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Merck
CN

48669

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

certified reference material, 200 μg/mL in methanol

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About This Item

Empirical Formula (Hill Notation):
C22H12
CAS Number:
193-39-5
Molecular Weight:
276.33
EC Number:
200-659-6
UNSPSC Code:
12352200
PubChem Substance ID:
329757394
Beilstein/REAXYS Number:
1879312
MDL number:
MFCD00152577

Key Documents

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InChI key

SXQBHARYMNFBPS-UHFFFAOYSA-N

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

SMILES string

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

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

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

signalword

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

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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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
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)
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)
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
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