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PIPERITONE |
| Synonyms. Piperitone; 6-Isopropyl-3-methylcyclohex-2-enone; p-Menth-1-en-3-one; 1-Methyl-4-isopropyl-1-cyclohexen-3-one; 3-Methyl-6-(1-methylethyl)-2-cyclohexen-1-one; 3-Carvomenthenone; |
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| PRODUCT IDENTIFICATION | |
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CAS RN |
89-81-6 |
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EINECS RN |
201-942-7 |
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FORMULA |
C10H16O |
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MOLE WEIGHT |
152.23 |
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H.S CODE |
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SMILES |
C1([C@@H](CCC(=C1)C)C(C)C)=O |
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CLASSIFICATION |
Ketone, Monoterpene |
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EXTRA NOTES |
Piperitone is a natural monoterpene ketone which is a component of some essential oils. Both stereoisomers, the D-form and the L-form, are known. The D-form has a peppermint-like aroma and has been isolated from the oils of plants from the genera Cymbopogon, Andropogon, and Mentha.[1] The L-form has been isolated from Sitka spruce. wikipedia |
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| PHYSICAL AND CHEMICAL PROPERTIES | |
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PHYSICAL STATE. |
yellow liquid |
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MELTING POINT |
<25 C |
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BOILING POINT |
233 C |
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DENSITY |
0.933 |
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SOLUBILITY IN WATER |
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| SOLVENT SOLUBILITY |
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VAPOR DENSITY |
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log P(octanol-water) |
2.85 |
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VAPOR PRESSURE |
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AUTOIGNITION TEMP |
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| pK |
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REFRACTIVE INDEX |
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FLASH POINT |
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| STABILITY AND REACTIVITY | |
| STABILITY | Stable under normal conditions. |
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INCOMPATIBLE MATERIALS |
Strong oxidizing agents |
| POLYMERIZATION |
Has not been reported |
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NFPA RATINGS |
Health: 1, Flammability: 0, Reactivity: 0 |
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| EXTERNAL LINKS & GENERAL DESCRIPTION |
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USA.gov - Piperitone Wikipedia Linking - Piperitone Google Scholar Search - Piperitone U.S. National Library of Medicine - Piperitone PubChem Compound Summary - Piperitone KEGG (Kyoto Encyclopedia of Genes and Genomes) - Piperitone ChEBI (http://www.ebi.ac.uk/chebi/) - Piperitone NCBI (http://www.ncbi.nlm.nih.gov/) - Piperitone EPA - Substance Registry Services - Piperitone |
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| SALES SPECIFICATION | |
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APPEARANCE |
yellow liquid |
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ASSAY |
98% min |
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BOILING POINT |
232 ~ 233 C |
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LOSS ON DRYING |
1% max |
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| TRANSPORT & REGULATORY INFORMATION | |
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UN NO. |
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| HAZARD CLASS |
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| PACKING GROUP | |
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| PACKING |
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Preserve in light-resistant and well-closed containers |
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