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125225-28-7

125225-28-7 Structure

125225-28-7 Structure
IdentificationBack 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 PropertiesBack 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)
Safety DataBack Directory
[HS Code ]

29339900
Hazard InformationBack 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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