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Merck
CN

45502

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:
Molecular Weight:
232.20
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
218-500-4
Beilstein/REAXYS Number:
2217354
MDL number:
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InChI key

RZILCCPWPBTYDO-UHFFFAOYSA-N

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)

SMILES string

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

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

Quality Level

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. It is also used for pre-emergence protection of bush fruits, citrus and asparagus.

Application

Fluometuron may be used as an analytical reference standard for the quantification of the analyte in environmental samples and vegetation 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

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品
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Handbook of Pesticide Toxicology: Principles and Agents, Volume 1, 1(2), 4109-4115 (2001)
Multiresidue HPLC methods for phenyl urea herbicides in water
Ruberu.RS, et al.
Journal of Agricultural and Food Chemistry, 48(9), 4109-4115 (2000)
Analysis of phenylurea herbicides from plants by GC/MS
Pena F, et al.
Talanta, 56(4), 727-734 (2002)
O S Mohamed et al.
Veterinary and human toxicology, 37(3), 214-216 (1995-06-01)
Twelve of fifteen 6-9-mo-old clinically healthy Desert sheep were given single or repeated daily doses of 25 to 4000 mg cotoran/kg by drench. Cotoran poisoning was characterized by grinding of the teeth, ruminal tympany, mydriasis, dyspnea, staggering, paresis of the
Beatriz Gámiz et al.
Journal of agricultural and food chemistry, 58(13), 7893-7901 (2010-06-16)
The use of pesticides in agriculture has become a source of pollution of soil and water in the last decades. Extensive pesticide transport losses due to leaching and runoff produce nonpoint source contamination of soils and water. One of the

Protocols

-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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