Liranaftate Bulk Powder
Purity:>99%
Product Name:Liranaftate Powder
Name:Liranaftate
Appearance:White Powder
Assay:HPLC99%
Application:Pharmaceutical
CAS:88678-31-3
Mf:C18h20n2o2s
MW:328.4286
Description
Liranaftate Bulk Powder information
| Product Name: | Liranaftate |
| Synonyms: | LNF;O-(5,6,7,8-tetrahydronaphthalen-2-yl) N-(6-methoxypyridin-2-yl)-N-methylcarbamothioate;carbamothioicacid,(6-methoxy-2-pyridinyl)methyl-,o-(5,6,7,8-tetrahydro-2-na;phthalenyl)ester;LIRANAFATE;LIRANAFTATE;M-732;(6-METHOXY-2-PYRIDINYL)-METHYLCARBAMOTHIOIC ACID O-(5,6,7,8-TETRAHYDRO-2-NAPHTHALENYL) ESTER |
| CAS: | 88678-31-3 |
| MF: | C18H20N2O2S |
| MW: | 328.43 |
| Mol File: | 88678-31-3.mol |
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What is Liranaftate Bulk Powder?
Tinea pedis treatment: It includes interdigital type, hyperkeratosis type and vesicular type foot infections.
Tinea corporis treatment: It is used for dermatophyte infections in smooth skin areas.
Treatment for tinea cruris: Targeting fungal infections in the groin and perineum.
Tinea manus treatment: Improve fungal lesions on the palms and fingers.
Treatment for pityriasis versicolor: Inhibit abnormal skin pigmentation caused by Malassezia.
Cutaneous candidiasis: Treating intercutaneous rashes and infections caused by Candida.
COA of Liranaftate
| Test Item | Specification | Result |
| Appearance | Visual inspection - white powder | Conforms |
| Identification | Infrared Spectroscopy (IR) / UV Spectroscopy (UV) - Matches reference standard | Matches reference standard |
| Assay (Content) | HPLC - 98.0% to 102.0% of labeled amount | 99.61% |
| Loss on Drying | Gravimetric Analysis at 105℃ - Not more than 0.5% | 0.19% |
| Residue on Ignition | Gravimetric Analysis - Not more than 0.1% | 0.02% |
| Heavy Metals | Not more than 20 ppm | 8ppm |
| Individual Impurity | HPLC - Not more than 2.0% | 1.03% |
| Total Impurities | HPLC - Not more than 5.0% | 1.19% |
| Microbial Limit | Total Aerobic Microbial Count (TAMC) - Not more than 1000 CFU/gTotal Yeasts and Molds Count (TYMC) - Not more than 100 CFU/gAbsence of Escherichia coli, Salmonella spp, and Staphylococcus aureus | 560CFU/g33CFU/gNot detected |
| Bacterial Endotoxins | LAL Test - Not more than 0.25 Endotoxin Units per mg | 0.15 Endotoxin Units per mg |
| Conclusion | Conform with enterprise specification. | |
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