Description

Tecovirimat is a potent antiviral agent specifically developed to combat orthopoxvirus infections. This compound is of critical importance in the pharmaceutical industry as a key active pharmaceutical ingredient (API) for the treatment of smallpox and related diseases. It is primarily required by pharmaceutical manufacturers, research institutions, and government stockpiling agencies focused on biodefense and public health preparedness.

Application

• Primary Active Pharmaceutical Ingredient (API) in antiviral drug formulations for the treatment of smallpox.
• Key component in biodefense and strategic national stockpile (SNS) programs for emergency preparedness.
• Research and development of therapeutics against other orthopoxviruses, such as monkeypox and cowpox.
• Use in preclinical and clinical studies to evaluate antiviral efficacy and pharmacokinetics.
• Reference standard for analytical method development and quality control in pharmaceutical laboratories.

Basic Information

Product Name	Tecovirimat
CAS No.	816458-31-8
Molecular Formula	C19H15F3N2O3
Molecular Weight	376.33 g/mol
Synonyms	Tecovirimat; ST-246; (N-{3,5-Dioxo-4-azatetracyclo[5.3.2.0^{2,6}.0^{8,10}]dodec-11-en-4-yl}-4-(trifluoromethyl)benzamide); 4-Trifluoromethyl-N-(3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl)-benzamide; Arestvyr; Tpoxx
EINECS	Contact for details

Quality Control

Our Tecovirimat is manufactured under strict quality management systems to ensure it meets the stringent requirements for pharmaceutical actives. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC and other pharmacopeial methods. A Certificate of Analysis (COA) is provided with each shipment, detailing compliance with agreed specifications.

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 to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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