TetrahymanoneCAS# 17822-06-9 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 17822-06-9 | SDF | Download SDF |
PubChem ID | 101124569 | Appearance | Powder |
Formula | C30H50O | M.Wt | 426.72 |
Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | (4aR,6aR,6aR,6bR,8aS,12aS,14aR,14bR)-4,4,6a,6b,9,9,12a,14b-octamethyl-2,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydro-1H-picen-3-one | ||
SMILES | CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C | ||
Standard InChIKey | IMOCDWIUBNNKCU-KYSSMBTOSA-N | ||
Standard InChI | InChI=1S/C30H50O/c1-25(2)15-9-16-27(5)20(25)12-18-29(7)22(27)10-11-23-28(6)17-14-24(31)26(3,4)21(28)13-19-30(23,29)8/h20-23H,9-19H2,1-8H3/t20-,21-,22+,23+,27-,28-,29+,30+/m0/s1 | ||
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 | Tetrahymanone is a natural product from Bradyrhizobium japonicum. |
Structure Identification | Sci Total Environ. 2014 Feb 1;470-471:180-92Occurrence and sources of polar lipid tracers in sediments from the Shatt al-Arab River of Iraq and the northwestern Arabian Gulf.[Pubmed: 24140688 ]
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Tetrahymanone Dilution Calculator
Tetrahymanone Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.3435 mL | 11.7173 mL | 23.4346 mL | 46.8691 mL | 58.5864 mL |
5 mM | 0.4687 mL | 2.3435 mL | 4.6869 mL | 9.3738 mL | 11.7173 mL |
10 mM | 0.2343 mL | 1.1717 mL | 2.3435 mL | 4.6869 mL | 5.8586 mL |
50 mM | 0.0469 mL | 0.2343 mL | 0.4687 mL | 0.9374 mL | 1.1717 mL |
100 mM | 0.0234 mL | 0.1172 mL | 0.2343 mL | 0.4687 mL | 0.5859 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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Occurrence and sources of polar lipid tracers in sediments from the Shatt al-Arab River of Iraq and the northwestern Arabian Gulf.[Pubmed:24140688]
Sci Total Environ. 2014 Feb 1;470-471:180-92.
Shallow surface sediment samples from the southern part of the Shatt al-Arab River estuary of Iraq and the northwestern Arabian Gulf were analyzed for polar lipid compounds including n-alkanoic acids, n-alkanols, steroids and triterpenoids. The results showed that the n-alkanoic acids, methyl n-alkanoates and n-alkanols typically ranged from C12 to C32 with total concentrations of 3.2 to 108.2 mug g(-1)dwt sample, from C12 to C30 with totals of 1.1 to 18.9 mug g(-1)dwt sample, and from C14 to C32 at 1.8 to 112.6 mug g(-1)dwt sample, respectively. Steroids and triterpenoids were detected and included stenols, stanols, stenones, stanones, tetrahymanol, Tetrahymanone and extended betabeta-hopanes. The total steroid concentrations ranged from 2.8 to 78.4 mug g(-1)dwt sample, whereas the triterpenoids varied from 0.05 to 7.6 mug g(-1)dwt sample. The simple regression analysis of the results and the spatial distribution patterns of the identified organic tracers indicated that the inter-compound relationships were related mainly to their major sources. Cluster analysis and principal component analysis (PCA) of data set showed that the sampling sites are similar. These sources were allochthonous (terrestrial vegetation), autochthonous (plankton residues and bacteria in the sediments) and anthropogenic (sewage and petroleum).