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Merck

D205001

9,10-Diphenylanthracene

97%

Synonym(s):

Anthracene

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CZK 1,920.00

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About This Item

Empirical Formula (Hill Notation):
C26H18
CAS Number:
1499-10-1
Molecular Weight:
330.42
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
24893609
EC Number:
216-105-1
Beilstein/REAXYS Number:
1914010
MDL number:
MFCD00001253

Key Documents

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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

100

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Show Differences

1 of 4

This Item
457888.205298.20109
9,10-Diphenylanthracene 97%

Sigma-Aldrich

D205001

9,10-Diphenylanthracene

9,10-Diphenylanthracene analytical standard

Supelco

45788

9,10-Diphenylanthracene

9,10-Diphenylanthracene for synthesis

Sigma-Aldrich

8.20529

9,10-Diphenylanthracene

Anthracene for synthesis

Sigma-Aldrich

8.20109

Anthracene

assay

97%

assay

-

assay

≥98.0% (HPLC)

assay

≥98.5% (GC)

form

powder

form

-

form

powder

form

solid

mp

245-248 °C (lit.)

mp

245-248 °C (lit.)

mp

247-252 °C

mp

213-217 °C

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

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)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK8674
STBK3211
STBJ8616
STBJ5682
STBH9409

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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)
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
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.
[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)
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