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Travoprost CAS 157283-68-6

Travoprost CAS 157283-68-6

CAS Number: 157283-68-6
Standard: In-House Standard
Travoprost is an ophthalmic solution used to reduce intraocular pressure in patients with glaucoma or ocular hypertension.
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Product Introduction

Travoprost API

High-Quality Ophthalmic Solution for Glaucoma and Ocular Hypertension

Product Details

CAS Number: 157283-68-6
Standard: In-House Standard

Travoprost is a highly effective ophthalmic API used to lower intraocular pressure (IOP) in patients with primary open-angle glaucoma and ocular hypertension. As a potent prostaglandin F2α analogue, it enhances uveoscleral outflow of aqueous humour, helping preserve the optic nerve and prevent progressive vision loss.

Key Specifications

Molecular Formula C26H35F3O6
Molar Mass 500.55
Density 1.245±0.06 g/cm³ (Predicted)
Boiling Point 584.8±50.0 °C (Predicted)
Flash Point 17°C
Vapor Pressure 1.61E-14 mmHg at 25°C
Appearance Ethanol Solution
Color Colourless to Light Beige
pKa 13.43±0.20 (Predicted)
Storage Condition Sealed in dry condition, stored below -20°C

Travoprost demonstrates strong selectivity and affinity for PGFP receptors and functions as a full agonist, making it a reliable and safe option for glaucoma therapy.

Applications of Travoprost

  • Glaucoma Treatment: Effectively reduces IOP while protecting the optic nerve and preventing permanent vision loss.
  • Ocular Hypertension: Lowers elevated eye pressure to reduce glaucoma risk.
  • Combination Therapy: Can be used alongside beta-blockers or carbonic anhydrase inhibitors for enhanced pressure control.
  • Pediatric Glaucoma (Off-Label): Used under strict medical supervision in rare pediatric cases.
  • Scientific Research: Supports studies on glaucoma mechanisms and development of new ophthalmic therapies.

Its once-daily dosing provides convenience, high efficacy, and minimal systemic side effects, positioning it among first-line glaucoma therapies.

Why Choose Our Travoprost API?

1. Extensive Production Experience

Established in 2013 with over ten years of pharmaceutical manufacturing expertise.

2. Complete GMP Manufacturing System

A 2,523 m² facility including a 365 m² Class D cleanroom, built fully according to GMP standards.

3. Strict Quality Control

Comprehensive quality assurance covering raw material testing, environmental monitoring, and production validation.

4. Excellent Customer Support

Technical assistance, regulatory documentation support, and responsive service to ensure smooth integration into your manufacturing process.

FAQs

Q1: Can we receive samples before placing an order?

Yes, samples are available for analytical evaluation. Please contact our sales team to request the required quantity.

Q2: Can we conduct a factory audit?

Absolutely. Customers are welcome to visit by prior appointment. Our team will fully support your quality audit process.

 

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