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Merck
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Key Documents

45637

Supelco

Propachlor

PESTANAL®, analytical standard

동의어(들):

2-Chloro-N-isopropylacetanilide

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About This Item

실험식(Hill 표기법):
C11H14ClNO
CAS Number:
Molecular Weight:
211.69
Beilstein:
2103903
EC Number:
MDL number:
UNSPSC 코드:
41116107
PubChem Substance ID:
NACRES:
NA.24

Grade

analytical standard

Quality Level

제품 라인

PESTANAL®

유통기한

limited shelf life, expiry date on the label

기술

HPLC: suitable
gas chromatography (GC): suitable

응용 분야

agriculture
environmental

형식

neat

SMILES string

CC(C)N(C(=O)CCl)c1ccccc1

InChI

1S/C11H14ClNO/c1-9(2)13(11(14)8-12)10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3

InChI key

MFOUDYKPLGXPGO-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Propachlor is a herbicide, widely used in oil seeds and crop planting.

애플리케이션

Propachlor may be used as an analytical reference standard for the quantification of the analyte in industrial wastewater samples and complex matrices using chromatography techniques.
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

Skull and crossbonesEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

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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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Multiresidue analysis of 240 pesticides in apple and lettuce by QuEChERS sample preparation and HPLC-MS/MS analysis
Wang.L, et al.
The Korean Journal of Pesticide Science, 46(5), 424-429 (2008)
Liquid-liquid extraction for sample preparation prior to gas chromatography and gas chromatography-mass spectrometry determination of herbicide and pesticide compounds
Mahara.MB, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 58(1), 31-38 (1998)
K L Davison et al.
Xenobiotica; the fate of foreign compounds in biological systems, 24(10), 1003-1012 (1994-10-01)
1. 14C-labelled propachlor, alachlor, butachlor, metolachlor, methoxypropachlor and some of their mercapturic acid pathway metabolites (MAP) were given to rat either by gavage or by perfusion into a renal artery. MAP metabolites were isolated from bile and urine. 2. Rat
Katrice A Lippa et al.
Journal of agricultural and food chemistry, 52(10), 3010-3021 (2004-05-13)
The ease with which alpha-chloroacetanilide herbicides undergo displacement reactions with strong nucleophiles, and their recalcitrance toward weak ones, is intimately related to their herbicidal properties and environmental chemistry. In this study, we investigate the kinetics and mechanisms of nucleophilic substitution
C S Liu et al.
The Science of the total environment, 416, 507-512 (2012-01-10)
The process of in situ chemical oxidation (ISCO) by persulfate (S(2)O(8)(2-)) can be accelerated by metal ion activation, which more effectively degrades subsurface pollutants by enhancing sulfate radical (SO(4)(-)) generation. This study compared the results of propachlor degradation by Cu(2+)

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