzo[j]fluoranthene, benzo[k]fluoranthene, and indeno-[1,2,3-cd]pyrene was evaluated in newborn CD-1 mice. The total doses of these non-alternant polycyclic aromatic hydrocarbons employed in this study ranged from 0.5 to 2.1 mumol per mouse. The results of this

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