4-(4-Chlorophenoxy)butanoic acid
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| Names | |
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| Preferred IUPAC name 4-(4-chlorophenoxy)butanoic acid | |
| Other names 4-CPB | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| EC Number | 
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| PubChem CID | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C10H11ClO3 | |
| Molar mass | 214.65 g·mol−1 | 
| Hazards | |
| GHS labelling: | |
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| Danger | |
| H302, H318 | |
| P264, P264+P265, P270, P280, P301+P317, P305+P354+P338, P317, P330, P501 | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
4-(4-Chlorophenoxy)butanoic acid is an herbicide. Its formula is C10H11ClO3. It is an approved substance under the name 4-CPB by the Weed Science Society of America.[1]
Uses
4-(4-Chlorophenoxy)butanoic acid has been used as a starting material to produce derivatives of benzoxepin, several of which are the subject of research due to their apparent sedative-hypnotic effects.[2]
References
- ^ "4-CPB". Compendium of Pesticide Common Names. British Crop Production Council. Retrieved January 30, 2025.
- ^ Abdel Gawad NM, Hassan GS, Georgey HH, El-Zorba HY (June 1, 2012). "Benzoxepin derivatives: design, synthesis, and pharmacological evaluation with sedative–hypnotic effect". Medicinal Chemistry Research. 21 (6): 747–759. doi:10.1007/s00044-011-9579-3. ISSN 1554-8120.