登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式(希尔记法):
C18H16ClNO5
化学文摘社编号:
分子量:
361.78
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
266-362-9
MDL number:
InChI key
PQKBPHSEKWERTG-UHFFFAOYSA-N
InChI
1S/C18H16ClNO5/c1-3-22-17(21)11(2)23-13-5-7-14(8-6-13)24-18-20-15-9-4-12(19)10-16(15)25-18/h4-11H,3H2,1-2H3
SMILES string
CCOC(=O)C(C)Oc1ccc(Oc2nc3ccc(Cl)cc3o2)cc1
grade
analytical standard
product line
PESTANAL®
quality
racemate
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
Quality Level
正在寻找类似产品? 访问 产品对比指南
相关类别
General description
Fenoxaprop-ethyl is a postemergence herbicide used for the control of annual and perennial weeds in crops. Its mode of action involves inhibiting the fatty acid biosynthesis in plant meristems, which in turn affects the activity of acetyl-coenzyme A carboxylase.
Application
Fenoxaprop-ethyl may be used as a reference standard for the determination of fenoxaprop-ethyl by high performance liquid chromatography (HPLC) with photometric detection and mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
农药列管产品
此项目有
Determination of fenoxaprop-ethyl in agricultural products by HPLC with photometric detection and mass spectrometry.
Ishimitsu S, et al.
Journal of Health Science, 49(6), 492-496 (2003)
Biodegradation of fenoxaprop-ethyl by an enriched consortium and its proposed metabolic pathway.
Dong W, et al.
International Biodeterioration & Biodegradation, 97, 159-167 (2015)
Cécile Petit et al.
Pest management science, 66(2), 168-177 (2009-09-29)
Repeated use of acetyl-CoA carboxylase (ACCase) inhibitors, especially fenoxaprop and clodinafop, since the late 1980s has selected for resistance in Alopecurus myosuroides Huds. (black-grass) in France. We investigated whether resistance to pinoxaden, a phenylpyrazoline ACCase inhibitor to be marketed in
Ian Cummins et al.
Plant biotechnology journal, 7(8), 807-820 (2009-09-17)
Safeners enhance the selectivity of graminicidal herbicides such as fenoxaprop ethyl in cereals, by increasing their rates of detoxification in the crop. While studying the selectivity of fenoxaprop ethyl in wheat, we determined that the safeners mefenpyr diethyl and fenchlorazole
Y Bakkali et al.
Journal of agricultural and food chemistry, 55(10), 4052-4058 (2007-04-19)
Fenoxaprop-p-ethyl (FE), 2-[4-[(6-chloro-2-benzoxazolyl)oxy]phenoxy] propanoate, ethyl ester (R), is an aryloxyphenoxypropionate herbicide for postemergence control of annual and perennial grasses in paddy fields; its site of action is acetyl-coenzyme A carboxylase (ACCase), an enzyme in fatty acids biosynthesis. The possible mechanism(s)
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持
