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Merck
CN

Q906

醌茜

96%

别名:

1,4-二羟基蒽醌

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关于此项目

经验公式(希尔记法):
C14H8O4
化学文摘社编号:
分子量:
240.21
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
201-368-7
Beilstein/REAXYS Number:
1914036
MDL number:
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产品名称

醌茜, 96%

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

SMILES string

Oc1ccc(O)c2C(=O)c3ccccc3C(=O)c12

vapor density

8.3 (vs air)

vapor pressure

1 mmHg ( 196.7 °C)

assay

96%

mp

198-199 °C (lit.)

pictograms

Environment

signalword

Warning

hcodes

pcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

存储类别

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

431.6 °F

flash_point_c

222 °C

ppe

Eyeshields, Faceshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

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Andrzej Blachecki et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(13), 1798-1810 (2017-04-28)
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
P Guiraud et al.
Ecotoxicology and environmental safety, 69(2), 296-305 (2007-01-30)
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
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+
N J Hao et al.
Mutation research, 328(2), 183-191 (1995-05-01)
The antimutagenicity of 17 natural and synthetic anthraquinones was determined using Salmonella typhimurium TA98 against 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) in the presence of Aroclor 1254-induced rat hepatic S9. In general, the relationship between the chemical structures of anthraquinones and their antimutagenicity was
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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