Dehydro-δ-tocopherolCAS# 802909-72-4 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 802909-72-4 | SDF | Download SDF |
| PubChem ID | 15839186 | Appearance | Oil |
| Formula | C27H44O2 | M.Wt | 400.65 |
| Type of Compound | Phenols | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 2,8-dimethyl-2-(4,8,12-trimethyltridecyl)chromen-6-ol | ||
| SMILES | CC1=C2C(=CC(=C1)O)C=CC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C | ||
| Standard InChIKey | FEGYJQTVMVOWKC-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C27H44O2/c1-20(2)10-7-11-21(3)12-8-13-22(4)14-9-16-27(6)17-15-24-19-25(28)18-23(5)26(24)29-27/h15,17-22,28H,7-14,16H2,1-6H3 | ||
| 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. Dehydro-δ-tocopherol shows antioxidant capacities. |
Dehydro-δ-tocopherol Dilution Calculator
Dehydro-δ-tocopherol Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.4959 mL | 12.4797 mL | 24.9594 mL | 49.9189 mL | 62.3986 mL |
| 5 mM | 0.4992 mL | 2.4959 mL | 4.9919 mL | 9.9838 mL | 12.4797 mL |
| 10 mM | 0.2496 mL | 1.248 mL | 2.4959 mL | 4.9919 mL | 6.2399 mL |
| 50 mM | 0.0499 mL | 0.2496 mL | 0.4992 mL | 0.9984 mL | 1.248 mL |
| 100 mM | 0.025 mL | 0.1248 mL | 0.2496 mL | 0.4992 mL | 0.624 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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Antioxidant dehydrotocopherols as a new chemical character of Stemona species.[Pubmed:15464160]
Phytochemistry. 2004 Oct;65(19):2719-29.
From the roots of various Stemona species four new dehydrotocopherols (chromenols) were isolated and their structures and stereochemistry elucidated by spectroscopic methods. The double bond between C-3 and C-4 proved to be a typical chemical character of the genus found in most of the species. Various C-methylations of the aromatic ring reflect differences in methyltransferase activities and agreed with the current species delimitations showing an exclusive accumulation of dehydro-delta-tocopherol for the Stemona tuberosa group, whereas different provenances of Stemona curtisii were characterized by dehydro-gamma-tocopherol accompanied by small amounts of dehydro-alpha-tocopherol. From Stemona collinsae all four tocopherols were isolated with a clear preponderance of dehydro-delta-tocopherol accompanied by smaller amounts of the rare dehydro-beta-tocopherol. Stemona burkillii and a group of unidentified species showed a weak accumulation trend towards dehydro-alpha-tocopherol, whereas Stemona cochinchinensis and especially Stemona kerrii clearly differed by a preponderance of chromanol derivatives. In Stemona cf. pierrei no tocopherols could be detected at all. Based on TLC tests and microplate assays with the free radical 2,2-diphenyl-1-picrylhydrazyl (DPPH*) the antioxidant capacities of all chromenol derivatives were comparable with that of alpha-tocopherol showing no significant differences among each other, except for a more rapid kinetic behaviour of the 5,7,8-methylated dehydro-alpha-tocopherol.
