45788
9,10-Diphenylanthracene
analytical standard
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About This Item
Fórmula empírica (Notação de Hill):
C26H18
Número CAS:
Peso molecular:
330.42
Beilstein:
1914010
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24
Produtos recomendados
grau
analytical standard
Nível de qualidade
prazo de validade
limited shelf life, expiry date on the label
técnica(s)
HPLC: suitable
gas chromatography (GC): suitable
pf
245-248 °C (lit.)
aplicação(ões)
environmental
formato
neat
cadeia de caracteres SMILES
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
chave InChI
FCNCGHJSNVOIKE-UHFFFAOYSA-N
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Descrição geral
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).
Aplicação
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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Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
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].
A D Malakhov et al.
Bioorganicheskaia khimiia, 25(12), 933-937 (2000-03-29)
Regression analysis of electrochemical data with expanding space grid digital simulation at spherical electrodes.
J V Arena et al.
Analytical chemistry, 58(7), 1481-1488 (1986-06-01)
M J Steinbeck et al.
The Journal of biological chemistry, 268(21), 15649-15654 (1993-07-25)
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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