Merck
CN
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文件

安全信息

31477

Supelco

甲羧除草醚

PESTANAL®, analytical standard

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别名:
5-(2,4-二氯苯氧基)-2-硝基苯甲酸甲酯
经验公式（希尔记法）:
C14H9Cl2NO5
CAS号:
42576-02-3
分子量:
342.13
Beilstein:
2170169
EC 号:
255-894-7
MDL编号:
MFCD00055314
PubChem化学物质编号:
329753781
NACRES:
NA.24

等级

analytical standard

质量水平

100

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

格式

neat

SMILES string

COC(=O)c1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+]([O-])=O

InChI

1S/C14H9Cl2NO5/c1-21-14(18)10-7-9(3-4-12(10)17(19)20)22-13-5-2-8(15)6-11(13)16/h2-7H,1H3

InChI key

SUSRORUBZHMPCO-UHFFFAOYSA-N

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相关类别

应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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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
GHS09

警示用语：

Warning

危险声明

H410

预防措施声明

P273 - P391 - P501

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

农药列管产品

分析证书(COA)

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Ana Catarina Almeida et al.
Aquatic toxicology (Amsterdam, Netherlands), 210, 117-128 (2019-03-09)
The widespread presence of herbicides in the aquatic environment has raised awareness about the need to develop further in depth ecotoxicological risk assessments, more specifically on potential effects on photosynthetic organisms as microalgae. The majority of the information available regarding
B M Francis
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 21(4), 303-317 (1986-08-01)
The teratogenicity of the diphenyl ether herbicide bifenox [2,4-dichlorophenyl 3'-carboxymethyl-4'-nitrophenyl ether] was compared to that of nitrofen [2,4-dichlorophenyl 4'-nitrophenyl ether] in rats and in mice. Neither compound increased prenatal mortality in mice. Because nitrofen causes both malformations that are compatible
B M Francis et al.
Teratology, 59(2), 69-80 (1999-03-09)
In an ongoing effort to delineate structure-activity relationships in the developmental toxicity of diphenyl ethers, we evaluated the maternal and developmental toxicity of 10 diphenyl ethers related to the herbicide nitrofen. All possible trichlorophenyl 4'-nitrophenyl ethers were evaluated, as were
D J Hoffman et al.
Journal of toxicology and environmental health, 34(3), 323-336 (1991-11-01)
Beginning the day after hatching, American kestrel (Falco sparverius) nestlings were orally dosed for 10 consecutive days with 5 microliters/g of corn oil (controls) or one of the diphenyl ether herbicides (nitrofen, bifenox, or oxyfluorfen) at concentrations of 10, 50
A Lubineau et al.
Carbohydrate research, 228(1), 191-203 (1992-04-10)
Glycosides (alpha- and beta-D-glucosides and -D-galactosides) derived from three pesticides, 2-tert-butyl-2,4-dinitrophenol,2,6-dibromo-4-cyanophenol, and 5-(2,4-dichlorophenoxy)-2-nitrobenzoic acid, were synthesized from 2,3,4,6-tetra-O-chloroacetyl-D-gluco- and -D-galactopyranose by use of the Mitsunobu reaction. It was shown that selectivity for the beta-D anomer increases with the pKa of
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