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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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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Andrzej Blachecki et al.
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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
Christopher Batchelor-McAuley et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(50), 19891-19895 (2011-11-24)
After 35 years the hunt for improved anthracycline antibiotics is unabated but has yet to achieve the levels of clinical success desired. Electrochemical techniques provide a large amount of kinetic and thermodynamic information, but the use of such procedures is
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Bioorganic & medicinal chemistry letters, 18(20), 5672-5675 (2008-09-19)
In eukaryotes, protein phosphorylation of serine, threonine or tyrosine residues by protein kinases plays an important role in many cellular processes. Members of the protein kinase CK1 family usually phosphorylate residues of serine that are close to other phosphoserine in
M M Fiallo et al.
Journal of inorganic biochemistry, 75(2), 105-115 (1999-08-18)
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+
X Ma et al.
Biochimica et biophysica acta, 781(1-2), 173-182 (1984-02-24)
The effect of dihydroxyanthraquinone (DHAQ), a new antitumor drug, on mammalian chromosome replication was investigated using simian virus 40 (SV40) as a model system. The maximum effect of inhibition on viral DNA synthesis was observed within 30-40 min after the
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