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Thermo Scientific™ Fluconazole 98%

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SKU: 455480250
UoM: Each
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LabMart Limited - Tamale
NS-246, Via, 4388 Tamale-Kumbungu Rd, Tamale, Northern Region, Ghana
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LabMart Limited
10 Rcecourse street, Accra, Greater Accra Region, Ghana
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MOQ : 1.0 Each
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Fluconazole is a synthetic, broad-spectrum triazole antifungal compound supplied at ≥98% purity, widely used in microbiological research, drug discovery, and fungal susceptibility assays. It exerts its fungistatic activity primarily through inhibition of fungal cytochrome P-450 enzyme sterol 14α-demethylase, disrupting ergosterol biosynthesis—a vital component of fungal cell membranes.

Due to its selectivity, fluconazole exhibits significantly lower inhibition of mammalian cytochrome P450 enzymes, making it a reliable tool in antifungal assays and fungal pathogenesis research.

Key Features

  • ≥98% HPLC purity
  • Inhibits cytochrome P450 14α-demethylase in fungal cells
  • Effective against Candida, Cryptococcus, and Coccidioides spp.
  • Supplied as a white to off-white crystalline powder
  • Highly soluble in DMSO, methanol, or ethanol for bioassays
  • Ideal for use as positive control in antifungal screening experiments
  • For Research Use Only (RUO)

Chemical & Physical Properties

PropertySpecification
CAS Number86386-73-4
IUPAC Name2-(2,4-difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol
Molecular FormulaC₁₃H₁₂F₂N₆O
Molecular Weight306.27 g/mol
Purity (HPLC)≥97.5%
Melting Point138–142 °C
AppearanceWhite to off-white crystalline powder
Loss on Drying≤1% (105 °C, 3 h)
SolubilitySoluble in DMSO, methanol, ethanol
StorageAmbient (store sealed and dry)

Packaging Options

Catalog No.Quantity
4554800101 g
4554800505 g

Applications

  • Fungal susceptibility testing (e.g., MIC assays)
  • Positive control in antifungal bioassays of plant or drug candidates
  • Model antifungal agent for studying ergosterol pathway inhibition
  • Used in research on Candida species, including C. albicans, C. glabrata, C. parapsilosis, and C. tropicalis
  • Studies on cytochrome P450 (CYP2C9) inhibition and drug metabolism

Mode of Action

Fluconazole inhibits fungal cytochrome P-450 sterol C-14 α-demethylation, a critical step in ergosterol synthesis. This leads to:

  • Accumulation of toxic 14α-methyl sterols
  • Disruption of cell membrane integrity
  • Inhibition of fungal growth (fungistatic effect)

Storage & Handling

  • Store in a cool, dry place in tightly closed container
  • Use appropriate PPE when handling powders
  • For laboratory research use only; not intended for therapeutic or diagnostic purposes

Supporting References

  1. Clancy, C.J. et al. Antimicrob. Agents Chemother. 2005, 49(8), 3171–3177.
  2. Matsui, K. et al. Mol. Pharmaceutics 2015, 12(7), 2418–2428.
  3. Bhardwaj, T. et al. J. Chem. Thermodyn. 2014, 78, 1–6.


Thermo Scientific’s Fluconazole, 98% offers a reliable and well-characterized antifungal agent for in vitro microbiological, biochemical, and pharmacological research. Its broad spectrum of activity, high purity, and defined mode of action make it a go-to control reagent for researchers investigating antifungal efficacy, resistance mechanisms, and drug-pathogen interactions.


Application: Cell culture
Storage Temperature: 2-8°C
Product Type: Antifungals
Product Brand: Thermo Fisher Scientific™, thermo Scientific
Product Grade: Analytical grade

Fluconazole is a synthetic, broad-spectrum triazole antifungal compound supplied at ≥98% purity, widely used in microbiological research, drug discovery, and fungal susceptibility assays. It exerts its fungistatic activity primarily through inhibition of fungal cytochrome P-450 enzyme sterol 14α-demethylase, disrupting ergosterol biosynthesis—a vital component of fungal cell membranes.

Due to its selectivity, fluconazole exhibits significantly lower inhibition of mammalian cytochrome P450 enzymes, making it a reliable tool in antifungal assays and fungal pathogenesis research.

Key Features

  • ≥98% HPLC purity
  • Inhibits cytochrome P450 14α-demethylase in fungal cells
  • Effective against Candida, Cryptococcus, and Coccidioides spp.
  • Supplied as a white to off-white crystalline powder
  • Highly soluble in DMSO, methanol, or ethanol for bioassays
  • Ideal for use as positive control in antifungal screening experiments
  • For Research Use Only (RUO)

Chemical & Physical Properties

PropertySpecification
CAS Number86386-73-4
IUPAC Name2-(2,4-difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol
Molecular FormulaC₁₃H₁₂F₂N₆O
Molecular Weight306.27 g/mol
Purity (HPLC)≥97.5%
Melting Point138–142 °C
AppearanceWhite to off-white crystalline powder
Loss on Drying≤1% (105 °C, 3 h)
SolubilitySoluble in DMSO, methanol, ethanol
StorageAmbient (store sealed and dry)

