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Merck
CN

04287

Supelco

草枯醚

PESTANAL®, analytical standard

别名:

1,3,5-Trichloro-2-(4-nitrophenoxy)benzene, 4-Nitrophenyl 2,4,6-trichlorophenyl ether

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关于此项目

经验公式(希尔记法):
C12H6Cl3N1O3
化学文摘社编号:
分子量:
318.54
Beilstein:
1890443
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
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等级

analytical standard

质量水平

产品线

PESTANAL®

方案

≥98% (HPLC)

保质期

limited shelf life, expiry date on the label

应用

agriculture
environmental

包装形式

neat

SMILES字符串

[O-][N+](=O)c1ccc(Oc2c(Cl)cc(Cl)cc2Cl)cc1

InChI

1S/C12H6Cl3NO3/c13-7-5-10(14)12(11(15)6-7)19-9-3-1-8(2-4-9)16(17)18/h1-6H

InChI key

XQNAUQUKWRBODG-UHFFFAOYSA-N

相关类别

一般描述

Chlornitrofen (Cnf) is a diphenyl-ether-derived pesticide belonging to the nitrophenyl chemical class of compounds. It is a pre-emergence herbicide used to control annual weeds and some perennials, including Eleocharis acicularis and Sagittaria pygmaea in rice fields. The mode of action of Cnf is by the inhibition of a vital enzyme, protoporphyrinogen oxidase (PPO).

应用

Chlornitrofen may be used as an analytical reference standard for the determination of the analyte in river water, air samples and tobacco by chromatography based techniques.

包装

Bottomless glass bottle. Contents are inside inserted fused cone.

分析说明

C-NMR and H-NMR conform to structure

其他说明

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

象形图

Environment

警示用语:

Warning

危险声明

预防措施声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

No data available

闪点(°C)

No data available

法规信息

农药列管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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N Hanioka et al.
Chemosphere, 30(7), 1297-1309 (1995-04-01)
The induction of hepatic drug-metabolizing enzymes by chlornitrofen (CNP) and CNP-amino was studied in the liver of male rats and mice. CNP-amino increased the activities of 7-pentoxyresorufin O-depentylase (PROD) and 7-benzyloxyresorufin O-debenzylase (BROD) as CYP2B1-dependent monooxygenase 3.6- and 4.1-fold in
Kotaro Minomo et al.
Chemosphere, 85(2), 188-194 (2011-07-08)
In Japan, Ayase River is one of the most polluted rivers by PCDDs, PCDFs and dioxin-like PCBs, which are referred to as dioxins in this paper. The water samples of the river were collected once per month for a year
Hiroyuki Kojima et al.
Environmental health perspectives, 111(4), 497-502 (2003-04-05)
Chlornitrofen (CNP) was widely used in large quantities as a herbicide in rice paddy fields in Japan during 1965-1994. Recently, there has been concern that chemicals in the environment may disrupt the endocrine function of wildlife and humans, but little
Y Hiraoka et al.
Hiroshima journal of medical sciences, 38(3), 125-129 (1989-09-01)
We investigated the effects of a diphenyl ether herbicide, a chlornitrophen (CNP) emulsion, on mouse fetuses. An MO emulsion was used as the experimental chemical twenty percent of this herbicide consisting of CNP. CNP and other components were extracted and
Biodegradation of herbicide chlornitrofen (CNP) and mutagenicity of its degradation products
Tanaka, Y
Water Science and Technology, 34, 15-20 (1994)

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