Imidacloprid olefin (CHEM059015)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-02 23:13:04 UTC | ||||||||
| Update Date | 2026-08-25 21:03:09 UTC | ||||||||
| Accession Number | CHEM059015 | ||||||||
| Identification | |||||||||
| Common Name | Imidacloprid olefin | ||||||||
| Class | Small Molecule | ||||||||
| Description | Imidacloprid olefin is an organic compound with the formula C9H8Cl1N5O2 and an average molecular weight of 253.65 g/mol. Imidacloprid olefin belongs to the halopyridines, a subclass of pyridines and derivatives within the organic compounds. It is categorized under the superclass of organoheterocyclic compounds. This substance is found in or released from one recorded source: agriculture and land management pesticides. Recorded exposure routes for this compound include inhalation, oral, and touch. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type |
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| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C9H8Cl1N5O2 | ||||||||
| Average Molecular Mass | 253.650 g/mol | ||||||||
| Monoisotopic Mass | 253.037 g/mol | ||||||||
| CAS Registry Number | 1115248-04-8 | ||||||||
| IUPAC Name | N-[1-[(6-chloropyridin-3-yl)methyl]imidazol-2-yl]nitramide | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | [O-][N+](=O)NC1=NC=CN1CC1=CC=C(Cl)N=C1 | ||||||||
| InChI Identifier | InChI=1S/C9H8ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-5H,6H2,(H,11,13) | ||||||||
| InChI Key | TYLCDJYHUVCRBH-UHFFFAOYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
