Tafluprost Active Pharmaceutical Ingredients

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Tafluprost Active Pharmaceutical Ingredients

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MOQ : 25 Kilograms

Tafluprost Active Pharmaceutical Ingredients Specification

Poisonous
No (handled as hazardous material)

Storage
Store at 2-8C, protect from light

Shelf Life
24 months

Structural Formula
Provided on request

Molecular Weight
452.53 g/mol

Molecular Formula
C25H34F2O5

Color
White to off-white

Particle Size
NMT 10 m (as per requirement)

Loss on Drying
NMT 0.5%

Boiling point
Not available/decomposes

Heavy Metal (%)
NMT 0.001%

Smell
Odorless

Taste
Not determined

Solubility
Soluble in organic solvents such as ethanol, DMSO

HS Code
29339900

Melting Point
Approx. 68-72C

Medicine Name
Tafluprost

Chemical Name
Tafluprost

CAS No
209860-87-7

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Treatment of glaucoma and ocular hypertension

Purity(%)
>=99%

Appearance
White to off-white powder

Physical Form
Solid

Identification
HPLC & IR Conforms

Related Substances
NMT 0.2%

Packing Details
1 g, 5 g, or as per customer requirements

Endotoxin Level
NMT 0.25 EU/mg

Microbial Limits
Total aerobic microbial count NMT 100 cfu/g

Optical Rotation
+30 to +40 (c=1, CHCl3)

Residual Solvents
Complies with ICH guidelines

Certificate of Analysis
Available on request

Tafluprost Active Pharmaceutical Ingredients Trade Information

Minimum Order Quantity
25 Kilograms

Payment Terms
Cash on Delivery (COD), Cash in Advance (CID), Cash Against Delivery (CAD)

Supply Ability
500 Kilograms Per Month

Delivery Time
5-7 Days

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

Main Domestic Market
All India

Tafluprost Active Pharmaceutical Ingredients About

Utilise this exclusive offer to procure dominant Tafluprost Active Pharmaceutical Ingredients, crafted to pharmaceutical-grade standards for phenomenal effectiveness in glaucoma and ocular hypertension treatment. Our top-notch Tafluprost offers outstanding purity at >=99%, supported by HPLC & IR identification, ensuring related substances NMT 0.2% and compliance with ICH for residual solvents. With microbial limits (NMT 100 cfu/g) and low endotoxin level (NMT 0.25 EU/mg), this affordable and quality API is available in 1 g, 5 g, or as per your requirement. Get it now from a leading exporter, supplier, and trader based in India!

Commercial Applications and Features of Tafluprost API

Tafluprost Active Pharmaceutical Ingredient is widely utilised in ophthalmic formulations for the effective management of glaucoma and ocular hypertension. As a highly refined API with a superb material profile, it boasts purity levels above 99%, white to off-white solid appearance, and optimal particle size. The ingredient's compliance with international standards ensures its ready adaptability for commerical manufacturing, offering robust performance in final pharmaceutical preparations. Dependable analytical certificates are available upon request for quality assurance.

Efficient Freight, Order Completion, and Goods Delivery

Our Tafluprost API is shipped promptly to ensure timely delivery and customer satisfaction. Standard freight options and specialized packing safeguard your order during goods transport. With flexible payment terms, transparent FOB Port options (India), and seamless order completion, we prioritize smooth logistics from order placement to final delivery. We strive to meet or exceed client expectations for reliability and speed, making sure your pharmaceutical operations remain uninterrupted and productive.

FAQ's of Tafluprost Active Pharmaceutical Ingredients:

Q: How is Tafluprost Active Pharmaceutical Ingredient utilized in medicine?

A: Tafluprost API is primarily used in the formulation of ophthalmic preparations for the treatment of glaucoma and ocular hypertension. It serves as a key active ingredient, ensuring potent therapeutic effects with excellent purity and safety.

Q: What are the quality and safety features of your Tafluprost API?

A: Our Tafluprost API meets strict quality criteria, including purity of >=99%, identification by HPLC & IR, related substances not exceeding 0.2%, microbial limits under 100 cfu/g, and compliance with ICH guidelines for residual solvents and endotoxins. These standards assure top-grade, safe pharmaceutical applications.

Q: When can I expect delivery after placing an order for Tafluprost API?

A: Delivery times depend on order size and location, but we strive for prompt order completion. Goods are dispatched via reliable freight options from our FOB Port in India, ensuring you receive your shipment within the stipulated timeframe.

Q: What payment terms and packing options are available?

A: We offer flexible payment terms and can pack Tafluprost API in 1 g, 5 g, or as per your custom requirements. Packing is designed to maintain product quality and safety during transport.

Q: Where can I get the Certificate of Analysis or structural formula for Tafluprost API?

A: The Certificate of Analysis and structural formula are provided upon request, ensuring transparency and assisting our clients in maintaining compliance with regulatory requirements.

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