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ChemicalBook > Product Catalogue >API >Synthetic Anti-infective Drugs >Antifungal Drugs >Oxiconazole nitrate

Oxiconazole nitrate

Oxiconazole nitrate Structure
  • ₹0
  • Product name: Oxiconazole nitrate
  • CAS: 64211-46-7
  • MF: C18H13Cl4N3O
  • MW: 429.13
  • EINECS:264-730-3
  • MDL Number:MFCD01727545
  • Synonyms:(Z)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone O-[(2,4-Dichlorophenyl)methyl]oxime Mononitrate;Myfungar;Oceral;Oxistat;Ro-13-8996;Sgd-301-76;Oxiconazole nitrate;(Z)-1-(2,4-Diehlorophenyl)-2-(1H-imidazol-1-y1)ethanone O-[(2,4-diehlorophenyl)methyl]oxime mononitrate
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :137-1380C
storage temp. :Refrigerator
solubility :Chloroform, Methanol (Sparingly)
form :Solid
color :Off-White
CAS DataBase Reference :64211-46-7(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
H332 Harmful if inhaled Acute toxicity,inhalation Category 4 Warning GHS hazard pictograms P261, P271, P304+P340, P312
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P271 Use only outdoors or in a well-ventilated area.
P301+P312 IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P304+P340 IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P312 Call a POISON CENTER or doctor/physician if you feel unwell.
P330 Rinse mouth.
P501 Dispose of contents/container to..…

Description

Oxiconazole is an antifungal imidazole that inhibits a broad spectrum of pathogenic yeasts and molds, including A. fumigatus, C. neoformans, C. albicans, and T. mentagrophytes. Its inhibitory action results from its ability to inhibit the synthesis of ergosterol, the major sterol of the fungal cell membrane.

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