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Merck
모든 사진(1)

주요 문서

45518

Supelco

Fenoxaprop-ethyl

PESTANAL®, analytical standard

동의어(들):

Ethyl 2-{4-[(6-chlorobenzoxazol-2-yl)oxy]phenoxy}propionate

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About This Item

실험식(Hill 표기법):
C18H16ClNO5
CAS Number:
Molecular Weight:
361.78
EC Number:
MDL number:
UNSPSC 코드:
41116107
PubChem Substance ID:
NACRES:
NA.24

Grade

analytical standard

Quality Level

제품 라인

PESTANAL®

품질

racemate

유통기한

limited shelf life, expiry date on the label

기술

HPLC: suitable
gas chromatography (GC): suitable

응용 분야

agriculture
environmental

형식

neat

SMILES string

CCOC(=O)C(C)Oc1ccc(Oc2nc3ccc(Cl)cc3o2)cc1

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

InChI key

PQKBPHSEKWERTG-UHFFFAOYSA-N

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관련 카테고리

일반 설명

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.

애플리케이션

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.

법적 정보

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

픽토그램

Exclamation markEnvironment

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

개인 보호 장비

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Biodegradation of fenoxaprop-ethyl by an enriched consortium and its proposed metabolic pathway.
Dong W, et al.
International Biodeterioration & Biodegradation, 97, 159-167 (2015)
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)
Yanfeng Zhang et al.
Journal of agricultural and food chemistry, 58(24), 12878-12884 (2010-12-03)
The enantioselective degradation behavior of fenoxaprop-ethyl (FE) and its chiral metabolite fenoxaprop (FA) in three soils under native conditions was investigated. Two pairs of enantiomers were analyzed by high-performance liquid chromatography (HPLC) with an amylose tri-(3,5-dimethylphenylcarbamate) (ADMPC) chiral column. The
Jing Lin et al.
Journal of agricultural and food chemistry, 55(18), 7626-7629 (2007-08-10)
Hydrolysis of fenoxaprop-p-ethyl (FE), a widely used herbicide, was studied in aqueous buffer solutions at pH ranging from 4.0 to 10.0. The degradation kinetics, strongly dependent on pH values, followed first-order kinetics. FE was relatively stable in neutral media, whereas
Ying Hou et al.
FEMS microbiology letters, 323(2), 196-203 (2011-11-19)
An enrichment culture which completely degraded fenoxaprop-ethyl (FE) was acquired by using FE as sole carbon source. An efficient FE-degrading strain T1 was isolated from the enrichment culture and identified as Rhodococcus sp. Strain T1 could degrade 94% of 100

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