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A8906

Sigma-Aldrich

Apigenin 7-O-neohesperidoside

Sinonimo/i:

Rhoifolin, Rhoifoloside

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About This Item

Formula empirica (notazione di Hill):
C27H30O14
Numero CAS:
17306-46-6
Peso molecolare:
578.52
Numero CE:
241-335-4
Numero MDL:
MFCD00016773
Codice UNSPSC:
12352201
ID PubChem:
24891380
NACRES:
NA.25

Stato

solid

Stringa SMILE

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2Oc3cc(O)c4C(=O)C=C(Oc4c3)c5ccc(O)cc5)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C27H30O14/c1-10-20(32)22(34)24(36)26(37-10)41-25-23(35)21(33)18(9-28)40-27(25)38-13-6-14(30)19-15(31)8-16(39-17(19)7-13)11-2-4-12(29)5-3-11/h2-8,10,18,20-30,32-36H,9H2,1H3/t10-,18+,20-,21+,22+,23-,24+,25+,26-,27+/m0/s1
RPMNUQRUHXIGHK-PYXJVEIZSA-N

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Applicazioni

Apigenin 7-O-neohesperidoside is a flavonoid found in plants such as Paeonia suffruticosa and Buddleja albiflora. Apigenin 7-O-neohesperidoside is useful as a reference compound in procedures for the separation and detection of flavonoids.

Altre note

To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.

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

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
023H0743

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Li-Juan Chen et al.
Journal of chromatography. A, 988(1), 95-105 (2003-03-22)
Four flavonoids, chrysin, baicalein, baicalein-7-O-glucoside, baicalein-7-O-diglucoside (Oroxylin B) and one unknown flavonoid have been isolated and purified for the first time in the seeds of Oroxylum indicum by high-speed counter-current chromatography with a two-phase solvent system composed of chloroform-methanol-water (8:10:5
Ye Tian et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 34(11), 1377-1380 (2009-09-24)
To screen effective constituents of Discocleidion rufescens against bacteria. Compounds were isolated by bioassay-guided fractionation method with various chromatographic methods and their structures were determined by spectral analysis and chemical evidence. Seven compounds were isolated from the Et2O and n-BuOH
Xiao Wang et al.
Journal of chromatography. A, 1075(1-2), 127-131 (2005-06-25)
Four flavonoids, apigenin-7-O-neohesperidoside, luteolin-7-O-glucoside, apigenin-7-O-glucoside and kaempferol-7-O-glucoside have been isolated and purified for the first time from the flowers of Paeonia suffruticosa by high-speed counter-current chromatography with a two-phase solvent system composed of ethyl acetate-ethanol-acetic acid-water (4:1:0.25:5, v/v). Then, 5
K Ishii et al.
Journal of chromatography. B, Biomedical applications, 655(2), 300-304 (1994-05-13)
A method for determining flavonoids in human plasma is presented for application to pharmacokinetic studies of two flavonoids, rhoifolin and daidzin. Isocratic reversed-phase high-performance liquid chromatography (HPLC) was used with genistin as an internal standard and solid-phase extraction using a
Meng-Hua Liu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 35(1), 56-61 (2012-06-28)
To investigate the impurities in naringin extracted from Citrus grandis 'Tomentosa'. High performance liquid chromatographies coupled with photodiode array and electrospray ionization mass spectrometry detectors (HPLC-PDA/ESI-MS/MS) were applied to investigate the impurities, and their structures were elucidated by spectral data

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