| Weight | 410.73 g/mol |
|---|---|
| Formula | C30H50 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 15 |
squalene
7683-64-9, 111-02-4, 11051-27-7
Score:
#301 in Biochemistry
,
#1110 in Biology
,
#1251 in Chemistry
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- Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squalene (Journal of the American Chemical Society, 1970)
- ENZYMATIC CYCLIZATION OF SQUALENE AND OXIDOSQUALENE TO STEROLS AND TRITERPENES (Chemical Reviews, 1993)
- Phenolic compounds and squalene in olive oils: the concentration and antioxidant potential of total phenols, simple phenols, secoiridoids, lignansand squalene (Food and Chemical Toxicology, 2000)
- Structure and function of a squalene cyclase. (Science, 1997)
- Allylamine derivatives: new class of synthetic antifungal agents inhibiting fungal squalene epoxidase (Science, 1984)
- Fatty acid profile, tocopherol, squalene and phytosterol content of walnuts, almonds, peanuts, hazelnuts and the macadamia nut. (International Journal of Food Sciences and Nutrition, 2004)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C
-
InChIKeyYYGNTYWPHWGJRM-UHFFFAOYSA-N
- Pubchem - squalene
- Wikipedia - squalene
Squalene is a natural 30-carbon organic compound originally obtained for commercial purposes primarily from shark liver oil (hence its name, as Squalus is a genus of sharks), although plant sources (primarily vegetable oils) are now used as well, including amaranth seed, rice bran, wheat germ, and olives. Yeast cells have been genetically engineered to produce commercially useful quantities of "synthetic" squalene. All plants and animals produce squalene as a biochemical intermediate, including humans.
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squalene
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