Description

7-Methyl-2,4-Diazaspiro[5.5]Undecane-1,3,5-Trione is a high-purity, specialized heterocyclic organic compound featuring a unique spirocyclic structure. This compound serves as a critical advanced pharmaceutical intermediate (API intermediate) and a versatile building block for medicinal chemistry research and development. It is primarily utilized by R&D chemists and process development scientists in the pharmaceutical, agrochemical, and fine chemical industries for the synthesis of novel active molecules.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of potential drug candidates, particularly those targeting central nervous system (CNS) disorders.
• Medicinal Chemistry Research: Used as a constrained scaffold to explore structure-activity relationships (SAR) and develop new chemical entities with improved pharmacological profiles.
• Agrochemical Synthesis: Serves as a precursor in the development of novel herbicides or insecticides, leveraging its heterocyclic core.
• Fine Chemical Production: Employed in the multi-step synthesis of complex, high-value specialty chemicals.
• Academic & Contract Research: Utilized in university and CRO (Contract Research Organization) labs for method development and novel compound library generation.

Basic Information

Product Name	7-Methyl-2,4-Diazaspiro[5.5]Undecane-1,3,5-Trione
CAS No.	67196-32-1
Molecular Formula	C10H14N2O3
Molecular Weight	210.23 g/mol
Synonyms	7-Methyl-2,4-diazaspiro[5.5]undecane-1,3,5-trione; 1,3-Diazaspiro[4.5]decane-2,4-dione, 8-methyl-; 8-Methyl-1,3-diazaspiro[4.5]decane-2,4-dione; Spirocyclic hydantoin derivative; 7-Methylspirohydantoin; MDUT
EINECS	Contact for details

Quality Control

Our 7-Methyl-2,4-Diazaspiro[5.5]Undecane-1,3,5-Trione is manufactured under a strict quality management system. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. Certificates of Analysis (COA) documenting full specifications are provided with every shipment. We support cGMP standards for pharmaceutical applications and can tailor purity grades to meet specific project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials such as strong acids, bases, and oxidizing agents. For long-term storage, consider an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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