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Esbiothrin

PESTANAL®, analytical standard

Synonym(s):

3-Allyl-2-methyl-4-oxo-2-cyclopentenyl chrysanthemate

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About This Item

Empirical Formula (Hill Notation):
C19H26O3
CAS Number:
584-79-2
Molecular Weight:
302.41
EC Number:
209-542-4
MDL number:
MFCD00045443
UNSPSC Code:
41116107
PubChem Substance ID:
329754485
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

format

neat

SMILES string

C\C(C)=C\[C@@H]1[C@@H](C(=O)O[C@H]2CC(=O)C(CC=C)=C2C)C1(C)C

InChI

1S/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3

InChI key

ZCVAOQKBXKSDMS-UHFFFAOYSA-N

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General description

Esbiothrin is a synthetic pyrethroid, which is widely used against household pests and in public health.

Application

Esbiothrin may be used as a reference standard for the determination of the analyte in electric-mosquito coils using gas chromatography (GC) technique.
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 + H332,H410

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG0866
BCCC2129
BCBT2206
BCBT2070
SZBE028XV

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Sublethal toxicity of esbiothrin relationship with total antioxidant status and in vivo genotoxicity assessment in fish (Cyprinus carpio L., 1758) using the micronucleus test and comet assay.
Selvi M, et al.
Environmental Toxicology, 28(11), 644-651 (2011)
April P Neal et al.
Toxicological sciences : an official journal of the Society of Toxicology, 116(2), 604-613 (2010-05-15)
Pyrethroid insecticides are one of the most widely used classes of insecticides. Previous studies revealed that pyrethroids potently affect the insect voltage-gated sodium (Na(+)) channel (VGSC), resulting in prolonged channel open time. However, recent findings have suggested that pyrethroids may
Hitoshi Kawada et al.
PLoS neglected tropical diseases, 3(3), e391-e391 (2009-03-11)
Pyrethroid resistance is envisioned to be a major problem for the vector control program since, at present, there are no suitable chemical substitutes for pyrethroids. Cross-resistance to knockdown agents, which are mainly used in mosquito coils and related products as
Bao-Lin Chu et al.
Journal of separation science, 31(22), 3911-3920 (2008-11-15)
A comparison between chiral cyclodextrin-modified microemulsion electrokinetic chromatography (CD-MEEKC) and cyclodextrin-modified micellar electrokinetic chromatography (CD-MEKC) for the enantiomeric separation of esbiothrin was carried out. For both methods, the separation conditions were optimized by varying CD types and concentration, running buffer
Araceli Vences-Mejía et al.
Toxicology mechanisms and methods, 22(1), 41-46 (2011-11-15)
The effect of transfluthrin (TF) or D-allethrin (DA) pyrethroid (PYR) vapors, often contained as main ingredients in two commercially available mosquito repellent mats, on cytochrome P450 (CYP) enzymes of rat brain and liver was assessed. Immunodetection of CYP2E1 and CYP3A2
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