D205001

9,10-Diphenylanthracene

Name: 9,10-Diphenylanthracene
Brand: ALDRICH

97%

Synonym(s):

Anthracene

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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	8.20529	8.20109	07671
Sigma-Aldrich D205001 9,10-Diphenylanthracene	Sigma-Aldrich 8.20529 9,10-Diphenylanthracene	Sigma-Aldrich 8.20109 Anthracene	Supelco 07671 Anthracene
assay 97%	assay ≥98.0% (HPLC)	assay ≥98.5% (GC)	assay -
form powder	form powder	form solid	form powder or crystals
mp 245-248 °C (lit.)	mp 247-252 °C	mp 213-217 °C	mp 210-215 °C (lit.)
Quality Level 100	Quality Level 200	Quality Level 200	Quality Level 300

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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The first soluble conjugated poly(2,6-anthrylene): synthesis and properties.

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.

Chemiluminescence from the decomposition of peroxymonocarbonate catalyzed by gold nanoparticles.

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

Determination of absolute chemiluminescence quantum yields for reactions of bis-(pentachlorophenyl) oxalate, hydrogen peroxide and fluorescent compounds.

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)

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)

[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)

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