Q906
Quinizarin
96%
Synonym(s):
1,4-Dihydroxyanthraquinone
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About This Item
Empirical Formula (Hill Notation):
C14H8O4
CAS Number:
Molecular Weight:
240.21
Beilstein:
1914036
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23
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Recommended Products
vapor density
8.3 (vs air)
vapor pressure
1 mmHg ( 196.7 °C)
Assay
96%
mp
198-199 °C (lit.)
SMILES string
Oc1ccc(O)c2C(=O)c3ccccc3C(=O)c12
InChI
1S/C14H8O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,15-16H
InChI key
GUEIZVNYDFNHJU-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 2
Flash Point(F)
431.6 °F
Flash Point(C)
222 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Titanium dioxide nanocomposites were synthesized in hierarchical architectures through the use of a 1,4-dihydroxyanthraquinone photosensitizer. In the first step, the dye was either incorporated into the TiO
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The interaction of Fe3+ with several anthracycline antitumour antibiotics has been reinvestigated. Absorption and circular dichroism (CD) measurements were carried out (i) in aqueous solution and (ii) in semi-aqueous MeOH to avoid the stacking of the anthracycline molecules. The Fe3+
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Anthracene (AC) is a non-mutagenic and non-carcinogenic, low-molecular-weight polycyclic aromatic hydrocarbon present in the environment. Its toxicity can be dramatically increased after solar-light exposure. Biotransformation capacities of AC by Tetrahymena pyriformis and a selection of eight micromycetes were studied, and
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