Determine the necessary mass, volume, or concentration for preparing a solution.
≥97%(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.
The stereoselective hydrogenation of 3-hexyn-1-ol was studied. Poly(N-vinyl-2-pyrrolidone)-stabilized Pd-nanoclusters showed an extraordinary catalytic performance in the selective hydrogenation of 3-hexyn-1-ol.
| Pubchem Sid | 488183723 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183723 |
| Sorrisi canonici | CCC#CCCO |
| IUPAC Name | hex-3-yn-1-ol |
| InChIKey | ODEHKVYXWLXRRR-UHFFFAOYSA-N |
| INCHI | 1S/C6H10O/c1-2-3-4-5-6-7/h7H,2,5-6H2,1H3 |
| Isomeri SMILES | CCC#CCCO |
| WGK Germania | 3 |
| Peso molecolare | 98.15 |
| Beilstein | 1(3)1986 |
| Reaxy-Rn | 1735911 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1735911&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 | Lipids and lipid-like molecules |
| Classe | Fatty Acyls |
| Subclass | Fatty alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty alcohols |
| Alternative Parents | Primary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. |
| 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 |
|---|---|---|---|
| Certificate of Analysis | Sep 19, 2025 | H157360 | |
| Certificate of Analysis | Sep 19, 2025 | H157360 | |
| Certificate of Analysis | Aug 19, 2025 | H157360 | |
| Certificate of Analysis | Aug 19, 2025 | H157360 | |
| Certificate of Analysis | Jul 16, 2024 | H157360 | |
| Certificate of Analysis | Jan 06, 2023 | H157360 | |
| Certificate of Analysis | Jul 30, 2022 | H157360 | |
| Certificate of Analysis | Jul 30, 2022 | H157360 |
| Indice di rifrazione | 1.45 |
|---|---|
| Punto di infiammabilità (°F) | 145.4 °F |
| Punto di infiammabilità (°C) | 64°C(lit.) |
| Punto di ebollizione (°C) | 161°C(lit.) |
| Peso molecolare | 98.140 g/mol |
| XLogP3 | 1.100 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 98.0732 Da |
| Monoisotopic Mass | 98.0732 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 82.800 |
| 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. Yun Fang, Yong Yan, Xiayan Wang, Guangsheng Guo. (2025) Bimetallic PdCu nanohybrid sheets for enhanced electrocatalytic selective semi-hydrogenation of alkynols. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.164620] |
| 2. Yuan Ren, Ruiyun Guo, Yanan Li, Zixin Ge, Yaohui Zhao, Jiapeng Huang, Qian Wang, Junhao Lu, Mingshang Jin. (2025) Carbon-Doped Lattice Interstitial Sites Enable Water-Driven Electrocatalytic Alkyne Semihydrogenation by Suppressing Subsurface Hydrogen. ACS Catalysis, [PMID:] [10.1021/acscatal.5c05096] |