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36176

Supelco

Neburon

PESTANAL®, analytical standard

Synonym(s):

N-Butyl-N′-(3,4-dichlorophenyl)-N-methylurea

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About This Item

Empirical Formula (Hill Notation):
C12H16Cl2N2O
CAS Number:
555-37-3
Molecular Weight:
275.17
Beilstein:
2733280
EC Number:
209-096-0
MDL number:
MFCD00018140
UNSPSC Code:
41116107
PubChem Substance ID:
329755320
NACRES:
NA.24

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

SMILES string

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

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)

InChI key

CCGPUGMWYLICGL-UHFFFAOYSA-N

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Application

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

Legal Information

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK2183
BCBZ7493
SZBE035XV
SZBB033XV
SZE6010X

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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)
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)
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