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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:
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. 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
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

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

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW2049

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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)
Analysis of phenylurea herbicides from plants by GC/MS
Pena F, et al.
Talanta, 56(4), 727-734 (2002)
Michael T Rose et al.
Chemosphere, 63(11), 1849-1858 (2005-12-07)
A pilot-scale, ponded wetland consisting of an open pond and a vegetated pond in series was constructed on a cotton farm in northern New South Wales, Australia, and assessed for its potential to remove pesticides from irrigation tailwater. Ten incubation
Sarah H Lancaster et al.
Journal of agricultural and food chemistry, 56(18), 8588-8593 (2008-08-30)
Laboratory experiments were conducted to describe the influence of glyphosate and fluometuron on soil microbial activity and to determine the effect of glyphosate on fluometuron degradation in soil and by Rhizoctonia solani. Soil and liquid medium were amended with formulated
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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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