Packaging Options

Catalog No.Quantity
4554800101 g
4554800505 g

Applications

  • Fungal susceptibility testing (e.g., MIC assays)
  • Positive control in antifungal bioassays of plant or drug candidates
  • Model antifungal agent for studying ergosterol pathway inhibition
  • Used in research on Candida species, including C. albicans, C. glabrata, C. parapsilosis, and C. tropicalis
  • Studies on cytochrome P450 (CYP2C9) inhibition and drug metabolism

Mode of Action

Fluconazole inhibits fungal cytochrome P-450 sterol C-14 α-demethylation, a critical step in ergosterol synthesis. This leads to:

  • Accumulation of toxic 14α-methyl sterols
  • Disruption of cell membrane integrity
  • Inhibition of fungal growth (fungistatic effect)

Storage & Handling

  • Store in a cool, dry place in tightly closed container
  • Use appropriate PPE when handling powders
  • For laboratory research use only; not intended for therapeutic or diagnostic purposes

Supporting References

  1. Clancy, C.J. et al. Antimicrob. Agents Chemother. 2005, 49(8), 3171–3177.
  2. Matsui, K. et al. Mol. Pharmaceutics 2015, 12(7), 2418–2428.
  3. Bhardwaj, T. et al. J. Chem. Thermodyn. 2014, 78, 1–6.


Thermo Scientific’s Fluconazole, 98% offers a reliable and well-characterized antifungal agent for in vitro microbiological, biochemical, and pharmacological research. Its broad spectrum of activity, high purity, and defined mode of action make it a go-to control reagent for researchers investigating antifungal efficacy, resistance mechanisms, and drug-pathogen interactions.


No resources are currently available for this product.

This will display Shipping & Return.

Fluconazole is a synthetic, broad-spectrum triazole antifungal compound supplied at ≥98% purity, widely used in microbiological research, drug discovery, and fungal susceptibility assays. It exerts its fungistatic activity primarily through inhibition of fungal cytochrome P-450 enzyme sterol 14α-demethylase, disrupting ergosterol biosynthesis—a vital component of fungal cell membranes.

Due to its selectivity, fluconazole exhibits significantly lower inhibition of mammalian cytochrome P450 enzymes, making it a reliable tool in antifungal assays and fungal pathogenesis research.

Key Features

  • ≥98% HPLC purity
  • Inhibits cytochrome P450 14α-demethylase in fungal cells
  • Effective against Candida, Cryptococcus, and Coccidioides spp.
  • Supplied as a white to off-white crystalline powder
  • Highly soluble in DMSO, methanol, or ethanol for bioassays
  • Ideal for use as positive control in antifungal screening experiments
  • For Research Use Only (RUO)

Chemical & Physical Properties

PropertySpecification
CAS Number86386-73-4
IUPAC Name2-(2,4-difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol
Molecular FormulaC₁₃H₁₂F₂N₆O
Molecular Weight306.27 g/mol
Purity (HPLC)≥97.5%
Melting Point138–142 °C
AppearanceWhite to off-white crystalline powder
Loss on Drying≤1% (105 °C, 3 h)
SolubilitySoluble in DMSO, methanol, ethanol
StorageAmbient (store sealed and dry)

Packaging Options

Catalog No.Quantity
4554800101 g
4554800505 g

Applications

  • Fungal susceptibility testing (e.g., MIC assays)
  • Positive control in antifungal bioassays of plant or drug candidates
  • Model antifungal agent for studying ergosterol pathway inhibition
  • Used in research on Candida species, including C. albicans, C. glabrata, C. parapsilosis, and C. tropicalis
  • Studies on cytochrome P450 (CYP2C9) inhibition and drug metabolism

Mode of Action

Fluconazole inhibits fungal cytochrome P-450 sterol C-14 α-demethylation, a critical step in ergosterol synthesis. This leads to:

  • Accumulation of toxic 14α-methyl sterols
  • Disruption of cell membrane integrity
  • Inhibition of fungal growth (fungistatic effect)

Storage & Handling

  • Store in a cool, dry place in tightly closed container
  • Use appropriate PPE when handling powders
  • For laboratory research use only; not intended for therapeutic or diagnostic purposes

Supporting References

  1. Clancy, C.J. et al. Antimicrob. Agents Chemother. 2005, 49(8), 3171–3177.
  2. Matsui, K. et al. Mol. Pharmaceutics 2015, 12(7), 2418–2428.
  3. Bhardwaj, T. et al. J. Chem. Thermodyn. 2014, 78, 1–6.


Thermo Scientific’s Fluconazole, 98% offers a reliable and well-characterized antifungal agent for in vitro microbiological, biochemical, and pharmacological research. Its broad spectrum of activity, high purity, and defined mode of action make it a go-to control reagent for researchers investigating antifungal efficacy, resistance mechanisms, and drug-pathogen interactions.


No resources are currently available for this product.

This will display Shipping & Return.

Specifications

Pack Size 1g, 5g, 25g