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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
BCCF3010
BCBS5817V
SZBD326XV
SZBA316XV
SZBA218X

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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)
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)
Ki Hun Park et al.
Food chemistry, 138(4), 2306-2311 (2013-03-19)
This paper describes a comparison of the properties of the three versions of the QuEChERS method (quick, easy, cheap, effective, rugged and safe) - the original (unbuffered), acetate-buffered, and citrate-buffered methods - for the determination of fenobucarb residues in beef
Profile of metal-binding proteins and heme oxygenase in red carp treated with heavy metals, pesticides and surfactants.
T Ariyoshi et al.
Bulletin of environmental contamination and toxicology, 44(4), 643-649 (1990-04-01)
T Miyaoka et al.
Journal of pharmacobio-dynamics, 9(9), 697-703 (1986-09-01)
The mechanism of potentiation of 2-sec-butylphenyl N-methylcarbamate (BPMC) toxicity by O,O-dimethyl O-(3-methyl-4-methylthiophenyl) phosphorothioate (fenthion) in mice was investigated in relation to BPMC metabolism in the liver. Simultaneous administration of BPMC and either one of the thiophosphates (fenthion, its sulfoxide and
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