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48499

Supelco

Indeno[1,2,3-cd]pyrene

analytical standard

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About This Item

Formule empirique (notation de Hill):
C22H12
Numéro CAS:
Poids moléculaire :
276.33
Numéro Beilstein :
1879312
Numéro CE :
Numéro MDL:
Code UNSPSC :
12000000
ID de substance PubChem :

Qualité

analytical standard

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 10 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

environmental

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

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

Clé InChI

SXQBHARYMNFBPS-UHFFFAOYSA-N

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Description générale

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.

Autres remarques

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.

Pictogrammes

Health hazard

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Carc. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Les clients ont également consulté

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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

Protocoles

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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