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Merck
Todas as fotos(2)

Documentos

74553

Supelco

Rubiadin

analytical standard

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C15H10O4
Número CAS:
Peso molecular:
254.24
Número do índice de cores:
75350
Beilstein:
1885558
Número MDL:
Código UNSPSC:
85151701
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

Ensaio

≥95.0% (HPLC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

food and beverages

formato

neat

cadeia de caracteres 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

chave InChI

IRZTUXPRIUZXMP-UHFFFAOYSA-N

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Aplicação

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

Pictogramas

Health hazardExclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Acute Tox. 4 Oral - Carc. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Visite a Biblioteca de Documentos

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
L R Comini et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 18(12), 1093-1095 (2011-06-15)
Searching for agents that could be effective in the treatment of cancer, special highlight has focused on the study of numerous plant-derived compounds. We previously demonstrated that anthraquinones (AQs) isolated from a vegetal species: Heterophyllaea pustulata Hook f. (Rubiaceae), such
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)
Susana C Núñez Montoya et al.
Toxicon : official journal of the International Society on Toxinology, 51(8), 1409-1415 (2008-06-03)
Heterophyllaea pustulata (Rubiaceae), a South American genus, is a phototoxic shrub that grows in the Andean mountain range of the northwest of Argentina, popularly known as "cegadera". Animals that ingest the aerial parts of this plant suffer a typical primary

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