Description

Ftibamzone is a potent antiviral compound with significant activity against a range of viral pathogens. This high-purity active pharmaceutical ingredient (API) is critical for the development and formulation of effective antiviral therapeutics. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on virology and antiviral drug discovery.

Application

• Antiviral Pharmaceutical Formulations: As a key active ingredient in the development of antiviral drugs.
• Virology Research: Used as a reference standard and research tool in academic and industrial laboratories studying viral replication mechanisms.
• Preclinical and Clinical Development: Serves as a critical component in the synthesis of drug candidates for antiviral therapy testing.
• Biochemical Assays: Employed in high-throughput screening and biochemical assays to identify and characterize antiviral activity.

Basic Information

Product Name	Ftibamzone
CAS No.	210165-00-7
Molecular Formula	C5H7N5O2S2
Molecular Weight	241.27 g/mol
Synonyms	Fti-Bz; 4-(4-Bromophenyl)-2-(2-((E)-((2,4-difluorophenyl)imino)methyl)-4-thiazolyl)thiazole; Thiazolylthiazole derivative; Antiviral agent Fti-Bz; FtiBz; Bromophenyl-difluorophenyl thiazolyl thiazole; Fti-Bz compound
EINECS	Contact for details

Quality Control

Our Ftibamzone is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. The product undergoes comprehensive analytical testing, including HPLC for assay and impurity profiling, to meet stringent pharmaceutical-grade specifications. A Certificate of Analysis (COA) detailing identity, purity, and related substances is provided with each shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

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%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 1.0%
Heavy Metals	≤ 20 ppm

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