| Identification | More | [Name]
2,6-DIHYDROXYANTHRAQUINONE | [CAS]
84-60-6 | [Synonyms]
2,6-DIHYDROXYANTHRA-9,10-QUINONE
2,6-DIHYDROXYANTHRAQUINONE
2,7 DIHYDROXYANTHRAQUINONE
ANTHRAFLAVIC ACID
10-Anthracenedione,2,6-dihydroxy-9
2,6-dihydroxy-10-anthracenedione
2,6-dihydroxy-anthraquinon
9,10-Anthracenedione, 2,6-dihydroxy-
Anthraflavin
Anthraquinone, 2,6-dihydroxy-
NSC-33531
ANTHRAFLAVIC ACID, TECH., 90%
2,6-Dihydroxyanthraquinone, tech., 94%
2,6-Dihydroxyanthraquinone, Anthraflavine
2,6-Dihydroxyanthraquinone ,94%
Anthraflaric acid
Anthrafravic acid | [EINECS(EC#)]
201-544-3 | [Molecular Formula]
C14H8O4 | [MDL Number]
MFCD00001228 | [Molecular Weight]
240.21 | [MOL File]
84-60-6.mol |
| Chemical Properties | Back Directory | [Appearance]
solid | [Melting point ]
>320 °C(lit.) | [Boiling point ]
342.92°C (rough estimate) | [density ]
1.3032 (rough estimate) | [refractive index ]
1.5430 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Soluble in DMSO | [form ]
powder to crystal | [pka]
6.72±0.20(Predicted) | [color ]
Light yellow to Brown to Dark green | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [InChIKey]
APAJFZPFBHMFQR-UHFFFAOYSA-N | [LogP]
3.360 (est) | [CAS DataBase Reference]
84-60-6(CAS DataBase Reference) | [EPA Substance Registry System]
9,10-Anthracenedione, 2,6-dihydroxy- (84-60-6) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
S36/37:Wear suitable protective clothing and gloves . | [WGK Germany ]
3
| [RTECS ]
CB6675000
| [Hazard Note ]
Irritant | [HS Code ]
29146990 |
| Hazard Information | Back Directory | [Chemical Properties]
solid | [Uses]
Anthraflavic acid can be used as a starting material to synthesize tetrahydroxy tetrathiafulvalene (TTF) derivatives, which are used as redox-active building blocks in supramolecular and materials science. It is also utilized to prepare phosphanylidene anthra[2,1-b]furans by reacting with dialkyl acetylenedicarboxylates and triphenylphosphine. | [Definition]
ChEBI: A dihydroxyanthraquinone that is anthracene substituted by hydroxy groups at C-3 and C-7 and oxo groups at C-9 and C-10. | [storage]
Store at -20°C |
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