Description

(S)-Lanoconazole is the single, active (S)-enantiomer of the broad-spectrum antifungal agent lanoconazole. This high-purity chiral compound is critical for advanced pharmaceutical research and development, offering superior specificity and reduced potential for side effects compared to racemic mixtures. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on developing next-generation topical antifungal treatments and studying sterol biosynthesis inhibition.

Application

• Active Pharmaceutical Ingredient (API) for topical antifungal creams, ointments, and solutions.
• Reference Standard in analytical chemistry for quality control and method development.
• Pharmacological Research for studying the mechanism of action of azole antifungals.
• Chiral Intermediate in the synthesis of more complex, enantiomerically pure drug molecules.
• Formulation Development for optimizing drug delivery systems targeting dermatological infections.

Basic Information

Product Name	(S)-Lanoconazole
CAS No.	133162-80-8
Molecular Formula	C14H7Cl2N3S2
Molecular Weight	352.27 g/mol
Synonyms	(S)-(-)-Lanoconazole; (S)-N-[4-(2,4-Dichlorophenyl)-1,3-dithiolan-2-ylidene]-2,6-dichlorobenzeneacetamide; (S)-Astat; (S)-NND-318; (S)-Lanoconazol; (S)-Dermaleve; (S)-Z-0515; (S)-Form of Lanoconazole
EINECS	Contact for details

Quality Control

Our (S)-Lanoconazole is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral purity verification by HPLC, to ensure it meets stringent specifications for pharmaceutical research. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and enantiomeric excess.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Enantiomeric Purity (Chiral HPLC)	≥99.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.