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About This Item
Empirical Formula (Hill Notation):
C26H18
CAS Number:
Molecular Weight:
330.42
Beilstein/REAXYS Number:
1914010
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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grade
analytical standard
Quality Level
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
mp
245-248 °C (lit.)
application(s)
environmental
format
neat
SMILES string
c1ccc(cc1)-c2c3ccccc3c(-c4ccccc4)c5ccccc25
InChI
1S/C26H18/c1-3-11-19(12-4-1)25-21-15-7-9-17-23(21)26(20-13-5-2-6-14-20)24-18-10-8-16-22(24)25/h1-18H
InChI key
FCNCGHJSNVOIKE-UHFFFAOYSA-N
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General description
9,10-Diphenylanthracene, an aromatic hydrocarbon, is a blue light emitting material that is used for the measurement of fluorescence quantum yields in dilute solutions. Its derivatives show potential candidature in organic light emitting diode (OLED) devices. It is also used as a fluorophore for the study of peroxyoxalate chemiluminescence (POCL).
Application
9,10-Diphenylanthracene may be used as an analytical standard for the determination of the analyte in fish and meat products by liquid chromatography (LC) as well as capillary gas chromatography-mass spectrometry (GC-MS) techniques. It may be used as an internal standard for the determination of halofantrine and desbutylhalofantrine in animal biological samples using on-line UV irradiation and POCL detection.
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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Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Abena Amponsaa-Karikari et al.
Biomedical chromatography : BMC, 23(1), 101-106 (2008-10-01)
A sensitive, selective and reliable method has been developed and validated for the determination of halofantrine and its metabolite desbutylhalofantrine in rat plasma using 9,10-diphenylanthracene as an internal standard. The method is based on peroxyoxalate chemiluminescence detection of hydrogen peroxide
Jin-Ming Lin et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(1), 126-132 (2008-11-11)
The decomposition of peroxymonocarbonate (HCO(4)(-)) has been investigated by flow-injection chemiluminescence (CL) method. An ultraweak CL was observed during mixing the bicarbonate and hydrogen peroxide solution in organic cosolvent. An appropriate amount of fluorescent organic compounds, such as dichlorofluorescein (DCF)
[Synthesis of novel fluorescent 9,10-bisphenylethynylanthracene-derived pseudonucleoside and its introduction into oligonucleotides].
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Bioorganicheskaia khimiia, 25(12), 933-937 (2000-03-29)
Regression analysis of electrochemical data with expanding space grid digital simulation at spherical electrodes.
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M J Steinbeck et al.
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The extracellular production of singlet oxygen (O2(1 delta g)) by stimulated macrophages was measured using a modification of our quantitative method initially developed to measure the intracellular production of O2(1 delta g) by neutrophils (Steinbeck, M. J., Khan, A. U.
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