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45502

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Fluometuron

PESTANAL®, analytical standard

Synonym(s):

1,1-Dimethyl-3-[3-(trifluoromethyl)phenyl]urea, Fluomethuron

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About This Item

Empirical Formula (Hill Notation):
C10H11F3N2O
CAS Number:
2164-17-2
Molecular Weight:
232.20
Beilstein/REAXYS Number:
2217354
EC Number:
218-500-4
MDL number:
MFCD00018012
UNSPSC Code:
41116107
PubChem Substance ID:
329756794
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

CN(C)C(=O)Nc1cccc(c1)C(F)(F)F

InChI

1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)

InChI key

RZILCCPWPBTYDO-UHFFFAOYSA-N

General description

Fluometuron belongs to the class of phenylurea herbicides, commonly employed for the control of broad-leaf weeds and grasses affecting crops such as cotton and sugarcane.[1] It is also used for pre-emergence protection of bush fruits, citrus and asparagus.[2]

Application

Fluometuron may be used as an analytical reference standard for the quantification of the analyte in environmental samples[3] and vegetation[2] using different chromatography techniques.
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

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW2049

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Analysis of phenylurea herbicides from plants by GC/MS
Pena F, et al.
Talanta, 56(4), 727-734 (2002)
Multiresidue HPLC methods for phenyl urea herbicides in water
Ruberu.RS, et al.
Journal of Agricultural and Food Chemistry, 48(9), 4109-4115 (2000)
Handbook of Pesticide Toxicology: Principles and Agents, Volume 1, 1(2), 4109-4115 (2001)
Michael T Rose et al.
Chemosphere, 72(7), 999-1005 (2008-06-10)
Field data shows that plants accelerate pesticide dissipation from aquatic systems by increasing sedimentation, biofilm contact and photolysis. In this study, a graphical model was constructed and calibrated with site-specific and supplementary data to describe the loss of two pesticides
D Kh Khamidov et al.
Tsitologiia, 33(4), 84-88 (1991-01-01)
Intracellular distribution of labeled cotoran was studied. 3H-cotoran was shown to penetrate through the nuclear membrane to accumulate uneventfully in the intranuclear components. An insignificant amount of 3H-cotoran was associated with the nucleoplasm and the outer nuclear membrane. At the
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Protocols

US EPA Method 632: HPLC Analysis of Pesticides on Ascentis® C18

-methylcarbamate 10 μg/mL; Diuron; Propham; Siduron; Methiocarb, analytical standard; Linuron 10 μg/mL; Swep 10 μg/mL; Chlorpropham 10 μg/mL; Barban; Neburon

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