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Documentos Principais

PS1016

Acifluorfen

analytical standard

Sinônimo(s):

5-(2-Chloro-α,α,α-trifluoro-p-tolyloxy)-2-nitrobenzoic acid, 5-[2-Chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid

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About This Item

Fórmula empírica (Notação de Hill):
C14H7ClF3NO5
Número CAS:
Peso molecular:
361.66
Beilstein:
2953865
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:

grau

analytical standard

embalagem

ampule of 250 mg

fabricante/nome comercial

Chem Service, Inc. PS-1016

aplicação(ões)

agriculture
environmental

cadeia de caracteres SMILES

OC(=O)c1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1[N+]([O-])=O

InChI

1S/C14H7ClF3NO5/c15-10-5-7(14(16,17)18)1-4-12(10)24-8-2-3-11(19(22)23)9(6-8)13(20)21/h1-6H,(H,20,21)

chave InChI

NUFNQYOELLVIPL-UHFFFAOYSA-N

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Descrição geral

Acifluorfen is a photobleaching herbicide, used as selective preemergence and postemergence weed control in soybean, peanuts and legumes. It causes the photooxidative destruction of pigments and lipids in sensitive plant species.

Aplicação

Acifluorfen may be used as a reference standard for the determination of aclonifen herbicide in water samples using high-performance liquid chromatography coupled with diode array tandem mass spectrometric detection.

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Acifluorfen effects on intermediates of chlorophyll synthesis in green cucumber cotyledon tissues.
Becerril J, et al.
Pesticide Biochemistry and Physiology, 35(2), 119-126 (1989)
Effects of acifluorfen on endogenous antioxidants and protective enzymes in cucumber (Cucumis sativus L.) cotyledons.
Kenyon W H, et al.
Plant Physiology, 79(3), 862-866 (1985)
Determination of diphenyl-ether herbicides and metabolites in natural waters using high-performance liquid chromatography with diode array tandem mass spectrometric detection.
Lagana A, et al.
Analytica Chimica Acta, 414(1-2), 79-94 (2000)
Lu Sun et al.
Amino acids, 37(3), 523-530 (2009-03-07)
Protoporphyrinogen IX oxidase (PPO), the last common enzyme of heme and chlorophyll biosynthesis, catalyses the oxidation of protoporphyrinogen IX to protoporphyrin IX, with FAD as cofactor. Among PPO, Bacillus subtilis PPO (bsPPO) is unique because of its broad substrate specificity
Nina Cedergreen et al.
Environmental toxicology and chemistry, 24(12), 3166-3172 (2006-02-01)
During the past two decades, the phenomenon of hormesis has gained increased recognition. To promote research in hormesis, a sound statistical quantification of important parameters, such as the level and significance of the increase in response and the range of

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