Doxofylline API

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Product Details:

Poisonous NO
Melting Point 119-122C
Structural Formula Available on request
Shelf Life 36 months
Storage Store in a cool, dry place, protected from light
Application Used in the treatment of asthma and COPD
Grade Pharmaceutical Grade
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Doxofylline API Price And Quantity

Minimum Order Quantity 100 Kilograms

Doxofylline API Product Specifications

Ph Level Neutral
Properties Non-hygroscopic, stable under recommended conditions, odorless
Product Type Active Pharmaceutical Ingredient
Smell Odorless
Molecular Weight 266.26 g/mol
Appearance White to off-white crystalline powder
Ingredients Doxofylline
Shape Crystalline
Solubility Soluble in water, methanol and slightly soluble in ethanol
Usage For formulation and research use only, not for direct human consumption
EINECS No 274-906-4
Physical Form Powder
CAS No 69975-86-6
Molecular Formula C11H14N4O4
Taste Bitter
Density 1.34 Gram per cubic centimeter(g/cm3)
HS Code 29393000
Grade Pharmaceutical Grade
Purity NLT 99% (By HPLC)
Application Used in the treatment of asthma and COPD
Shelf Life 36 months
Storage Store in a cool, dry place, protected from light
Structural Formula Available on request
Poisonous NO
Melting Point 119-122C

Residual Solvents Complies with ICH guidelines
Loss on Drying NMT 0.5%
Impurity Profile Complies with pharmacopeial standards
Endotoxin Level < 0.25 EU/mg
Particular Risks/Safety Handle using proper personal protective equipment, avoid inhalation
Identification IR, HPLC, conforms to standard
Heavy Metals NMT 10 ppm
Packaging HDPE drums with double polybag or as per customer requirement
Certificate of Analysis Provided with each batch
Assay NLT 99.0% (on anhydrous basis)
Boiling Point Decomposes before boiling
Microbial Limits Total aerobic microbial count NMT 1000 cfu/g, Total yeast & moulds NMT 100 cfu/g

Doxofylline API Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Grab Yours now-introducing our crackerjack Doxofylline API, a glorious solution masterfully crafted for excellence in pharmaceutical applications! Redeem this last chance to secure a product with an assay of NLT 99% purity, spotless impurity profile, and conformity to rigorous pharmacopeial standards. Packaged securely in HDPE drums with double polybags, it is odorless, non-hygroscopic, and features a neutral pH and density of 1.34 g/cm3. With industry-leading microbial and endotoxin limits, each batch comes with a Certificate of Analysis. Ideal for formulation and research-your opportunity awaits!

Features & Applications of Doxofylline API

Our Doxofylline API stands out with its non-hygroscopic, stable, and odorless crystalline powder form. Masterfully developed for formulation and research, it is commonly used in the treatment of asthma and COPD. The material boasts remarkable solubility in water and methanol, an assuring low heavy metals content, and complies with ICH residual solvent standards. Its long 36-month shelf life ensures reliability, while storage in cool, dry conditions guarantees consistent performance.

Certifications, Payment Terms, and Dispatch Process

Each batch of Doxofylline API is issued with a Certificate of Analysis to guarantee consistency and safety. Proposal amounts reflect the lowest price, providing undeniable value. Efficient dispatching and timely delivery are ensured via your preferred FOB port in India. Flexible payment terms can be discussed to suit your business needs-whether you are a distributor, exporter, importer, manufacturer, service provider, supplier, trader, or wholesaler.

FAQ's of Doxofylline API:

Q: How should Doxofylline API be stored for maximum shelf life?

A: Store Doxofylline API in a cool, dry place, protected from light, to maintain its stability and ensure the full 36-month shelf life.

Q: What usage is recommended for this Doxofylline API?

A: This API is intended strictly for formulation and research purposes and is not meant for direct human consumption.

Q: Where does your Doxofylline API comply in terms of safety and standards?

A: Our Doxofylline API conforms to pharmacopeial standards, complies with ICH residual solvent guidelines, and is provided with a detailed Certificate of Analysis for every batch.

Q: What is the process to procure Doxofylline API from your company?

A: Initiate an inquiry, discuss the proposal amount and payment terms, confirm the order, and we will dispatch your product from the preferred FOB port in India promptly.

Q: What are the benefits of using your Doxofylline API in formulations?

A: With high assay purity (NLT 99%), low impurity levels, and strict microbial and heavy metal limits, it provides a reliable ingredient for producing quality asthma and COPD treatments.

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