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1,2-Disinapoylglucose

CAS# 91095-79-3

1,2-Disinapoylglucose

Catalog No. BCX0985----Order now to get a substantial discount!

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Quality Control of 1,2-Disinapoylglucose

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Chemical structure

1,2-Disinapoylglucose

Chemical Properties of 1,2-Disinapoylglucose

Cas No. 91095-79-3 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C28H32O14 M.Wt 592.55
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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.

1,2-Disinapoylglucose Dilution Calculator

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1,2-Disinapoylglucose Molarity Calculator

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Preparing Stock Solutions of 1,2-Disinapoylglucose

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.6876 mL 8.4381 mL 16.8762 mL 33.7524 mL 42.1905 mL
5 mM 0.3375 mL 1.6876 mL 3.3752 mL 6.7505 mL 8.4381 mL
10 mM 0.1688 mL 0.8438 mL 1.6876 mL 3.3752 mL 4.2191 mL
50 mM 0.0338 mL 0.1688 mL 0.3375 mL 0.675 mL 0.8438 mL
100 mM 0.0169 mL 0.0844 mL 0.1688 mL 0.3375 mL 0.4219 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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References on 1,2-Disinapoylglucose

Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules.[Pubmed:28239412]

Biotechnol Biofuels. 2017 Feb 17;10:40.

BACKGROUND: Monolignol-like molecules can be integrated into lignin along with conventional monolignol units, and it has been shown that the incorporation of non-canonical subunits can be used to generate hydrolysable lignin by introduction of ester linkages into the polymer and that this type of lignin is more easily removable. Disinapoyl esters (DSEs), which to some degree resemble the monolignol sinapyl alcohol, may be promising lignin modifying units for this purpose. As a first step toward determining whether this goal is achievable, we manipulated metabolic flux in Arabidopsis to increase the amounts of DSEs by overexpressing sinapoylglucose:sinapoylglucose sinapoyltransferase (SST) which produces two main DSEs, 1,2-Disinapoylglucose, and another compound we identify in this report as 3,4-disinapoyl-fructopyranose. RESULTS: We succeeded in overproducing DSEs by introducing an SST-overexpression construct into the sinapoylglucose accumulator1 (sng1-6) mutant (SST-OE sng1-6) which lacks several of the enzymes that would otherwise compete for the SST substrate, sinapoyglucose. Introduction of cinnamyl alcohol dehydrogenase-c (cad-c) and cad-d mutations into the SST-OE sng1-6 line further increased DSEs. Surprisingly, a reduced epidermal fluorescence (ref) phenotype was observed when SST-OE sng1-6 plants were evaluated under UV light, which appears to have been induced by the sequestration of DSEs into subvacuolar compartments. Although we successfully upregulated the accumulation of the target DSEs, we did not find any evidence showing the integration of DSEs into the cell wall. CONCLUSIONS: Our results suggest that although phenylpropanoid metabolic engineering is possible, a deeper understanding of sequestration and transport mechanisms will be necessary for successful lignin engineering through this route.

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