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D146706

Sigma-Aldrich

9,10-Dimethylanthracene

99%

Sinonimo/i:

9,10-Dimethylanthracene

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About This Item

Formula empirica (notazione di Hill):
C16H14
Numero CAS:
781-43-1
Peso molecolare:
206.28
Beilstein:
1909028
Numero CE:
212-308-4
Numero MDL:
MFCD00001262
Codice UNSPSC:
12352100
ID PubChem:
24893449
NACRES:
NA.22

Saggio

99%

Forma fisica

crystals

Punto di fusione

182-184 °C (lit.)

Stringa SMILE

Cc1c2ccccc2c(C)c3ccccc13

InChI

1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3
JTGMTYWYUZDRBK-UHFFFAOYSA-N

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Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H312 + H332,H317,H334

Consigli di prudenza

P280 - P302 + P352 + P312

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Resp. Sens. 1 - Skin Sens. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG7840
BCCF1277
BCCC8932
BCBX0857
BCBS5555V

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9,10-Diphenylanthracene for synthesis

Sigma-Aldrich

8.20529

9,10-Diphenylanthracene

Rubrene powder

Sigma-Aldrich

R2206

Rubrene

9,10-Bis(phenylethynyl)anthracene 97%

Sigma-Aldrich

264199

9,10-Bis(phenylethynyl)anthracene

9-Phenylanthracene 98%

Sigma-Aldrich

P18004

9-Phenylanthracene

9,10-Diphenylanthracene analytical standard

Supelco

45788

9,10-Diphenylanthracene

Alan Sholto et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(3), 344-351 (2008-04-05)
Six amphiphilic silicon phthalocyanines (SiPc's) axially linked to a dimethylated amino alkyl group of varying length have been examined for their potential suitability as photosensitizers for photodynamic therapy (PDT). This group of molecules was chosen because the length of the
David Bailey et al.
Chemical communications (Cambridge, England), (20)(20), 2569-2571 (2005-05-19)
Irradiating 2,3,6,7-tetraphenylanthracene in the presence of 9,10-dimethylanthracene leads to exclusive formation of the cross-dimer. No photochemical reaction is observed when either of these chromophores is irradiated in the absence of the other.
E Gross et al.
Photochemistry and photobiology, 57(5), 808-813 (1993-05-01)
Two new sensitizers are introduced for a potential use in photodynamic therapy: Zn(2+)- and MG(2+)-tetrabenzoporphyrin (ZnTBP and MgTBP). A comparative study of the quantum yields of singlet oxygen generation (phi delta) of hematoporphyrin derivative (HpD), Photofrin II (PF-II), Zn(2+)-phthalocyanine tetrahydroxyl
E W Vogel et al.
Mutation research, 250(1-2), 291-298 (1991-09-01)
A set of six Drosophila strains was developed, by inducing by chemical treatment with N-ethyl-N-nitrosourea (ENU) new white and, in some strains, yellow mutations in 3 wild-type (WT) and 3 insecticide-resistant (IR) populations. These strains were previously shown to vary
M Elisa Milanesio et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(9), 926-933 (2003-10-17)
A novel 5-[4-(trimethylammonium)phenyl]-10,15,20-tris(2,4,6-trimethoxyphenyl)porphyrin iodide (2) has been synthesized. A positive charge was incorporated at a peripheral position to increase the amphiphilic character of the structure. The photodynamic effect of the cationic porphyrin 2 was compared with that of non-charged 5-(4-aminophenyl)-10,15,20-tris(2,4,6-trimethoxyphenyl)porphyrin
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