50594-66-6
50594-66-6
Chemical Structure
Acifluorfen
- CAS No.: 50594-66-6
- Formula:C14H7ClF3NO5
- Molecular Weight:361.66
IUPAC Name: 5-(2-chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoic acid
InChIKey: NUFNQYOELLVIPL-UHFFFAOYSA-N
SMILES: O=C(O)C1=CC(OC2=CC=C(C(F)(F)F)C=C2Cl)=CC=C1[N+]([O-])=O
Biological Activity: Acifluorfen, a protoporphyrinogen oxidase (PROTOX) inhibitor herbicide, promotes the accumulation of protoporphyrin IX (PPIX), and induces tumors in the rodent liver. Acifluorfen causes strong photooxidative destruction of pigments and lipids in sensitive plant species[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Acifluorfen | 98.95% | Acifluorfen, a protoporphyrinogen oxidase (PROTOX) inhibitor herbicide, promotes the accumulation of protoporphyrin IX (PPIX), and induces tumors in the rodent liver. Acifluorfen causes strong photooxidative destruction of pigments and lipids in sensitive plant species. | ||||||||||||||||||||
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Acifluorfen (Standard) | ≥98% | Acifluorfen (Standard) is the analytical standard of Acifluorfen. This product is intended for research and analytical applications. Acifluorfen, a protoporphyrinogen oxidase (PROTOX) inhibitor herbicide, promotes the accumulation of protoporphyrin IX (PPIX), and induces tumors in the rodent liver. Acifluorfen causes strong photooxidative destruction of pigments and lipids in sensitive plant species. | ||||||||||||||||||||
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References
- [1]. Kuwata K, et al. Involvement of Mouse Constitutive Androstane Receptor in Acifluorfen-Induced Liver Injury and Subsequent Tumor Development. Toxicol Sci. 2016;151(2):271-285. [Content Brief]
- [2]. Hong T, et al. Exposure to acifluorfen induces developmental toxicity in the early life stage of zebrafish. Comp Biochem Physiol C Toxicol Pharmacol. 2024 Jul;281:109909. [Content Brief]
Keywords
