Nadifloxacin
Price 100 INR/ Kilograms
Nadifloxacin Specification
- Storage
- Store in a cool, dry, well-ventilated place away from light
- Boiling point
- Not applicable (decomposes before boiling)
- Molecular Weight
- 388.40 g/mol
- Melting Point
- 221-225C
- Poisonous
- No, when used as directed
- Shelf Life
- 2 years
- Solubility
- Slightly soluble in water, freely soluble in methanol, soluble in dimethyl sulfoxide (DMSO)
- Structural Formula
- See image
- Heavy Metal (%)
- Not more than 0.001%
- Smell
- Odorless
- Loss on Drying
- Not more than 0.5%
- Color
- White to off-white
- Molecular Formula
- C19H21FN4O4
- HS Code
- 29419090
- Medicine Name
- Nadifloxacin
- Chemical Name
- ()-9-Fluoro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid
- CAS No
- 124858-35-1
- Type
- Other
- Grade
- Other
- Usage
- Pharmaceutical intermediate; Topical antibiotic used for skin infections
- Purity(%)
- 98%
- Appearance
- White to off-white crystalline powder
- Physical Form
- Solid
- Packaging
- Fiber drum with inner double plastic bags or as required
- Stability
- Stable under recommended storage conditions
- Refractive Index
- Not applicable (solid)
- Residual Solvents
- Below ICH limits
- Application
- Active pharmaceutical ingredient (API) for topical formulations
- Microbial Limit
- Complies with pharmacopeial standards
- Manufacturing Process
- Synthetic
- Impurity Content
- Complies with pharmacopeial standards
Nadifloxacin Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
About Nadifloxacin
Features and Application of Nadifloxacin
Nadifloxacin is esteemed for its meritorious properties and is manufactured via a synthetic process with strict controls. Primarily used as an API in topical antibiotic formulations, it targets skin infections effectively. Its resplendent quality is reflected in its crystalline appearance and high purity. Utilized by healthcare professionals and pharmaceutical companies, Nadifloxacin offers safe, odorless application on affected areas. The site of application is generally the skin, and its usage brings rapid relief with minimal side effects, making it a popular choice.
Export Markets, Valuation, and Certifications
Nadifloxacin is celebrated in prime export markets across Asia, Europe, and North America. Offering quick dispatches, it meets stringent certifications and complies with global standards. The asking price is determined through transparent valuation, ensuring competitive rates for distributors and traders. Samples are provided as per policy to guarantee meritorious quality, and certifications authenticate its pharmacopoeial compliance and stability. Trusted by importers, Nadifloxacins purity and reliability facilitate seamless transactions and repeat business worldwide.
FAQs of Nadifloxacin:
Q: How is Nadifloxacin commonly used in pharmaceuticals?
A: Nadifloxacin is primarily used as an active pharmaceutical ingredient in topical formulations, serving as an antibiotic to treat various skin infections.Q: What process is involved in the manufacturing of Nadifloxacin?
A: Nadifloxacin is produced through a synthetic manufacturing process, ensuring purity, safety, and compliance with pharmacopeial standards.Q: When should Nadifloxacin be applied?
A: Nadifloxacin should be applied as directed by healthcare professionals, usually to the affected skin areas in accordance with prescription requirements for treating bacterial infections.Q: Where can Nadifloxacin be exported and distributed?
A: Nadifloxacin is distributed and exported globally, with main markets including Asia, Europe, and North America, subject to regulatory approvals and certifications.Q: What are the benefits of using Nadifloxacin?
A: Benefits include high purity, compliance with international standards, proven effectiveness against skin infections, and a favorable safety profile when used as recommended.Q: How is the quality of Nadifloxacin validated before exporting?
A: Quality is validated through extensive certifications, compliance with pharmacopeial standards, and rigorous testing for impurity content, microbial limits, and stability.
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