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5-Oxaspiro[3.5]Nonan-8-Amine Hydrochloride(Wxc08738S1) CAS NO 1309366-17-3


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CAS No.:1309366-17-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

5-Oxaspiro[3.5]Nonan-8-Amine Hydrochloride (Wxc08738S1) is a high-purity, advanced pharmaceutical intermediate featuring a unique spirocyclic amine structure. This compound is valued for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in central nervous system (CNS) and antiviral research. It is primarily sought by R&D chemists and process development scientists in the pharmaceutical and biotechnology industries for constructing complex molecular architectures.

Application

  • Pharmaceutical Intermediate: A key chiral building block for the synthesis of novel drug candidates targeting neurological disorders.
  • Organic Synthesis Reagent: Used in medicinal chemistry for constructing complex spirocyclic and bridged ring systems.
  • Agrochemical Research: Serves as a precursor in the development of new pesticides and herbicides with specific activity profiles.
  • Ligand and Catalyst Development: Utilized in the preparation of specialized ligands for asymmetric catalysis and metal-organic frameworks (MOFs).
  • Academic & R&D: Employed in university and institutional research for studying structure-activity relationships (SAR) and new synthetic methodologies.
  • Fine Chemical Production: Integrated into multi-step synthesis processes for high-value specialty chemicals.

Basic Information

Product Name 5-Oxaspiro[3.5]Nonan-8-Amine Hydrochloride (Wxc08738S1)
CAS No. 1309366-17-3
Molecular Formula C8H16ClNO
Molecular Weight 177.67 g/mol
Synonyms 8-Amino-5-oxaspiro[3.5]nonane hydrochloride; 5-Oxaspiro[3.5]nonan-8-amine, hydrochloride; Spiro[3.5]nonan-8-amine, 5-oxa-, hydrochloride; WXC08738S1; 1309366-17-3; 5-Oxa-spiro[3.5]nonan-8-ylamine hydrochloride
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Quality Control

Every batch of 5-Oxaspiro[3.5]Nonan-8-Amine Hydrochloride is manufactured under strict quality management systems. Our products undergo rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency meet the exacting standards required for pharmaceutical R&D. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with each shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed under an inert atmosphere after opening to prevent degradation.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (NMR) Conforms to structure
Purity (HPLC) ≥ 98.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Single Unknown Impurity (HPLC) ≤ 0.5%
Total Impurities (HPLC) ≤ 2.0%

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

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