|Source:||From Rhodopseudomonas palustris.|
|Biological Activity or Inhibitors:|| 1. Tetrahymanol, the most likely precursor of gammacerane, occurs ubiquitously in marine sediments.
|Solvent:||Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.|
|Storage:||Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: email@example.com
|After receiving:||The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.|
|1 mg||5 mg||10 mg||20 mg||25 mg|
|1 mM||2.3324 mL||11.6621 mL||23.3242 mL||46.6483 mL||58.3104 mL|
|5 mM||0.4665 mL||2.3324 mL||4.6648 mL||9.3297 mL||11.6621 mL|
|10 mM||0.2332 mL||1.1662 mL||2.3324 mL||4.6648 mL||5.831 mL|
|50 mM||0.0466 mL||0.2332 mL||0.4665 mL||0.933 mL||1.1662 mL|
|100 mM||0.0233 mL||0.1166 mL||0.2332 mL||0.4665 mL||0.5831 mL|
Geochimica Et Cosmochimica Acta, 1989, 53(11):3073-3079.
|Tetrahymanol, the most likely precursor of gammacerane, occurs ubiquitously in marine sediments[Reference: WebLink]|
|Tetrahymanol has been identified in several sediment samples from different depositional environments by gas chromatography-mass spectrometry and by coinjections with an authentic standard. Together with literature data this shows that Tetrahymanol is likely to be widespread, which is in accordance with the ubiquitous occurrence of its presumed diagenetic product, gammacerane, in more mature sediments and crude oils. The diagenetic conversion of Tetrahymanol to gammacerane most likely proceeds via dehydration and subsequent hydrogenation. The intermediate in this conversion, gammacer-2-ene, has been synthesized, and its presence in one sample confirmed by coinjections. The identification of Tetrahymanol in marine sediments indicates either that protozoa of the genus Tetrahymena are widely distributed or that Tetrahymanol is also a natural product of organisms other than Tetrahymena.|
Microbiology, 1990, 136(12):2551-2553.
|Tetrahymanol from the phototrophic bacterium Rhodopseudomonas palustris: First report of a gammacerane triterpene from a prokaryote[Reference: WebLink]|
|Tetrahymanol, a rare triterpene from the gammacerane series, previously detected only in a few scattered eukaryotic taxa, has been isolated for the first time from the phototrophic bacterium Rhodopseudomonas palustris. This extends the significance of geochemical markers from this series, which are abundant in marine sediments and palaeohypersaline environments.|