2-Imidazolidinone

2-Imidazolidinone | Technical Product Data & Wholesale Sourcing:

2-Imidazolidinone functions primarily as a heterocyclic intermediate in organic synthesis. It provides a stable ethylene urea moiety utilized in the preparation of active pharmaceutical ingredients (APIs), specialty polymers, and industrial auxiliaries. Supplied in commercial quantities for batch chemical processing.

Product Specifications:
Chemical Name: 2-Imidazolidinone
CAS Registry Number: 128-53-0
Molecular Formula: C3H6N2O
Molecular Weight: 86.09 g/mol
Structural Formula: 5-membered cyclic urea ring containing two secondary amine nitrogens flanked by a carbonyl group.

Chemical & Physical Properties:
Appearance: White to off-white crystalline powder or needles
Assay (Purity): >= 99.0% (determined by HPLC / Titrimetry)
Melting Point: 199°C - 202°C
Loss on Drying (Moisture): <= 0.5% (Karl Fischer method)
Residue on Ignition (Ash): <= 0.1%
Solubility: Soluble in water and polar organic solvents; practically insoluble in non-polar solvents.

Applications:
Pharmaceutical Synthesis: Acts as an intermediate for constructing nitrogen-containing heterocycles in active pharmaceutical ingredients (APIs).
Resin Manufacturing: Used in the production of formaldehyde scavengers and crease-resistant wet-strength resins for the textile and paper industries.
Specialty Chemicals: Serves as a building block for corrosion inhibitors and customized organic synthesis reagents.

Pharmaceutical Manufacturing Relevance:
Synthesized under controlled reaction parameters to minimize residual impurities, this grade aligns with requirements for downstream API precursors. Trace impurity profiles are monitored to support analytical method validation and regulatory filing support (DMF reference packages available upon request).

Grade & Quality Requirements:
Standard Grade: Synthesis Grade (>= 99.0% purity)
Regulatory Status: Manufactured in accordance with ISO 9001 certified processes. REACH pre-registered/registered profiles available for EU importing compliance. 

Quality Control:
Every production batch undergoes analytical verification prior to release. Testing protocols utilize high-performance liquid chromatography (HPLC) for assay determination, differential scanning calorimetry (DSC) for melting point verification, and Karl Fischer titration for moisture control. Representative retention samples are archived for 24 months.

Technical Documents:
COA (Certificate of Analysis): Batch-specific analytical data sheet provided with every shipment, detailing exact assay, moisture, and melting point results. Downloadable sample COA documents accessible via client portal.
SDS (Safety Data Sheet): Comprehensive GHS-compliant hazard, handling, and storage documentation accessible in regional compliance formats. Downloadable GHS SDS documents available.
TDS (Technical Data Sheet): Summary of physical constants, recommended handling conditions, and storage parameters. Downloadable technical data sheets available.

Packaging & Storage: 

Standard Packaging: 25 kg fiber drums lined with dual polyethylene moisture-barrier bags. Custom super-sack (bulk bag) configurations available for high-volume manufacturing sites.
Storage Conditions: Store in a cool, dry, well-ventilated area away from strong oxidizing agents. Keep containers tightly sealed to prevent moisture absorption.
Shelf Life: 24 months from the date of manufacture when stored under specified conditions.

Supply & Procurement:
MOQ (Minimum Order Quantity): 100 kg (standard drum configuration).
Sample Policy: 100g to 500g analytical samples available for laboratory evaluation and method validation.
Lead Time:
Spot orders: Dispatch within 3 to 5 business days from verified warehouse inventory.
Scheduled contract orders: Staggered delivery windows managed via annual supply agreements.
Bulk Supply: Scalable production capacity supporting metric ton (MT) scale annual volume requirements with stable pricing models.

OEM / Custom Specification:
Custom particle size reduction (milling/micronization), specific packaging weights, and tailored impurity threshold testing protocols can be accommodated for qualified volume contracts. Technical discussions require consultation with our process engineering team.

Request a Quote:
Submit specification requirements, annual volume forecasts, and destination port details to receive a commercial quotation including freight terms (FOB/CIF) and current lead times.

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