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45488

Supelco

Fenobucarb

PESTANAL®, analytical standard

Synonym(s):

BPMC

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About This Item

Empirical Formula (Hill Notation):
C12H17NO2
CAS Number:
3766-81-2
Molecular Weight:
207.27
Beilstein:
2052332
EC Number:
223-188-8
MDL number:
MFCD00053081
UNSPSC Code:
41116107
PubChem Substance ID:
329756780
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

CCC(C)c1ccccc1OC(=O)NC

InChI

1S/C12H17NO2/c1-4-9(2)10-7-5-6-8-11(10)15-12(14)13-3/h5-9H,4H2,1-3H3,(H,13,14)

InChI key

DIRFUJHNVNOBMY-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 markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>212.0 °F

Flash Point(C)

> 100 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL1474
BCCF3010
BCBS5817V
SZBD326XV
SZBA316XV

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Huan Wu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 174, 301-306 (2016-12-18)
A convenient fluorescence quenching method for determination of Quizalofop-p-ethyl(Qpe) was proposed in this paper. Eosin Y(EY) is a red dye with strong green fluorescence (λex/λem=519/540nm). The interaction between EY, Pd(II) and Qpe was investigated by fluorescence spectroscopy, resonance Rayleigh scattering(RRS)
Nguyen Thanh Tam et al.
Environmental science and pollution research international, 25(14), 13226-13234 (2016-06-03)
Organophosphates (e.g. chlorpyrifos ethyl) and carbamates (e.g. fenobucarb) are commonly used to control a wide range of pests in rice fields of the Mekong Delta in Vietnam. This study assesses the combined effect of chlorpyrifos ethyl (CPF) and fenobucarb (F)
Yuko Ito et al.
Journal of chromatography. A, 1187(1-2), 53-57 (2008-02-26)
Dual counter-current chromatography (dual CCC)-tandem mass spectrometry (MS/MS) was successfully performed with a newly designed spiral column for dual CCC. The small column capacity required for directly coupling with electrospray MS/MS was accomplished by forming a rectangular spiral groove on
Yuko Ito et al.
Journal of chromatography. A, 1108(1), 20-25 (2006-02-01)
Dual counter-current chromatography (dual CCC) has been successfully applied to rapid sample preparation for the simultaneous determination of residual carbaryl, fenobucarb and methomyl in vegetable oil and citrus fruit. The citrus fruit samples were extracted with n-hexane solution containing stable
Rashmi Sharma et al.
Insect biochemistry and molecular biology, 34(5), 425-432 (2004-04-28)
Toxicity to o-sec-butylphenyl methylcarbamate compound (BPMC) was analyzed in the rice brown planthopper, Nilaparvata lugens, using a differential proteomics approach of identifying proteins on two dimensional-polyacrylamide gel electrophoresis (2D-PAGE). Proteome analysis from BPMC-treated brown planthopper resulted in the modulation of
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