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Geranyl acetate information


Geranyl acetate
Skeletal formula
Ball-and-stick model
Names
Preferred IUPAC name
(2E)-3,7-Dimethylocta-2,6-dien-1-yl acetate
Other names
Geraniol acetate; Geranyl ethanoate
Identifiers
CAS Number
  • 105-87-3 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:5331 ☒N
ChemSpider
  • 1266019 checkY
ECHA InfoCard 100.003.038 Edit this at Wikidata
PubChem CID
  • 1549026
UNII
  • 3W81YG7P9R checkY
CompTox Dashboard (EPA)
  • DTXSID0020654 Edit this at Wikidata
InChI
  • InChI=1S/C12H20O2/c1-10(2)6-5-7-11(3)8-9-14-12(4)13/h6,8H,5,7,9H2,1-4H3/b11-8+ checkY
    Key: HIGQPQRQIQDZMP-DHZHZOJOSA-N checkY
  • InChI=1/C12H20O2/c1-10(2)6-5-7-11(3)8-9-14-12(4)13/h6,8H,5,7,9H2,1-4H3/b11-8+
    Key: HIGQPQRQIQDZMP-DHZHZOJOBM
SMILES
  • O=C(OC/C=C(/CC/C=C(\C)C)C)C
Properties
Chemical formula
 C12H20O2
Molar mass 196.290 g·mol−1
Density 0.916 g/cm3 at 15 °C
Melting point < 25 °C (77 °F; 298 K)
Boiling point 240 to 245 °C (464 to 473 °F; 513 to 518 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Geranyl acetate is a terpenoid. It is a colorless liquid with a pleasant floral or fruity rose aroma. It is a colorless liquid but commercial samples can appear yellowish. Geranyl acetate is insoluble in water but soluble in organic solvents. Several hundred tons are produced annually.[2]

  1. ^ Geranyl acetate, Good Scents Company
  2. ^ Sell, Charles S. (2006). "Terpenoids". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.2005181602120504.a01.pub2. ISBN 0471238961.

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including piperitone, phellandrene, citral, methyl cinnamate and geranyl acetate. The European Medicines Agency Committee on Herbal Medicinal Products...

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Odakkali

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aromatic plants. Scientists here have identified two herbs rich in geranyl acetate, giving off the smell of rope. They are found in the hills of Munnar...

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Thymus pannonicus

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isomerase. IPP and DMAPP condense to give geranyl pyrophosphate, the precursor to monoterpenes and monoterpenoids. Geranyl pyrophosphate is also converted to...

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C12H20O2

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of essential oil components, including geranial, methyl geranate, geranyl acetate, limonene, phellandrene, neral, terpinolene and geraniol. Brazil and...

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Limonene

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give the ketone-containing carvone. In nature, limonene is formed from geranyl pyrophosphate, via cyclization of a neryl carbocation or its equivalent...

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Eriocephalus africanus

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Thymus zygis

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isomerase. Geranyl pyrophosphate is the precursor to monoterpenes (and hence monoterpenoids). Elimination of the pyrophosphate group from geranyl pyrophosphate...

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Eucalyptus macarthurii

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Linalool

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linalool are referred to as linalyl, e.g. linalyl pyrophosphate, an isomer of geranyl pyrophosphate. The word linalool is based on linaloe (a type of wood) and...

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