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Art. -Nr.: HY-N13089

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Pyrethrolone

Pyrethrolone is a pyrethrolone-type component found in the flowers of Tanacetum cinerariifolium and constitutes a component of natural pyrethrins. Pyrethrolone is generated through the desaturation of jasmolone catalyzed by the cytochrome P450 enzyme TcPYS (CYP82Q3). Pyrethrolone is used in insecticide-related research.

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CAS. Nr.: 487-67-2
Formel: C₁₁H₁₆O₂
Molecular Weight:180.24

Speicherung:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (270 KB)

Pyrethrolone Chemical Structure

CAS. Nr.: 487-67-2

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biologische Aktivität
- Beschreibung
- In Vitro
Chemical Information
Reinheit & Dokumentation
Verweise
Calculators
Help & FAQs
Classifications
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Biologische Aktivität

Beschreibung

In Vitro

Pyrethrolone is the active component of pyrethrin extracts, which exhibit strong contact toxicity against locusts and grasshoppers by interfering with voltage-gated sodium channels, causing rapid paralysis and death^[1].
Pyrethrolone is produced from jasmone in N. benthamiana leaves co-expressing TcJMH and DN144246^[2].
Pyrethrolone is produced by co-expression of TcJMH and TcPYS in transgenic Arabidopsis thaliana^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS. Nr. 487-67-2
Molecular Weight 180.24
Formel C₁₁H₁₆O₂
SMILES

CC/C=C\CC1=C([C@H](CC1=O)O)C
Structure Classification
- Others
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

Please store the product under the recommended conditions in the Certificate of Analysis.

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (270 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Mbuyiswa AA, et al. Botanical defence: medicinal plants as botanical insecticides against Locustana pardalina Walker (Orthoptera: Acrididae). Frontiers in Insect Science. 2026 Jul 30;6:1833553.

[2]. Li W, et al. Pyrethrin Biosynthesis: The Cytochrome P450 Oxidoreductase CYP82Q3 Converts Jasmolone To Pyrethrolone. Plant physiology. 2019 Nov;181(3):934-944. [Content Brief]

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Bioz

Keywords

MOQ

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100 mg

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