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Merck
CN

D146706

9,10-Dimethylanthracene

99%

Synonym(s):

9,10-Dimethylanthracene

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About This Item

Empirical Formula (Hill Notation):
C16H14
CAS Number:
781-43-1
Molecular Weight:
206.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893449
EC Number:
212-308-4
Beilstein/REAXYS Number:
1909028
MDL number:
MFCD00001262

Key Documents

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Product Name

9,10-Dimethylanthracene, 99%

assay

99%

InChI key

JTGMTYWYUZDRBK-UHFFFAOYSA-N

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

SMILES string

Cc1c2ccccc2c(C)c3ccccc13

form

crystals

mp

182-184 °C (lit.)

Quality Level

100

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pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN5540
BCCK4289
BCCG7840
BCCF1277
BCCC8932

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A smart polysaccharide/drug conjugate for photodynamic therapy.
So Young Park et al.
Angewandte Chemie (International ed. in English), 50(7), 1644-1647 (2011-02-11)
Sankarasharma Devipriya et al.
Chemico-biological interactions, 162(2), 106-113 (2006-07-19)
Administration of quercetin, a common polyphenolic component of many vascular and edible plants including vegetables, fruits and tea significantly reduced the tumor volume in rats induced for mammary carcinoma using dimethyl benz (a) anthracene (DMBA). Dose response was assessed, by
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)
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
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.
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