|
HS Code |
920303 |
| Chemical Name | 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide |
| Molecular Formula | C9H16N2O |
| Molecular Weight | 168.24 g/mol |
| Cas Number | 1638-94-0 |
| Appearance | White to off-white solid |
| Melting Point | 102-104°C |
| Solubility | Soluble in organic solvents, slightly soluble in water |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Synonyms | TPC, TEMPAMINE |
| Smiles | CC1(C)C(N(C(C1(C)C)=O))C |
As an accredited 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide, 25g," featuring hazard symbols and lot number for reference. |
| Shipping | 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide is shipped in tightly sealed containers, protected from moisture and light. It should be packaged according to chemical safety regulations, with appropriate labelling and documentation. Transport typically follows guidelines for non-hazardous organic compounds, ensuring secure handling to prevent spills or contamination during transit. |
| Storage | 2,2,5,5-Tetramethyl-3-pyrroline-3-carboxamide should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen, and kept away from moisture, heat, and direct sunlight. Store at room temperature or as specified by the supplier, in a cool, dry, and well-ventilated area. Avoid exposure to oxidizing agents and incompatible substances to maintain stability and safety. |
Applications of 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide in Industrial Manufacturing2,2,5,5-Tetramethyl-3-pyrroline-3-carboxamide provides specialized performance in select industrial segments, where its stable nitroxide functional group delivers oxidative resistance or controlled radical processes. As an original manufacturer, we have worked directly with global downstream partners to support formulation development, compliance documentation, and technical audits for the following application scenarios. 1. Polymer Stabilizers for Polyolefin ManufacturingIn polyolefin extrusion and film production, this compound functions as a hindered amine light stabilizer. Manufacturers dose it during compounding to prolong polymer life under UV and thermal exposure, maintaining mechanical and appearance properties through multiple processing cycles. The amide functionality reinforces polymer compatibility, providing targeted stabilization in outdoor applications, agricultural films, and packaging substrates. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Free Radical Scavenger in Acrylic Paints and CoatingsCoatings formulators include this compound as a free radical scavenger to slow yellowing, chalking, and gloss loss in exterior-grade acrylic emulsions. It enters the production phase before pigment grind or after polymer dispersion synthesis, relying on its steric protection to improve shelf-life and UV resistance without impacting rheology. Its integration helps coating manufacturers meet accelerated weathering performance benchmarks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Spin Trap Agent for Analytical ESR ReagentsContract research organizations and analytical laboratories use this molecule as a spin trap in electron spin resonance (ESR) assays to detect reactive oxygen and nitrogen species. The crystalline amide structure ensures purity and reproducibility, supporting precise identification of transient radicals during kinetic studies for pharmaceutical, food, and polymer oxidation investigations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Catalyst Intermediate for Controlled Radical PolymerizationAdvanced polymerization labs and specialty chemical producers utilize this compound as an intermediate ligand or initiator for nitroxide-mediated radical polymerization (NMP) processes, particularly in well-defined styrenic and (meth)acrylic block copolymer synthesis. Its steric structure enables tailored control over polymer chain length distribution and end-group functionality, supporting high-purity elastomer and thermoplastic elastomer workflows. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Oxygen Scavenger for Specialty Food Packaging FilmsIn multilayer oxygen barrier packaging, processors employ this amide derivative within the core or tie layer to scavenge residual oxygen, slowing oxidation and spoilage of sensitive food products. Blended during film extrusion, it responds to internal and external oxygen ingress, especially in modified atmosphere packaging, minimizing undesired taste changes and shelf-life reduction in high-fat or delicate food goods. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In our laboratories, the synthesis of 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide reflects years of focused research and direct manufacturing experience. This chemical, sometimes written as TMPCA, stands out among pyrroline derivatives for its stability and application spectrum. Over decades, we have seen firsthand how steady demand from research groups and specialty chemical companies has shaped small-batch process improvements and attention to trace-level purity concerns.
Chemical synthesis of this pyrroline carboxamide doesn’t leave much room for shortcuts. The path from starting ketones and ammonium derivatives to the final product brings challenges at every catalytic step. Each batch runs under controlled temperature and pressure, avoiding contamination by oxygen and moisture, two constant threats to sensitive nitrogen rings. Every time we finish a batch, our analytical team looks closely at the byproduct profile. NMR and LC-MS results guide us back to the reactors whenever they find anything unexpected. Chemical manufacturing isn’t abstract or remote; it’s a daily discipline, and TMPCA remains one of those molecules that rewards attention to detail.
Our standard release for 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide favors a crystalline solid, off-white in appearance, with a purity of not less than 98% by HPLC assay. Over the years, we have had requests for different presentations, mostly from formulation specialists interested in solubility or process chemistry research. We guarantee freshly produced material with a low residual solvent profile, keeping moisture well below 0.5% and storing everything under inert gas to guard against degradation. Only real-world production trials have taught us where this product is prone to picking up trace water or discoloration, and we respond to those factors before anything leaves our facility.
