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Merck

48499

Supelco

Indeno[1,2,3-cd]pyrene

analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C22H12
Número de CAS:
Peso molecular:
276.33
Beilstein/REAXYS Number:
1879312
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 10 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

neat

storage temp.

2-30°C

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

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General description

Indeno[1,2,3-cd]pyrene is a polycyclic aromatic hydrocarbon, which is a major environmental pollutant. It can be formed via incomplete combustion of organic matter.

Application

Indeno[1,2,3-cd]pyrene may be used as an analytical standard for the determination of the analyte in sewage sludge, solvent solutions and food extracts, water, and oil samples by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Ion Mobility: TWCCSN2 value of 154.8 Å2 [M+H]+

The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.

TWCCS measurements are expected to be within 2% of this reference value.

P/N 48499 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.

pictograms

Health hazard

signalword

Warning

hcodes

Hazard Classifications

Carc. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Certificados de análisis (COA)

Lot/Batch Number

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Los clientes también vieron

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Identification of mutagenic metabolites of indeno [1, 2, 3-cd] pyrene formed in vitro with rat liver enzymes
Rice.EJ, et al.
Cancer Research, 45, 5421-5425 (1985)
Polycyclic aromatic hydrocarbons in the diet
Phillips.HD
Mutation Research. Genetic Toxicology and Environmental Mutagenesis, 443, 139-147 (1999)
PAH source fingerprints for coke ovens, diesel and, gasoline engines, highway tunnels, and wood combustion emissions
Khalili.RM, et al.
Atmospheric Environment, 29, 533-542 (1995)
José Angel Gómez-Ruiz et al.
Analytical and bioanalytical chemistry, 393(6-7), 1697-1707 (2009-01-10)
Three different stationary phases were investigated for the analysis of the 15 + 1 EU-priority polycyclic aromatic hydrocarbons (PAHs) by gas chromatography-mass spectrometry. In addition to the most commonly used 5% phenyl methylpolysiloxane, a mid-polar phase (50% phenyl methylpolysiloxane) and
Gianfranco Diletti et al.
Journal of chromatography. A, 1062(2), 247-254 (2005-02-01)
A gas chromatographic (GC) method with mass spectrometry detection (MS) for the determination of eight polycyclic aromatic hydrocarbons (PAHs) in olive pomace oil has been developed. The oil was diluted with n-pentane and extracted by liquid-liquid partition with dimethyl sulphoxide

Protocolos

US EPA Method 610 describes the analysis of polynuclear aromatic hydrocarbons (commonly referred to as PAHs or PNAs) by both HPLC and GC.

HPLC Analysis of PAHs on SUPELCOSIL™ LC-PAH

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