1646-88-4
1646-88-4
Chemical Structure
Aldicarb sulfone
- CAS No.: 1646-88-4
- Formula:C7H14N2O4S
- Molecular Weight:222.26
IUPAC Name: (E)-2-methyl-2-(methylsulfonyl)propanal O-methylcarbamoyl oxime
InChIKey: YRRKLBAKDXSTNC-WEVVVXLNSA-N
SMILES: CC(S(=O)(C)=O)(C)/C=N/OC(NC)=O
Biological Activity: Aldicarb sulfone is one of the metabolites of the carbamate pesticide Aldicarb and has insecticidal activity. Aldicarb sulfone is also an inhibitor of cholinesterase[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Aldicarb sulfone | 99.46% | Aldicarb sulfone is one of the metabolites of the carbamate pesticide Aldicarb and has insecticidal activity. Aldicarb sulfone is also an inhibitor of cholinesterase. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Aldicarb sulfone (Standard) | ≥98% | Aldicarb sulfone (Standard) is the analytical standard of Aldicarb sulfone (HY-17530). This product is intended for research and analytical applications. Aldicarb sulfone is one of the metabolites of the carbamate pesticide Aldicarb and has insecticidal activity. Aldicarb sulfone is also an inhibitor of cholinesterase. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Aldicarb sulfone-13C2,d3 | Aldicarb sulfone-13C2,d3 is the deuterium and 13C labeled Aldicarb sulfone (HY-17530). Aldicarb sulfone is one of the metabolites of the carbamate pesticide Aldicarb and has insecticidal activity. Aldicarb sulfone is also an inhibitor of cholinesterase. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Huang SP, et al. Effects of aldicarb and its sulfoxide and sulfone on the biology of Tylenchulus semipenetrans. J Nematol. 1978 Jan;10(1):100-6. [Content Brief]
- [2]. Burgess J L, et al. Aldicarb poisoning: a case report with prolonged cholinesterase inhibition and improvement after pralidoxime therapy. Archives of internal medicine, 1994, 154(2): 221-224.
