≥98%(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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Rotational Raman spectra of 1,3,5-trifluorobenzene has been studied under high resolution using a single mode argon laser as the exciting source. Proton and fluorine magnetic resonance spectra of 1,3,5-trifluorobenzene in a nematic liquid crystal has been analyzed.
1,3,5-Trifluorobenzene was used in the synthesis of (-)-epicatechin and its 3-O-gallate
| Pubchem Sid | 504751864 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751864 |
| Canonical Smiles | C1=C(C=C(C=C1F)F)F |
| IUPAC Name | 1,3,5-trifluorobenzene |
| InChIKey | JXUKFFRPLNTYIV-UHFFFAOYSA-N |
| INCHI | 1S/C6H3F3/c7-4-1-5(8)3-6(9)2-4/h1-3H |
| Isomeric SMILES | C1=C(C=C(C=C1F)F)F |
| WGK Germany | 2 |
| PubChem CID | 9745 |
| UN Number | 1993 |
| Packing Group | II |
| Molecular Weight | 132.09 |
| Reaxy-Rn | 1906457 |
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 | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Halobenzenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fluorobenzenes |
| Alternative Parents | Aryl fluorides Organofluorides Hydrofluorocarbons Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Fluorobenzene - Aryl halide - Aryl fluoride - Hydrofluorocarbon - Hydrocarbon derivative - Organofluoride - Organohalogen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as fluorobenzenes. These are compounds containing one or more fluorine atoms attached to a benzene ring. |
| 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 |
|---|---|---|---|
 A2203093 | Certificate of Analysis | Oct 13, 2025 | T161824 |
| I2508578 | Certificate of Analysis | Aug 12, 2025 | T161824 |
| I2508577 | Certificate of Analysis | Aug 12, 2025 | T161824 |
| I2501552 | Certificate of Analysis | Aug 12, 2025 | T161824 |
| I2501544 | Certificate of Analysis | Aug 12, 2025 | T161824 |
| I2501543 | Certificate of Analysis | Aug 12, 2025 | T161824 |
| I2501527 | Certificate of Analysis | Aug 12, 2025 | T161824 |
| I2501525 | Certificate of Analysis | Aug 12, 2025 | T161824 |
| I2124447 | Certificate of Analysis | Jul 10, 2025 | T161824 |
| I1910144 | Certificate of Analysis | Jun 12, 2023 | T161824 |
| G1924061 | Certificate of Analysis | May 15, 2023 | T161824 |
| G2322903 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| G2322892 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| G2322890 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| G2322889 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| G2322885 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| G2322884 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| G2322880 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| G2322877 | Certificate of Analysis | Feb 09, 2023 | T161824 |
| Solubility | Insoluble in water. |
|---|---|
| Sensitivity | Heat sensitive |
| Refractive Index | 1.414 |
| Flash Point(°F) | 19.4 °F |
| Flash Point(°C) | -7°C |
| Boil Point(°C) | 76°C |
| Melt Point(°C) | -5.5°C |
| Molecular Weight | 132.080 g/mol |
| XLogP3 | 2.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 132.019 Da |
| Monoisotopic Mass | 132.019 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 63.300 |
| 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. Mingsheng Qin, Ziqi Zeng, Qiang Wu, Xiaowei Liu, Qijun Liu, Shijie Cheng, Jia Xie. (2023) 1,3,5-Trifluorobenzene endorsed EC-free electrolyte for high-voltage and wide-temperature lithium-ion batteries. Journal of Energy Chemistry, [PMID:] [10.1016/j.jechem.2023.06.003] |
| 2. Ma Baochen, Zhang Haikuo, Li Ruhong, Zhang Shuoqing, Chen Long, Zhou Tao, Wang Jinze, Zhang Ruixin, Ding Shouhong, Xiao Xuezhang, Deng Tao, Chen Lixin, Fan Xiulin. (2024) Molecular-docking electrolytes enable high-voltage lithium battery chemistries. Nature Chemistry, [PMID:39009795] [10.1038/s41557-024-01585-y] |
| 3. Xiaoxia Zhang, Congmei Chen, Meng Rong. (2025) Fluorinated tetraphenyladamantane-based microporous organic polymers for efficient CO2 and organic vapors capture. MICROPOROUS AND MESOPOROUS MATERIALS, [PMID:] [10.1016/j.micromeso.2025.113667] |
| 4. Sa Xue, Xiangyang Liu, Yongqi Liu, Maogang He. (2026) Dual-Interphase Modulation with a Locally Concentrated Ionic Liquid Electrolyte toward High-Performance Lithium Metal Batteries. ACS Applied Materials & Interfaces, [PMID:41571589] [10.1021/acsami.5c20150] |
