![]() Quinizarin structure
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Common Name | Quinizarin | ||
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CAS Number | 81-64-1 | Molecular Weight | 240.211 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 465.3±40.0 °C at 760 mmHg | |
Molecular Formula | C14H8O4 | Melting Point | 198-199 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 249.3±23.8 °C | |
Symbol |
![]() GHS09 |
Signal Word | Warning |
Use of QuinizarinQuinizarin (1,4-Dihydroxyanthraquinone), a part of the anticancer agents such as Doxorubicin, Daunorubicin, and Adriamycin, interacts with DNA by intercalating mode (Kd=86.1 μM). Quinizarin is used as a fungicide and pesticide chemical and has shown the ability to inhibit tumor cell growth[1][2]. |
Name | quinizarin |
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Synonym | More Synonyms |
Description | Quinizarin (1,4-Dihydroxyanthraquinone), a part of the anticancer agents such as Doxorubicin, Daunorubicin, and Adriamycin, interacts with DNA by intercalating mode (Kd=86.1 μM). Quinizarin is used as a fungicide and pesticide chemical and has shown the ability to inhibit tumor cell growth[1][2]. |
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Related Catalog | |
In Vitro | 1,4-Dihydroxyanthraquinone (1,4-DHAQ, a fluorophore) doped cellulose (CL) (denoted as 1,4-DHAQ@CL) microporous nanofiber film has been achieved via simple electrospinning and subsequent deacetylating, and used for highly sensitive and selective fluorescence detection of Cu(2+) in aqueous solution[1]. |
References |
[2]. Dominic Cheuk, et al. Investigation into solid and solution properties of quinizarin. |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 465.3±40.0 °C at 760 mmHg |
Melting Point | 198-199 °C(lit.) |
Molecular Formula | C14H8O4 |
Molecular Weight | 240.211 |
Flash Point | 249.3±23.8 °C |
Exact Mass | 240.042252 |
PSA | 74.60000 |
LogP | 4.47 |
Vapour density | 8.3 (vs air) |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.733 |
Water Solubility | <1 g/L (20 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
![]() GHS09 |
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Signal Word | Warning |
Hazard Statements | H410 |
Precautionary Statements | P273-P501 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
Hazard Codes | Xi |
Risk Phrases | R36/37/38 |
Safety Phrases | S22-S24/25 |
RIDADR | UN 3077 9 / PGIII |
WGK Germany | 2 |
RTECS | CB6600000 |
Packaging Group | II; III |
Hazard Class | 4.1 |
HS Code | 2914610000 |
Precursor 9 | |
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DownStream 9 | |
HS Code | 2914610000 |
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Summary | 2914610000 anthracene-9,10-dione。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。Lowest tariff:5.5%。General tariff:30.0% |
In vitro inhibition of Streptococcus mutans biofilm formation on hydroxyapatite by subinhibitory concentrations of anthraquinones.
Antimicrob. Agents Chemother. 51 , 1541-4, (2007) We report that certain anthraquinones (AQs) reduce Streptococcus mutans biofilm formation on hydroxyapatite at concentrations below the MIC. Although AQs are known to generate reactive oxygen species,... |
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Synthesis and activity of substituted anthraquinones against a human filarial parasite, Brugia malayi.
J. Med. Chem. 48 , 2822-30, (2005) Lymphatic filariasis (elephantiasis) is a global public health problem caused by the parasitic nematodes Wuchereria bancrofti and Brugia malayi. We have previously reported anthraquinones from daylily... |
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Synthesis of glycoside derivatives of hydroxyanthraquinone with ability to dissolve and inhibit formation of crystals of calcium oxalate. Potential compounds in kidney stone therapy.
Eur. J. Med. Chem. 45 , 1001-7, (2010) Synthesis of glycosyl derivatives of hydroxyanthraquinones (6-10) potentially useful for kidney stone therapy is presented. These compounds were analyzed as inhibitors of calcium oxalate crystals form... |
MFCD00001209 |
EINECS 201-368-7 |
1,4-hydroxyanthraquinone |
QUINIZARINE |
DSD ACID |
smokeoranger |
1,4-Dihydroxy-9,10-anthraquinone |
Quinizarin |
Chinizarin |
1,4-Dihydroxy-9,10-anthracene-dione |
1,4-Dihydroxyanthraquinone |
9,10-Anthracenedione, 1,4-dihydroxy- |
Quinizalin |
QUINAZARIN |
1,4-Doa |
1,4-dihydroxyanthracene-9,10-dione |
quiniazarine |