Travoprost API
High-Purity Intermediate for Ophthalmic Formulation Development
Travoprost is supplied as a high-purity intermediate Active Pharmaceutical Ingredient (API) designed for ophthalmic eye-drop formulation workflows. This product is intended strictly for laboratory, analytical, and formulation development use, with emphasis on material performance, stability, and batch consistency rather than clinical application.
Our focus is on how the material behaves during real-world lab handling, including solvent compatibility, reproducibility, and storage stability - helping formulation and QC teams work with confidence.
Key Specifications
157283-68-6
Pale crystalline solid or viscos oil (dependent on storage conditions)
≥ 98% (HPLC), lot-verified and documented on Certificate of Analysis (COA)
Compatible with commonly used organic solvents (refer to TDS for solvent matrix)
Short-term: 2–8 °C | Long-term: −20 °C | Protect from light and moisture
Small evaluation quantities, bulk production sizes, and custom vialing available
COA, MSDS/TDS, impurity profile, and stability summary
Technical & Laboratory Advantages
Defined Stability Windows
Material behavior is documented under standard laboratory conditions to support realistic in-use timelines.
Analytical Fingerprinting
HPLC chromatograms and retention-time markers are provided for reliable QC comparison.
Solvent Compatibility Guidance
Bench-tested solvent and co-solvent recommendations help avoid incompatibilities during formulation.
Pilot-Scale Quantities
Small packs support method development and feasibility studies while minimizing material waste.
Export & Packaging Flexibility
Shipping and packaging can be adapted to temperature control and regulatory needs.
Recommended Supply Workflow
Conduct solubility testing, sterile filtration trials, and short-term stability studies.
Compare COA and HPLC data with internal references. Extended impurity or stability reports can be requested.
Finalize packaging format, lead time, and order bulk quantities.
Handling & Storage Best Practices
▸ Unpack under low-light conditions and record batch details in your LIMS.
▸ Allow shipments to equilibrate to storage temperature before sampling.
▸ Use recommended solvent systems from the technical data sheet; avoid high-pH buffers.
▸ Prepared solutions should be used promptly or aliquoted and frozen according to internal SOPs.
Frequently Asked Questions
Q: Can I order a small sample before committing to bulk quantities?
A: Yes. Evaluation samples are available for QC testing and formulation development.
Q: What documentation is included with each shipment?
A: Each order includes a COA, TDS/MSDS, and impurity/stability summary. Extended analytical reports are available upon request.
Q: Do you offer custom packaging for production-scale orders?
A: Yes. Vial size, labeling, and packaging configurations can be customized to meet process and regulatory requirements.
Ready to Source Travoprost API?
We support both R&D and commercial-scale manufacturing needs with high-quality, traceable Travoprost API - from evaluation samples through to bulk supply.
Contact our team to discuss how Travoprost API fits into your ophthalmic formulation pipeline.
Hot Tags: travoprost cas 157283-68-6, China travoprost cas 157283-68-6 manufacturers, suppliers, factory, Human APIs, 130209-82-4, 39746-00-4, 157283-68-6, 155206-00-1, Carboprost Trometamina
