≥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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488186868 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488186868 |
| Sonrisas canónicas | C1=C(C(=CC(=C1F)F)F)N |
| IUPAC Name | 2,4,5-trifluoroaniline |
| InChIKey | QMYVWJVVVMIBMM-UHFFFAOYSA-N |
| INCHI | 1S/C6H4F3N/c7-3-1-5(9)6(10)2-4(3)8/h1-2H,10H2 |
| Isómeros SMILES | C1=C(C(=CC(=C1F)F)F)N |
| WGK Alemania | 3 |
| PubChem CID | 94953 |
| Peso molecular | 147.1 |
| Beilstein | 12(4)1115 |
| Reaxy-Rn | 2085734 |
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 |
| Clase | Benzene and substituted derivatives |
| Subclass | Aniline and substituted anilines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aniline and substituted anilines |
| Alternative Parents | Fluorobenzenes Aryl fluorides Primary amines Organopnictogen compounds Organofluorides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aniline or substituted anilines - Halobenzene - Fluorobenzene - Aryl halide - Aryl fluoride - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organofluoride - Organohalogen compound - Amine - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 H2217748 | Certificate of Analysis | Jun 08, 2026 | T161787 |
| H2217749 | Certificate of Analysis | Jun 08, 2026 | T161787 |
| H2217750 | Certificate of Analysis | Jun 08, 2026 | T161787 |
| H2217753 | Certificate of Analysis | Jun 08, 2026 | T161787 |
| H1731078 | Certificate of Analysis | Apr 09, 2025 | T161787 |
| Punto de fusión (°C) | 60 °C |
|---|---|
| Peso molecular | 147.100 g/mol |
| XLogP3 | 1.500 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Exact Mass | 147.03 Da |
| Monoisotopic Mass | 147.03 Da |
| Topological Polar Surface Area | 26.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 120.000 |
| 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. Tu Hong, Tian Bihong, Chen Shunshun, Xu Jingyi, Yang Jianrong, Zhao Zhichao, Chen Shunhong, Wu Jian. (2025) Enhancing photocatalytic efficiency through surface modification to manipulate internal electron-hole distribution. npj Clean Water, 8 (1): (1-10). [PMID:] [10.1038/s41545-025-00480-4] |
