imazapic
3-pyridinecarboxylic acid, 2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-methyl-
Identification
| Name | imazapic |
| CAS Number | 104098-48-8 |
| FDA UNII | K98N09T10R |
| Molecular Formula | C14 H17 N3 O3 |
| Molecular Weight | 275.30809000 |
| MDL Number | MFCD04307828 |
| Nikkaji Number | J754.490A |
Regulatory
Physical Properties
| Appearance | off-white to tan powder (est) |
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 434.20 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.000000 mmHg @ 25.00 °C. (est) |
| Flash Point | 422.00 °F. TCC ( 216.40 °C. ) (est) |
| logP (o/w) | 2.470 |
| Soluble in | water, 132.5 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | herbicides / pesticides |
| Recommendation for imazapic usage levels up to | not for fragrance use. |
| Recommendation for imazapic flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2-[4,5-
dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-methyl-3-pyridinecarboxylic acid
imazameth
imazamethapyr
imazmethapyr
5-
methyl-2-(4-methyl-5-oxidanylidene-4-propan-2-yl-1H-imidazol-2-yl)pyridine-3-carboxylic acid
5-
methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)-3-pyridinecarboxylic acid
5-
methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)pyridine-3-carboxylic acid
5-
methyl-2-[4-methyl-4-(methylethyl)-5-oxo(2-imidazolin-2-yl)]pyridine-3-carboxylic acid
5-
methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid
5-
methyl-2-[5-methyl-5-(1-methylethyl)-4-oxo-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid
2-(4-iso
propyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-methylnicotinic acid
2-(4-iso
propyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-methylnicotinic acid
2-(5-iso
propyl-5-methyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-methylnicotinic acid
3-
pyridinecarboxylic acid, 2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl)-5-methyl-
3-
pyridinecarboxylic acid, 2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-methyl-
3-
pyridinecarboxylic acid, 2-[4,5-dihydro-5-methyl-5-(1-methylethyl)-4-oxo-1H-imidazol-2-yl]-5-methyl-
PubMed:
Toxicological responses of Cyprinus carpio after exposure to a commercial herbicide containing imazethapyr and imazapic.
PubMed:
Bioavailability of diuron, imazapic and isoxaflutole in soils of contrasting textures.
PubMed:
Isolation, characterization of a strain capable of degrading imazethapyr and its use in degradation of the herbicide in soil.
PubMed:
Molecular and biochemical characterization of an induced mutation conferring imidazolinone resistance in sunflower.
PubMed:
Photolysis pathway of imazapic in aqueous solution: ultrahigh resolution mass spectrometry analysis of intermediates.
PubMed:
Comparative genotoxicity evaluation of imidazolinone herbicides in somatic cells of Drosophila melanogaster.
PubMed:
Responses of enantioselective characteristics of imidazolinone herbicides and Chiralcel OJ column to temperature variations.
PubMed:
High-performance liquid chromatographic separation of imidazolinone herbicide enantiomers and their methyl derivatives on polysaccharide-coated chiral stationary phases.
PubMed:
A new method for in-situ monitoring of the underground development of Orobanche cumana in sunflower (Helianthus annuus) with a mini-rhizotron.
PubMed:
Imidazolinone-tolerant crops: history, current status and future.
PubMed:
Cross-resistance to imidazolinone herbicides in chlorsulfuron-resistant Raphanus raphanistrum.
PubMed:
Haptens and monoclonal antibodies for immunoassay of imidazolinone herbicides.
PubMed:
Capillary electrophoresis determinative and LC-MS confirmatory method for screening selected imidazolinone herbicides from soil.