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Frova CAS NO 158930-17-7


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CAS No.:158930-17-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Frova CAS NO 158930-17-7 is a high-purity active pharmaceutical ingredient (API) with significant therapeutic applications. This compound is critical for the development and production of advanced pharmaceutical formulations targeting specific neurological pathways. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development of innovative treatments. Our supply ensures consistent quality and reliable availability for global commercial and clinical-scale production.

Application

  • Pharmaceutical API: Primary active ingredient in prescription medications for neurological conditions.
  • Neurological Research: Key reference standard and investigational compound in preclinical and clinical studies.
  • Formulation Development: Used in the R&D of solid oral dosage forms such as tablets and capsules.
  • Generic Drug Manufacturing: Serves as the core component for producing bioequivalent generic versions.
  • Contract Manufacturing (CMO): Supplied to contract development and manufacturing organizations for client-specific projects.
  • Analytical Standard: High-purity grade used for method development, validation, and quality control testing in analytical laboratories.

Basic Information

Product Name Frova
CAS No. 158930-17-7
Molecular Formula C14H17NO2S
Molecular Weight 263.35 g/mol
Synonyms Frovatriptan; Frovatriptan Succinate; (R)-Frovatriptan; SB-209509; 3-[2-(Dimethylamino)ethyl]-5-(pyrrolidin-1-ylsulfonylmethyl)-1H-indole; 5-[[(2R)-1-Methylpyrrolidin-2-yl]methanesulfonyl]-1H-indole-3-ethanamine
EINECS Contact for details

Quality Control

Our Frova is manufactured under strict quality management systems to meet the rigorous standards of the pharmaceutical industry. Every batch is subjected to comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling via advanced techniques like HPLC and GC. A Certificate of Analysis (COA) detailing all test results is provided with each shipment to ensure full traceability and compliance with cGMP guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment. For long-term storage, consider using desiccants.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference standard
Identification (HPLC) Retention time matches reference
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Related Substances (HPLC) Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5%
Heavy Metals ≤ 20 ppm

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

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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.