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D205001

Sigma-Aldrich

9,10-Diphenylanthracene

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
Beilstein:
1914010
EC Number:
216-105-1
MDL number:
MFCD00001253
UNSPSC Code:
12352103
PubChem Substance ID:
24893609
NACRES:
NA.23

Assay

97%

form

powder

mp

245-248 °C (lit.)

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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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 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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

D205001-5G-A:
D205001-VAR-A:
D205001-100G-A:
D205001-BULK-A:
D205001-500G-A:
D205001-500MG-A:
D205001-1G-A:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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.
M J Steinbeck et al.
The Journal of biological chemistry, 267(19), 13425-13433 (1992-07-05)
To determine if singlet oxygen (O2(1 delta g)) is produced by neutrophils (PMNs) during the process of phagocytosis, glass beads were coated with a specific chemical trap for O2(1 delta g), 9,10-diphenylanthracene (DPA). Singlet oxygen, but not other reactive oxygen
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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