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Merck
CN

36176

草不隆

PESTANAL®, analytical standard

别名:

N-丁基-N′-(3,4-二氯苯基)-N-甲基脲

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关于此项目

经验公式(希尔记法):
C12H16Cl2N2O
化学文摘社编号:
分子量:
275.17
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
209-096-0
Beilstein/REAXYS Number:
2733280
MDL number:
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产品名称

草不隆, PESTANAL®, analytical standard

InChI key

CCGPUGMWYLICGL-UHFFFAOYSA-N

InChI

1S/C12H16Cl2N2O/c1-3-4-7-16(2)12(17)15-9-5-6-10(13)11(14)8-9/h5-6,8H,3-4,7H2,1-2H3,(H,15,17)

SMILES string

CCCCN(C)C(=O)Nc1ccc(Cl)c(Cl)c1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

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相关类别

Legal Information

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

Application

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

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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R H Hill et al.
Archives of environmental health, 36(1), 11-14 (1981-01-01)
The presence of 3,3', 4,4'-tetrachloroazobenzene (TCAB) was determined by high performance liquid chromatography in 3, 4-dichloroaniline and herbicides made therefrom. The concentrations of TCAB in 3, 4-dichloroanilines and in different herbicides from a variety of manufacturers ranged from 9 to
A Di Muccio et al.
Ecotoxicology and environmental safety, 8(6), 511-515 (1984-12-01)
The levels of 3,3',4,4'-tetrachloroazobenzene (TCAB) and 3,3',4,4'-tetrachloroazoxybenzene (TCAOB) were determined by gas chromatography-electron capture detection in 20 samples of 3,4-dichloroaniline-derived herbicides. The concentrations of TCAB in technical grade propanil, diuron, linuron, and neburon from a variety of manufacturers ranged from
Recovery of Nostoc muscorum previously exposed to some triazine and phenylurea herbicides.
H Abou-Waly et al.
Bulletin of environmental contamination and toxicology, 50(5), 665-673 (1993-05-01)
T Tamiri et al.
Biomedical & environmental mass spectrometry, 14(1), 39-42 (1987-01-01)
The application of gas chromatography/mass spectrometry to three thermally labile phenylurea pesticides is reported. Using alcohols as solvents the decomposition of the pesticides is followed by a reaction in which esters of N-(3,4-dichlorophenyl)carbamic acid are formed. As these reactions occur
Temperature dependence of neburon mass spectra using thermospray or a moving-belt interface.
T Cairns et al.
Rapid communications in mass spectrometry : RCM, 1(6), 90-92 (1987-10-01)

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