≥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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
4-Chloro-3-fluorophenol is hydroxylated at both ortho positions to yield different products.
4-Chloro-3-fluorophenol was used in the synthesis of 4-chloro-3-fluoro catechol.
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 | Phenols |
| Subclass | Halophenols |
| Intermediate Tree Nodes | Chlorophenols |
| Direct Parent | P-chlorophenols |
| Alternative Parents | M-fluorophenols Fluorobenzenes Chlorobenzenes 1-hydroxy-2-unsubstituted benzenoids Aryl fluorides Aryl chlorides Organooxygen compounds Organofluorides Organochlorides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | 4-chlorophenol - 3-fluorophenol - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organofluoride - Organohalogen compound - Organochloride - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as p-chlorophenols. These are chlorophenols carrying a iodine at the C4 position of the 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 |
|---|---|---|---|
 F1419060 | Certificate of Analysis | Jan 27, 2026 | C122588 |
| C2218144 | Certificate of Analysis | Jan 19, 2026 | C122588 |
| C2218147 | Certificate of Analysis | Jan 19, 2026 | C122588 |
| K1702131 | Certificate of Analysis | Jun 12, 2025 | C122588 |
| I2407161 | Certificate of Analysis | Jun 22, 2024 | C122588 |
| I2407176 | Certificate of Analysis | Jun 22, 2024 | C122588 |
| I2407179 | Certificate of Analysis | Jun 22, 2024 | C122588 |
| F2425017 | Certificate of Analysis | Feb 18, 2022 | C122588 |
| Flash Point(°F) | 235.4 °F |
|---|---|
| Flash Point(°C) | >110℃(230°F) |
| Boil Point(°C) | 84°C/4.4mmHg |
| Melt Point(°C) | 54 °C |
| Molecular Weight | 146.540 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 145.993 Da |
| Monoisotopic Mass | 145.993 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 99.100 |
| 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 |
