Tetrahymanol

Tetrahymanol
Product Name Tetrahymanol
CAS No.: 2130-17-8
Catalog No.: CFN96625
Molecular Formula: C30H52O
Molecular Weight: 428.74 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: From Rhodopseudomonas palustris.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Tetrahymanol, the most likely precursor of gammacerane, occurs ubiquitously in marine sediments.
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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: service@chemfaces.com

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.
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    Geochimica Et Cosmochimica Acta, 1989, 53(11):3073-3079.
    Tetrahymanol, the most likely precursor of gammacerane, occurs ubiquitously in marine sediments[Reference: WebLink]

    METHODS AND RESULTS:
    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.
    CONCLUSIONS:
    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.
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