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229148

Sigma-Aldrich

Purpurin

Dye content 90 %

Sinônimo(s):

1,2,4-Trihydroxyanthraquinone, Hydroxylizaric acid, Verantin

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About This Item

Fórmula empírica (Notação de Hill):
C14H8O5
Número CAS:
Peso molecular:
256.21
Número do índice de cores:
58205
Beilstein:
1887127
Número CE:
Número MDL:
Código UNSPSC:
12171500
ID de substância PubChem:
NACRES:
NA.47

Ensaio

>70-85% (HPLC)

forma

powder

composição

Dye content, 90%

Impurezas

1-3% DMF

pf

253-256 °C (lit.)

solubilidade

NH4OH: 1 mg/mL, clear to turbid

λmax

515 nm
521 nm (2nd)

aplicação(ões)

diagnostic assay manufacturing
hematology
histology

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

Oc1cc(O)c2C(=O)c3ccccc3C(=O)c2c1O

InChI

1S/C14H8O5/c15-8-5-9(16)14(19)11-10(8)12(17)6-3-1-2-4-7(6)13(11)18/h1-5,15-16,19H

chave InChI

BBNQQADTFFCFGB-UHFFFAOYSA-N

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Descrição geral

Purpurin (1, 2, 4-trihydroxyanthraquinone) is the key pigment present in the roots of Indian madder (Rubia cordifolia). This pigment produces colors, with distinctive heat and light resistant properties.

Aplicação

Nuclear stain in histology

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Optimization of microwave-assisted extraction for alizarin and purpurin in Rubiaceae plants and its comparison with conventional extraction methods.
Dabiri M
Journal of Separation Science, 28, 387-396 (2005)
Dyeing studies with hydroxyanthraquinones extracted from Indian madder. Part 1: Dyeing of nylon with purpurin
Gupta D
Coloration Technology (2001)
H Melhus et al.
Experimental cell research, 197(1), 119-124 (1991-11-01)
To establish a suitable experimental system for studies of the interaction of retinol-binding protein (RBP) with transthyretin (TTR) we have expressed the corresponding cDNAs in HeLa cells. To investigate whether complex formation might occur already in the endoplasmic reticulum (ER)
E Takahashi et al.
Mutation research, 480-481, 139-145 (2001-08-17)
We have previously demonstrated the inhibitory effect of chlorophyllin, a green food additive, on the genotoxicities of various carcinogens in Drosophila. Recently, we reported that purpurin, a component of a red food additive produced from madder root (Rubia tinctorium), inhibits
Eizo Takahashi et al.
Mutation research, 508(1-2), 147-156 (2002-10-16)
Recently we have shown that anthraquinone food pigments such as purpurin and alizarin suppress the genotoxic activities of several mutagens including heterocyclic amines and polycyclic aromatic hydrocarbons in the Drosophila DNA repair test and in the Ames test. To investigate

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