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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
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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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