Skip to Content
Merck
All Photos(1)

Documents

ERI-001

Supelco

Indeno[1,2,3-cd]pyrene

vial of 25 mg, analytical standard, Cerilliant®

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C22H12
CAS Number:
193-39-5
Molecular Weight:
276.33
Beilstein:
1879312
EC Number:
205-893-2
MDL number:
MFCD00152577
UNSPSC Code:
41116107
PubChem Substance ID:
329799592

grade

analytical standard

packaging

vial of 25 mg

manufacturer/tradename

Cerilliant®

application(s)

environmental
forensics and toxicology

format

neat

storage temp.

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

InChI key

SXQBHARYMNFBPS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Legal Information

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

Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H351

Hazard Classifications

Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
J E Rice et al.
Cancer research, 45(11 Pt 1), 5421-5425 (1985-11-01)
Indeno[1,2,3-cd]pyrene (IP) is a major environmental pollutant which is carcinogenic on mouse skin and in rat lung. Unlike benzo(a)pyrene, IP is a nonalternant polycyclic aromatic hydrocarbon which is devoid of a bay region. IP was mutagenic in Salmonella typhimurium TA100
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service