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Merck
CN

48669

Supelco

Indeno[1,2,3-c,d]pyrene solution

new

certified reference material, 200 μg/mL in methanol

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About This Item

Empirical Formula (Hill Notation):
C22H12
CAS Number:
Molecular Weight:
276.33
Beilstein:
1879312
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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grade

certified reference material
TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

200 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

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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Application

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

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup

Regulatory Information

危险化学品
This item has

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’.

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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
Nitration of indeno[1,2,3-cd]pyrene and mutagenic activities of related compounds.
M Minabe et al.
Chemical research in toxicology, 2(6), 357-358 (1989-11-01)
E H Pfeiffer et al.
Zentralblatt fur Bakteriologie, Mikrobiologie und Hygiene. 1. Abt. Originale B, Hygiene, 179(6), 574-585 (1984-12-01)
The possible destruction in the soil of PAH present in sewage sludge-garbage composts in considerable amounts has been studied under various conditions. Sandy and loamy soil were mixed with the compost and kept in a climate chamber at 20 degrees
Indeno [1,2,3-cd]pyrene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 373-378 (1983-12-01)
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.

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