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Merck
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重要文件

36947

Supelco

茚并[1,2,3-c,d]芘 溶液

100 μg/mL in cyclohexane, analytical standard

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About This Item

經驗公式(希爾表示法):
C22H12
CAS號碼:
分子量::
276.33
Beilstein:
1879312
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

儲存期限

limited shelf life, expiry date on the label

濃度

100 μg/mL in cyclohexane

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

environmental

形式

single component solution

儲存溫度

2-8°C

SMILES 字串

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 密鑰

SXQBHARYMNFBPS-UHFFFAOYSA-N

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應用

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

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分析證明 (COA)

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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)
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, 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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