Geraniol
IUPAC name	3,7-Dimethylocta-2,6-dien-1-ol
Identifiers
CAS number	106-24-1 Y
EC number	203-377-1
SMILES	CC(C)=CCC/C(C)=C/CO
Properties
Molecular formula	C10H18O
Molar mass	154.25 g/mol
Density	0.889 g/cm3
Melting point	15 °C
Boiling point	229 °C
Solubility in water	Insoluble
Y (what is this?)  (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Geraniol is a monoterpenoid and an alcohol. It is the primary part of rose oil, palmarosa oil, and citronella oil (Java type). It also occurs in small quantities in geranium, lemon, and many other essential oils. It appears as a clear to pale-yellow oil which is insoluble in water, but soluble in most common organic solvents. It has a rose-like odor and is commonly used in perfumes. It is used in flavors such as peach, raspberry, grapefruit, red apple, plum, lime, orange, lemon, watermelon, pineapple and blueberry.

Contents 1 Use 2 Biochemistry 3 Reactions 4 Health and safety 5 Related compounds 6 References 7 External links

[edit] Use

Research has shown geraniol to be an effective plant-based mosquito repellent.^[1][2] On the other hand, it can attract bees as it is produced by the scent glands of honey bees to help them mark nectar-bearing flowers and locate the entrances to their hives.

Although geraniol and other flavor compounds are found naturally in well aged tobacco, geraniol is listed in a 1994 report from cigarette companies as one of the 599 additives to cigarettes to improve their flavor.^[3]

[edit] Biochemistry

The functional group based on geraniol (essentially geraniol lacking the terminal -OH) is called geranyl. It is important in biosynthesis of other terpenes. It is a by product of the metabolism of sorbate and thus is a very unpleasant contaminant of wine if bacteria are allowed to grow in wine.

[edit] Reactions

In acidic solutions, geraniol is converted to the cyclic terpene alpha-terpineol.

[edit] Health and safety

Geraniol should be avoided by people with perfume allergy.^[4]

[edit] Related compounds

• Citral, the corresponding aldehyde
• Nerol, the double bond isomer
• Rhodinol, a related terpene alcohol
• Geranyl pyrophosphate
• Geranylgeranyl pyrophosphate

[edit] References

[edit] External links

• Extensive page containing Geraniol properties, animations, links