≥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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
1-Fluorooctane undergoes C-F bond-cleavage reaction with phenyl magnesium chloride to give n-octylbenzene. It reacts rapidly with trimethylsilyl iodide to give corresponding octyl iodides and trimethylsilyl fluoride.
| Pubchem Sid | 504751899 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751899 |
| Kanonisches Lächeln | CCCCCCCCF |
| IUPAC Name | 1-fluorooctane |
| InChIKey | DHIVLKMGKIZOHF-UHFFFAOYSA-N |
| INCHI | 1S/C8H17F/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3 |
| Isomere SMILES | CCCCCCCCF |
| WGK Deutschland | 3 |
| RTECS | RG9700000 |
| UN-Nummer | 1993 |
| Verpackungsgruppe | III |
| Molekulargewicht | 132.22 |
| Reaxy-Rn | 1697462 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697462&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 | Organohalogen compounds |
| Klasse | Organofluorides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organofluorides |
| Alternative Parents | Hydrofluorocarbons Hydrocarbon derivatives Alkyl fluorides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hydrofluorocarbon - Hydrocarbon derivative - Organofluoride - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as organofluorides. These are compounds containing a chemical bond between a carbon atom and a fluorine atom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 C2307414 | Certificate of Analysis | Dec 16, 2022 | F170468 |
| C2307415 | Certificate of Analysis | Dec 16, 2022 | F170468 |
| G2315497 | Certificate of Analysis | Dec 16, 2022 | F170468 |
| H2402026 | Certificate of Analysis | Dec 16, 2022 | F170468 |
| Flammpunkt (°F) | 107.6 °F |
|---|---|
| Flammpunkt (°C) | 42 °C |
| Siedepunkt (°C) | 142-146°C |
| Molekulargewicht | 132.220 g/mol |
| XLogP3 | 4.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 6 |
| Exact Mass | 132.131 Da |
| Monoisotopic Mass | 132.131 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 43.800 |
| 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. Bin Zhang, Ke Yue, Ke Wang, Guohao Zhao, Wenbin Huang, Tao Li, Jianmin Luo, Ying Xu, Xinyong Tao. (2025) In situ engineered organic–inorganic bilayer solid electrolyte interphase enabling lithium metal batteries over 15,000-hour lifespan. eScience, [PMID:] [10.1016/j.esci.2025.100479] |
