≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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.
1,2,6-Hexanetriol is used as moisturizing agent (cremes), as solvent (pharmaceuticals) and as crosslinker in plastics. It is used as rocket propellant. It acts as wetting agent of tobacco and special hydraulic fluid. It is used in the production of alkyd resins, celluloid, polyurethane and synthetic rubber.
| Pubchem Sid | 504751473 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751473 |
| Sorrisi canonici | C(CCO)CC(CO)O |
| IUPAC Name | hexane-1,2,6-triol |
| InChIKey | ZWVMLYRJXORSEP-UHFFFAOYSA-N |
| INCHI | 1S/C6H14O3/c7-4-2-1-3-6(9)5-8/h6-9H,1-5H2 |
| Isomeri SMILES | C(CCO)CC(CO)O |
| WGK Germania | 1 |
| RTECS | MO4650000 |
| Numero UN | 1208 |
| Peso molecolare | 134.17 |
| Beilstein | 1304479 |
| Reaxy-Rn | 1304479 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1304479&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 | Secondary alcohols Polyols Primary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty alcohol - Secondary alcohol - Polyol - 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 |
|---|---|---|---|
 G2227049 | Certificate of Analysis | May 19, 2026 | H105564 |
| G2227048 | Certificate of Analysis | May 19, 2026 | H105564 |
| K2518591 | Certificate of Analysis | Nov 06, 2025 | H105564 |
| K2518590 | Certificate of Analysis | Nov 06, 2025 | H105564 |
| K2518588 | Certificate of Analysis | Nov 06, 2025 | H105564 |
| K2518587 | Certificate of Analysis | Nov 06, 2025 | H105564 |
| F2609021 | Certificate of Analysis | Nov 06, 2025 | H105564 |
| A2206644 | Certificate of Analysis | Oct 13, 2025 | H105564 |
| A2206638 | Certificate of Analysis | Oct 13, 2025 | H105564 |
| G2115216 | Certificate of Analysis | Apr 03, 2025 | H105564 |
| G2115214 | Certificate of Analysis | Apr 03, 2025 | H105564 |
| D2515674 | Certificate of Analysis | Mar 29, 2024 | H105564 |
| I2511095 | Certificate of Analysis | Sep 27, 2023 | H105564 |
| J2313375 | Certificate of Analysis | Sep 27, 2023 | H105564 |
| J2313626 | Certificate of Analysis | Sep 27, 2023 | H105564 |
| J2313627 | Certificate of Analysis | Sep 27, 2023 | H105564 |
| G2227022 | Certificate of Analysis | Jul 05, 2022 | H105564 |
| F23061459 | Certificate of Analysis | Jul 05, 2022 | H105564 |
| G2227050 | Certificate of Analysis | Jul 05, 2022 | H105564 |
| C1805036 | Certificate of Analysis | Jan 27, 2022 | H105564 |
| Solubilità | Miscible in water and acetone. Soluble in methanol. |
|---|---|
| Sensibilità | Moisture sensitive. |
| Indice di rifrazione | 1.476 |
| Punto di infiammabilità (°F) | 174.2 °F |
| Punto di infiammabilità (°C) | 198℃ |
| Punto di ebollizione (°C) | 178°C |
| Punto di fusione (°C) | 25-32°C |
| Peso molecolare | 134.170 g/mol |
| XLogP3 | -0.700 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 134.094 Da |
| Monoisotopic Mass | 134.094 Da |
| Topological Polar Surface Area | 60.700 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 56.300 |
| 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. Yang Xiong, Lili Liu, Chengyao Hu, Junxiao Yang, Yawen Huang. (2023) Hot-Pressing/Salt-Leaching Method Assisted by Boronic Ester Dynamic Bond to Prepare Vitrimer Foams with Ultra-Low Relative Permittivity and Superhydrophobic Performance. MACROMOLECULAR CHEMISTRY AND PHYSICS, 224 (14): (2300042). [PMID:] [10.1002/macp.202300042] |