The molecular formula, C9H18N2O, gives it a predictable profile in NMR and mass spectrometry. This matters for everyone who works with it in an analytical lab or feeds it into a new synthetic route. Our plant samples every lot by both classic wet chemistry and modern liquid chromatography, catching even small outliers in specification. No generic approach gives customers confidence; only direct and repeated testing works.
2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide owes much of its reputation to its status in the synthesis of nitroxide radicals. In our own development runs, oxidation steps proceed with predictable efficiency because this molecule’s rigid, bulky ring sterically protects the sensitive amide group. Researchers in chemical biology value this product for building spin labels used in electron paramagnetic resonance (EPR) experiments, where stable, well-behaved radicals make or break a study’s data. It’s satisfying seeing the compound we manufacture drive discovery in protein structure, membrane studies, or radical trapping investigations.
Manufacturing the carboxamide form, compared to esters or acids of 2,2,5,5-tetramethyl-3-pyrroline, means working with a more hydrolytically stable product. Colleagues running reactions in aqueous environments or launching it into complex reaction media come back with positive feedback about shelf life and compatibility. Several industrial clients choose this specific amide thanks to its balance between reactivity (in oxidation) and resistance to unwanted side reactions. Compared to 2,2,6,6-tetramethylpiperidine derivatives, our product has a smaller ring size and a distinct suite of physical properties, which makes a real impact on spin labeling and polymer stabilization effectiveness.
Years of hands-on process chemistry inform our perspective on pyrroline compared to piperidine scaffolds or less hindered nitroxide sources. 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide stands apart for its lower molecular weight and the way its structure brings rigidity without unwelcome steric blockage. While piperidine-based nitroxides like TEMPO claim the spotlight in bulk oxidation and polymer chemistry, our product has carved out its niche where smaller, more agile molecules matter. This difference becomes obvious in biochemistry labs relying on EPR for clean, precisely located spin probes, or in polymer research, where compatible backbone structures keep additives from phase separating.
Market landscapes make it easy to lose sight of what’s happening at the bench level. We routinely field technical questions about differences between related compounds; real users want data on reactivity, shelf-life, or storage practices. TMPCA maintains a stable solid form for years under proper conditions, and we have seen no evidence of rapid decomposition even under challenging storage situations. Its ability to survive freeze-thaw cycles or exposure to minor process upsets gives formulators added confidence relative to more fragile nitroxide sources.
No chemical product exists in a vacuum. Manufacturing carboxamide derivatives at scale brings pressure from three sides: economic constraints, worker and community safety standards, and new sustainability benchmarks. Running larger reactors to produce 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide each month, we track solvent use, reaction energy, and emissions intensely. Our production staff aim for processes that both meet customer specifications and strike a balance with regulations and good stewardship.
One practical difficulty emerges around waste minimization. Pyrroline-ring creation brings chances for unwanted byproducts—either over-oxidized impurities or side-chain scrambling—especially in less experienced hands. Our teams keep batch records stretching back many years. Routinely, we tweak catalyst ratios or change base sources to reduce waste. As a manufacturer, direct involvement with every reaction phase makes a difference, and we collect feedback after each production run. This commitment to continuous improvement sits at the core of our operation.
We also invest in hazard reduction around amine and ketone handling, an area where training and vigilance cannot lapse. Standard personal protective equipment and gas scrubbing installations form part of our plant culture, not only to comply with regulations but because every team member deserves the right to a safe work environment. As we grow, our plant safety committees evaluate each new process step, weighing both chemical and physical hazards, and searching for greener synthesis options.
There’s a lesson we take from decades producing specialty chemicals: being close to the end user sharpens every decision. Academics and industrial customers alike want detailed, practical advice. Our teams answer technical questions about drying, dissolution, or compatibility with common lab solvents. Working chemists have asked how TMPCA compares to related carboxylates or alkoxyamides for a specific synthetic route, or whether our crystalline grades dissolve completely in cold tetrahydrofuran. We run pilot-scale dissolutions and dry-down cycles ourselves to give straight answers.
Sometimes a research group requires an unusual grading—ultra-high purity or a specific isotopic makeup. We rely on modular synthesis steps and dedicated cleaning regimens to avoid cross-contamination or reagent carryover. By listening to users, each product cycle grows more robust, with feedback informing tweaks to crystallization, drying, or final handling. No two lots ever run on autopilot.
