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Potassium 1,2,3,6-Tetrahydro-1,3-Dimethyl-2,6-Dioxo-7H-Purine-7-Acetate CAS NO 62026-29-3
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CAS No.:62026-29-3
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Potassium 1,2,3,6-Tetrahydro-1,3-Dimethyl-2,6-Dioxo-7H-Purine-7-Acetate is a high-purity potassium salt derivative of a xanthine-based compound, offering enhanced solubility and stability for advanced formulation work. This specialized chemical is critical for researchers and manufacturers requiring a precisely defined and reliable active pharmaceutical ingredient (API) intermediate or reference standard. It is primarily utilized in the pharmaceutical and life science sectors for the development and production of novel therapeutic agents.
Application
- Pharmaceutical Intermediate: Serves as a key building block in the synthesis of advanced pharmaceutical compounds, particularly those targeting neurological and cardiovascular pathways.
- Reference Standard: Used in analytical laboratories for method development, validation, and quality control testing of related APIs and finished drug products.
- Biochemical Research: Employed in life science research to study purinergic signaling, enzyme inhibition, and other receptor-level interactions.
- Preclinical Development: Utilized in the formulation of compounds for pharmacological and toxicological studies during drug discovery.
Basic Information
| Product Name | Potassium 1,2,3,6-Tetrahydro-1,3-Dimethyl-2,6-Dioxo-7H-Purine-7-Acetate |
| CAS No. | 62026-29-3 |
| Molecular Formula | C9H9KN4O4 |
| Molecular Weight | 276.30 g/mol |
| Synonyms | Potassium 7-Acetyl-1,3-dimethylxanthine; Potassium Acefyllinate; Potassium Theophylline-7-acetate; 7-(Carboxymethyl)theophylline Potassium Salt; Acetylline Potassium; 1,3-Dimethyl-7-(potassiumoxycarbonylmethyl)xanthine; Theophylline-7-acetic acid potassium salt |
| EINECS | Contact for details |
Quality Control
Our Potassium 1,2,3,6-Tetrahydro-1,3-Dimethyl-2,6-Dioxo-7H-Purine-7-Acetate is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets stringent specifications for pharmaceutical R&D use. Certificates of Analysis (COA) with detailed HPLC, NMR, and elemental analysis data are provided to guarantee traceability and batch-to-batch consistency.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time conforms to reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Water Content (KF) | ≤ 2.0% |
| Heavy Metals | ≤ 20 ppm |
| Residue on Ignition | ≤ 0.1% |
| Related Substances (HPLC) | Individual impurity ≤ 0.5%; Total impurities ≤ 1.5% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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