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Esbiothrin

PESTANAL®, analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C19H26O3
Numéro CAS:
584-79-2
Poids moléculaire :
302.41
Numéro CE :
209-542-4
Numéro MDL:
MFCD00045443
Code UNSPSC :
41116107
ID de substance PubChem :
329754485
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Format

neat

Chaîne SMILES 

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

Clé InChI

ZCVAOQKBXKSDMS-UHFFFAOYSA-N

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Description générale

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.

Informations légales

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Exclamation markEnvironment
GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H302 + H332,H410

Classification des risques

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

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG0866
BCCC2129
BCBT2206
BCBT2070
SZBE028XV

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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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