Product Information
- 3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol
- 3,7,11,15-Tetramethyl-1,6,10,14-cetene-3-ol
- 3,7,11,15-Tetramethyl-3-hydroxy-1,6,10,14-hexadecatetraene
- (6E)-3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraen-3-ol
- (6E,10E)-3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol
- (6E,10E)-3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraen-3-ol
- (E,E)-3,7,11,15-Tetramethyl-1,6,10,14-Hexadecatetraen-3-ol
- (E,E)-Geranyllinalool
- (±)-Geranyllinalool
- 1,6,10,14-Hexadecatetraen-3-ol, 3,7,11,15-tetramethyl-, (E,E)-
- See more synonyms
- 1,6,10,14-hexadecatetraen-3-ol, 3,7,11,15-tetramethyl-, (6E)-
- 1,6,10,14-hexadecatetraen-3-ol, 3,7,11,15-tetramethyl-, (6E,10E)-
- Geranyl inalool
- Geranyl linalool
- Linalool, geranyl-
Applications Geranyl Linalool is am aliphatic genaryl derivative. Geranyl Linalool unlike other genaryl derivatives showed poor inhibitory activity against carotenoid synthesis in Synechococcus. Geranyl Linalool was identified as a testosterone-dependent volatile compound in the preputial gland of rat Rattus norvegicus.
References Juettner, F. et al.: Zeitsch. Naturforsch. C J. Biosci., 38C, 387 (1983); Ponmanickam, P. et al.: Gen. Comp. Endocrinol., 167, 35 (2010):
Chemical properties
Technical inquiry about: TR-G367750 Geranyl Linalool
If you want to request a quotation or place an order, please instead add the desired products to your cart and then request a quotation or order from the cart. It is faster, cheaper, and you will be able to benefit from the available discounts and other advantages.