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Merck
CN

33613

Supelco

烯丙酰草胺

PESTANAL®, analytical standard

别名:

N,N-二烯丙基二氯乙酰胺, 二氯丙烯胺

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About This Item

经验公式(希尔记法):
C8H11Cl2NO
CAS号:
分子量:
208.09
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

包装形式

neat

SMILES字符串

ClC(Cl)C(=O)N(CC=C)CC=C

InChI

1S/C8H11Cl2NO/c1-3-5-11(6-4-2)8(12)7(9)10/h3-4,7H,1-2,5-6H2

InChI key

YRMLFORXOOIJDR-UHFFFAOYSA-N

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相关类别

一般描述

Dichlormid belongs to the class of dichloroacetamide safeners used to provide good protection on maize, wheat and rice grain against injury caused by pre-emergence applications of butachlor, metolachlor, chloroacetanilide and thiocarbamate.

应用

Dichlormid may be used as an analytical reference standard for the determination of the contaminant, dichlormid in animal muscle samples using gel permeation chromatography cleanup (GPC) followed by gas chromatography/mass spectrometry (GS/MS), and column chromatography tandem MS (LC/MS/MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

推荐产品

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

法律信息

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

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

Lot/Batch Number

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D C Holt et al.
Planta, 196(2), 295-302 (1995-01-01)
The safener-induced maize (Zea mays L.) glutathione S-transferase, GST II (EC 2.5.1.18) and another predominant isoform, GST I, were purified from extracts of maize roots treated with the safeners R-25788 (N,N-diallyl-2-dichloroacetamide) or R-29148 (3-dichloroacetyl-2,2,5-trimethyl-1,3-oxazolidone). The isoforms GST I and GST
Effects of the herbicide sethoxydim and the safener dichlormid on lipid synthesis and acetyl-CoA carboxylase activity of grain sorghum.
Hatzios KK.
Zeitschrift fur Naturforschung C, 46(9-10), 934-938 (1991)
The Pesticide Encyclopedia (2014)
Adam Baldwin et al.
Journal of experimental botany, 54(385), 1289-1294 (2003-03-26)
The thiocarbamates, such as pebulate (S-propyl butyl (ethyl) thiocarbamate) are a well-established class of herbicides. They inhibit fatty acid elongation, which is necessary for the biosynthesis of constituents of surface waxes and suberin and this has been proposed to be
Shiful Islam et al.
PloS one, 12(11), e0187504-e0187504 (2017-11-03)
Glutathione S-transferase (GST) refers to one of the major detoxifying enzymes that plays an important role in different abiotic and biotic stress modulation pathways of plant. The present study aimed to a comprehensive genome-wide functional characterization of GST genes and

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