Latanoprost Tris-triethylsilyl-Ether

Latanoprost Tris(triethylsilyl) Ether

CAS No. 477884-78-9
MF: C44H82O5Si3
Molecular weight 775.38
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Product Name
Latanoprost Tris-triethylsilyl- Ether
Appearance
Colorless oil Liquid
Specification
 95%
Test Method
HPLC
Storage
Keep in a cool, dry, dark location in a tightly sealed container or cylinder.
Shelf Time
24 months

Latanoprost Tris-triethylsilyl-Ether is a chemically modified derivative of latanoprost,

a widely used prostaglandin analog for treating glaucoma and ocular hypertension.

this compound serves as a reference standard or analytical impurity in pharmaceutical research and quality control processes.

Latanoprost Tris-triethylsilyl-Ether is primarily utilized to ensure the purity, stability, and consistency of latanoprost-based formulations during manufacturing and regulatory evaluations.

Pharmaceutical Quality Control
As a high-purity reference material, Latanoprost Tris-triethylsilyl-Ether enables precise identification and quantification of impurities in latanoprost drug products. It is critical for compliance with ICH guidelines (e.g., Q3A/B) on impurity profiling and batch-to-batch consistency.
Analytical Method Development
This compound is used to validate chromatographic methods (e.g., HPLC, LC-MS) for detecting trace impurities in ophthalmic formulations. Its unique silyl ether modification enhances stability during analysis, ensuring reliable results in method qualification studies.
Latanoprost Tris-triethylsilyl-Ether Stability Testing
Latanoprost Tris-triethylsilyl-Ether aids in assessing degradation pathways of latanoprost under varying storage conditions (e.g., temperature, humidity). This data supports shelf-life determination and packaging optimization for commercial products.
Latanoprost Tris-triethylsilyl-Ether Regulatory Submissions
Pharmaceutical companies include this compound in regulatory filings (e.g., ANDA, NDA) to demonstrate comprehensive impurity control strategies, meeting requirements from agencies like the FDA and EMA