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D146706

Sigma-Aldrich

9,10-Dimethylanthracene

99%

Sinônimo(s):

9,10-Dimethylanthracene

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About This Item

Fórmula empírica (Notação de Hill):
C16H14
Número CAS:
781-43-1
Peso molecular:
206.28
Beilstein:
1909028
Número CE:
212-308-4
Número MDL:
MFCD00001262
Código UNSPSC:
12352100
ID de substância PubChem:
24893449
NACRES:
NA.22

Nível de qualidade

100

Ensaio

99%

Formulário

crystals

pf

182-184 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

JTGMTYWYUZDRBK-UHFFFAOYSA-N

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Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Danger

Frases de perigo

H312 + H332,H317,H334

Declarações de precaução

P280 - P302 + P352 + P312

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCG7840
BCCF1277
BCCC8932
BCBX0857
BCBS5555V

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Sigma-Aldrich

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9-Phenylanthracene 98%

Sigma-Aldrich

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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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