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HS Code |
171023 |
| Chemical Name | Diethyl Aminomalonate Hydrochloride |
| Cas Number | 13433-00-6 |
| Molecular Formula | C7H15ClN2O4 |
| Molecular Weight | 226.66 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 139-143 °C |
| Solubility | Soluble in water and ethanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | Diethyl 2-aminomalonate hydrochloride |
| Smiles | CCOC(=O)C(N)C(=O)OCC.Cl |
As an accredited Diethyl Aminomalonate Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g white crystalline powder is securely sealed in a labeled amber glass bottle with a screw cap, stored within a protective cardboard box. |
| Shipping | Diethyl Aminomalonate Hydrochloride is shipped in tightly sealed containers protected from moisture and light. The packaging complies with chemical safety regulations to prevent leaks or contamination. It is transported as a non-hazardous solid, typically with appropriate labeling. Temperature control is maintained at ambient conditions, avoiding excessive heat or humidity during transit. |
| Storage | Diethyl Aminomalonate Hydrochloride should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Store at room temperature, ideally between 15–25°C (59–77°F). Ensure proper labeling and restrict access to trained personnel only. |
Applications of Diethyl Aminomalonate Hydrochloride in Industrial ManufacturingAs a specialized manufacturer of Diethyl Aminomalonate Hydrochloride, we supply this intermediate to global B2B clients who demand consistent quality and traceability for regulated downstream processes. Below we present major industrial applications, each reflecting authentic use in advanced synthesis across pharmaceutical and fine chemical production lines. 1. Pharmaceutical Active Pharmaceutical Ingredient SynthesisDiethyl Aminomalonate Hydrochloride serves as a key building block for the synthesis of several pyrimidine and purine analogues in the pharmaceutical sector, notably in the production of antineoplastic and antiviral compounds. Process chemists value its clean amination profile for introducing the aminomalonate backbone during nucleobase elaboration. Its integration supports multi-step active pharmaceutical ingredient (API) synthesis, where lot traceability and compliance with pharmacopeial grades are mandatory. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingThis material acts as a specialized C-N backbone extender in the preparation of substituted heterocyclic intermediates for crop protection chemistry. Downstream agrochemical production often employs it in the synthesis of triazine and pyrimidine motifs, which are integral to selective herbicides and fungicides. Consistent particle size and controlled chloride counterion level are scrutinized due to process sensitivity at scale. Industry compliance standards
Typical usage ratio
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3. Specialty Dye and Pigment Intermediate ProductionWithin the pigment and specialty dye sectors, this compound aids as a chain-integrating monomeric intermediate for developing high-stability azo and anthraquinone chromophores. Manufacturers apply it during multi-point coupling reactions for colorant molecules destined for solvent- and acid-fast textile dyes. Material qualification ensures limited trace contaminants that could affect final shade persistence and lightfastness. Industry compliance standards
Typical usage ratio
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4. Fine Chemical Building Block for Amino Acid DerivativesThis intermediate finds targeted use in peptide and amino acid derivative synthesis, where its bifunctional aminomalonate group enables construction of non-natural amino acid analogs. Fine chemical companies incorporate it into linear and cyclic peptide workflows to achieve site-specific backbone modifications, required for next-gen catalysts and biochemical probes. Lot-to-lot homogeneity is essential to maintain analytical performance for subsequent chromatographic purification. Industry compliance standards
Typical usage ratio
Downstream process integration
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Diethyl aminomalonate hydrochloride, known across labs and process lines for decades, is best described as a chemist’s tool for building value into molecules. As manufacturers, we have watched this intermediate become a staple in multi-step syntheses where both reliability and adaptability matter. Its structure opens routes to complex targets, like amino acids, pharmaceutical actives, and agrochemical ingredients. Our expertise lies in translating this molecular versatility into large-batch, reproducible results for downstream innovators.
