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Anthraflavic acid - technical grade, 90%, high purity , CAS No.84-60-6

  • technical grade
  • ≥90%
Item Number
A477097
Grouped product items
SKUSizeAvailabilityPrice Qty
A477097-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$209.90

Basic Description

Synonyms2,6-Dihydroxyanthraquinone|Anthraflavic acid|84-60-6|2,6-dihydroxyanthracene-9,10-dione|Anthraflavin|9,10-Anthracenedione, 2,6-dihydroxy-|2,6-Dihydroxyanthra-9,10-quinone|Az-F|NSC-33531|2,6-dihydroxy-9,10-anthraquinone|2,6-DIHYDROXY-ANTHRAQUINONE|2,6-dihy
Specifications & Puritytechnical grade, ≥90%
Gradetechnical grade
Product Description

Description

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.

Associated Targets

ESR1 Tclin Estrogen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ESR2 Tclin Estrogen receptor beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT2B15 Tbio UDP-glucuronosyltransferase 2B15 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A4 Tbio UDP-glucuronosyltransferase 1-4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAOB Tclin Amine oxidase [flavin-containing] B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A3 Tbio UDP-glucuronosyltransferase 1-3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT2A1 Tbio UDP-glucuronosyltransferase 2A1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 2,6-dihydroxyanthracene-9,10-dione
INCHI InChI=1S/C14H8O4/c15-7-1-3-9-11(5-7)14(18)10-4-2-8(16)6-12(10)13(9)17/h1-6,15-16H
InChi Key APAJFZPFBHMFQR-UHFFFAOYSA-N
Canonical SMILES C1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C=C(C=C3)O
Isomeric SMILES C1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C=C(C=C3)O
RTECS CB6675000
PubChem CID 6776
Molecular Weight 240.21
Beilstein 8(4)3272
Reaxy-Rn 2054127

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Chemical and Physical Properties

Melt Point(°C)330°C(lit.)

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

RTECS CB6675000
Reaxy-Rn 2054127

Related Documents

References

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2. A D Ayrton,D F Lewis,C Ioannides,R Walker.  (1987-12-18)  Anthraflavic acid is a potent and specific inhibitor of cytochrome P-448 activity..  Biochimica et biophysica acta,  916  ((3)): (328-331).  [PMID:3689794]
3. D F Liberman,R C Fink,F L Schaefer,R J Mulcahy,A A Stark.  (1982-06-01)  Mutagenicity of anthraquinone and hydroxylated anthraquinones in the Ames/Salmonella microsome system..  Applied and environmental microbiology,  43  ((6)): (1354-1359).  [PMID:7103489]
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8. María Elena Sánchez-Vergara,Juan Carlos Alonso-Huitron,Arturo Rodriguez-Gómez,Jerry N Reider-Burstin.  (2012-08-28)  Determination of the optical GAP in thin films of amorphous dilithium phthalocyanine using the Tauc and Cody models..  Molecules (Basel, Switzerland),  17  ((9)): (10000-10013).  [PMID:22922272]
9. Jie Liu,Hantang Zhang,Huanli Dong,Lingqiang Meng,Longfeng Jiang,Lang Jiang,Ying Wang,Junsheng Yu,Yanming Sun,Wenping Hu,Alan J Heeger.  (2015-12-02)  High mobility emissive organic semiconductor..  Nature communications,  (10032-10032).  [PMID:26620323]
10. Ranjith Kumar Manoharan,Jin-Hyung Lee,Yong-Guy Kim,Jintae Lee.  (2017-11-01)  Alizarin and Chrysazin Inhibit Biofilm and Hyphal Formation by.  Frontiers in cellular and infection microbiology,  (447-447).  [PMID:29085811]
11. Trang Thi Huyen Nguyen,Ramesh Prasad Pandey,Prakash Parajuli,Jang Mi Han,Hye Jin Jung,Yong Il Park,Jae Kyung Sohng.  (2018-08-30)  Microbial Synthesis of Non-Natural Anthraquinone Glucosides Displaying Superior Antiproliferative Properties..  Molecules (Basel, Switzerland),  23  ((9)):   [PMID:30154376]
12. Katarzyna Lech,Emilia Fornal.  (2020-07-19)  A Mass Spectrometry-Based Approach for Characterization of Red, Blue, and Purple Natural Dyes..  Molecules (Basel, Switzerland),  25  ((14)):   [PMID:32679693]
13. Evan Wenbo Zhao,Erlendur Jónsson,Rajesh B Jethwa,Dominic Hey,Dongxun Lyu,Adam Brookfield,Peter A A Klusener,David Collison,Clare P Grey.  (2021-01-22)  Coupled In Situ NMR and EPR Studies Reveal the Electron Transfer Rate and Electrolyte Decomposition in Redox Flow Batteries..  Journal of the American Chemical Society,  143  ((4)): (1885-1895).  [PMID:33475344]
14. H Mukhtar,M Das,W A Khan,Z Y Wang,D P Bik,D R Bickers.  (1988-05-01)  Exceptional activity of tannic acid among naturally occurring plant phenols in protecting against 7,12-dimethylbenz(a)anthracene-, benzo(a)pyrene-, 3-methylcholanthrene-, and N-methyl-N-nitrosourea-induced skin tumorigenesis in mice..  Cancer research,  48  ((9)): (2361-2365).  [PMID:3128399]
15. A D Ayrton,C Ioannides,R Walker.  (1988-11-01)  Induction of rat hepatic cytochrome P-450 I proteins by the antimutagen anthraflavic acid..  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association,  26  ((11-12)): (909-915).  [PMID:3209131]
16. A D Ayrton,C Ioannides,R Walker.  (1988-03-01)  Anthraflavic acid inhibits the mutagenicity of the food mutagen IQ: mechanism of action..  Mutation research,  207  ((3-4)): (121-125).  [PMID:3282161]
17. M Das,W A Khan,P Asokan,D R Bickers,H Mukhtar.  (1987-02-01)  Inhibition of polycyclic aromatic hydrocarbon-DNA adduct formation in epidermis and lungs of SENCAR mice by naturally occurring plant phenols..  Cancer research,  47  ((3)): (767-773).  [PMID:3802081]
18. H Matsuda,H Shimoda,T Morikawa,M Yoshikawa.  (2001-07-19)  Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): structure-requirement of hydroxyanthraquinones for estrogenic activity..  Bioorganic & medicinal chemistry letters,  11  ((14)): (1839-1842).  [PMID:11459643]

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