Ethyl beta-D-fructofuranosideCAS# 1820-84-4 |
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| Cas No. | 1820-84-4 | SDF | Download SDF |
| PubChem ID | 11769694 | Appearance | Powder |
| Formula | C8H16O6 | M.Wt | 208.2 |
| Type of Compound | Saccharides | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (2R,3S,4S,5R)-2-ethoxy-2,5-bis(hydroxymethyl)oxolane-3,4-diol | ||
| SMILES | CCOC1(C(C(C(O1)CO)O)O)CO | ||
| Standard InChIKey | KQQFKZUGBOQKLW-OOJXKGFFSA-N | ||
| Standard InChI | InChI=1S/C8H16O6/c1-2-13-8(4-10)7(12)6(11)5(3-9)14-8/h5-7,9-12H,2-4H2,1H3/t5-,6-,7+,8-/m1/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. |
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| 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. |
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| 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. | ||
| Description | 1. Ethyl beta-D-fructofuranoside shows positive anti-tumor cells migration effects. |
Ethyl beta-D-fructofuranoside Dilution Calculator
Ethyl beta-D-fructofuranoside Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.8031 mL | 24.0154 mL | 48.0307 mL | 96.0615 mL | 120.0768 mL |
| 5 mM | 0.9606 mL | 4.8031 mL | 9.6061 mL | 19.2123 mL | 24.0154 mL |
| 10 mM | 0.4803 mL | 2.4015 mL | 4.8031 mL | 9.6061 mL | 12.0077 mL |
| 50 mM | 0.0961 mL | 0.4803 mL | 0.9606 mL | 1.9212 mL | 2.4015 mL |
| 100 mM | 0.048 mL | 0.2402 mL | 0.4803 mL | 0.9606 mL | 1.2008 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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Purification of fructooligosaccharides by immobilized yeast cells and identification of ethyl beta-D-fructofuranoside as a novel glycoside formed during the process.[Pubmed:23186684]
Bioresour Technol. 2013 Mar;132:365-9.
A yeast strain (XS1) capable of selective utilization of fructooligosaccharides (FOSs) syrup was identified as Wickerhamomyces anomala. Cells of W. anomala XS1 were immobilized in calcium alginate and incubated with an FOS mixture at 30 degrees C. The purity of the FOS increased from 54.4% to 80.1% (w/w) as 93.6% of monosaccharides were metabolized while the oligosaccharides were not affected. The immobilized yeast cells could be recycled 10 times and the corresponding batch treatments achieved FOS purities around 80%. Thus, the method could be promising for large-scale purification of FOS syrup at low cost. A byproduct formed by the yeast was identified as Ethyl beta-D-fructofuranoside by MS and NMR spectroscopy.
Fructose-derived carbohydrates from Alisma orientalis.[Pubmed:19521916]
Nat Prod Res. 2009;23(11):1013-20.
Nine fructose-derived carbohydrates were obtained from the methanol extract from the rhizome of Alisma orientalis. On the basis of spectroscopic analysis, their structures were determined to be alpha-D-fructofuranose (1), beta-D-fructofuranose (2), ethyl alpha-D-fructofuranoside (3), Ethyl beta-D-fructofuranoside (4), 5-hydroxymethyl-furaldehyde (5), sucrose (6), raffinose (7), stachyose (8) and verbascose (9), along with two oligosaccharides of manninotriose (10) and verbascotetraose (11). Compounds 3, 4 and 7-11 were isolated from this plant for the first time. A hypothetical biosynthesis pathway among these isolated carbohydrates (1-11) was briefly introduced.
Use of the yeast Hansenula polymorpha (Pichia angusta) to remove contaminating sugars from ethyl beta-D-fructofuranoside produced during sucrose ethanolysis catalysed by invertase.[Pubmed:16232429]
J Biosci Bioeng. 1999;87(1):82-6.
Alkyl glycosides are interesting intermediates for the production of biodegradable surfactants. Synthesis of Ethyl beta-D-fructofuranoside by invertase-catalysed ethanolysis of sucrose has been extensively reported in literature. However, this procedure yields mixtures of glucose, fructose, sucrose and Ethyl beta-D-fructofuranoside. Purification of Ethyl beta-D-fructofuranoside from such mixtures by chromatographic methods is laborious, difficult to scale up and requires organic solvents. The yeast Hansenula polymorpha grows rapidly on glucose, fructose and sucrose. Sucrose hydrolysis in this yeast is catalysed by an intracellular alpha-glucosidase ('maltase'); consequently, H. polymorpha should be unable to hydrolyse Ethyl beta-D-fructofuranoside. Indeed, aerobic cultivation of H. polymorpha on sugar mixtures obtained by invertase-catalysed ethanolysis of sucrose resulted in the complete removal of contaminating sugars, leaving Ethyl beta-D-fructofuranoside as the sole organic compound in culture supernatants. Pure Ethyl beta-D-fructofuranoside was recovered from the supernatants by mixed-bed ion exchange chromatography with an 86% yield.