We produce this compound with a close eye on batch-to-batch consistency. Over the years, direct feedback from project chemists and scale-up engineers has shaped our approach. Customers often highlight that small impurities can ruin downstream steps or require laborious purification. Because of this, attention sits on several key metrics: purity above 98%, controlled particle size, and low residual solvents. No universal specification fits every application, but we have sharpened our methods to deliver tight reproducibility on color, flow, and yield. Product texture may seem trivial, though clumping and caking frustrate operators trying to achieve quick, dust-free dissolution. Simple details—how it pours, disperses, or stores—connect directly to our day-to-day improvements. We now adopt closed-system drying to stabilize moisture content, helping extend shelf life and prevent cake build-up under variable warehouse climates.
Our facility started making diethyl aminomalonate hydrochloride due to mounting demand from custom synthesis clients. They described hurdles with on-site preparation—sometimes hazardous—using raw diethyl malonate and ammonia derivatives. By preparing and purifying at scale, we remove the operational risks and allow chemists to focus on end-stage transformations. End-users employ our compound to craft amino acid analogs, intermediates for antihypertensive agents, and heterocyclic scaffolds. Its reactivity, based on active methylene and amino functional groups, permits quick derivatization, alkylation, or cyclization. In medicinal chemistry, it offers a launching pad for alpha-amino acid and peptide mimetic synthesis due to its protected nature and ease of deprotection when needed.
Outside pharmaceutical circles, diethyl aminomalonate hydrochloride acts as a precursor in crop protection R&D. Here, the repeatability of reactions often decides whether a synthetic plan is viable for pilot trials or process transfer. We regularly collaborate with process chemists to tweak crystal forms, solvent systems, or drying conditions, responding to project-specific needs without abrupt changes between production runs.
Those less familiar with the nuances of functionalized malonate derivatives might see only subtle differences, but hands-on use clarifies why diethyl aminomalonate hydrochloride merits separate attention from analogs like diethyl acetamidomalonate or even raw diethyl malonate. For one, the hydrochloride salt handles more safely than free bases, offering improved stability when stored under ambient conditions. We have witnessed fewer degradation problems and less off-gassing during long-haul shipments. Also, compared to the parent diethyl malonate, the aminomalonate core delivers both nucleophilic and electrophilic handles, reducing the steps in typical synthetic plans. Process teams have demonstrated two-cycle savings in certain pharmaceutical intermediates by starting with aminomalonate as a protected amino donor instead of crafting the group in situ from ammonia.
The acetyl-protected analog, diethyl acetamidomalonate, does act as a key alternative in peptide and nucleotide chemistry. Still, our data and first-hand troubleshooting have shown that acetamido protection sometimes introduces stubborn side products, plus deprotection steps that complicate waste handling. Conversely, hydrochloride salt formation strips away these difficulties, yielding a compound more predictable for scale-up and registration batches, especially under tight project deadlines.
Quality in fine chemical manufacturing hinges on what we control—which is nearly everything from raw feedstock to sealed packaging. We carefully source diethyl malonate and establish chain-of-custody for all incoming materials. During conversion, our operators check temperature and pH at every addition stage, drawing on years of hands-on chemical practice to catch any deviation early. Modern analytical tools confirm chemical identity, purity, and water content, but our most experienced team members still rely on physical cues—smell, color shift, the texture during crystallization. Simple tests, such as “squeeze powder for flow” or “watch dissolution speed”, still uncover issues faster than a spectrometer alone. In our daily QC meetings, plant staff scrutinize both in-spec and borderline samples, recalling past production challenges and resolution methods.
Repeat orders from multinational pharma teams and university R&D projects confirm that reliability builds trust. New project leads often ask about change control; we keep detailed batch records for traceability. For both regulated and investigative buyers, quality audits welcome walk-throughs and Q&A with our plant chemists, not just a slide deck from a sales office.
Industrial chemists know that hazards do not only stem from headline materials but also from their intermediates and side products. Our experience reveals that diethyl aminomalonate hydrochloride, as a salt, provides process safety: less volatility, a lower inhalation risk, and a reduced chance of unwanted side reactions during shipping or storage. The compound’s solubility profile lends itself to controlled addition into aqueous or alcoholic solution, allowing metered feeds with little dust formation. Users who previously struggled with corrosive or reactive bases report smoother processes, specifically in semi-batch reactors that lack advanced containment.
