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Merck
CN

34314

Bifenthrin

PESTANAL®, analytical standard, mixture of isomers

Synonym(s):

3-[(1Z)-2-Chloro-3,3,3-trifluoro-1-propenyl]-2,2-dimethylcyclopropanecarboxylic acid (2-methylbiphenyl-3-yl)methyl ester

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About This Item

Empirical Formula (Hill Notation):
C23H22ClF3O2
CAS Number:
Molecular Weight:
422.87
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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grade

analytical standard

Quality Level

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

CC1(C)C(C(OCC2=C(C)C(C3=CC=CC=C3)=CC=C2)=O)C1/C=C(Cl)/C(F)(F)F

InChI

1S/C23H22ClF3O/c1-14-16(10-7-11-17(14)15-8-5-4-6-9-15)12-19(28)21-18(22(21,2)3)13-20(24)23(25,26)27/h4-11,13,18,21H,12H2,1-3H3/b20-13+

InChI key

URDFVRKNOVHDTP-DEDYPNTBSA-N

General description

Bifenthrin (BF) is a pyrethroid insecticide widely used in urban and agricultural applications.

Application

Bifenthrin may be used as an analytical reference standard for the determination of the analyte in vegetables, ground and sea water and tea samples by various 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


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Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Sens. 1 - STOT RE 1

target_organs

Nervous system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品

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Simple, rapid solid-phase extraction procedure for the determination of ultra-trace levels of pyrethroids in ground and sea water by liquid chromatography/electrospray ionization mass spectroscopy.
Gil?Garcia MD, et al.
Rapid Communications in Mass Spectrometry, 20(16), 2395-2403 (2006)
Dissipation behavior of bifenthrin residues in tea and its brew.
Tewary DK, et al.
Food Control, 16(3), 231-237 (2005)
The effect of bifenthrin on the dopaminergic pathway in juvenile rainbow trout (Oncorhynchus mykiss).
Crago J and Schlenk D
Aquatic Toxicology (Amsterdam, Netherlands), 162, 66-72 (2015)



Global Trade Item Number

SKUGTIN
34314-100MG04061835352807