omega-hydroxyemodin
9,10-anthracenedione, 1,3,8-trihydroxy-6-(hydroxymethyl)-
Identification
| Name | omega-hydroxyemodin |
| CAS Number | 481-73-2 |
| FDA UNII | O2H2Z421AP |
| Molecular Formula | C15 H10 O6 |
| Molecular Weight | 286.23990000 |
| Nikkaji Number | J13.188A |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 672.30 °C. @ 760.00 mm Hg (est) |
| Flash Point | 706.00 °F. TCC ( 374.40 °C. ) (est) |
| logP (o/w) | 3.380 (est) |
| Soluble in | water, 95.38 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for omega-hydroxyemodin usage levels up to | not for fragrance use. |
| Recommendation for omega-hydroxyemodin flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
9,10-
anthracenedione, 1,3,8-trihydroxy-6-(hydroxymethyl)-
citreorosein
w-
hydroxyemodin
1,3,8-
trihydroxy-6-(hydroxymethyl)-9,10-anthracenedione
1,3,8-
trihydroxy-6-(hydroxymethyl)-9,10-anthraquinone
1,3,8-
trihydroxy-6-(hydroxymethyl)-9,10-dihydroanthracene-9,10-dione
1,3,8-
trihydroxy-6-(hydroxymethyl)anthracene-9,10-dione
1,3,8-
trihydroxy-6-hydroxymethyl anthraquinone
1,3,8-
trihydroxy-6-hydroxymethylanthraquinone
PubMed:
Calmodulin inhibitors from Aspergillus stromatoides.
PubMed:
Differences in pharmacokinetics and ex vivo antioxidant activity following intravenous and oral administrations of emodin to rats.
PubMed:
Characterization of emodin metabolites in Raji cells by LC-APCI-MS/MS.
PubMed:
Structural elucidation of in vitro metabolites of emodin by liquid chromatography-tandem mass spectrometry.
PubMed:
Six immunosuppressive features from an ascomycete, Zopfiella longicaudata, found in a screening study monitored by immunomodulatory activity.
PubMed:
Neuraminidase inhibitors from Reynoutria elliptica.
PubMed:
Biotransformation of the anthraquinones emodin and chrysophanol by cytochrome P450 enzymes. Bioactivation to genotoxic metabolites.
PubMed:
omega-Hydroxyemodin, a major hepatic metabolite of emodin in various animals and its mutagenic activity.
PubMed:
Studies in the biochemistry of micro-organisms: Emodic acid (4:5:7-trihydroxyanthraquinone-2-carboxylic acid) and omega-hydroxyemodin (4:5:7-trihydroxy-2-(hydroxymethyl)-anthraquinone), metabolic products of a strain of Penicillium cyclopium Westling.