≥99%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normale 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.
| Pubchem Sid | 504752288 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752288 |
| Sorrisi canonici | CC(CC=C)O |
| IUPAC Name | pent-4-en-2-ol |
| InChIKey | ZHZCYWWNFQUZOR-UHFFFAOYSA-N |
| INCHI | 1S/C5H10O/c1-3-4-5(2)6/h3,5-6H,1,4H2,2H3 |
| Isomeri SMILES | CC(CC=C)O |
| WGK Germania | 3 |
| PubChem CID | 12247 |
| Peso molecolare | 86.13 |
| Beilstein | 1839740 |
| Reaxy-Rn | 1839744 |
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 |
| Classe | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Secondary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 F2315408 | Certificate of Analysis | Jun 26, 2023 | P160534 |
| F2315416 | Certificate of Analysis | Jun 26, 2023 | P160534 |
| F2316721 | Certificate of Analysis | Jun 26, 2023 | P160534 |
| F2316728 | Certificate of Analysis | Jun 26, 2023 | P160534 |
| F2316812 | Certificate of Analysis | Jun 26, 2023 | P160534 |
| F2316841 | Certificate of Analysis | Jun 26, 2023 | P160534 |
| Indice di rifrazione | 1.42 |
|---|---|
| Punto di infiammabilità (°F) | 86 °F |
| Punto di infiammabilità (°C) | 30°C(lit.) |
| Punto di ebollizione (°C) | 116°C(lit.) |
| Peso molecolare | 86.130 g/mol |
| XLogP3 | 1.100 |
| 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 | 41.200 |
| 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. Siyang Yan, Ruilin Feng, Jiaxu Liu, Chenxi Bai, Yanlong Qi. (2024) Stereocatalytic Effect of CeO2 for the Synthesis of trans-3-Penten-2-ol. ChemCatChem, [PMID:] [10.1002/cctc.202401605] |
