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Diethyl Aminomalonate Hydrochloride

    • Product Name Diethyl Aminomalonate Hydrochloride
    • Alias DAM HCl
    • Einecs 226-322-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of Diethyl Aminomalonate Hydrochloride

    Applications of Diethyl Aminomalonate Hydrochloride in Industrial Manufacturing

    As 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 Synthesis

    Diethyl 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

    • ICH Q7 GMP for APIs
    • European Pharmacopoeia (Ph. Eur.) General Chapter 5.10
    • U.S. Pharmacopeia (USP) General Notices for synthetic intermediates
    • FDA 21 CFR Part 211 (where directly relevant in quality oversight)

    Typical usage ratio

    • In nucleobase intermediate synthesis: 0.85–1.10 molar equivalents to initial substrate depending on reaction route and yield optimization.

    Downstream process integration

    • Charged as an amination substrate into refluxing alcohol/amine media in mid-stage heterocycle ring closures.
    • Introduced prior to protective group manipulation in stepwise total syntheses.

    Final product types

    • Anticancer APIs (e.g., purine analog drugs such as mercaptopurine derivatives)
    • Antiviral nucleotide analogues
    • Cytostatic active substances for pharmaceuticals

    2. Agrochemical Intermediate Manufacturing

    This 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

    • FAO/WHO Specifications for Pesticide Technical Grade
    • ISO 9001:2015-certified QC for raw materials in crop protection
    • Regulatory assessment to EU Regulation 1107/2009 for plant protection products
    • REACH registration for intermediate use

    Typical usage ratio

    • For C5–C6 ring introduction: standard range is 0.95–1.25 molar equivalents to chloroheterocycle reactant, optimized based on impurity control and downstream conversion value.

    Downstream process integration

    • Added during condensation and amination stages of triazine derivative synthesis after initial raw material validation.
    • Sample analysis for unreacted starting material before downstream methylation or halogenation.

    Final product types

    • Selective herbicide intermediates
    • Fungicidal precursor compounds
    • Heterocyclic agrochemical actives

    3. Specialty Dye and Pigment Intermediate Production

    Within 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

    • OEKO-TEX® Standard 100 for restricted substance listing in dyes
    • ISO 9001:2015 quality management for pigment raw materials
    • EN 71-3 (Toys Safety) regarding heavy metal and amine contaminants in pigments
    • ZDHC Manufacturing Restricted Substances List (MRSL) compliance checkpoints

    Typical usage ratio

    • Chain-coupling steps: typically 0.7–1.2 equivalents per coupling site, adjusted for mono- versus bis-amine dye frameworks and side product minimization.

    Downstream process integration

    • Reaction charged as nucleophilic amine donor at controlled low temperatures to maintain chromophore selectivity.
    • QC phase sampling prior to ring closure and diazotization to measure conversion.

    Final product types

    • Textile azo dyes
    • Anthraquinone-based colorants for technical fibers
    • Solvent-resistant and acid-fast pigments

    4. Fine Chemical Building Block for Amino Acid Derivatives

    This 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

    • ISO 13485:2016 for fine chemicals in analytical/diagnostic uses
    • European Pharmacopoeia (Ph. Eur.) 5.10 for impurities
    • Internal QC protocols for chiral purity and trace residual solvents (GC-MS)
    • REACH registration for laboratory-grade applications

    Typical usage ratio

    • 0.6–1.0 molar equivalents per targeted amino acid or peptide coupling site, fine-tuned based on end-use purity and stereocontrol requirements.

    Downstream process integration

    • Introduced during early peptide elongation or cyclization steps under controlled base conditions.
    • Fed into amidation and deprotection phases prior to solid-phase purification or freeze-drying.

    Final product types

    • Non-standard amino acid building blocks
    • Modified peptides for analytical chemistry applications
    • Catalytic probe molecules and biochemical assay substrates
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    Certification & Compliance
    More Introduction

    Diethyl Aminomalonate Hydrochloride: Rethinking a Fundamental Intermediate

    Building Blocks with a Purpose

    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.

    Model and Specifications Shaped by Experience

    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.

    A Route to Specialty and R&D Applications

    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.

    Standing Apart from Similar Intermediates

    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, Experience, and Trust

    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.

    Safety and Handling in Perspective

    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.

    Innovation and Continuous Feedback

    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.

    Meeting Global and Local Demand with Adaptability

    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.

    Environmental Stewardship, Cost, and Waste

    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.

    The Human Element

    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.

    Looking Forward

    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.