Description

Spiro[4.4]Nonan-1-Ol, 6-Amino-, (1R,5R,6R)-Rel- (9Ci) is a chiral, functionalized spirocyclic compound of significant interest in advanced organic synthesis. This molecule matters as a sophisticated building block, offering a rigid, three-dimensional scaffold with both amino and hydroxyl functional groups for precise chemical modifications. Pharmaceutical and agrochemical R&D teams need it for developing novel active ingredients, particularly where stereochemistry and molecular shape are critical for biological activity.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new therapeutic agents, including central nervous system (CNS) drugs and enzyme inhibitors.
• Agrochemical Synthesis: Used in creating novel pesticides and herbicides where the spirocyclic structure can contribute to unique modes of action and environmental stability.
• Asymmetric Catalysis Ligand Precursor: Serves as a starting material for synthesizing chiral ligands and organocatalysts used in enantioselective transformations.
• Material Science Research: Investigated as a monomer or additive for creating polymers with specific thermal or mechanical properties due to its rigid backbone.
• Chemical Biology Probe Development: Utilized in constructing molecular probes to study protein-ligand interactions and biological pathways.

Basic Information

Product Name	Spiro[4.4]Nonan-1-Ol, 6-Amino-, (1R,5R,6R)-Rel- (9Ci)
CAS No.	575342-75-5
Molecular Formula	C9H17NO
Molecular Weight	155.24 g/mol
Synonyms	(1R,5R,6R)-6-Aminospiro[4.4]nonan-1-ol; rel-(1R,5R,6R)-6-Aminospiro[4.4]nonan-1-ol; 6-Aminospiro[4.4]nonan-1-ol (rel-(1R,5R,6R)-); Spiro[4.4]nonan-1-ol, 6-amino-, (1R,5R,6R)-rel-; (1R,5R,6R)-rel-6-Amino-spiro[4.4]nonane-1-ol; 575342-75-5; Amino Spiro Nonanol Derivative
EINECS	Contact for details

Quality Control

Our production of Spiro[4.4]Nonan-1-Ol, 6-Amino-, (1R,5R,6R)-Rel- (9Ci) adheres to stringent quality management protocols. Each batch undergoes comprehensive analytical testing, including chiral HPLC for enantiomeric excess (ee) and standard purity assays, to ensure it meets the exacting requirements of research and process development. Certificates of Analysis (COA) with detailed chromatographic data are available upon request to support your quality assurance and regulatory documentation.

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 nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption, which can affect stability and handling properties. For long-term storage, consider using desiccants.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Enantiomeric Excess (Chiral HPLC)	≥ 98.0% ee
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%

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