Bisoprolol Fumarate
Price 100 INR/ Kilograms
Bisoprolol Fumarate Specification
- Loss on Drying
- 0.5%
- Molecular Formula
- C18H31NO4.C4H4O4
- Storage
- Store below 25C in a tightly closed container, protected from light and moisture
- Taste
- Characteristic, bitter
- Ph Level
- No data available
- Poisonous
- No (when used as prescribed)
- Solubility
- Freely soluble in water, methanol; very slightly soluble in dichloromethane
- Smell
- Odorless
- EINECS No
- 620-237-2
- Color
- White
- Heavy Metal (%)
- 0.001%
- Boiling point
- Not applicable (decomposes)
- Melting Point
- 100-105C
- HS Code
- 29420090
- Particle Size
- Typically 2080 mesh
- Molecular Weight
- 486.55 g/mol
- Shelf Life
- 2-3 years if stored properly
- Structural Formula
- See image or literature reference
- Medicine Name
- Bisoprolol Fumarate
- Chemical Name
- Bisoprolol Fumarate
- CAS No
- 104344-23-2
- Type
- Other
- Grade
- Other
- Usage
- Used as an antihypertensive agent and in the management of chronic heart failure
- Purity(%)
- 99%
- Appearance
- White or almost white crystalline powder
- Physical Form
- Solid
- pKa
- 9.5 (approx)
- Residual Solvents
- Meet regulatory limits
- Stability
- Stable under normal storage conditions
- Polymorphism
- Exists
- Impurities
- Complies with pharmacopeial standards
- Specific Rotation
- No data provided
- Therapeutic Category
- Beta-blocker (selective 1-adrenoceptor antagonist)
- Related Substances
- 0.1%
- Identification
- Conforms to standards (IR, HPLC, TLC)
- Packing
- Usually packed in double polyethylene bags in fiber drums
- Bulk Density
- 0.4 - 0.6 g/cm3
Bisoprolol Fumarate Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
About Bisoprolol Fumarate
Usage & Applications of Bisoprolol Fumarate
Bisoprolol Fumarate is widely utilized as an antihypertensive agent and in the management of chronic heart failure. Suitable for pharmaceutical formulation, its material features include high stability, excellent bulk density, and certified purity. The application surfaces are typically oral dosage forms designed for direct human administration. Its exceptional solubility in water and methanol offers versatility in medication production, while the bitter taste and odorless nature ensure patient compliance in finished products.
Shipping, Arrival and Packaging Details
Bisoprolol Fumarate is shipped through major global FOB ports, ensuring prompt arrival and secure handling. The main domestic market covers widespread regions, benefiting local manufacturers and suppliers. Packaging details entail double polyethylene bags placed in strong fiber drums to protect against moisture and light during transit and storage, with no extra charge for premium packaging. The product is delivered with careful attention to regulations, maximizing quality and shelf-life on arrival.
FAQs of Bisoprolol Fumarate:
Q: How is Bisoprolol Fumarate typically used in medical treatment?
A: Bisoprolol Fumarate is commonly prescribed for the management of hypertension and chronic heart failure, acting as a selective beta-blocker to reduce heart workload and control blood pressure.Q: What makes Bisoprolol Fumarate an exceptional choice for pharmaceutical applications?
A: Its high purity (99%), compliance with pharmacopeial standards, stability under normal storage conditions, and selective 1-adrenoceptor antagonism make Bisoprolol Fumarate a crowning choice for safe and effective medications.Q: When should Bisoprolol Fumarate be stored to maintain its shelf life?
A: To maintain optimal shelf life of 23 years, Bisoprolol Fumarate should be stored below 25C in a tightly closed container protected from light and moisture.Q: Where can Bisoprolol Fumarate be shipped and what is the packaging?
A: Bisoprolol Fumarate is shipped globally via major FOB ports, packaged securely in double polyethylene bags within fiber drums to ensure product integrity and easy handling.Q: What are the material features of Bisoprolol Fumarate that benefit manufacturers?
A: The material features include stable crystalline solid form, high water solubility, low impurities, and compliance with pharmaceutical standards, facilitating safe formulation and broad application.Q: How does the process guarantee product purity and safety?
A: Stringent identification methods (IR, HPLC, TLC) are used, and the product meets all regulatory standards for residual solvents, heavy metals, and related substances, ensuring purity and safety throughout the supply chain.
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