≥85%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488187457 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488187457 |
| Sonrisas canónicas | CC1=CCC(CC1)C(C)(C)OC(=O)C |
| IUPAC Name | 2-(4-methylcyclohex-3-en-1-yl)propan-2-yl acetate |
| InChIKey | IGODOXYLBBXFDW-UHFFFAOYSA-N |
| INCHI | 1S/C12H20O2/c1-9-5-7-11(8-6-9)12(3,4)14-10(2)13/h5,11H,6-8H2,1-4H3 |
| Isómeros SMILES | CC1=CCC(CC1)C(C)(C)OC(=O)C |
| RTECS | OT0200000 |
| PubChem CID | 111037 |
| Peso molecular | 196.29 |
| Beilstein | 6(4)252 |
| Reaxy-Rn | 3198769 |
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 Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | P-menthane monoterpenoid - Monocyclic monoterpenoid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 H2205327 | Certificate of Analysis | May 18, 2026 | T162412 |
| H2205329 | Certificate of Analysis | May 18, 2026 | T162412 |
| H2205330 | Certificate of Analysis | May 18, 2026 | T162412 |
| D2122039 | Certificate of Analysis | Feb 07, 2025 | T162412 |
| I2504627 | Certificate of Analysis | Jul 10, 2024 | T162412 |
| I2504628 | Certificate of Analysis | Jul 10, 2024 | T162412 |
| E23081237 | Certificate of Analysis | Jan 10, 2023 | T162412 |
| E23081238 | Certificate of Analysis | Jan 10, 2023 | T162412 |
| E23081242 | Certificate of Analysis | Jan 10, 2023 | T162412 |
| E23081254 | Certificate of Analysis | Jan 10, 2023 | T162412 |
| E23081330 | Certificate of Analysis | Jan 10, 2023 | T162412 |
| Índice de refracción | 1.47 |
|---|---|
| Punto de inflamación (°F) | 115°C(lit.) |
| Punto de inflamación (°C) | 115°C(lit.) |
| Punto de ebullición (°C) | 94°C/4mmHg(lit.) |
| Peso molecular | 196.290 g/mol |
| XLogP3 | 2.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 196.146 Da |
| Monoisotopic Mass | 196.146 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 251.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Zhong-Lei Meng, Ru-Si Wen, Xiao-Rui Huang, Rong-Xiu Qin, Yi-Ming Hu, Yong-Hong Zhou. (2022) Synthesis of Terpineol from Alpha-Pinene Catalyzed by α-Hydroxy Acids. MOLECULES, 27 (3): (1126). [PMID:35164391] [10.3390/molecules27031126] |
| 2. Xiya Feng, Hongwei Wang, Zhirong Wang, Pimiao Huang, Jianquan Kan. (2021) Discrimination and characterization of the volatile organic compounds in eight kinds of huajiao with geographical indication of China using electronic nose, HS-GC-IMS and HS-SPME-GC–MS. FOOD CHEMISTRY, [PMID:34865919] [10.1016/j.foodchem.2021.131671] |
