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Merck

45637

Supelco

プロパクロール

PESTANAL®, analytical standard

別名:

2-クロロ-N-イソプロピルアセトアニリド

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About This Item

実験式(ヒル表記法):
C11H14ClNO
CAS番号:
分子量:
211.69
Beilstein:
2103903
EC Number:
MDL番号:
UNSPSCコード:
41116107
PubChem Substance ID:
NACRES:
NA.24

グレード

analytical standard

品質水準

製品種目

PESTANAL®

シェルフライフ

limited shelf life, expiry date on the label

テクニック

HPLC: suitable
gas chromatography (GC): suitable

アプリケーション

agriculture
environmental

フォーマット

neat

SMILES記法

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

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関連するカテゴリー

詳細

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

アプリケーション

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.

法的情報

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

ピクトグラム

Skull and crossbonesEnvironment

シグナルワード

Danger

危険有害性の分類

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

保管分類コード

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

WGK

WGK 3

個人用保護具 (PPE)

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


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以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

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+)

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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