Caffeine IP BP USP EP

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Product Details:

Shelf Life 5 years
Color White
Taste Bitter
Particle Size 40-80 mesh
Poisonous Non-poisonous
Ph Level 5.5 - 7.0
Storage Store in a cool, dry place
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Caffeine IP BP USP EP Price And Quantity

Minimum Order Quantity 100 Kilograms

Caffeine IP BP USP EP Product Specifications

Poisonous Non-poisonous
Ph Level 5.5 - 7.0
Storage Store in a cool, dry place
Taste Bitter
Particle Size 40-80 mesh
Type Active Pharmaceutical Ingredient (API)
Physical Form Powder
Usage Pharmaceutical, Stimulant, Research
Appearance White crystalline powder
Shelf Life 5 years
Color White
Grade IP/BP/USP/EP
Medicine Name Caffeine IP BP USP EP
Purity(%) 99% min
Smell Odorless
Loss on Drying 0.5%
Molecular Formula C8H10N4O2
HS Code 29393000
Chemical Name 1,3,7-Trimethylxanthine
Melting Point 234-239C
Molecular Weight 194.19 g/mol
EINECS No 200-362-1
Solubility Soluble in water, alcohol, chloroform
Boiling point 178C (sublimes)
CAS No 58-08-2
Heavy Metal (%) 0.001%
Structural Formula C8H10N4O2

Refractive Index 1.688
pKa 14.0
Residual Solvent Meets ICH guidelines
Microbial Limit Tests Complies with pharmacopeia standards
Stability Stable under recommended storage conditions
Packaging Size 25kg/drum
Density 1.23 g/cm3

Caffeine IP BP USP EP Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Discover the hot-selling Caffeine IP BP USP EP, now available at a reduced price for an unbeatable deal! This classic Active Pharmaceutical Ingredient (API) features enviable purity at 99% minimum and comes in a convenient 25kg drum. With exceptional stability, a pKa of 14.0, superb solubility in water and alcohols, and compliance with ICH and pharmacopeia microbial standards, it supports both pharmaceutical and advanced research needs. The white, crystalline, odorless powder is non-poisonous, boasts a five-year shelf life, and meets stringent global quality norms-making it the premium choice for distributors, manufacturers, and suppliers across India.

User Guidance and Application Sites

Caffeine IP BP USP EP is favored by pharmaceutical companies, research institutions, and laboratories. This versatile stimulant is typically administered orally or used in tablet and capsule formulations. For research purposes, precise dosing is recommended, always adhering to protocol guidelines. This product is applied primarily in medicinal preparations and scientific experiments, ensuring maximum efficacy and safety across a range of pharmaceutical and research settings.

Sample Policy and Certifications: Swift, Reliable Service

We provide express shipping for samples of Caffeine IP BP USP EP, ensuring prompt outlay and transparent handling of shipped goods. Every batch adheres to IP, BP, USP, and EP certifications, guaranteeing top-tier quality. Our main export markets span the globe, particularly North America, Europe, and Asia. Rigorous compliance with international standards assures that clients receive only the best pharmaceutical-grade caffeine with each order.

FAQ's of Caffeine IP BP USP EP:

Q: How should Caffeine IP BP USP EP be safely stored?

A: Caffeine IP BP USP EP should be stored in a cool, dry place and kept in the original sealed drum to maintain stability and preserve its five-year shelf life.

Q: What are the recommended uses of this caffeine product?

A: It is primarily used as a pharmaceutical stimulant in medications, as well as for various laboratory and research applications where high purity and compliance are essential.

Q: When can I expect to receive my sample order?

A: With express shipping, sample orders are typically dispatched promptly so you receive your goods quickly, depending on your location and shipping preferences.

Q: Where does your Caffeine IP BP USP EP export to?

A: Our main export markets include North America, Europe, and Asia, and we frequently supply to leading pharmaceutical companies and research organizations worldwide.

Q: What certifications does this caffeine product carry?

A: Caffeine IP BP USP EP meets the stringent standards of IP, BP, USP, and EP pharmacopeias, as well as ICH guidelines for residual solvents and quality.

Q: How does the process ensure compliance with pharmaceutical standards?

A: Each batch undergoes rigorous testing for microbial limits, heavy metals, particle size, and other critical parameters to comply with international pharmacopeial requirements.

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