EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

rubiadin 1-methyl ether
9,10-anthracenedione, 3-hydroxy-1-methoxy-2-methyl-

Supplier Sponsors

Name:3-hydroxy-1-methoxy-2-methylanthracene-9,10-dione
CAS Number: 7460-43-7Picture of molecule3D/inchi
FDA UNII: MK2IXH6AUE
Nikkaji Web:J533.633C
XlogP3-AA:2.80 (est)
Molecular Weight:268.26844000
Formula:C16 H12 O4
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
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Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 502.16 °C. @ 760.00 mm Hg (est)
Flash Point: 379.00 °F. TCC ( 193.00 °C. ) (est)
logP (o/w): 2.073 (est)
Soluble in:
 water, 5.742 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
Rubiadin-1-methyl ether 98%
BOC Sciences
For experimental / research use only.
Rubiadin-1-methyl ether >98%
Odor: characteristic
Use: Source from herbs of Paederia scandens (Lour.) Merr. Rubiadin 1-methyl ether enhance adipocyte differentiation in 3T3-L1 cells. antineoplastic
Coompo
For experimental / research use only.
Rubiadin 1-methyl Ether from Plants ≥96%
 
Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for rubiadin 1-methyl ether usage levels up to:
 not for fragrance use.
 
Recommendation for rubiadin 1-methyl ether flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :96191
National Institute of Allergy and Infectious Diseases:Data
3-hydroxy-1-methoxy-2-methylanthracene-9,10-dione
Chemidplus:0007460437
 
References:
 3-hydroxy-1-methoxy-2-methylanthracene-9,10-dione
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):96191
Pubchem (sid):135053303
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
HMDB (The Human Metabolome Database):Search
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 found in nature
 
Synonyms:
9,10-anthracenedione, 3-hydroxy-1-methoxy-2-methyl-
3-hydroxy-1-methoxy-2-methyl-9,10-anthracene dione
3-hydroxy-1-methoxy-2-methyl-anthraquinone
3-hydroxy-1-methoxy-2-methylanthra-9,10-quinone
3-hydroxy-1-methoxy-2-methylanthracene-9,10-dione
 rubiadin-1-methyl ether
 

Articles:

PubMed:[Anthraquinones from the roots of Knoxia valerianoides].
PubMed:Anthraquinones from Morinda officinalis roots enhance adipocyte differentiation in 3T3-L1 cells.
PubMed:Photodynamic activity of anthraquinones isolated from Heterophyllaea pustulata Hook f. (Rubiaceae) on MCF-7c3 breast cancer cells.
PubMed:Anthraquinones with antiplasmodial activity from the roots of Rennellia elliptica Korth. (Rubiaceae).
PubMed:Antiosteoporotic activity of anthraquinones from Morinda officinalis on osteoblasts and osteoclasts.
PubMed:Anthraquinones from the roots of Prismatomeris malayana.
PubMed:Antiosteoporotic chemical constituents from Er-Xian Decoction, a traditional Chinese herbal formula.
PubMed:[Chemical constituents from root of Prismatomeris tetrandra].
PubMed:Biological activity of Anthraquinones and Triterpenoids from Prismatomeris fragrans.
PubMed:Natural anthraquinones probed as Type I and Type II photosensitizers: singlet oxygen and superoxide anion production.
PubMed:Pharmacological and toxicological activity of Heterophyllaea pustulata anthraquinone extracts.
PubMed:Antimalarials from Stephania venosa, Prismatomeris sessiliflora, Diospyros montana and Murraya siamensis.
PubMed:Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of morinda elliptica.
PubMed:Anthraquinones from Neonauclea calycina and their inhibitory activity against DNA topoisomerase II.
PubMed:Effects of three compounds extracted from Morinda lucida on Plasmodium falciparum.
PubMed:[Anthraquinones isolated from Morinda officinalis and Damnacanthus indicus].
PubMed:[Chemical constituents of Morinda officinalis How].
 
Notes:
isolated from the stem bark and roots of morinda lucida.
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