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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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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)
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
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
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