Description

Actarit

Actarit is a small-molecule pharmaceutical compound used in research, analytical development, and regulated drug-development programs where material identity, purity, documentation readiness, and dependable sourcing are essential. It is also known as 4-Acetylaminophenylacetic acid and has the molecular formula C₁₀H₁₁NO₃, a molecular weight of approximately 193.20 g/mol, and CAS Registry Number 18699-02-0. Actarit is
• A small-molecule pharmaceutical and research compound
• Also identified as 4-Acetylaminophenylacetic acid
• Suitable for analytical evaluation, formulation research, process development, and qualified manufacturing programs
• Supported by technical and safety documentation for supplier qualification and internal review
Actarit is an Anilide and Acetamide-related compound that has been investigated and used as a disease-modifying antirheumatic drug in certain markets. Published formulation research describes Actarit as a white or nearly white crystalline powder with limited water solubility and reports its evaluation in conventional and controlled-release oral tablet systems.
The compound may be evaluated in pharmaceutical research involving oral solid dosage forms, modified-release delivery systems, analytical reference work, process-development studies, and other controlled programs. A published study investigated double-layer osmotic pump tablets containing Actarit to address the short plasma half-life and concentration fluctuations associated with conventional tablets. This work illustrates the importance of solubility, release behavior, polymer selection, osmotic agents, coating design, and dosage-form performance when Actarit is considered for formulation development.
For organizations looking to buy Actarit, supplier qualification should extend beyond price and immediate availability. A qualified Actarit supplier should provide clear information regarding chemical identity, assay, appearance, related substances, water content, residual solvents, elemental impurities, particle characteristics, storage requirements, and other grade-specific controls. Customers should review the current specification and Certificate of Analysis before purchase because the chemical name alone does not establish suitability for a specific pharmaceutical, analytical, or research application.
CarboMer approaches Actarit sourcing with a regulation-first and manufacturing-centered perspective. Research and development teams benefit from a supplier capable of supporting material evaluation, analytical method development, formulation screening, and scale-up planning. Quality professionals require traceable lot documentation and clearly defined acceptance criteria. Procurement teams need confidence that the selected material can be purchased consistently as demand progresses from laboratory quantities to larger development or qualified production requirements.
Actarit should be handled under appropriate laboratory or manufacturing controls. Available Safety Data Sheets classify some commercially supplied research grades as harmful if swallowed and capable of causing skin and eye irritation. Personnel should therefore review the current Safety Data Sheet and use suitable engineering controls, protective equipment, and site-specific procedures when receiving, sampling, weighing, transferring, or processing the material.
The material is supported by standard technical documentation, including a Certificate of Analysis, Safety Data Sheet, and related product information where applicable. Available analytical methods, impurity limits, storage conditions, retest periods, and regulatory support should be confirmed for the individual grade before ordering. Batch-to-batch consistency, traceability, and controlled handling remain central to effective material sourcing and downstream development performance.
The material is packaged in appropriate containers selected to protect its quality from contamination, moisture, and environmental exposure during storage and transportation. Packaging formats, minimum order quantities, availability, and lead times may be discussed according to research, development, and qualified manufacturing requirements.
As with all CarboMer products, customers receive responsive technical communication and documentation support intended to advance material qualification, formulation development, scale-up, and long-term supply planning.