Record Information |
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Version | 1.0 |
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Creation date | 2015-10-09 22:32:03 UTC |
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Update date | 2017-01-19 02:36:33 UTC |
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FoodComEx ID | PC000706 |
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FoodDB Record | FDB014923 |
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Chemical Information |
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Name | p-Mentha-1,8-dien-7-ol |
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Description | Perillyl alcohol is a monoterpene isolated from the essential oils of lavendin, peppermint, spearmint, cherries, celery seeds, and several other plants. In animal studies it has been shown to regress pancreatic, mammary, and liver tumors, to exhibit possible application as a chemopreventative agent for colon, skin, and lung cancer, and as a chemotherapeutic agent for neuroblastoma, and prostate and colon cancer.(PMID: 9855569) [HMDB]. p-Mentha-1,8-dien-7-ol is found in many foods, some of which are caraway, ginger, german camomile, and sweet bay. |
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CAS Number | 536-59-4 |
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Structure | |
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Synonyms | Synonym | Source |
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1-Hydroxymethyl-4-isopropenyl-1-cyclohexene | ChEBI | 1-Hydroxymethyl-4-isopropenylcyclohexene | db_source | 1-Perillalcohol | ChEBI | 1,8-P-Menthadien-7-ol | HMDB | 4-(1-Methylethenyl)-1-cyclohexene-1-methanol | ChEBI | 4-(1-Methylethenyl)-1-cyclohexene-1-methanol, 9CI | db_source | 4-Isopropenyl-1-cyclohexene carbinol | ChEBI | 4-Isopropenyl-cyclohex-1-ene-1-methanol | HMDB | 4-Isopropenylcyclohex-1-en-1-ylmethanol | ChEBI | Dihydrocuminic alcohol | HMDB | Dihydrocuminyl alcohol | db_source | Dihydrocuminyl alcoholn | ChEBI | Hydrocumin alcohol | HMDB | Iso-carveol | HMDB | NSC 641066 | db_source | Para-mentha-1,8-dien-7-ol | HMDB | Perill alcohol | HMDB | Perilla alcohol | db_source | Perillic alcohol | db_source | Perillol | db_source | Perillyl alcohol | db_source |
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Chemical Formula | C10H16O |
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IUPAC name | [4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol |
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InChI Identifier | InChI=1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,10-11H,1,4-7H2,2H3 |
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InChI Key | NDTYTMIUWGWIMO-UHFFFAOYSA-N |
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Isomeric SMILES | CC(=C)C1CCC(CO)=CC1 |
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Average Molecular Weight | 152.237 |
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Monoisotopic Molecular Weight | 152.120115135 |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. |
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Kingdom | Organic compounds |
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Super Class | Lipids and lipid-like molecules |
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Class | Prenol lipids |
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Sub Class | Monoterpenoids |
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Direct Parent | Menthane monoterpenoids |
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Alternative Parents | |
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Substituents | - P-menthane monoterpenoid
- Monocyclic monoterpenoid
- Organic oxygen compound
- Hydrocarbon derivative
- Primary alcohol
- Organooxygen compound
- Alcohol
- Aliphatic homomonocyclic compound
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Molecular Framework | Aliphatic homomonocyclic compounds |
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External Descriptors | |
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Physico-Chemical Properties - Experimental |
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Property | Value | Reference |
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Experimental logP | Not Available | |
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Experimental Water Solubility | Not Available | |
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Melting Point | Not Available | |
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Foods of Origin |
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Food | Content Range | Average | Reference |
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Food | | | Reference |
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Production Data |
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Production Method | commercial |
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Production Method Reference | Not Available |
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Production Method Reference File | Not Available |
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Quantity Available | Production upon request, up to 3 g |
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Delivery Time | Not Available |
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Storage Form | liquid |
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Storage Conditions | -80°C |
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Stability | Not Available |
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Purity | Not Available |
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Spectra |
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Spectral Data Upon Request | Not Available |
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Provider Information |
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Commercial Vendors |
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AKSci | 8575AJ |
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