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9-[(2R)-3α-Hydroxy-4β-(Hydroxymethyl)Tetrahydrofuran-2β-Yl]-9H-Purine-6-Amine CAS NO 19200-56-7


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CAS No.:19200-56-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

9-[(2R)-3α-Hydroxy-4β-(Hydroxymethyl)Tetrahydrofuran-2β-Yl]-9H-Purine-6-Amine is a high-purity nucleoside analog of significant interest in advanced pharmaceutical research and development. This compound serves as a critical building block and reference standard for the synthesis of novel antiviral and anticancer agents. It is primarily utilized by research institutions and pharmaceutical companies engaged in the development of nucleoside-based therapeutics. The material's defined stereochemistry and purity are essential for ensuring reproducible biological activity and research outcomes.

Application

  • Pharmaceutical Intermediate: A key synthetic precursor in the production of nucleoside analog drugs targeting viral infections and cancer.
  • Biochemical Research: Used as a reference standard and substrate in enzymatic studies, metabolic pathway analysis, and molecular biology research.
  • Antiviral Drug Development: Serves as a core scaffold for the research and synthesis of potential antiviral agents.
  • Oncology Research: Investigated for its role and derivatives in the development of chemotherapeutic agents.
  • Process Development & Scale-up: Employed in process chemistry for route scouting, optimization, and analytical method development.
  • Academic Research: Utilized in university and institutional labs for fundamental studies in medicinal chemistry and pharmacology.

Basic Information

Product Name 9-[(2R)-3α-Hydroxy-4β-(Hydroxymethyl)Tetrahydrofuran-2β-Yl]-9H-Purine-6-Amine
CAS No. 19200-56-7
Molecular Formula C11H15N5O3
Molecular Weight 265.27 g/mol
Synonyms 9-[(2R,3S,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-amine; (2R,3S,4R,5R)-2-(6-Amino-9H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol; Adenosine, 2'-deoxy-; 2'-Deoxyadenosine; dA; 2'-dA; Deoxyadenosine; Cordycepin precursor analog
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Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards for research and pharmaceutical applications. Each batch is analyzed using advanced chromatographic and spectroscopic techniques to confirm identity, purity, and potency. Certificates of Analysis (COA) are available upon request, detailing comprehensive testing results. We adhere to strict quality management protocols to ensure batch-to-batch consistency and reliability for your critical research and development needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and purity. Avoid exposure to excessive heat and humidity.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (HPLC) Conforms to reference standard
Assay (HPLC) ≥98.0%
Water Content (KF) ≤1.0%
Residue on Ignition ≤0.1%
Heavy Metals ≤10 ppm
Related Substances (HPLC) Total impurities ≤2.0%

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

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