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Canolol

CAS# 28343-22-8

Canolol

Catalog No. BCC8371----Order now to get a substantial discount!

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Quality Control of Canolol

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Chemical structure

Canolol

3D structure

Chemical Properties of Canolol

Cas No. 28343-22-8 SDF Download SDF
PubChem ID 35960 Appearance Powder
Formula C10H12O3 M.Wt 180
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 4-ethenyl-2,6-dimethoxyphenol
SMILES COC1=CC(=CC(=C1O)OC)C=C
Standard InChIKey QHJGZUSJKGVMTF-UHFFFAOYSA-N
Standard InChI InChI=1S/C10H12O3/c1-4-7-5-8(12-2)10(11)9(6-7)13-3/h4-6,11H,1H2,2-3H3
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.

Canolol Dilution Calculator

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Canolol Molarity Calculator

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Preparing Stock Solutions of Canolol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.5556 mL 27.7778 mL 55.5556 mL 111.1111 mL 138.8889 mL
5 mM 1.1111 mL 5.5556 mL 11.1111 mL 22.2222 mL 27.7778 mL
10 mM 0.5556 mL 2.7778 mL 5.5556 mL 11.1111 mL 13.8889 mL
50 mM 0.1111 mL 0.5556 mL 1.1111 mL 2.2222 mL 2.7778 mL
100 mM 0.0556 mL 0.2778 mL 0.5556 mL 1.1111 mL 1.3889 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 Canolol

INHIBITORY MECHANISM AGAINST OXIDATIVE STRESS AND BIOLOGICAL ACTIVITIES OF CANOLOL.[Pubmed:29474758]

Acta Pol Pharm. 2017 Jan;74(1):25-29.

Canolol is a decarboxylated derivative of sinapic acid. Due to lipophilic nature, Canolol is an excellent orally bioavailable phenol. It mainly occurs in roasted rapeseeds. It is documented in the literature as a potent antioxidant and safe for human health. The mode of antioxidant activity of Canolol involves the suppression of various free radicals such as 02, ONOO and 'OOH. As evident from the literature, few studies have been carried out to explore the free radical scavenging activity of Canolol. Thus, the objective of this review article is to summarize the available literature about free radical scavenging potential of this promising phenol to pave the path for further investigations about biological activities of Canolol.

A Two-Step Bioconversion Process for Canolol Production from Rapeseed Meal Combining an Aspergillus niger Feruloyl Esterase and the Fungus Neolentinus lepideus.[Pubmed:29036919]

Microorganisms. 2017 Oct 14;5(4). pii: microorganisms5040067.

Rapeseed meal is a cheap and abundant raw material, particularly rich in phenolic compounds of biotechnological interest. In this study, we developed a two-step bioconversion process of naturally occurring sinapic acid (4-hydroxy-3,5-dimethoxycinnamic acid) from rapeseed meal into Canolol by combining the complementary potentialities of two filamentous fungi, the micromycete Aspergillus niger and the basidiomycete Neolentinus lepideus. Canolol could display numerous industrial applications because of its high antioxidant, antimutagenic and anticarcinogenic properties. In the first step of the process, the use of the enzyme feruloyl esterase type-A (named AnFaeA) produced with the recombinant strain A. niger BRFM451 made it possible to release free sinapic acid from the raw meal by hydrolysing the conjugated forms of sinapic acid in the meal (mainly sinapine and glucopyranosyl sinapate). An amount of 39 nkat AnFaeA per gram of raw meal, at 55 degrees C and pH 5, led to the recovery of 6.6 to 7.4 mg of free sinapic acid per gram raw meal, which corresponded to a global hydrolysis yield of 68 to 76% and a 100% hydrolysis of sinapine. Then, the XAD2 adsorbent (a styrene and divinylbenzene copolymer resin), used at pH 4, enabled the efficient recovery of the released sinapic acid, and its concentration after elution with ethanol. In the second step, 3-day-old submerged cultures of the strain N. lepideus BRFM15 were supplied with the recovered sinapic acid as the substrate of bioconversion into Canolol by a non-oxidative decarboxylation pathway. Canolol production reached 1.3 g/L with a molar yield of bioconversion of 80% and a productivity of 100 mg/L day. The same XAD2 resin, when used at pH 7, allowed the recovery and purification of Canolol from the culture broth of N. lepideus. The two-step process used mild conditions compatible with green chemistry.

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