Description

3'-Butylspiro[Tetralin-2,4'-Imidazolidine]-2',5'-Dione is a specialized spirocyclic organic compound featuring a fused tetralin and imidazolidinedione structure. This unique molecular architecture makes it a valuable advanced intermediate for the synthesis of complex heterocyclic molecules in pharmaceutical research and development. It is primarily sought by R&D chemists and process development scientists in the fine chemical and pharmaceutical industries for creating novel active pharmaceutical ingredients (APIs) and other high-value chemical entities.

Application

• Pharmaceutical Intermediate: A key building block for the synthesis of novel drug candidates, particularly those targeting central nervous system (CNS) disorders.
• Organic Synthesis Research: Used in academic and industrial R&D to explore new spirocyclic and fused-ring chemical spaces for material science and medicinal chemistry.
• Fine Chemical Production: Serves as a precursor for manufacturing specialized fine chemicals with specific stereochemical or functional properties.
• Agrochemical Research: Potential intermediate in the development of new agrochemicals, such as herbicides or fungicides, with novel modes of action.
• Ligand and Catalyst Development: The rigid spirocyclic framework can be utilized to develop novel chiral ligands or organocatalysts for asymmetric synthesis.

Basic Information

Product Name	3'-Butylspiro[Tetralin-2,4'-Imidazolidine]-2',5'-Dione
CAS No.	110176-42-6
Molecular Formula	C₁₆H₂₀N₂O₂
Molecular Weight	272.34 g/mol
Synonyms	3'-Butylspiro[tetralin-2,4'-imidazolidine]-2',5'-dione; Spiro[tetralin-2,4'-imidazolidine]-2',5'-dione, 3'-butyl-; 3'-n-Butylspiro[tetralin-2,4'-imidazolidine]-2',5'-dione; 3'-Butyl-1,3-diazaspiro[4.5]decane-2,4-dione (tetralin fused); Butylspiroimidazolidinedione; 110176-42-6; 3'-Butylspiro(tetralin-2,4'-imidazolidine)-2',5'-dione
EINECS	Contact for details

Quality Control

Our production of 3'-Butylspiro[Tetralin-2,4'-Imidazolidine]-2',5'-Dione adheres to stringent quality management protocols to ensure batch-to-batch consistency and high purity. All materials undergo rigorous analytical testing, including HPLC, NMR, and MS, to confirm identity and purity. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with each shipment. We support cGMP compliance for pharmaceutical applications and can tailor quality documentation to meet specific client or regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Keep away from heat, sparks, and open flame. For long-term storage, consider storing under an inert atmosphere to maintain product integrity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
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.