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P36959

Sigma-Aldrich

N-Phenylurea

97%

Synonym(s):

Phenylcarbamide

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About This Item

Linear Formula:
C6H5NHCONH2
CAS Number:
64-10-8
Molecular Weight:
136.15
Beilstein:
1934615
EC Number:
200-576-5
MDL number:
MFCD00007944
UNSPSC Code:
12352100
PubChem Substance ID:
24898443
NACRES:
NA.22

vapor density

>1 (vs air)

Assay

97%

form

solid

mp

145-147 °C (lit.)

SMILES string

NC(=O)Nc1ccccc1

InChI

1S/C7H8N2O/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)

InChI key

LUBJCRLGQSPQNN-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Wei-Hsiang Chen et al.
Environmental science. Processes & impacts, 17(12), 2092-2100 (2015-11-06)
The objective of this study was to investigate the formation of different nitrosamines during chlorination or chloramination (chlor(am)ination) of five phenylurea herbicides (fluometuron, diuron, linuron, metobromuron, and propanil), with the effects of disinfection approaches, additional inorganic nitrogen, and reaction pH
P Palma et al.
The Science of the total environment, 488-489, 208-219 (2014-05-20)
The purpose of this study was to evaluate the potential impact of the pesticides detected in the Alqueva reservoir (Guadiana Basin, South Iberian Peninsula) on the aquatic organisms belonging to this ecosystem. For this purpose, the occurrence and risk assessment
Pankaj Aggarwal et al.
Journal of chromatography. A, 1364, 96-106 (2014-09-07)
Highly cross-linked monolithic networks (i.e., polyethylene glycol diacrylate, PEGDA) synthesized from monomers containing varying ethylene oxide chain lengths were fabricated inside fused silica capillary columns for use in liquid chromatography (LC) of small molecules. Tergitol was used as a surfactant
Shu-Ling Lin et al.
Talanta, 147, 199-206 (2015-11-26)
In this study, recently developed 1,6-hexanediol ethoxylate diacrylate (HEDA)-based polymeric monoliths were utilized as sorbents for efficient extraction of phenylurea herbicides (PUHs) from water samples. The HEDA-based monolithic sorbents were prepared in a fused silica capillary (0.7mm i.d., 4.5-cm long)

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