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74553

Supelco

Rubiadin

analytical standard

Synonym(s):

1,3-Dihydroxy-2-methyl-9,10-anthracenedione, 1,3-Dihydroxy-2-methylanthraquinone

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About This Item

Empirical Formula (Hill Notation):
C15H10O4
CAS Number:
117-02-2
Molecular Weight:
254.24
Colour Index Number:
75350
Beilstein/REAXYS Number:
1885558
MDL number:
MFCD02752095
UNSPSC Code:
85151701
PubChem Substance ID:
329764989
NACRES:
NA.24

grade

analytical standard

Quality Level

100

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

SMILES string

O=C1C2=C(C=C(O)C(C)=C2O)C(C3=CC=CC=C31)=O

InChI

1S/C15H10O4/c1-7-11(16)6-10-12(13(7)17)15(19)9-5-3-2-4-8(9)14(10)18/h2-6,16-17H,1H3

InChI key

IRZTUXPRIUZXMP-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

hcodes

H302,H351

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5984
BCCH0913
BCCG0519
BCBV9117
BCCB5418

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Guntupalli M Mohana Rao et al.
Journal of ethnopharmacology, 103(3), 484-490 (2005-10-11)
The hepatoprotective effects of rubiadin, a major constituent isolated from Rubia cordifolia Linn., were evaluated against carbon tetrachloride (CCl4)-induced hepatic damage in rats. Rubiadin at a dose of 50, 100 and 200 mg/kg was administered orally once daily for 14
Kaoru Inoue et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 47(4), 752-759 (2009-01-27)
Madder color (MC) has been shown to exert carcinogenic potential in the rat kidney in association with degeneration, karyomegaly, increased cell proliferation of renal tubule cells and increased renal 8-OHdG levels. To clarify the causal relationship of components and metabolites
M Usai et al.
Natural product research, 24(7), 626-632 (2010-04-20)
The isolation, characterisation and quantification of anthraquinones, from hypogeal apparatus of Rubia peregrina L. (Wild Madder) growing wild in Sardinia (Italy) are described. The present study allowed us to perform an easy and fast HPLC analytical method for the detection
B Blömeke et al.
Mutation research, 265(2), 263-272 (1992-02-01)
Rubia tinctorum L., a medicinal plant used for the treatment of kidney and bladder stones, contains a characteristic spectrum of 9,10-anthraquinone derivatives, which are substituted in only one of the aromatic benzo rings. The majority of the anthraquinones present in
Y Kawasaki et al.
Chemical & pharmaceutical bulletin, 40(6), 1504-1509 (1992-06-01)
Twenty compounds were isolated from the roots of Rubia tinctorum which are used as a commercial source of madder color. Among these compounds, mollugin (1), 1-hydroxy-2-methylanthraquinone (2), 2-ethoxymethylanthraquinone(11), rubiadin (13), 1,3-dihydroxyanthraqunone (14), 7-hydroxy-2-methylanthraquinone (16), lucidin (17), 1-methoxymethylanthraquinone (18) and lucidin-3-O-primeveroside
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