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Sigma-Aldrich

Oeninchlorid

≥90% (HPLC)

Synonym(e):

Cyclaminchlorid, Malvidin-3-β-D-glucopyranosid, Malvidin-3-O-glucosidchlorid

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About This Item

Empirische Formel (Hill-System):
C23H25ClO12
CAS-Nummer:
7228-78-6
Molekulargewicht:
528.89
EG-Nummer:
230-631-9
MDL-Nummer:
MFCD00185576
UNSPSC-Code:
12352200
PubChem Substanz-ID:
57652436
NACRES:
NA.25

Assay

≥90% (HPLC)

Form

powder

Anwendung(en)

metabolomics
vitamins, nutraceuticals, and natural products

SMILES String

[Cl-].COc1cc(cc(OC)c1O)-c2[o+]c3cc(O)cc(O)c3cc2O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O

InChI

1S/C23H24O12.ClH/c1-31-14-3-9(4-15(32-2)18(14)27)22-16(7-11-12(26)5-10(25)6-13(11)33-22)34-23-21(30)20(29)19(28)17(8-24)35-23;/h3-7,17,19-21,23-24,28-30H,8H2,1-2H3,(H2-,25,26,27);1H/t17-,19-,20+,21-,23-;/m1./s1

InChIKey

YDIKCZBMBPOGFT-DIONPBRTSA-N

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Allgemeine Beschreibung

Oenin chloride/malvidin-3-O-glucoside is an anthocyanin content, present at high level in Vitis vinifera young red wines. It helps in defining the colour of wine.

Biochem./physiol. Wirkung

Anthocyanin. Studied for its neuroprotective properties.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Delphinidin-3-glucosidchlorid phyproof® Reference Substance

PHL89627

Delphinidin-3-glucosidchlorid

Keracyaninchlorid analytical standard

Supelco

36428

Keracyaninchlorid

Peonidin-3-O-glucosidchlorid analytical standard

Supelco

42008

Peonidin-3-O-glucosidchlorid

Alessandra Maestro et al.
Cardiovascular research, 85(1), 175-183 (2009-08-27)
Ingestion of flavonoid-rich beverages acutely affects endothelial function, causing vasodilation. This effect might be dependent on flavonoid transport into the endothelium. We investigated flavonoid uptake into vascular endothelial cells and whether this was mediated by bilitranslocase (TC 2.A.65.1.1), a bilirubin-specific
M S Dopico-García et al.
Talanta, 75(5), 1190-1202 (2008-07-01)
Phenolic profile of 10 different varieties of red "Vinho Verde" grapes (Azal Tinto, Borraçal, Brancelho, Doçal, Espadeiro, Padeiro de Basto, Pedral, Rabo de ovelha, Verdelho and Vinhão), from Minho (Portugal) were studied. Nine Flavonols, four phenolic acids, three flavan-3-ols, one
Nour-Eddine Es-Safi et al.
Journal of agricultural and food chemistry, 56(12), 4584-4591 (2008-05-24)
Two new colorless phenolic compounds were formed from malvidin 3- O-glucoside incubated in an ethanolic solution. Their structures were characterized by means of one- and two-dimensional NMR analysis and through electrospray ionization-mass spectrometry. As compared to the structure of the
Petros Kneknopoulos et al.
Journal of agricultural and food chemistry, 59(3), 1005-1011 (2011-01-11)
Anthocyanins and their related compounds were extracted from grape skins of Pinot noir, using 50% aqueous methanol, and purified by solid phase extraction chromatography using XAD-7 resin to obtain a pigment-rich fraction. This fraction was subjected to multilayer coil countercurrent
Stefanos Koundouras et al.
Journal of agricultural and food chemistry, 57(17), 7805-7813 (2009-09-03)
Compositional changes of skin and seed phenolic compounds and berry glycosylated aroma precursors were measured in Vitis vinifera L. cv. Cabernet Sauvignon onto 1103P and SO4 rootstocks, in three irrigation regimes (FI, 100% of evapotranspiration; DI, 50% of evapotranspiration; and
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