share

Carafiban CAS NO 177563-40-5


Unit Price:

CAS No.:177563-40-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Carafiban is a high-purity, non-peptide platelet aggregation inhibitor belonging to the glycoprotein IIb/IIIa receptor antagonist class. This compound is of significant interest in pharmaceutical research and development for its potent antiplatelet activity. It serves as a critical intermediate or active pharmaceutical ingredient (API) for researchers and manufacturers developing next-generation antithrombotic agents. The global demand for such specialized intermediates is driven by the ongoing need for improved cardiovascular therapeutics.

Application

  • Pharmaceutical Intermediate: Primary use as a key building block in the synthesis of advanced antithrombotic drug candidates.
  • Biochemical Research: Used as a reference standard or tool compound in studies of platelet physiology and thrombosis mechanisms.
  • API Development: Serves as the core active moiety in the development and scale-up of finished dosage forms targeting arterial thrombosis.
  • Preclinical Studies: Employed in animal models to evaluate efficacy and safety profiles of novel antiplatelet therapies.
  • Process Chemistry: Utilized in route scouting and optimization for the commercial manufacturing of glycoprotein IIb/IIIa antagonists.

Basic Information

Product Name Carafiban
CAS No. 177563-40-5
Molecular Formula C20H28N4O4S
Molecular Weight 420.53 g/mol
Synonyms Carafiban; L-734,217; (2S)-2-[(4-{4-[(Aminosulfonyl)amino]phenyl}-1-piperidinyl)carbonyl]amino]-3-(1-naphthalenyl)propanoic acid; N-[(1S)-1-[[(4-{4-[(Aminosulfonyl)amino]phenyl}-1-piperidinyl)carbonyl]amino]-2-(1-naphthyl)ethyl]glycine; L 734217; L734217.
EINECS Contact for details

Quality Control

Our Carafiban is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity, suitable for research and development purposes. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. While produced to meet exacting internal standards, we can discuss alignment with specific pharmacopeial guidelines (e.g., ICH Q3A/B, USP) based on project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

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

Advanced R&D Expertise

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