Pulegone

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Pulegone[1]
Image:Pulegone.png
IUPAC name (R)-5-Methyl-2-(1-methylethylidine)cyclohexanone
Other names p-Menth-4(8)-en-3-one
delta-4(8)-p-menthen-3-one
Identifiers
CAS number 89-82-7
PubChem 442495
SMILES C[C@@H]1CCC(=C(C)C)C(=O)C1
Properties
Molecular formula C10H16O
Molar mass 152.23 g/mol
Appearance Colorless oil
Density 0.9346 g/cm3
Boiling point

224 °C, 497 K, 435 °F

Solubility in water Insoluble
Solubility in Ethanol
Ether
Chloroform
Miscible
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Pulegone is a naturally occurring organic compound obtained from the essential oils of a variety of plants such as Nepeta cataria (catnip), Mentha piperita, and pennyroyal.[2][3] It is classified as a monoterpene.

Pulegone is a clear colorless oily liquid and has a pleasant odor similar to pennyroyal, peppermint and camphor. It is used in flavoring agents, in perfumery, and in aromatherapy.

References

  1. Merck Index, 11th Edition, 7955.
  2. Grundschober, F. (1979) Literature review of pulegone. Perfum. Flavorist, 4, 15–17.
  3. Sullivan, J.B., Rumack, B.H., Thomas, H., Peterson, R.G. & Brysch, P. (1979) Pennyroyal oil poisoning and hepatotoxicity. J. Am. Med. Assoc., 242, 2873–2874.

External links

de:Pulegonuk:Пулегон

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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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