D205001
9,10-Diphenylanthracene
97%
Synonym(s):
Anthracene
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C26H18
CAS Number:
Molecular Weight:
330.42
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
216-105-1
Beilstein/REAXYS Number:
1914010
MDL number:
Product Name
9,10-Diphenylanthracene, 97%
InChI key
FCNCGHJSNVOIKE-UHFFFAOYSA-N
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
SMILES string
c1ccc(cc1)-c2c3ccccc3c(-c4ccccc4)c5ccccc25
assay
97%
form
powder
mp
245-248 °C (lit.)
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
- Achieving spin-triplet exciton transfer between silicon and molecular acceptors for photon upconversion.: This research demonstrates the transfer of triplet excitons from silicon to 9,10-diphenylanthracene, a key mechanism for photon upconversion technologies that could revolutionize solar energy harvesting and optoelectronic devices (Xia et al., 2020).
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Weibin Cui et al.
Chemical communications (Cambridge, England), (8)(8), 1017-1019 (2008-02-20)
The first soluble conjugated poly(2,6-anthrylene) with 9,10-diphenyl-anthracene as the repeating unit is reported; photophysical studies reveal that this polymer represents a novel well-conjugated system.
Jin-Ming Lin et al.
The journal of physical chemistry. B, 112(26), 7850-7855 (2008-06-12)
In this work, an online preparation of peroxymonocarbonate was formed innovatively, which offered the reliable intermediate for further investigation. Gold colloids with nanoparticles of different sizes were found to enhance the chemiluminescence (CL) of the peroxymonocarbonate-eosin Y system, and the
C L Catherall et al.
Journal of bioluminescence and chemiluminescence, 3(3), 147-154 (1989-07-01)
Absolute chemiluminescence quantum yields (phi CL) for reactions of bis-(pentachlorophenyl) oxalate (PCPO), hydrogen peroxide (H2O2) and 9:10 diphenyl anthracene (DPA) have been determined. A fully corrected chemiluminescence monitoring spectrometer was calibrated for spectral sensitivity using the chemiluminescence of the bis-(pentachlorophenyl)
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)
J R Lakowicz et al.
Analytical biochemistry, 160(2), 471-479 (1987-02-01)
We describe a general method to correct for contaminant fluorescence when using the technique of frequency-domain fluorometry. The method can be applied regardless of the origin of the background signal, from scattered light, impurity fluorescence, or both. The procedure requires
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service