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Merck
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重要文件

48570

Supelco

analytical standard

同義詞:

苯并[def]菲

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About This Item

經驗公式(希爾表示法):
C16H10
CAS號碼:
分子量::
202.25
Beilstein:
1307225
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
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等級

analytical standard

品質等級

CofA

current certificate can be downloaded

包裝

ampule of 5000 mg

技術

HPLC: suitable
gas chromatography (GC): suitable

mp

145-148 °C (lit.)

應用

environmental

形式

neat

儲存溫度

2-30°C

SMILES 字串

c1cc2ccc3cccc4ccc(c1)c2c34

InChI

1S/C16H10/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h1-10H

InChI 密鑰

BBEAQIROQSPTKN-UHFFFAOYSA-N

基因資訊

human ... CYP1A2(1544)

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一般說明

Pyrene belongs to polycyclic aromatic hydrocarbon group. These are organic compounds which have two or more fused benzene rings in linear, angular and cluster arrangements. Pyrene is a four ring PAH.[1]
Pyrene is a neat reference standard, which may be used for environmental analysis.

應用

Pyrene may be used as an analytical reference standard for the quantification of the analyte in environmental tobacco smoke samples using high-performance liquid chromatography technique.[2]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

象形圖

Environment

訊號詞

Warning

危險聲明

防範說明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

435.2 °F

閃點(°C)

224 °C

個人防護裝備

Eyeshields, Gloves


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分析證明 (COA)

Lot/Batch Number

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Semivolatile and particulate polycyclic aromatic hydrocarbons in environmental tobacco smoke: cleanup, speciation, and emission factors
Gundel AL, et al.
Environmental Science & Technology, 259(6), 1602-1614 (1995)
Yanna Liang
Pyrene Degradation by Mycobacterium Sp Kms: Biochemical Pathway, Enzymatic Mechanisms, and Humic Acid Effect, 1- 4 (2010)
Pentti Somerharju
Chemistry and physics of lipids, 116(1-2), 57-74 (2002-07-03)
Pyrene is one of the most frequently used lipid-linked fluorophores. Its most characteristic features are a long excited state lifetime and (local) concentration-dependent formation of excimers. Pyrene is also hydrophobic and thus does not significantly distort the conformation of the
Michael E Østergaard et al.
Chemical Society reviews, 40(12), 5771-5788 (2011-04-14)
Pyrene-functionalized oligonucleotides (PFOs) are increasingly explored as tools in fundamental research, diagnostics and nanotechnology. Their popularity is linked to the ability of pyrenes to function as polarity-sensitive and quenchable fluorophores, excimer-generating units, aromatic stacking moieties and nucleic acid duplex intercalators.
Intramolecular pyrene excimer fluorescence: a probe of proximity and protein conformational change.
S S Lehrer
Methods in enzymology, 278, 286-295 (1997-01-01)

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