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Aripiprazole CAS NO 129722-12-9
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CAS No.:129722-12-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Aripiprazole CAS NO 129722-12-9 is a high-purity atypical antipsychotic active pharmaceutical ingredient (API) of significant therapeutic importance. It is a critical component in the formulation of medications used to treat major psychiatric disorders, offering a unique pharmacological profile. This compound is essential for pharmaceutical manufacturers and research institutions engaged in the development and production of neuropsychiatric treatments.
Application
- Pharmaceutical API: Primary active ingredient in the manufacture of antipsychotic tablets, orally disintegrating tablets, and injectable solutions.
- Neuropsychiatric Drug Development: Key intermediate for research into novel treatments for schizophrenia, bipolar disorder, and major depressive disorder.
- Generic Drug Production: Sourcing for the formulation of bioequivalent generic versions of branded antipsychotic medications.
- Clinical Research Materials: Used as a reference standard and raw material in pharmacokinetic and pharmacodynamic studies.
- Precision Medicine Formulations: Component in the development of tailored dosage forms and combination therapies.
- Analytical Standard: Serves as a high-purity standard for quality control testing in pharmaceutical laboratories.
Basic Information
| Product Name | Aripiprazole |
| CAS No. | 129722-12-9 |
| Molecular Formula | C23H27Cl2N3O2 |
| Molecular Weight | 448.39 g/mol |
| Synonyms | 7-{4-[4-(2,3-Dichlorophenyl)-1-piperazinyl]butoxy}-3,4-dihydro-2(1H)-quinolinone; Abilify; OPC-14597; BMY-14802; Aripiprazolum; UNII-82VFR53I78; Aristada (extended-release injectable); BMS-337039 |
| EINECS | Contact for details |
Quality Control
Our Aripiprazole is manufactured under strict quality management systems, targeting compliance with major pharmacopoeial standards such as USP and ICH Q7 guidelines. Every batch undergoes comprehensive analytical testing including identification, assay, impurity profiling, and residual solvent analysis. A Certificate of Analysis (COA) documenting all test results is provided with each shipment to ensure full traceability and regulatory support for your projects.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a low-humidity environment to prevent degradation. For long-term storage, consider the use of desiccants.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference standard |
| Identification (HPLC) | Retention time conforms to reference standard |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Related Substances (HPLC) | Individual impurity: ≤ 0.15% Total impurities: ≤ 0.5% |
| Heavy Metals | ≤ 20 ppm |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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