2,6-DIHYDROXY-ANTHRAQUINONE

Modify Date: 2026-07-01 23:18:35

2,6-DIHYDROXY-ANTHRAQUINONE Structure
2,6-DIHYDROXY-ANTHRAQUINONE structure
Common Name 2,6-DIHYDROXY-ANTHRAQUINONE
CAS Number 84-60-6 Molecular Weight 240.211
Density 1.5±0.1 g/cm3 Boiling Point 442.1±35.0 °C at 760 mmHg
Molecular Formula C14H8O4 Melting Point >320 °C(lit.)
MSDS Chinese USA Flash Point 235.3±22.4 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 2,6-DIHYDROXY-ANTHRAQUINONE


Anthraflavic acid, a flavonoid, is a potent IQ mutagenicity inhibitor by virtue of its ability to inhibit both its microsomal and cytosolic activation pathways. Anthraflavic acid is a potent and specific cytochrome P-448 inhibitor activity an enzyme system closely associated with the activation of many chemical carcinogens[1].

 Names

Name anthraflavic acid
Synonym More Synonyms

 2,6-DIHYDROXY-ANTHRAQUINONE Biological Activity

Description Anthraflavic acid, a flavonoid, is a potent IQ mutagenicity inhibitor by virtue of its ability to inhibit both its microsomal and cytosolic activation pathways. Anthraflavic acid is a potent and specific cytochrome P-448 inhibitor activity an enzyme system closely associated with the activation of many chemical carcinogens[1].
Related Catalog
References

[1]. Ayrton AD, et al. Anthraflavic acid inhibits the mutagenicity of the food mutagen IQ: mechanism of action. Mutat Res. 1988 Mar-Apr;207(3-4):121-5.

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 442.1±35.0 °C at 760 mmHg
Melting Point >320 °C(lit.)
Molecular Formula C14H8O4
Molecular Weight 240.211
Flash Point 235.3±22.4 °C
Exact Mass 240.042252
PSA 74.60000
LogP 3.36
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.733
InChIKey APAJFZPFBHMFQR-UHFFFAOYSA-N
SMILES O=C1c2ccc(O)cc2C(=O)c2ccc(O)cc21
Stability Stable. Incompatible with strong oxidizing agents.

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CB6675000
CHEMICAL NAME :
Anthraquinone, 2,6-dihydroxy-
CAS REGISTRY NUMBER :
84-60-6
BEILSTEIN REFERENCE NO. :
2054127
LAST UPDATED :
199701
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C14-H8-O4
MOLECULAR WEIGHT :
240.22
WISWESSER LINE NOTATION :
L C666 BV IVJ DQ LQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
180 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value

MUTATION DATA

TYPE OF TEST :
Mutation in microorganisms
TEST SYSTEM :
Bacteria - Salmonella typhimurium
DOSE/DURATION :
100 ug/plate
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 40,203,1976

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases S26-S37/39
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS CB6675000
HS Code 2914690090

 Synthetic Route

 Customs

HS Code 2914690090
Summary 2914690090 other quinones。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

 Articles14

More Articles
Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): structure-requirement of hydroxyanthraquinones for estrogenic activity.

Bioorg. Med. Chem. Lett. 11(14) , 1839-42, (2001)

The methanolic extract from the roots of Polygonum (P.) cuspidatum was found to enhance cell proliferation at 30 or 100 microg/mL in MCF-7, an estrogen-sensitive cell line. By bioassay-guided separati...

Mutagenicity of anthraquinone and hydroxylated anthraquinones in the Ames/Salmonella microsome system.

Appl. Environ. Microbiol. 43(6) , 1354-9, (1982)

The mutagenicity of anthracene, anthraquinone, and four structurally similar compounds of each was evaluated in the Ames/Salmonella microsome assay. Anthraquinone was shown to be mutagenic for strains...

A compact optical instrument with artificial neural network for pH determination.

Sensors (Basel.) 12 , 6746-63, (2012)

The aim of this work was the determination of pH with a sensor array-based optical portable instrument. This sensor array consists of eleven membranes with selective colour changes at different pH int...

 2,6-DIHYDROXY-ANTHRAQUINONEBioassay

View more

Name: Cytotoxicity against human Raji cells assessed as cell viability at 10 molar ratio
Source: ChEMBL
Target: Raji
External Id: CHEMBL1018461
Name: Compound was tested for enhancement of proliferation of MCF-7 cell line at a concentr...
Source: ChEMBL
Target: Estrogen receptor beta
External Id: CHEMBL708330
Name: HIV Enzyme Data
Source: NIAID
Target: N/A
External Id: HIV Enzyme Data
Name: Compound was tested for enhancement of proliferation of MCF-7 cell line at a concentr...
Source: ChEMBL
Target: Estrogen receptor beta
External Id: CHEMBL708332
Name: Compound was tested for enhancement of proliferation of MCF-7 cell line at a concentr...
Source: ChEMBL
Target: Estrogen receptor beta
External Id: CHEMBL708331
Name: In vitro inhibitory activity against Plasmodium falciparum D6
Source: ChEMBL
Target: Plasmodium falciparum
External Id: CHEMBL856674
Name: Inhibition of 12-O-tetradecanoylphorbol-13-acetate induced EBV-early antigen activati...
Source: ChEMBL
Target: N/A
External Id: CHEMBL938674
Name: Ratio of Ki for inhibition of His-tagged HSD17B13 (unknown origin) using LTB3 as subs...
Source: ChEMBL
Target: N/A
External Id: CHEMBL5051774
Name: Inhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reductio...
Source: ChEMBL
Target: UDP-glucuronosyltransferase 1A1
External Id: CHEMBL3531465
Name: Inhibition of His-tagged HSD17B13 (unknown origin) using LTB3 as substrate incubated ...
Source: ChEMBL
Target: N/A
External Id: CHEMBL5051776
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 Synonyms

2,6-DIHYDROXY-ANTHRAQUINONE
2,6-Dihydroxy-9,10-anthraquinone
EINECS 201-544-3
2,6-DIHYDROXYANTHRAQUINONE
MFCD00001228
2,6-Dihydroxyanthracene-9,10-dione
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