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Fluconazole, 99%

Fluconazole, CAS # 86386-73-4, is a synthetic triazole with antifungal activity against some species of Candida. It also shows inhibitory activity against cytochrome P-450 enzymes and it is a demethylase. | CAS: 86386-73-4 | C13H12F2N6O | 306.277 g/mol

$233.01 - $2,155.44

Chemical Identifiers

CAS 86386-73-4
Molecular Formula C13H12F2N6O
Molecular Weight (g/mol) 306.277
MDL Number MFCD00274549
InChI Key RFHAOTPXVQNOHP-UHFFFAOYSA-N
Synonym fluconazole, diflucan, triflucan, elazor, biozolene, biocanol, fungata, fluconazol, fluconazolum, flucazol
PubChem CID 3365
ChEBI CHEBI:46081
IUPAC Name 2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazol-1-yl)propan-2-ol
SMILES C1=CC(=C(C=C1F)F)C(CN2C=NC=N2)(CN3C=NC=N3)O
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Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAJ6201503
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Thermo Scientific Chemicals
J6201503
1 g N/A
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AAJ6201506
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Thermo Scientific Chemicals
J6201506
5 g N/A
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AAJ6201514
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Thermo Scientific Chemicals
J6201514
25 g N/A
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Description

Description

Fluconazole is used to treat a variety of fungal infections, especially Candida infections of the vagina (yeast infections), mouth, throat and bloodstream. It is also used by the people having weak immune system such as persons with neutropenia due to cancer chemotherapy, transplanted patients and premature infants.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Description

  • Fluconazole, 98% is a triazole compound showing antifungal activity mainly against Candida, Coccidioides, and Cryptococcus species
  • It has been shown to inhibit fungal cytochrome P-450 sterol C-14 α-demethylation, resulting in the accumulation of fungal 14 α-methyl sterols, the loss of normal fungal sterols, and associated fungistatic activity
  • It also inhibits cytochrome P450 family 2 subfamily c member 9 (CYP2C9)
  • Mammalian cell demethylation is much less susceptible to fluconazole inhibition

Applications

  • Fluconazole has fungistatic activity against many fungal strains including Candida albicans, Candida glabrata, Candida parapsilosis, Candida tropicalis, and Cryptococcus neoformans.
  • Fluconazole interferes with fungal ergosterol synthesis and downregulates the metallothionein gene
  • In biological experiments, this compound has been used to assess minimum inhibitory concentration in (MIC)-fungal assays
  • It has also been used as a positive control in antifungal assay of plants
Specifications

Chemical Identifiers

86386-73-4
306.277
RFHAOTPXVQNOHP-UHFFFAOYSA-N
3365
2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazol-1-yl)propan-2-ol
C13H12F2N6O
MFCD00274549
fluconazole, diflucan, triflucan, elazor, biozolene, biocanol, fungata, fluconazol, fluconazolum, flucazol
CHEBI:46081
C1=CC(=C(C=C1F)F)C(CN2C=NC=N2)(CN3C=NC=N3)O

Specifications

86386-73-4
White
C13H12F2N6O
1 g
fluconazole, diflucan, triflucan, elazor, biozolene, biocanol, fungata, fluconazol, fluconazolum, flucazol
RFHAOTPXVQNOHP-UHFFFAOYSA-N
2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazol-1-yl)propan-2-ol
3365
306.27
Crystalline Powder
138°C to 140°C
1.05
MFCD00274549
14,4122
Soluble indimethylsulfoxide and ethanol.
C1=CC(=C(C=C1F)F)C(CN2C=NC=N2)(CN3C=NC=N3)O
306.277
CHEBI:46081
99%
Fluconazole
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Safety and Handling

Safety and Handling

GHS H Statement
H302-H315-H319-H335
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P201-P202-P264b-P270-P280i-P281-P301+P312-P302+P352-P305+P351+P338-P308+P313-P330-P332+P313-P362-P501c

H302-H315-H319-H360D

RTECSNumber : XZ4810000

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only