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8,9-Dihydroxy-10-isobutyryloxythymol

CAS# 107109-97-7

8,9-Dihydroxy-10-isobutyryloxythymol

Catalog No. BCN7974----Order now to get a substantial discount!

Product Name & Size Price Stock
8,9-Dihydroxy-10-isobutyryloxythymol:5mg Please Inquire In Stock
8,9-Dihydroxy-10-isobutyryloxythymol:10mg Please Inquire In Stock
8,9-Dihydroxy-10-isobutyryloxythymol:20mg Please Inquire In Stock
8,9-Dihydroxy-10-isobutyryloxythymol:50mg Please Inquire In Stock

Quality Control of 8,9-Dihydroxy-10-isobutyryloxythymol

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Chemical structure

8,9-Dihydroxy-10-isobutyryloxythymol

3D structure

Chemical Properties of 8,9-Dihydroxy-10-isobutyryloxythymol

Cas No. 107109-97-7 SDF Download SDF
PubChem ID 14427472 Appearance Powder
Formula C14H20O5 M.Wt 268.31
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [2,3-dihydroxy-2-(2-hydroxy-4-methylphenyl)propyl] 2-methylpropanoate
SMILES CC1=CC(=C(C=C1)C(CO)(COC(=O)C(C)C)O)O
Standard InChIKey HGIHDUILBYERQC-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H20O5/c1-9(2)13(17)19-8-14(18,7-15)11-5-4-10(3)6-12(11)16/h4-6,9,15-16,18H,7-8H2,1-3H3
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.

Source of 8,9-Dihydroxy-10-isobutyryloxythymol

The herbs of Inula cappa

Biological Activity of 8,9-Dihydroxy-10-isobutyryloxythymol

Description1. 8,9-Dihydroxy-10-isobutyryloxythymol shows in vitro antibacterial and antifungal effects.
TargetsAntifection

8,9-Dihydroxy-10-isobutyryloxythymol Dilution Calculator

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8,9-Dihydroxy-10-isobutyryloxythymol Molarity Calculator

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Preparing Stock Solutions of 8,9-Dihydroxy-10-isobutyryloxythymol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.727 mL 18.6352 mL 37.2703 mL 74.5406 mL 93.1758 mL
5 mM 0.7454 mL 3.727 mL 7.4541 mL 14.9081 mL 18.6352 mL
10 mM 0.3727 mL 1.8635 mL 3.727 mL 7.4541 mL 9.3176 mL
50 mM 0.0745 mL 0.3727 mL 0.7454 mL 1.4908 mL 1.8635 mL
100 mM 0.0373 mL 0.1864 mL 0.3727 mL 0.7454 mL 0.9318 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 8,9-Dihydroxy-10-isobutyryloxythymol

Asterisulphoxide and asterisulphone: two new antibacterial and antifungal metabolites from the Tunisian Asteriscus maritimus (L.) Less.[Pubmed:24824823]

Nat Prod Res. 2014;28(18):1418-26.

Two new sulphur-containing metabolites, asterisulphoxide 1 and asterisulphone 2, together with six known compounds, coniferaldehyde 4, 4-hydroxy-2-methoxybenzaldehyde 3, methylcaffeate 5, isobutyrate 10-isobutyryloxy-8,9-epoxythymyle 6, 8,9-Dihydroxy-10-isobutyryloxythymol 7 and 8-hydroxy-9,14-diisobutyryloxythymol 8, were isolated from Asteriscus maritimus roots. Their structures were elucidated on the basis of spectroscopic evidence and comparison with authentic samples. Compounds 1-8 were assessed for their in vitro antibacterial activity against Pseudomonas aureofasciens, Burkholderia glathei, Bacillus pumilus and their antifungal effects against Aspergillus flavus, Aspergillus niger, Penicillium digitatum, Botrytis cinerea and Fusarium oxysporum f. sp. lycopersici, using the disc diffusion method (20 muL/disc). A remarkable inhibition zone 10-15 mm of the growth of the bacterial and fungal agents was observed. The obtained results suggest that the isolated compounds could be promising abiotic antimicrobial agents.

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