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Cyanidin 3-O-arabinoside

CAS# 792868-19-0

Cyanidin 3-O-arabinoside

2D Structure

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Quality Control of Cyanidin 3-O-arabinoside

3D structure

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Cyanidin 3-O-arabinoside

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Chemical Properties of Cyanidin 3-O-arabinoside

Cas No. 792868-19-0 SDF Download SDF
PubChem ID 131752259 Appearance Powder
Formula C20H19O10 M.Wt 419.4
Type of Compound Anthocyanins Storage Desiccate at -20°C
Synonyms Cyanidin 3-b-L-arabinoside
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)chromenylium-5,7-diol
SMILES C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(O4)CO)O)O)O)O)O)O
Standard InChIKey SBBFXSBQYRSIPP-GNBUJSLZSA-O
Standard InChI InChI=1S/C20H18O10/c21-7-16-17(26)18(27)20(30-16)29-15-6-10-12(24)4-9(22)5-14(10)28-19(15)8-1-2-11(23)13(25)3-8/h1-6,16-18,20-21,26-27H,7H2,(H3-,22,23,24,25)/p+1/t16-,17-,18+,20-/m0/s1
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Cyanidin 3-O-arabinoside Dilution Calculator

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Cyanidin 3-O-arabinoside Molarity Calculator

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Preparing Stock Solutions of Cyanidin 3-O-arabinoside

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.3844 mL 11.9218 mL 23.8436 mL 47.6872 mL 59.609 mL
5 mM 0.4769 mL 2.3844 mL 4.7687 mL 9.5374 mL 11.9218 mL
10 mM 0.2384 mL 1.1922 mL 2.3844 mL 4.7687 mL 5.9609 mL
50 mM 0.0477 mL 0.2384 mL 0.4769 mL 0.9537 mL 1.1922 mL
100 mM 0.0238 mL 0.1192 mL 0.2384 mL 0.4769 mL 0.5961 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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Background on Cyanidin 3-O-arabinoside

Cyanidin 3-arabinoside belongs to the class of organic compounds known as anthocyanidin-3-o-glycosides. These are phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3-position. Cyanidin 3-arabinoside is considered to be a practically insoluble (in water) and relatively neutral molecule. Cyanidin 3-arabinoside has been primarily detected in urine. Within the cell, cyanidin 3-arabinoside is primarily located in the cytoplasm. Outside of the human body, cyanidin 3-arabinoside can be found in a number of food items such as apple, gooseberry, black chokeberry, and redcurrant. This makes cyanidin 3-arabinoside a potential biomarker for the consumption of these food products.
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References on Cyanidin 3-O-arabinoside

Characterization of cyanidin- and quercetin-derived flavonoids and other phenolics in mature saskatoon fruits (Amelanchier alnifolia Nutt.).[Pubmed:17994693]

J Agric Food Chem. 2007 Dec 12;55(25):10414-24.

In order to further characterize the anthocyanins, flavonols, and other phenolics present in mature saskatoon ( Amelanchier alnifolia Nutt.) fruit, extracts were characterized using high-performance liquid chromatography, gas chromatography, and liquid chromatography-mass spectrometry. Cyanidin 3-O-galactoside, cyanidin 3-O-glucoside, Cyanidin 3-O-arabinoside, and cyanidin 3-O-xyloside were identified as the four major anthocyanins in the mature fruit. The quercetin-derived flavonols, quercetin 3-O-glucoside, quercetin 3-O-galactoside, quercetin 3-O-arabinoside, quercetin 3-O-xyloside, quercetin 3-O-arabinoglucoside, quercetin 3-O-robinobioside, and quercetin 3-O-rutinoside were also identified in mature fruit extracts. In addition, two chlorogenic acid isomers (hydroxycinnamates), 3-O-caffeoylquinic acid and 5-O-caffeoylquinic acid were detected. The total content of the anthocyanin-, flavonol-, and hydroxycinnamate-type phenolics detected in mature 'Smoky' saskatoon fruit was 140, 25, and 96 mg/100 g fresh weight, respectively. These data further our knowledge of the phenolic composition of mature saskatoon fruit, and as anthocyanins, flavonols, and hydroxycinnamates exhibit antioxidant activities, the presence and levels of these classes of phenolics will aid in the understanding of the potential health-beneficial effects of saskatoon fruits in the human diet.

Anthocyanins from black currants (Ribes nigrum L.).[Pubmed:12009991]

J Agric Food Chem. 2002 May 22;50(11):3228-31.

Fifteen anthocyanin structures are reported from an extract of black currant berries (Ribes nigrum L.). These are the 3-O-glucosides and the 3-O-rutinosides of pelargonidin, cyanidin, peonidin, delphinidin, petunidin, and malvidin, Cyanidin 3-O-arabinoside, and the 3-O-(6' '-p-coumaroylglucoside)s of cyanidin and delphinidin. The anthocyanins were characterized by means of size exclusion chromatography, high-performance liquid chromatography, UV-visible spectroscopy, and electrospray mass spectrometry. The four main pigments (the 3-O-glucosides and the 3-O-rutinosides of delphinidin and cyanidin) made up >97% of the total anthocyanin content. The minor pigments were enriched from the extract by successive partition against ethyl acetate and by gel fractionation. These chromatographic steps were successfully used to isolate the acylated anthocyanins from the ethyl acetate layer and to separate Cyanidin 3-O-arabinoside from the mixture of anthocyanins. The amounts of anthocyanin rutinosides were found to be higher than the amount of the corresponding glucosides for all detected pigments having the same aglycon moiety.

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