Active dialogue with the chemical sciences community keeps our manufacturing responsive. Synthetic organic researchers tell us where yield bottlenecks or crystalline stability issues slow their workflows. Some mention success using TMPCA’s carboxamide group for coupling reactions or radical generation, while others find unique spin label strategies not manageable with bulkier, less reactive nitroxides. Repeating these syntheses in-house, our R&D chemists confirm or contradict field results, letting us update our documentation in ways that traders and middlemen simply can’t match.
Biology groups bring another perspective, focusing on how TMPCA-initiated radical species interact with proteins or cell membranes. Their feedback on solubility, side chain persistence, or labeling efficiency directly shapes our specification targets and storage guidelines. We invest in collaborative projects, lending technical samples to groups with innovative protocols, then integrate their data to improve our production. The product’s adaptability to both organic and aqueous systems often gets cited as an advantage over traditional spin label synthons.
A chemical manufacturer’s job doesn’t end with shipping. Every pouch or drum of carboxamide carries months of preparation—right sourcing, careful production, critical drying procedures, airtight packaging, and prompt shipment. We store TMPCA stocks under nitrogen in amber containers, cooling inventory even in transit during summer months. Well-defined procedures for weighing, aliquoting, and transferring keep even small lab-scale customers from thermal or moisture upsets.
Field experiences taught us the folly of cutting corners on storage conditions. Early in our production history, minor lapses in desiccant choice led to detectable hydrolysis products by the time samples reached customers. Careful overhaul of packaging standards brought those incidents to zero, and each incident became a training case for the next generation of plant scientists. Our goal every season revolves around maintaining trust through chemical quality.
Traceability and regulatory transparency anchor our approach to production. In a business where off-quality lots risk loss of customer trust or regulatory review, we maintain lot-level documentation easily accessible for customer review. We prefer up-to-date testing protocols that account not only for regulatory standards in our home markets, but also for destination markets. Only actual production records and regular audits build confidence in the reliability of a specialty chemical product like TMPCA.
Recent years have brought increased attention to the environmental impact of synthetic nitroxide and carboxamide production. We address this through process optimization, solvent recovery, and waste treatment upgrades. Changes to purification methods, including switchovers to more environmentally benign solvents, result from both commercial pressure and our own desire to minimize environmental footprint. In one recent batch cycle, solvent recycling alone brought down net emissions by nearly 20%—this kind of result drives internal motivation as much as outside regulation.
As a manufacturer aiming for both scale and technical distinction, we watch global markets for trends in nitroxide chemistry and specialty amide research. Our sales and R&D personnel track literature and patent filings for emerging applications of 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide in pharmaceuticals, advanced polymer formulation, or EPR label synthesis. In the last few years, increasing usage in biomedical imaging and radical scavenger applications has expanded the customer base. Broadening use brings new technical demands—different particle size cuts, alternative purities, and specialty packaging requests.
We support direct collaboration with research groups seeking scale-up from bench to pilot-scale runs. Challenges here often relate to reproducibility and purity drift as batch size increases. Upon request, we walk through each scale-up scenario with hands-on analytical work, not just literature-based advice. This approach cuts risk for downstream users and shows respect for chemical development as more than just a commodity transaction.
Foresight matters—much as regulatory or safety pressures have improved over the years, we expect new demands around green chemistry and carbon footprint to keep changing production routines for carboxamide derivatives. Our team dedicates a set budget to process R&D, constantly measuring energy and material flows to lower both cost and impact.
Real trust in specialty chemicals follows a line from the reactor vessel to the customer’s bench. Sourcing TMPCA from us means access to production records, batch-specific analytical reports, and direct technical support from the same staff who designed the processes and grew the crystals. Distributors and catalog companies rarely match that level of engagement.
Over the years, customers from biotechnology to advanced materials have come to appreciate the benefits of dealing directly with the maker. Immediate answers on impurity control, new packaging, or certificate of analysis formats build the relationship beyond business terms. We encourage customers to visit our plant, audit our records, or challenge us with new technical demands. Only a real manufacturer can respond with process changes or special runs tailored to emerging scientific challenges.
Decades spent manufacturing 2,2,5,5-Tetramethyl-3-Pyrroline-3-Carboxamide have shown that technical progress, safety, and user-focused innovation rely on honest engagement with both the chemistry and the people using it. Our operations blend careful synthesis, tight analytical controls, and active dialogue with a fast-changing field. Compared to less specialized pyrroline or piperidine derivatives, this chemical keeps earning its place on the lab bench for researchers and formulators demanding consistency, stability, and tailored physical properties.
Direct manufacturing experience grants perspective on the evolution of both process efficiency and customer needs. Making this carboxamide means constant vigilance, a willingness to improve, and a practical respect for every bench chemist, process engineer, or researcher relying on clean, predictable chemicals. The story of each batch begins in the reactors and concludes in the discoveries and products built by our customers—a link forged by attention, not abstraction.