Direkt zum Inhalt
Merck
Alle Fotos(3)

Dokumente

D205001

Sigma-Aldrich

9,10-Diphenyl-anthracen

97%

Synonym(e):

Anthracene

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(3)

About This Item

Empirische Formel (Hill-System):
C26H18
CAS-Nummer:
1499-10-1
Molekulargewicht:
330.42
Beilstein:
1914010
EG-Nummer:
216-105-1
MDL-Nummer:
MFCD00001253
UNSPSC-Code:
12352103
PubChem Substanz-ID:
24893609
NACRES:
NA.23

Assay

97%

Form

powder

mp (Schmelzpunkt)

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

InChIKey

FCNCGHJSNVOIKE-UHFFFAOYSA-N

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Verwandte Kategorien

Anwendung


  • 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).

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

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.
Alle zugehörigen Dokumente anzeigen

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.