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Linalool

Linalool
Skeletal formula
Ball-and-stick model
Names
IUPAC name
3,7-dimethylocta-1,6-dien-3-ol
Identifiers
78-70-6 YesY
126-91-0 (R) N
126-90-9 (S) N
3D model (Jmol) Interactive image
ChEBI CHEBI:17580 YesY
ChEMBL ChEMBL25306 YesY
ChemSpider 13849981 YesY
ECHA InfoCard 100.001.032
2469
PubChem 6549
443158 (R)
67179 (S)
UNII D81QY6I88E YesY
Properties
C10H18O
Molar mass 154.25 g/mol
Density 0.858 – 0.868 g/cm3
Melting point < −20 °C (−4 °F; 253 K)
Boiling point 198 to 199 °C (388 to 390 °F; 471 to 472 K)
1.589 g/l
Hazards
NFPA 704
Flammability code 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g., diesel fuel Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point 55 °C (131 °F; 328 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

Linalool (/lˈnælˌɒl, l-, -lˌɔːl, -ləˌwɒl, -ləˌwl/ or /ˌlɪnəˈll/) refers to two enantiomers of a naturally occurring terpene alcohol found in many flowers and spice plants. These have multiple commercial applications, the majority of which are based on its pleasant scent (floral, with a touch of spiciness). It has other names such as β-linalool, linalyl alcohol, linaloyl oxide, p-linalool, allo-ocimenol, and 3,7-dimethyl-1,6-octadien-3-ol.


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