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D146706

Sigma-Aldrich

9,10-Dimethylanthracene

99%

Synonym(s):

9,10-Dimethylanthracene

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About This Item

Empirical Formula (Hill Notation):
C16H14
CAS Number:
Molecular Weight:
206.28
Beilstein:
1909028
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

crystals

mp

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

InChI key

JTGMTYWYUZDRBK-UHFFFAOYSA-N

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Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M Fernandez et al.
Mutation research, 298(1), 31-41 (1992-11-01)
We evaluated the influence of near-ultraviolet light (UVA) on the cytotoxicity and genotoxicity of 7 polycyclic aromatic hydrocarbons (PAH) in larvae of the amphibian Pleurodeles waltl. Benz[a]anthracene (BA), 7,12-benz[a]anthraquinone (BAQ) and anthracene (Ac) proved to be lethal at low doses
M Roslaniec et al.
Journal of photochemistry and photobiology. B, Biology, 57(2-3), 149-158 (2001-01-12)
The spectroscopy and photophysics of several hypericin and helianthrone derivatives were studied in methanol and when bound to liposomes. The singlet oxygen quantum yields (phi(delta)) were measured indirectly relative to Rose Bengal and hematoporphyrin IX, employing 9,10-dimethylanthracene as a singlet
R K Saini et al.
Drug and chemical toxicology, 31(4), 459-471 (2008-10-14)
A single intratracheal instillation of 9,10-dimethyl benz(a)anthracene (DMBA) at 3 different doses of 5, 10, and 20 mg/kg body weight to Balb/c mice for 12 weeks had caused a significant incidence of pulmonary tumors along with inflammatory changes. The number
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)
Shimshon Ben Dror et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 8(3), 354-361 (2009-03-04)
In this work we investigate the localization and photophysical properties of twelve synthetically derived chlorins in artificial membranes, with the goal of designing more effective photosensitizers for photodynamic therapy (PDT). The studied chlorins incorporate substituents of varying lipophilicity at the

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