≥98%(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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
3-Methyl-3-buten-1-ol is a volatile aliphatic alcohol found in the extracts of basil and thyme leaves, immature mangaba fruits and some honey samples.
| Pubchem Sid | 488181761 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181761 |
| Sonrisas canónicas | CC(=C)CCO |
| IUPAC Name | 3-methylbut-3-en-1-ol |
| InChIKey | CPJRRXSHAYUTGL-UHFFFAOYSA-N |
| INCHI | 1S/C5H10O/c1-5(2)3-4-6/h6H,1,3-4H2,2H3 |
| Isómeros SMILES | CC(=C)CCO |
| WGK Alemania | 1 |
| RTECS | EM9473100 |
| Número ONU | 1987 |
| Grupo de embalaje | III |
| Peso molecular | 86.13 |
| Beilstein | 1071240 |
| Reaxy-Rn | 1071239 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1071239&ln= |
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 | Organic oxygen compounds |
| Clase | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Primary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hydrocarbon derivative - Primary alcohol - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl). |
| External Descriptors | Fatty alcohols |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F1819100 | Certificate of Analysis | Jan 27, 2026 | M158231 |
| G2101287 | Certificate of Analysis | Apr 02, 2025 | M158231 |
| G2101288 | Certificate of Analysis | Apr 02, 2025 | M158231 |
| K2525498 | Certificate of Analysis | Jul 20, 2024 | M158231 |
| K2525499 | Certificate of Analysis | Jul 20, 2024 | M158231 |
| K2210332 | Certificate of Analysis | Nov 01, 2022 | M158231 |
| K2210333 | Certificate of Analysis | Nov 01, 2022 | M158231 |
| K2210334 | Certificate of Analysis | Nov 01, 2022 | M158231 |
| K2210335 | Certificate of Analysis | Nov 01, 2022 | M158231 |
| K2210336 | Certificate of Analysis | Nov 01, 2022 | M158231 |
| L2417145 | Certificate of Analysis | Nov 01, 2022 | M158231 |
| D2320225 | Certificate of Analysis | Jul 06, 2021 | M158231 |
| D2320226 | Certificate of Analysis | Jul 06, 2021 | M158231 |
| G2101286 | Certificate of Analysis | Jul 06, 2021 | M158231 |
| Índice de refracción | 1.433 |
|---|---|
| Punto de inflamación (°F) | 107.6 °F |
| Punto de inflamación (°C) | 42°C |
| Punto de ebullición (°C) | 130-132 °C |
| Peso molecular | 86.130 g/mol |
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 86.0732 Da |
| Monoisotopic Mass | 86.0732 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 47.900 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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. Cong Qiu, Yang Liu, Yangbao Wu, Linguo Zhao, Jianjun Pei. (2021) Biochemical Characterization of a Novel Prenyltransferase from Streptomyces sp. NT11 and Development of a Recombinant Strain for the Production of 6-Prenylnaringenin. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:34793146] [10.1021/acs.jafc.1c06094] |
| 2. Li Guangjian, Liang Hui, Gao Ruichen, Qin Ling, Xu Pei, Huang Mingtao, Zong Min-Hua, Cao Yufei, Lou Wen-Yong. (2024) Yeast metabolism adaptation for efficient terpenoids synthesis via isopentenol utilization. Nature Communications, 15 (1): (1-12). [PMID:39537637] [10.1038/s41467-024-54298-8] |
| 3. Shuxing Zhou, Chunlin Li, Li Li, Feng Xie, Karyne M. Rogers, Yuwei Yuan, Jun Huang. (2025) Differentiating volatile compounds in soy sauce that regulate the attractiveness of flesh flies (Parasarcophaga dux). FOOD CHEMISTRY, [PMID:41027210] [10.1016/j.foodchem.2025.146504] |
| 4. Kefa Hu, Zhipeng Qi, Xiaode Huang, Lei Wang, Xiaomeng Zhang, Shaoheng Tang. (2026) De novo biosynthesis of lavandulol and lavandulyl acetate in Escherichia coli. JOURNAL OF BIOTECHNOLOGY, [PMID:41619942] [10.1016/j.jbiotec.2026.01.014] |
| 5. Guangjian Li, Pan Li, Zhiyao Wang, Jiayan Lyu, Mei Li, Pengsheng Yang, Jingwen Zhou, Yufei Cao, Wen-Yong Lou. (2026) Rewiring prenyl donor supply for orthogonal synthesis of prenylated compounds in yeast. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2026.173977] |