We have seen that clear labeling, closed transfer systems, and guided operator training prevent most incidents at scale. Years ago, we transitioned from static-prone plastic packaging to lined steel drums to combat accidental discharge and ensure stricter moisture seals. The changes stemmed less from regulation and more from seeing material lost to environmental pickups and clump formation. Few end-users notice packaging until it causes stoppages, but day-to-day manufacturing reinforces the value of proactive handling.
Chemical manufacturing never stands still. Innovations in biocatalysis, green chemistry, and continuous flow processes keep raising the bar for what intermediates like diethyl aminomalonate hydrochloride must achieve. We hold regular technical forums with downstream chemists to discuss flow reactor compatibility, potential for solvent substitution, or alternative work-ups to simplify mother liquor handling. If a customer designs a new ligand or building block that tests the limits of our process, our team reviews syntheses at both the benchtop and pilot scales, drawing on plant logs and batch histories.
Small changes in impurity profiles can stall a registration batch or trigger a failed validation in GMP settings. Our chemists keep a log of “minor major” adjustments: filtration tweaks, solvent swaps, or seeding optimizations, and share resulting data with our partners. Decades of work show that trace residue management—maybe 0.1% by GC-MS—impacts both solid handling and API purity, often more than anticipated on a tech transfer sheet alone.
No market sits still. Our main customer base covers large pharmaceutical companies and smaller, innovation-driven start-ups, each with their own purchasing patterns and regulatory needs. Some run kilo campaigns for weeks, others draw a single drum every six months for library generation or reference material production. International demand sometimes spikes on the heels of successful clinical trials. Readiness for fluctuations matters more than forecasts. Buffer stocks and rapid crystallization methods let us scale up or down on short notice without quality drift.
We partner with supply chain managers, regulatory teams, and synthetic chemists to keep the pipeline predictable. Advanced notice on purity upgrades or alternate packaging handles most challenges before they reach the bottleneck stage. Every project we support reflects the compound’s journey through multiple hands and process tweaks, each aiming for a better, reproducible outcome downstream.
Years ago, chemical intermediates attracted little scrutiny beyond their immediate process role, but priorities shifted with mounting environmental awareness. Waste minimization, energy conservation, and solvent recycle programs now shape daily routines on our plant floor. Our diethyl aminomalonate hydrochloride process runs closed-loop solvent recovery and heat integration—steps that lower both cost and footprint. Waste acid and solvent streams undergo in-plant neutralization and water treatment before external discharge. Not every competitor takes this approach, but our internal audits and community ties make it non-negotiable.
Cost remains a constant challenge, squeezed by rising raw material prices and tighter labor markets. Rather than chase lowest-cost formulas that threaten quality, we invest in process efficiency—batch yield optimizations, down-time reduction, and improved analytics that highlight preventive maintenance needs. Scraps from reprocessing or filter cake go to approved disposal rather than landfill, supporting both our audit requirements and our own view of responsible manufacturing.
Behind every drum of diethyl aminomalonate hydrochloride stand teams who have mastered not only recipes but also relationships. Customers prefer open lines to the plant, not a faceless web portal. We host calls with formulators testing new routes, discuss how the reactivity profile impacts their next stage, and dive into crystallization details rarely found in textbooks. Lessons from veteran operators—how slight pH shifts affect oiling out, or what color hazes signal side-reactions—shape both our training and our product’s reputation.
Most of all, confidence in an intermediate builds over time. Sourcing decisions mean more than price per kilo once buyers weigh lost time, troubleshooting, and material replacement costs. Our deepest partnerships result from transparency: not overselling flexibility, not promising zero issues, but demonstrating readiness to solve problems shoulder-to-shoulder. That commitment keeps this venerable intermediate fresh in the minds of today’s—and tomorrow’s—synthetic chemists.
The journey of diethyl aminomalonate hydrochloride traces a path through invention, scale-up, process refinement, and continual adaptation. End users push boundaries in drug discovery and synthesis, and it’s our responsibility as producers to match that momentum with technical depth, reliability, and honesty. Every kilo that ships out reflects years of hands-on learning and an ongoing commitment to customer success. In a crowded market of lookalike intermediates, real-world performance and practical support mark the difference between “another barrel” and a true enabling compound.