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Key Documents

74553

Supelco

Rubiadin

analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C15H10O4
Numéro CAS:
Poids moléculaire :
254.24
Numéro C.I. (Colour Index):
75350
Numéro Beilstein :
1885558
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Pureté

≥95.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

food and beverages

Format

neat

Chaîne SMILES 

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

Clé InChI

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.

Pictogrammes

Health hazardExclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Carc. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

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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