Oxyphyllenodiol ACAS# 363610-30-4 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
| Cas No. | 363610-30-4 | SDF | Download SDF |
| PubChem ID | N/A | Appearance | Powder |
| Formula | C14H22O3 | M.Wt | 238.36 |
| Type of Compound | Sesquiterpenoids | 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. |
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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. | ||
Oxyphyllenodiol A Dilution Calculator
Oxyphyllenodiol A Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.1953 mL | 20.9767 mL | 41.9533 mL | 83.9067 mL | 104.8834 mL |
| 5 mM | 0.8391 mL | 4.1953 mL | 8.3907 mL | 16.7813 mL | 20.9767 mL |
| 10 mM | 0.4195 mL | 2.0977 mL | 4.1953 mL | 8.3907 mL | 10.4883 mL |
| 50 mM | 0.0839 mL | 0.4195 mL | 0.8391 mL | 1.6781 mL | 2.0977 mL |
| 100 mM | 0.042 mL | 0.2098 mL | 0.4195 mL | 0.8391 mL | 1.0488 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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[Study on content of two sesquiterpenes in Alpinia oxyphylla].[Pubmed:23236757]
Zhongguo Zhong Yao Za Zhi. 2012 Sep;37(17):2589-93.
OBJECTIVE: To develop an HPLC method for determining Oxyphyllenodiol A (1) and teuhetenone A (2) contained in Alpinia oxyphylla and to compare the contents of the two components contained in medicinal materials and prepared herbal medicines in pieces sold in the market and different fractions. METHOD: HPLC and Waters sunfire C18 column (4. 6 mm x 250 mm, 5 microm) were adopted for gradient elute with the mobile phase of acetonitrile and water. The flow rate was 1.0 mL x min(-1) and the detection wavelength was 250 nm. RESULT: 1 and 2 showed a good linear relationship within the range of 0.1296 - 0.8640 microg and 0.1635 - 1.0900 microg respectively, with the average recoveries of 99.08% and 97.80%. Their content ranges were 0.0059% - 0.0149% and 0.0080% - 0.0164% in different samples. The mean value of 1 and 2 were 0.0085% and 0.0104% in the whole fruits, and 0.0137% and 0.0157% in the seeds. They were undetected in the nutshells. CONCLUSION: The method is so precise, accurate and highly reproducible that it can be used to determine the contents of Oxyphyllenodiol A and teuhetenone A in A. oxyphylla. The contents of the two components are mainly extracted from the seeds, with certain difference among different samples. There are a higher contents and no significant difference in the salted and raw seeds.
Absolute stereostructures of novel norcadinane- and trinoreudesmane-type sesquiterpenes with nitric oxide production inhibitory activity from Alpinia oxyphylla.[Pubmed:11514174]
Bioorg Med Chem Lett. 2001 Aug 20;11(16):2217-20.
Novel 14-norcadinane-type sesquiterpenes, oxyphyllenodiols A and B, and 11,12,13-trinoreudesmane-type sesquiterpenes, oxyphyllenones A and B, were isolated from the methanolic extract of kernels of Alpinia oxyphylla. The absolute stereostructures of these norsesquiterpenes were determined on the basis of physicochemical and chemical evidence. In addition, Oxyphyllenodiol A and oxyphyllenone A were found to inhibit the NO production in lipopolysaccharide-activated macrophages.
