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Rivenprost CAS NO 256382-08-8


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CAS No.:256382-08-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Rivenprost is a synthetic prostaglandin analog, a high-purity active pharmaceutical ingredient (API) identified by CAS NO 256382-08-8. This compound is valued for its potent and selective biological activity, making it a critical intermediate in advanced pharmaceutical research and development. It is primarily utilized by pharmaceutical companies and research institutions focused on developing novel therapeutics in areas such as ophthalmology and vascular biology.

Application

  • Pharmaceutical API: Serves as a key active ingredient in the formulation of prescription ophthalmic solutions for treating glaucoma and ocular hypertension.
  • Biomedical Research: Used as a reference standard and pharmacological tool in preclinical studies investigating prostaglandin receptor pathways and cellular signaling.
  • Drug Discovery: Acts as a crucial intermediate in the synthetic route for developing next-generation prostaglandin-based therapeutics.
  • Analytical Standard: Employed in quality control laboratories for method development, validation, and assay calibration via HPLC or LC-MS.

Basic Information

Product Name Rivenprost
CAS No. 256382-08-8
Molecular Formula C23H31NO5
Molecular Weight 401.50 g/mol
Synonyms Rivenprost; Travoprost Impurity C; AL-6221; 7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3R)-3-hydroxy-4-(3-trifluoromethylphenoxy)but-1-en-1-yl]cyclopentyl]-N-ethylhept-5-enamide; 5-Heptenamide, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-buten-1-yl]cyclopentyl]-N-ethyl-; Travoprost Related Compound C
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Quality Control

Our Rivenprost is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) confirming compliance with in-house pharmacopeial standards are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at controlled room temperature (15-25°C) to prevent oxidation and degradation. The container should be kept in a cool, dry, and well-ventilated area.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Loss on Drying ≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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Trusted Manufacturer

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.