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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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크기 선택

250 MG
₩107,286

₩107,286


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

크기 선택

보기 변경
250 MG
₩107,286

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

₩107,286


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

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.[1] Its mode of action involves inhibiting the fatty acid biosynthesis in plant meristems, which in turn affects the activity of acetyl-coenzyme A carboxylase.[2]

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.[3]
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


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문서 라이브러리 방문

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
Anping Zhang et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 43(3), 231-236 (2008-03-28)
Cyclodextrins (CDs), a class of cyclic oligosaccharide molecules containing a variety of chiral centre, are capable of recognizing enantiomeric molecules through the formation of inclusion complexes. In this work, we selected three types of CDs, beta-CD and its two derivatives
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

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