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Send InquiryIBUPROFEN IP/BP/USP
MOQ : 25 Kilograms
IBUPROFEN IP/BP/USP Specification
- Storage
- Store in a tightly closed container, protected from light and moisture, at room temperature
- Density
- 1.038 Gram per cubic centimeter(g/cm3)
- Molecular Formula
- C13H18O2
- Solubility
- Practically insoluble in water, freely soluble in organic solvents such as acetone, ethanol, methanol, chloroform
- Purity
- >= 99 %
- Melting Point
- 75-78 C
- Ph Level
- Neutral (5.5 7.5 in 1% aqueous solution)
- Product Type
- Active Pharmaceutical Ingredient
- Structural Formula
- C13H18O2
- Smell
- Odorless
- Physical Form
- Solid
- HS Code
- 29163990
- CAS No
- 15687-27-1
- Usage
- Used in formulation of oral tablets, capsules, suspensions
- Poisonous
- NO
- Taste
- Characteristic
- Shape
- Crystalline
- Ingredients
- Ibuprofen
- Shelf Life
- 5 years from date of manufacture
- Properties
- White or almost white crystalline powder, Odorless, Non-hygroscopic, Stable under recommended storage
- Appearance
- White crystalline powder
- Grade
- IP/BP/USP
- EINECS No
- 239-784-6
- Application
- Pharmaceuticals; anti-inflammatory, analgesic, antipyretic
- Molecular Weight
- 206.28 g/mol
- Microbial Limits
- As per IP/BP/USP requirements
- Impurity Level
- NMT 0.5%
- Loss on Drying
- NMT 0.5%
- pKa
- 4.91
- Assay
- 99.0-101.0% (on dried basis)
- Boiling Point
- 157-158C at 0.15 mmHg
- Packaging
- HDPE drums or fiber drums with double polyethylene liners, 25 kg or as required
- Residual Solvents
- Complies with pharmacopeial limits
- Chloride Content
- NMT 0.02%
- Specific Rotation
- Not specified as it is a racemic mixture
- Heavy Metals
- NMT 10 ppm
IBUPROFEN IP/BP/USP Trade Information
- Minimum Order Quantity
- 25 Kilograms
- Supply Ability
- 25 Kilograms Per Day
- Delivery Time
- 1 Days
About IBUPROFEN IP/BP/USP
IBUPROFEN IP/BP/USPis a widely recognized nonsteroidal anti-inflammatory drugthat provides effective relief from pain, inflammation, and fever. Its popularity stems from its ability to target discomfort caused by headaches, muscle aches, arthritis, and menstrual cramps. Ibuprofen works by reducing the production of certain chemicals in the body that cause inflammation and pain. Its trusted by individuals seeking swift relief without a prescription. IBUPROFEN IP/BP/USPcomes in various forms, including tablets and capsules, offering convenience and rapid action when needed.
Premium Quality and Compliance
Ibuprofen IP/BP/USP is manufactured to meet the international standards set by IP, BP, and USP, ensuring superior efficacy and safety. The product is assessed for impurities, solvents, heavy metals, and microbial content according to regulatory limits. Its chemical stability and purity guarantee optimal performance in pharmaceutical formulations.
Applications and Versatility
Widely used in the pharmaceutical industry, this grade of Ibuprofen is formulated into oral dosage forms such as tablets, capsules, and suspensions. Its anti-inflammatory, analgesic, and antipyretic effects are well-documented, offering relief from pain, fever, and various inflammatory conditions. Its consistent quality makes it a preferred choice for large-scale manufacturing and export.
Safe Packaging and Extended Shelf Life
Ibuprofen IP/BP/USP is packaged securely in HDPE drums or fiber drums with double polyethylene liners, protecting it from light and moisture. This ensures product integrity throughout transportation and storage. With a shelf life of five years from the date of manufacture, it remains stable and effective under recommended storage conditions.
FAQs of IBUPROFEN IP/BP/USP:
Q: How is Ibuprofen IP/BP/USP typically used in pharmaceutical formulations?
A: Ibuprofen IP/BP/USP serves as an active pharmaceutical ingredient in the creation of oral tablets, capsules, and suspensions. Its high purity ensures that it delivers reliable anti-inflammatory, analgesic, and antipyretic effects.Q: What quality control processes are followed for Ibuprofen IP/BP/USP?
A: The product undergoes rigorous testing for impurities (NMT 0.5%), heavy metals (NMT 10 ppm), residual solvents (compliant with pharmacopeial limits), chloride content, and microbial limits in accordance with IP, BP, and USP standards to ensure patient safety.Q: When should Ibuprofen IP/BP/USP be stored to maintain its efficacy?
A: Ibuprofen IP/BP/USP should always be stored in tightly closed containers, protected from light and moisture, and kept at room temperature. These conditions help preserve its stability and maintain its five-year shelf life.Q: Where is Ibuprofen IP/BP/USP manufactured and exported?
A: This grade of Ibuprofen is manufactured and supplied in India, and is exported globally to various countries for use by the pharmaceutical industry.Q: What is the benefit of using Ibuprofen IP/BP/USP with a purity of at least 99%?
A: A purity level of 99% or higher minimizes the risk of impurities, enhances safety, and supports consistent pharmacological performance, making it suitable for stringent pharmaceutical applications.Q: Which packaging options are available for Ibuprofen IP/BP/USP?
A: It is supplied in secure HDPE drums or fiber drums with double polyethylene liners, typically in 25 kg packs or customized sizes, ensuring safe transportation and storage.Q: What distinguishes Ibuprofen IP/BP/USP from other grades?
A: Its compliance with international pharmacopoeial standards (IP/BP/USP), high purity, confirmed stability, and strict regulatory adherence set it apart as an optimal choice for pharmaceutical manufacturing.
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RDR PHARMACHEM PRIVATE LIMITED
GST : 27AALCR5725M1ZR
GST : 27AALCR5725M1ZR
A-307, Rustomjee Central Park, Andheri Kurla Road, Andheri East,Mumbai - 400093, Maharashtra, India
Phone :08045803314
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