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Chemodex
Deltamethrin
84
CHF
CHF 84.00
In stock
CDX-D0619-M250250 mgCHF 84.00
| Product Details | |
|---|---|
| Product Type | Chemical |
| Properties | |
| Formula |
C22H19Br2NO3 |
| MW | 505.2 |
| CAS | 52918-63-5 |
| RTECS | GZ1233000 |
| Source/Host Chemicals | Synthetic. |
| Purity Chemicals | ≥97% (HPLC) |
| Appearance | White to light yellow powder. |
| Solubility | Soluble in DMSO (15 mg/ml) or ethanol (1 mg/ml). Insoluble in water. |
| Identity | Determined by 1H-NMR. |
| Declaration | Manufactured by Chemodex. |
| Other Product Data |
Click here for Original Manufacturer Product Datasheet |
| InChi Key | OWZREIFADZCYQD-DXCJPMOASA-N |
| Smiles | O=C(O[C@H](C#N)C1=CC=CC(OC2=CC=CC=C2)=C1)[C@H]3C(C)(C)[C@H]3/C=C(Br)/Br |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +20°C |
| Long Term Storage | +20°C |
| Handling Advice | Protect from light and moisture. |
| Use/Stability | Stable for at least 2 years after receipt when stored at RT. |
| Documents | |
| MSDS | Inquire |
| Product Specification Sheet | |
| Datasheet |
 Download PDF |
Description
Deltamethrin belongs to the class of synthetic pyrethroids, which are being widely used as insecticides. Deltamethrin acts on voltage-gated sodium channels (VGSCs) and voltage-gated calcium channels (VGCCs) that are the primary targets of these chemicals for toxicity to insects. Deltamethrin can increase neurotransmitter release which is associated with elevated levels of intrasynaptosomal free Ca2+ and protein phosphorylation activities. It acts as a potent inhibitor of calcineurin (protein phosphatase 2B), which results in cellular hyperexcitability by causing non-mutated calcium channels to remain open for an extended period of time allowing an abundance of Ca2+ to enter the cell. It also modulates sodium channels in the nerve cell membrane. It keeps the Na+ channels in an open state for a long time resulting to hyperactivity of the nervous system in mammals and insects. This compound can be used as a reference compound for analytical studies.
Product References
(1) K. Chinn & T. Narahashi; J. Physiol. 380, 191 (1986) | (2) E. Enan & F. Matsumura; Biochem. Pharmacol. 43, 1777 (1992) | (3) T. Narahashi; Trends Pharmacol. Sci. 13, 236 (1992) | (4) E. Enan & F. Matsumura; Biochem. Pharmacol. 45, 703 (1993) | (5) S.B. Symington & J.M. Clark; Pest. Biochem. Physiol. 82, 1 (2005) | (6) J.M. Clark & S.B. Symington; Invert. Neurosci. 7, 3 (2007) | (7) R. Zeng, et al.; Pestic. Biochem. Physiol. 138, 84 (2017) | (8) S.N. Bothe & A. Lampert; Toxicol. Appl. Pharmacol. 428, 115676 (2021)