≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
( R )-(+)-Pulegone, a monoterpene ketone found in the essential oil of pennyroyal, can induce abortion.
Application
( R )-(+)-Pulegone may be used as a starting material to synthesize: (2 S ,4 R ,6 R ,8 S )-2,4,8-trimethyl-1,7-dioxaspiro[5.5]undecane, a spiroketal ( R )-(+)-citronellic acid, an intermediate to prepare leucine-d 3 (+)-fawcettidine, a lycopodium alkaloid
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 376388.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit .com/metlin.
| Sonrisas canónicas | CC1CCC(=C(C)C)C(=O)C1 |
|---|---|
| IUPAC Name | (5R)-5-methyl-2-propan-2-ylidenecyclohexan-1-one |
| InChIKey | NZGWDASTMWDZIW-MRVPVSSYSA-N |
| INCHI | 1S/C10H16O/c1-7(2)9-5-4-8(3)6-10(9)11/h8H,4-6H2,1-3H3/t8-/m1/s1 |
| Isómeros SMILES | C[C@@H]1CCC(=C(C)C)C(=O)C1 |
| WGK Alemania | 3 |
| RTECS | OT0261000 |
| PubChem CID | 442495 |
| Peso molecular | 152.24 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Clase | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Menthane monoterpenoids |
| Alternative Parents | Monocyclic monoterpenoids Cyclic ketones Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound |
| Descripción | This compound 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. |
| External Descriptors | Menthane monoterpenoids |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 D2403475 | Certificate of Analysis | Jan 26, 2024 | R434327 |
| D2403476 | Certificate of Analysis | Jan 26, 2024 | R434327 |
| D2403477 | Certificate of Analysis | Jan 26, 2024 | R434327 |
| D2403525 | Certificate of Analysis | Jan 26, 2024 | R434327 |
| D2403526 | Certificate of Analysis | Jan 26, 2024 | R434327 |
| D2403527 | Certificate of Analysis | Jan 26, 2024 | R434327 |
| Solubilidad | Soluble in alcohol 、ether、chloroform； insoluble in water |
|---|---|
| Índice de refracción | 1.49 |
| Rotación específica [α] | 23° (neat) |
| Punto de inflamación (°F) | 179.6 °F |
| Punto de inflamación (°C) | 82°C |
| Punto de ebullición (°C) | 224 °C |
| Peso molecular | 152.230 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 152.12 Da |
| Monoisotopic Mass | 152.12 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 197.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Huimin Liao, Jinghong Wang, Feiran Chen, Le Ya, Ningke Fan, Yinghua Shu, Zhenggao Xiao, Zhenyu Wang. (2024) Salicylic acid functionalized chitosan nanocomposite increases bioactive components and insect resistance of Agastache rugosa. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, [PMID:39477584] [10.1016/j.pestbp.2024.106131] |
