Identification | Back Directory | [Name]
IPCONAZOLE | [CAS]
125225-28-7 | [Synonyms]
knf-317 Ipcozole IPCONAZOLE Ipconazole [iso] Ipconazole Solution IPCONAZOLE STANDARD ipconazole (bsi, pa e-iso) Ipconazole@100 μg/mL in Acetonitrile Ipconazole@1000 μg/mL in Acetonitrile Ipconazole Solution in Methanol, 100μg/mL 2-((4-Chlorophenyl)methyl)-5-(1-methylethyl)-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol Cyclopentanol, 2-((4-chlorophenyl)methyl)-5-(1-methylethyl)-1-(1H-1,2,4-triazol-1-ylmethyl)- | [Molecular Formula]
C18H24ClN3O | [MDL Number]
MFCD01635119 | [MOL File]
125225-28-7.mol | [Molecular Weight]
333.861 |
Chemical Properties | Back Directory | [Melting point ]
86~92℃ | [Boiling point ]
486.0±41.0 °C(Predicted) | [density ]
1.24±0.1 g/cm3(Predicted) | [vapor pressure ]
3.58 x l0-6 Pa (isomer pair I);
6.99 x l0-6Pa (isomer pair 11) (25 °C) | [pka]
13.76±0.60(Predicted) | [Water Solubility ]
6.93 mg l-1 (20 °C) | [EPA Substance Registry System]
Ipconazole (125225-28-7) |
Hazard Information | Back Directory | [Uses]
Ipconazole controls a wide range of seed diseases in rice and other
crops and is particularly effective against 'Bakanae disease', Helminthosporum
leaf spot and blast on rice. | [Definition]
ChEBI: A member of the class of cyclopentanols carrying 1,2,4-triazol-1-ylmethyl, 4-chlorobenzyl and isopropyl substituents at positions 1, 2 and 5 respectively. Used to control a range of seed diseases in rice, vegetables and other, mainly non-food, crops. | [Metabolic pathway]
Ipconazole is a mixture of two geometric isomer pairs (lRS,2SR,5RS)
(I) and (lRS,2SR,5SR) (Ⅱ). They differ in the orientation of the hydroxy,
benzyl and isopropyl groups. The ratio of I : II in the technical product is
90 : 10 and the two-component isomer pairs are of equal activity. The
metabolism of ipconazole in plants and animals involves oxidation at the
benzylic and isopropyl groups to yield alcohols which may be further
oxidised to the corresponding ketones or carboxylic acids (or lactones).
The resulting array of metabolites can be expected to be stereochemically
more complex than the original isomer mixture. | [Degradation]
Ipconazole is stable towards hydrolysis and is thermally stable. |
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