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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)
C L Qiao et al.
Journal of medical entomology, 36(6), 666-670 (1999-12-11)
Organophosphate (OP) insecticides have been used widely to control Culex pipiens L. populations and this has led to the emergence of OP-resistance. Predominantly, resistance in Cx. pipiens is caused by over-production of nonspecific esterases, such as Est beta 1(1) and
H Kobayashi et al.
Toxicology letters, 29(2-3), 153-159 (1985-12-01)
Mice showed no toxic signs after a single injection of o-sec-butylphenyl methylcarbamate (BPMC, 10 mg/kg) or 2-isopropoxyphenyl-N-methylcarbamate (propoxur, 2 mg/kg). Each dose of BPMC or propoxur caused an increase in acetylcholine content and a decrease in acetylcholinesterase activity in the
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
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