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PS1016

Acifluorfen

analytical standard

Sinonimo/i:

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

Formula empirica (notazione di Hill):
C14H7ClF3NO5
Numero CAS:
50594-66-6
Peso molecolare:
361.66
Beilstein:
2953865
Numero CE:
256-634-5
Numero MDL:
MFCD00143541
Codice UNSPSC:
41116107
ID PubChem:
24899078

Grado

analytical standard

Confezionamento

ampule of 250 mg

Produttore/marchio commerciale

Chem Service, Inc. PS-1016

applicazioni

agriculture
environmental

Stringa SMILE

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)
NUFNQYOELLVIPL-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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.

Avvertenze

Danger

Indicazioni di pericolo

H302,H315,H318,H410

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number

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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)
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)
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)
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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