1-{2-[(2,6-Dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazol-1-ium nitrate

Name	isoconazole nitrate
Synonyms	Fazol R 15454 24168-96-5 Adestan G 100 Gyno-Travogen isoconazole nitrate Imidazole, 1-[2,4-dichloro-b-[(2,6-dichlorobenzyl)oxy]phenethyl]-, mononitrate (8CI) 1-{2-[(2,6-Dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazol-1-ium nitrate 1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-1H-imidazolium nitrate 1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-1h-imidazole mononitrate 1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-3H-imidazol-1-ium nitrate 1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-, mononitrate (9CI)
CAS	24168-96-5
EINECS	246-051-4
InChI	InChI=1/C18H14Cl4N2O.NO3/c19-12-4-5-13(17(22)8-12)18(9-24-7-6-23-11-24)25-10-14-15(20)2-1-3-16(14)21;2-1(3)4/h1-8,11,18H,9-10H2;/q;-1/p+1

Molecular Formula	C18H15Cl4N3O4
Molar Mass	479.14
Melting Point	178-182°C
Boling Point	178-182℃
Solubility	Very slightly soluble in water, soluble in methanol, slightly soluble in ethanol (96 per cent).
Appearance	White crystal or crystalline powder
Color	White to Off-White
Merck	14,5160
Storage Condition	Sealed in dry,2-8°C
Use	Broad-spectrum antifungal agents
In vitro study	Isoconazole nitrate also exerts several other effects on the fungal membrane, which are independent of inhibition of the ergosterol synthesis. Isoconazole nitrate (ISN) causes a rapid reduction of cellular adenosine triphosphate (ATP) within 10 min of in vitro exposure. Isoconazole nitrate (1, 10 μg/mL) induces a blockade of cell division in vitro by its action on synthesis and organisation of the cell membrane. Isoconazole nitrate (50, 100 μg/mL), ISN induced necrosis and death of fungal cells.

RTECS

NI4772000

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1-{2-[(2,6-Dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazol-1-ium nitrate Request for Quotation