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Supelco

9,10-Diphenylanthracene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C26H18
CAS Number:
Molecular Weight:
330.42
Beilstein:
1914010
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Customers Also Viewed

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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