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LGM Pharma |
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- Vagistat
-
-
2026-09-11
- CAS:65899-73-2
- Min. Order: 1KG
- Purity: 99%-101%; EP
- Supply Ability: 500kg
- Vagistat USP/EP/BP
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- $1.10
-
2026-08-20
- CAS:65899-73-2
- Min. Order: 1g
- Purity: 99.9%
- Supply Ability: 100 Tons Min
- Tioconazole
-
- $45.00
-
2026-07-27
- CAS:65899-73-2
- Purity: 99.81%
- Supply Ability: 10g
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| | Vagistat Basic information |
| Product Name: | Vagistat | | Synonyms: | (+-)-1-(2,4-dichloro-beta-((2-chloro-3-ethenyl)oxy)phenethyl)imidazole;1-(2-((2-chloro-3-thienyl)methoxy)-2-(2,4-dichlorophenyl)ethyl)-1h-imidazol;vagistat;1-[2-[(2-chlorothiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)-ethyl]imidazole;1H-Imidazole, 1-[2-[(2-chloro-3-thienyl)methoxy]-2-(2,4-dichlorophenyl)ethyl]- (9CI);Fungibacid;Gyno-Trosyd;New Straitus U | | CAS: | 65899-73-2 | | MF: | C16H13Cl3N2OS | | MW: | 387.71 | | EINECS: | 265-973-8 | | Product Categories: | AGRYLIN;Antifungal;Active Pharmaceutical Ingredients | | Mol File: | 65899-73-2.mol |  |
| | Vagistat Chemical Properties |
| Melting point | 79-81oC | | Boiling point | 534.5±50.0 °C(Predicted) | | density | 1.3115 (rough estimate) | | refractive index | 1.6000 (estimate) | | RTECS | NI4480000 | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | solubility | Very slightly soluble in water, very soluble in methylene chloride, freely soluble in alcohol. | | form | powder | | pka | 6.66±0.12(Predicted) | | color | white to off-white | | Cosmetics Ingredients Functions | ANTIMICROBIAL | | InChI | InChI=1S/C16H13Cl3N2OS/c17-12-1-2-13(14(18)7-12)15(8-21-5-4-20-10-21)22-9-11-3-6-23-16(11)19/h1-7,10,15H,8-9H2 | | InChIKey | QXHHHPZILQDDPS-UHFFFAOYSA-N | | SMILES | C1N(CC(OCC2C=CSC=2Cl)C2=CC=C(Cl)C=C2Cl)C=CN=1 | | CAS DataBase Reference | 65899-73-2(CAS DataBase Reference) |
| Hazard Codes | Xn | | Risk Statements | 22 | | RIDADR | UN3077 | | WGK Germany | 3 | | HazardClass | 9 | | HS Code | 2934990002 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Repr. 2
Skin Sens. 1 |
| | Vagistat Usage And Synthesis |
| Description | Tioconazole is an antifungal agent, closely related to
miconazole. Tioconazole is effective in the topical
treatment of superficial fungal infections and appears to be more potent than
miconazole against Candida and Trichophyton species. | | Chemical Properties | White powder EINECS: 265-973-8 | | Originator | Pfizer (United Kiugdom) | | Uses | antithrombotic | | Uses | Tioconazole is an antifungal that is more active than Fluconazole (F421000) or Voriconazole (V760000) against Candida glabrata mutant strains. Antifungal (topical). | | Uses | Potent inhibitor of cytochrome-P450 | | Indications | Topical treatment of mycoses of the skin induced or sustained by fungi such as dermatophytes and yeasts. In addition, tioconazole is indicated for therapy of vulvovaginal mycoses caused by Candida species and Candida (Torulopsis) glabrata. | | Definition | ChEBI: A member of the class of imidazoles that comprises 2-(2,4-dichlorophenyl)ethylimidazole carrying an additional (2-chloro-3-thienyl)methoxy substituent at position 2. | | Manufacturing Process | A solution of 1-(2,4-dichlorophenyl)-2-(1-imidazolyl)ethanol (1.5 g, 5.8 mmol)
dissolved in dry tetrahydrofuran (10 ml) was added to a stirred suspension of
sodium hydride (0.39 g, as 80% dispersion in oil, 16 mmol) in dry
tetrahydrofuran (10 ml) and warmed to 70°C for 90 minutes.
The mixture was cooled in ice and a solution of 2-chloro-3-
chloromethylthiophene (8.8 mmol) in dry tetrahydrofuran was added. The
mixture was heated at 70°C for 3 hours and allowed to stir at room
temperature overnight. The solvent was removed under vacuum and the
residue stirred with dry ether (200 ml). The ether solution was filtered
through Celite and saturated with hydrogen chloride gas to precipitate an oil
which was solidified by trituration with ether and ethyl acetate. The solid
product was collected and recrystallized from a mixture of acetone and
diisopropyl ether to give the product, melting point 168°C to 170°C. | | Brand name | TROSYL | | Therapeutic Function | Antifungal | | Antimicrobial activity | Tioconazole is a broad-spectrum imidazole antimycotic with activity against almost all species of pathogenic fungi. | | Pharmacokinetics | Tioconazole is normally not absorbed after topical application to the skin [173]. On vaginal application of an ovulum containing 300 mg tioconazole, a serum concentration of 21 μg/mL was observed after 8 h. | | Clinical Use | 1-[2-[(2-chloro-3-thienyl)methoxy]2-(2,4-dichlorophenyl)-ethyl]-1H-imidazole (Vagistat) is used for the treatment ofvulvovaginal candidiasis. A vaginal ointment containing6.5% of the free base is available. Tioconazole is more effectiveagainst Torulopsis glabrata than are other azoles. | | Side effects | Local irritations such as itching, burning sensations, erythema, and dermatitis, and allergic reactions may occur in rare cases and are mainly due to the galenic formulation. |
| | Vagistat Preparation Products And Raw materials |
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