Linalool
Linalool je prirodni terpenski alkohol koji je prisutan u mnogim cvetajućim i začinskim biljkama. On ima mnoštvo komercijalnih primena, većina kojih se bazira na prijatnom mirisu. Njegova druga imena su: β-linalool, linalil alkohol, linaloil oksid, p-linalool, alo-ocimenol, i 2,6-dimetil-2,7-oktadien-6-ol.

Priroda

Preko 200 biljnih vrsta proizvodi linalool. One su uglavnom iz porodica -{Lamiaceae}- (menta, mirišljave trave), -{Lauraceae}- (lavor, cimet, palisandrovo drvo), i -{Rutaceae}- (citrusno voće).

Enantiomeri
Linalool ima stereogeni centar na -{C}-3 i stoga postoje dva stereoizomera: (-{R}-)-(–)-linalool je takođe poznat kao likareol i (-{S}-)-(+)-linalool ili koriandrol.

Literatura
-{
 Casabianca H, Graff JB, Faugier V, Fleig F, Grenier C (1998) Enantiomeric distribution studies of linalool and linalyl acetate. A powerful tool for authenticity control of essential oils. HRC J High Res Chrom 21:107-112
 Lewinshon E, Schalechet F, Wilkinson J, Matsui K,  Tadmor Y, Nam K,  Amar O, Lastochkin E, Larkov O, Ravid U, Hiatt W, Gepstein S, Pichersky E (2001) Enhanced levels of the aroma and flavor compound S-linalool by metabolic engineering of the terpenoid pathway in tomato fruits. Plant Physiol 127:1256–1265
 Pengelly, Andrew.  The Constituents of Medicinal Plants. 2nd Ed.  2004. CABI Publishing, U.S.A. and UK.
 Raguso RA, Pichersky E (1999) A day in the life of a linalool molecule: chemical communication in a plant-pollinator system. Part 1: linalool biosynthesis in flowering plants.  Plant Species Biol 14:95-120
 Akio Nakamura, Satoshi Fujiwara, Ichiro Matsumoto and Keiko Abe. Stress Repression in Restrained Rats by (R)-(−)-Linalool Inhalation and Gene Expression Profiling of Their Whole Blood Cells. J. Agric. Food Chem., 2009, 57 (12), pp 5480–5485.
}-

Reference

Vidi još 
 Lavanda
 -{Zanthoxylum simulans}-

Spoljašnje veze 

 -{Comprehensive data sheet}-
 

Укуси
Алкохоли
Инсектицидни биљни токсини
Алкени
Монотерпени
Linalool je prirodni terpenski alkohol koji je prisutan u mnogim cvetajućim i začinskim biljkama . On ima mnoštvo komercijalnih primena , većina kojih se bazira na prijatnom mirisu . Njegova druga imena su : β-linalool , linalil alkohol , linaloil oksid , p-linalool , alo-ocimenol , i6-dimetil-2,7-oktadien-6-ol . Priroda Prekobiljnih vrsta proizvodi linalool . One su uglavnom iz porodica -{ Lamiaceae }- ( menta , mirišljave trave ) , -{ Lauraceae }- ( lavor , cimet , palisandrovo drvo ) , i -{ Rutaceae }- ( citrusno voće ) . Enantiomeri Linalool ima stereogeni centar na -{ C } -3 i stoga postoje dva stereoizomera : ( -{ R }-) -( – ) -linalool je takođe poznat kao likareol i ( -{ S }- ) -( + ) -linalool ili koriandrol. Literatura - { Casabianca H , Graff JB , Faugier V , Fleig F , Grenier CEnantiomeric distribution studies of linalool and linalyl acetate . A powerful tool for authenticity control of essential oils . HRC J High Res Chrom107-112 Lewinshon E , Schalechet F , Wilkinson J , Matsui K , Tadmor Y , Nam K , Amar O , Lastochkin E , Larkov O , Ravid U , Hiatt W , Gepstein S , Pichersky EEnhanced levels of the aroma and flavor compound S-linalool by metabolic engineering of the terpenoid pathway in tomato fruits . Plant Physiol1256–1265 Pengelly , Andrew . The Constituents of Medicinal Plants.d Ed . CABI Publishing , U.S.A. and UK . Raguso RA , Pichersky EA day in the life of a linalool molecule : chemical communication in a plant-pollinator system . Part linalool biosynthesis in flowering plants . Plant Species Biol95-120 Akio Nakamura , Satoshi Fujiwara , Ichiro Matsumoto and Keiko Abe . Stress Repression in Restrained Rats by ( R) -( − ) -Linalool Inhalation and Gene Expression Profiling of Their Whole Blood Cells . J. Agric . Food Chem .,( 12 ) , pp5485 . }- Reference Vidi još Lavanda -{ Zanthoxylum simulans }- Spoljašnje veze -{ Comprehensive data sheet }- Укуси Алкохоли Инсектицидни биљни токсини Алкени Монотерпени