≥98% 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
application：
10-Undecen-1-ol is used as a flavoring agent. It reacts with tosylated beta-cyclodextrin to prepare beta-cyclodextrin undecenylether. It is used in the synthesis of 10-Undecenylacrylat by reacting with acryloyl and triethylamine. It reacts with carbon monoxide in the presence of dicobalt octacarbonyl and pyridine as a base at pressures greater than 150 bar and temperatures in the range of 100 to 2000C to linear and branched polyesters having relatively high molecular weights (Mn> 10,000 g / mol) in good yields.
| Pubchem Sid | 488180722 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180722 |
| Canonical Smiles | C=CCCCCCCCCCO |
| IUPAC Name | undec-10-en-1-ol |
| InChIKey | GIEMHYCMBGELGY-UHFFFAOYSA-N |
| INCHI | 1S/C11H22O/c1-2-3-4-5-6-7-8-9-10-11-12/h2,12H,1,3-11H2 |
| Isomeric SMILES | C=CCCCCCCCCCO |
| WGK Germany | 2 |
| RTECS | YQ2985000 |
| PubChem CID | 8185 |
| Molecular Weight | 170.29 |
| Beilstein | 1753225 |
| Reaxy-Rn | 1753225 |
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 |
| Class | 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 |
| Description | 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 | Date | Item |
|---|---|---|---|
 G2417675 | Certificate of Analysis | Apr 07, 2026 | U106482 |
| H2211556 | Certificate of Analysis | Feb 04, 2026 | U106482 |
| H2211557 | Certificate of Analysis | Feb 04, 2026 | U106482 |
| H2211558 | Certificate of Analysis | Feb 04, 2026 | U106482 |
| H2211559 | Certificate of Analysis | Feb 04, 2026 | U106482 |
| A2517124 | Certificate of Analysis | Jan 21, 2025 | U106482 |
| G2417672 | Certificate of Analysis | Apr 29, 2024 | U106482 |
| L1706049 | Certificate of Analysis | Jun 07, 2023 | U106482 |
| G2103267 | Certificate of Analysis | Apr 12, 2023 | U106482 |
| G2103268 | Certificate of Analysis | Apr 12, 2023 | U106482 |
| G1918082 | Certificate of Analysis | Feb 06, 2023 | U106482 |
| Solubility | Miscible with alcohol and ether. Immiscible with water |
|---|---|
| Refractive Index | 1.446-1.453 |
| Flash Point(°F) | 257 °F |
| Flash Point(°C) | 93℃ |
| Boil Point(°C) | 245-248°C |
| Melt Point(°C) | -3°C |
| Molecular Weight | 170.290 g/mol |
| XLogP3 | 4.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 9 |
| Exact Mass | 170.167 Da |
| Monoisotopic Mass | 170.167 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 89.000 |
| 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. Xuan Xin, Mengmeng Zhang, Xiao-Feng Li, Guanglei Zhao. (2019) Biocatalytic Synthesis of Lipophilic Baicalin Derivatives as Antimicrobial Agents. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:31564105] [10.1021/acs.jafc.9b04667] |
| 2. Changchang Zhang, Yong Kuai, Heming Cheng, Xiang Liu, Liang Ma. (2017) Covalent bonding of grafted polymer brushes of poly(poly(ethylene glycol) monomethacrylate) on surface of silicon quantum dots and the activation of the end hydroxyls. Arabian Journal of Chemistry, [PMID:] [10.1016/j.arabjc.2016.12.022] |
| 3. Chenyang Xia, Bowen Lu, Qi Xu, Nanxin Shen, Qiancheng Liao, Jiyun Cui, Baiyang Wang, Yueyang Sun, Changjiang Dong, Fei Gan. (2025) Structural and Mechanistic Insights into Dual Deprotonation by an Engineered GPP Methyltransferase: Discovery of Methyltransferases Generating Noncanonical Prenyl Diphosphates. ACS Catalysis, [PMID:] [10.1021/acscatal.5c03939] |
