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A7819612

Tolnaftate , ≥98% , 2398-96-1

Synonym(s):
Methyl-(3-methylphenyl)carbamothioic acid O-2-naphthyl ester;Tolnaftate

CAS NO.:2398-96-1

Empirical Formula: C19H17NOS

Molecular Weight: 307.41

MDL number: MFCD00056611

EINECS: 219-266-6

Pack Size Price Stock Quantity
1G RMB44.00 In Stock
5G RMB87.20 In Stock
25G RMB308.00 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 110.5-111.5°C
Boiling point: 453.4±38.0 °C(Predicted)
Density  1.1328 (rough estimate)
refractive index  1.6970 (estimate)
storage temp.  Sealed in dry,2-8°C
solubility  Soluble in chloroform at 50 mg/ml. Sparingly soluble in ethanol or methanol
form  powder
pka -0.35±0.50(Predicted)
color  white to off-white
Water Solubility  <0.1 g/100 mL at 22 ºC
λmax 258nm(MeOH)(lit.)
Merck  14,9519
InChIKey FUSNMLFNXJSCDI-UHFFFAOYSA-N
LogP 5.142 (est)
NIST Chemistry Reference Tolnaftate(2398-96-1)
EPA Substance Registry System Tolnaftate (2398-96-1)

Description and Uses

Tolnaftate is a thiocarbamate antifungal agent. It is active against clinical isolates of the dermatophytes T. rubrum, T. mentagraphytes, T. verrucosum, E. floccosum, and M. canis (MIC50s = 50, 100, 6, 50, and 50 ng/ml, respectively), as well as 18 additional yeast and filamentous fungi species (MIC = 0.003-0.8 μg/ml)., Tolnaftate also reduces aflatoxin production in A. parasiticus in a concentration-dependent manner. It inhibits squalene epoxidase with an IC50 value of 12.5 μg/ml in a cell-free assay.

Tolnaftate is used to study the mechanism of ergosterol (sterol) biosynthesis at the rate-limiting step of squalene epoxidase inhibition. Tolnaftate is clinically used to treat cutaneous infections such as athlete?s foot, jock itch, and ringworm1. It also has been used as a comparator compound for antifungal efficiency studies.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
WGK Germany  2
RTECS  FD8891300
TSCA  Yes
HazardClass  IRRITANT
HS Code  2930206050
Toxicity LD50 in mice, rats (g/kg): >10, >6 orally; >6, >4 s.c. (Hashimoto)

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