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74553

Supelco

Rubiadin

analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C15H10O4
Numero CAS:
117-02-2
Peso molecolare:
254.24
Colour Index:
75350
Beilstein:
1885558
Numero MDL:
MFCD02752095
Codice UNSPSC:
85151701
ID PubChem:
329764989
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥95.0% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Stringa SMILE

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
IRZTUXPRIUZXMP-UHFFFAOYSA-N

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Applicazioni

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

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H351

Classi di pericolo

Acute Tox. 4 Oral - Carc. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG0519
BCBV9117
BCCB5418
BCCB1295
BCBV6448

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Wei-Hua Huang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 33(5), 524-526 (2008-06-10)
To investigate the chemical constituents from Hedyotis diffusa. The compounds were isolated and purified by various chromatographic techniques and identified by their physicochemical properties and spectral data. Eight compounds were isolated and identified as octadecyl (E)-p-coumarate (1), p-E-methoxy-cinnamic acid (2)
Jian-shuang Jiang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 30(22), 1751-1753 (2006-02-14)
To study the chemical constituents from root of Prismatomeris tetrandra. Compounds were isolated by chromatographic techniques on silica gel column. Their structures were elucidated by chemical and spectral methods. Six compounds were identified as 1-hydroxy-2-methylanthraquinone (I), 2-hydoxy-3-methoxyanthraquinone (II), 1, 3-dihydroxy-2-methoxyanthraquione
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
Y B Tripathi et al.
Indian journal of biochemistry & biophysics, 35(5), 313-316 (1999-07-20)
The inhibition of FeSO4 induced lipid peroxidation in rat liver by alcoholic extract of Rubia cordifolia and by one of its constituent rubiadin (1, 3-dihydroxy-2-methyl anthraquinone) (pure form) has been compared. Both have been found to inhibit lipid peroxidation in
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