Doxofylline
Price 100 INR/ Kilograms
Doxofylline Specification
- Loss on Drying
- NMT 0.5%
- Taste
- Bitter
- Particle Size
- NMT 10 micron
- Poisonous
- NO
- Molecular Formula
- C11H14N4O4
- Melting Point
- >200C
- Shelf Life
- 36 months
- Storage
- Store in cool, dry place away from sunlight
- Structural Formula
- C11H14N4O4
- Smell
- Odorless
- Color
- White
- Heavy Metal (%)
- NMT 0.001%
- HS Code
- 2939
- Molecular Weight
- 266.26 g/mol
- EINECS No
- 274-662-1
- Solubility
- Slightly soluble in water, freely soluble in methanol, practically insoluble in ether
- Medicine Name
- Doxofylline
- Chemical Name
- 7-(1,3-dioxolan-2-ylmethyl)-theophylline
- CAS No
- 69975-86-6
- Type
- Other
- Grade
- Other
- Usage
- Used as a bronchodilator in treatment of asthma and COPD
- Purity(%)
- 99% min
- Appearance
- White or almost white powder
- Physical Form
- Powder
- Identification
- IR spectrum complies with reference standard
- Stability
- Stable under recommended storage conditions
- Standard
- USP/EP/BP/Ph. Eur.
- Related Substances
- Total impurities NMT 0.5%
- Application
- Pharmaceutical API
- Packing
- HDPE drums with double polyethylene bags
- Assay (by HPLC)
- Not less than 99.0%
- Specific Optical Rotation
- Not applicable (achiral)
- Microbial Limit
- As per pharmacopeial specifications
- Residual Solvents
- Complies with ICH guidelines
Doxofylline Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
About Doxofylline
Doxofylline: Advanced Features for Pharmaceutical Excellence
Doxofylline is expertly engineered with strict assay control, minimal impurities (NMT 0.5%), and compliance with all ICH and pharmacopeial guidelines. Its utility spans pharmaceutical and manufacturing applications, serving as an essential API for formulating bronchodilators. Ideal for bulk pharmaceutical plants and research laboratories, the powder features a controlled particle size, robust stability, and reliable storage attributes, cementing its status as an indispensable product for pioneering medical applications.
Doxofylline Samples, Packaging, and Supply Valuation
Doxofylline samples are available for domestic market evaluation, enabling stakeholders to analyse quality before confirming bulk supply. HDPE drums with double polyethylene bags provide optimal packaging to maintain purity from manufacturer to end-user. With a dependable supply ability, the sale price is determined by order volume, delivery terms, and market valuation. Exporters, importers, and local distributors can readily access this high-value API for sustained supply and seamless bulk shipments.
FAQs of Doxofylline:
Q: How is the purity of Doxofylline assured?
A: Doxofyllines purity is ensured by HPLC assay, with a specification of not less than 99.0%. Each batch undergoes rigorous identification and impurity testing to guarantee compliance with international standards.Q: What are the main applications of Doxofylline?
A: Doxofylline is primarily utilised in pharmaceutical formulations as a bronchodilator, aiding in the treatment of asthma and COPD in both clinical and bulk production settings.Q: When should Doxofylline be stored, and under what conditions?
A: Doxofylline should be stored in a cool, dry place away from sunlight. These conditions help maintain its stability and quality throughout the 36-month shelf life.Q: Where does Doxofylline comply with relevant quality standards?
A: Doxofylline complies with multiple international pharmacopeial standards, including USP, EP, BP, and Ph. Eur., as well as ICH guidelines for residual solvents and impurity levels.Q: What is the process to obtain a sample for evaluation?
A: Interested distributors or manufacturers may request a sample. The sample enables thorough evaluation, valuation, and quality analysis prior to confirming wholesale purchase or long-term supply agreements.Q: What benefits does advance purchase of Doxofylline provide?
A: Advance Purchase offers preferential access, better utilisation of offers, and ensures uninterrupted bulk supply, securing first-class API for pharmaceutical production and research needs.
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