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Dokumente

D146706

Sigma-Aldrich

9,10-Dimethyl-anthracen

99%

Synonym(e):

9,10-Dimethylanthracene

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About This Item

Empirische Formel (Hill-System):
C16H14
CAS-Nummer:
781-43-1
Molekulargewicht:
206.28
Beilstein:
1909028
EG-Nummer:
212-308-4
MDL-Nummer:
MFCD00001262
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24893449
NACRES:
NA.22

Assay

99%

Form

crystals

mp (Schmelzpunkt)

182-184 °C (lit.)

SMILES String

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

InChIKey

JTGMTYWYUZDRBK-UHFFFAOYSA-N

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Verwandte Kategorien

Piktogramme

Health hazardExclamation mark
GHS08,GHS07

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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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
M A Spanó et al.
Mutagenesis, 16(5), 385-394 (2001-08-17)
The wing somatic mutation and recombination test (SMART) using Drosophila melanogaster was employed to determine the recombinagenic and mutagenic activity of four chemicals in an in vivo eukaryotic system. Two different crosses involving the wing cell markers mwh and flr(3)
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
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
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