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Ethyl 3-Aminopropanoate Hydrochloride

    • Product Name Ethyl 3-Aminopropanoate Hydrochloride
    • Alias Ethyl β-aminopropionate hydrochloride
    • Einecs EINECS 244-365-1
    • 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

    789527

    Product Name Ethyl 3-Aminopropanoate Hydrochloride
    Cas Number 4263-80-1
    Molecular Formula C5H12ClNO2
    Molecular Weight 153.61
    Appearance White to off-white crystalline powder
    Melting Point 116-120°C
    Solubility Soluble in water and ethanol
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Synonyms Beta-Alanine ethyl ester hydrochloride
    Shelf Life 2 years under recommended conditions
    Hazard Statements Irritant

    As an accredited Ethyl 3-Aminopropanoate Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging consists of a 25-gram white powder, sealed in a labeled, airtight amber glass bottle with hazard and safety information.
    Shipping Ethyl 3-Aminopropanoate Hydrochloride is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is typically packed in amber glass bottles or HDPE containers, cushioned to avoid breakage. The shipment complies with chemical transport regulations, including clear labeling, and is delivered under standard temperature conditions unless otherwise specified by the supplier.
    Storage **Ethyl 3-Aminopropanoate Hydrochloride** should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area, ideally at room temperature (15–25°C). Avoid sources of ignition and incompatible materials such as strong oxidizers. Ensure proper labeling and observe all standard laboratory chemical hygiene and safety practices.
    Application of Ethyl 3-Aminopropanoate Hydrochloride

    Applications of Ethyl 3-Aminopropanoate Hydrochloride in Industrial Manufacturing

    Ethyl 3-Aminopropanoate Hydrochloride serves as a practical intermediate in advanced chemical synthesis, supporting various industrial segments. As a direct manufacturer with experience in global supply, we understand actual downstream usage patterns, formulation considerations, and process requirements.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Ethyl 3-Aminopropanoate Hydrochloride is valued in pharmaceutical manufacturing, specifically as a key building block for certain neurologically active APIs. Global API producers incorporate this material during multi-step syntheses, exploiting its reactivity in amide coupling or alkylation reactions. It often enters the process after protection/deprotection steps, ensuring high purity for regulatory documentation. Material quality directly affects yield and impurity profiles in the final pharmaceutical compound.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US FDA cGMP Guidelines
    • European Pharmacopoeia (Ph. Eur.) compliance for raw materials
    • Chinese Pharmacopoeia (ChP) for local manufacturing

    Typical usage ratio

    • Typically 1.0–1.25 molar equivalent relative to target moiety; adjusted per synthesis route.
    • Exact proportion determined by stoichiometry and process specification; excessive use minimized for purification efficiency.

    Downstream process integration

    • Added post-initial alkylation or reductive amination step.
    • Neutralized hydrochloride salt ensures controlled reaction kinetics.
    • Monitored by HPLC to verify complete consumption before next step.
    • Final product proceeds through successive intermediate isolations and purifications.

    Final product types

    • CNS-active API molecules (e.g., GABA analogues, anticonvulsants)
    • Nootropic agent precursors
    • Specialty pharmaceutical intermediates exported to regulated markets
    • Neurological drug candidates in clinical R&D

    2. Crop Protection Active Ingredient Synthesis

    This raw material is frequently used in the synthesis of specialty agrochemical actives, such as certain γ-aminobutyric acid (GABA) analogs with insecticidal or acaricidal activity. Major agrochemical manufacturers integrate it during core structure-building stages, where its aminoester functionality allows rapid chain extension and selective chemical transformations. Environmental and worker safety regulations require accurate traceability for all starting materials in this sector.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for the Quality Control of Pesticides
    • ISO 9001:2015 for agrochemicals production
    • REACH (EC 1907/2006) pre-registration for use in European Union markets
    • Local Ministry of Agriculture active ingredient registration requirements

    Typical usage ratio

    • Used at 0.9–1.1 molar equivalent, based on aldehyde or acid chloride reactant
    • Adjusted according to reaction design (batch or continuous)
    • Excess avoided to reduce waste treatment costs

    Downstream process integration

    • Introduced at the amination or condensation stage in multi-step synthesis
    • Reacted under inert atmosphere to ensure stable product formation
    • Purification by solvent extraction and recrystallization before further transformation
    • In-process control via GC and NMR confirmation

    Final product types

    • Systemic insecticides
    • Mite control actives for horticultural applications
    • Custom-tuned analogs for patent-protected formulations
    • Intermediates for multipurpose field crop protection products

    3. Fine Chemical Synthesis for Specialty Polymers

    In the field of specialty polymer development, downstream processors use Ethyl 3-Aminopropanoate Hydrochloride for introducing amino-functionalized side chains. This enables chain extension or cross-linking in custom polyamides and polyurethanes, especially for high-performance coatings and adhesives. Controlled dosage prevents uncontrolled gelation and maximizes material strength without defects.

    Industry compliance standards

    • ISO 9001:2015 certified formulation management
    • RoHS 2011/65/EU substance restrictions for electronics- and appliance-grade materials
    • EU REACH compliance for polymer intermediates
    • UL Yellow Card requirements for polymer materials, as applicable

    Typical usage ratio

    • 0.5%–2% by weight relative to total monomer mixture
    • Adjusted based on target amine functionality and desired polymer flexibility
    • Controlled via automated dosing systems

    Downstream process integration

    • Metered into reactor during monomer mixing phase
    • Directly participates in chain extension or as co-monomer in step-growth polymerization
    • In-process sampling for molecular weight and amine content monitoring
    • Washing and curing steps remove residuals prior to extrusion or casting

    Final product types

    • Electronically insulating polymer films
    • Solvent-resistant coating systems for automotive and marine markets
    • High-bond adhesives with functional end-groups
    • Specialty polyamides for 3D-printing filaments

    4. Building Block for Peptide Synthesis

    In the peptide synthesis sector, research and diagnostic reagent manufacturers select Ethyl 3-Aminopropanoate Hydrochloride as a protected amino acid analog or as a precursor for further derivatization steps. The hydrochloride salt guarantees purity and solubility, essential for reproducible automated solid-phase peptide synthesis (SPPS). Careful process alignment is necessary to avoid side-chain hydrolysis and maintain sequence fidelity throughout the elongation cycles.

    Industry compliance standards

    • ISO 13485:2016 for medical device reagents
    • US Pharmacopoeia (USP) for peptide starting materials (where applicable)
    • ISO/IEC 17025 for analytical quality control in laboratory manufacturing
    • GLP (Good Laboratory Practice) for research reagent production

    Typical usage ratio

    • Used at 1.0 molar equivalent relative to peptide chain position per cycle
    • Adjusted for sequence length and resin loading capacity
    • Excess minimized to simplify downstream purification

    Downstream process integration

    • Incorporated during side-chain elongation step in SPPS or liquid-phase peptide synthesis
    • Deprotection and coupling monitored via UV and HPLC
    • Followed by acidolytic cleavage and purification before freeze-drying
    • QC checks include purity, mass spectrometry confirmation, and sequence verification

    Final product types

    • Research-grade peptide fragments
    • Peptide-based enzyme substrates
    • Diagnostic marker reference materials
    • Custom peptide analogs for pharmaceutical discovery
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    Certification & Compliance
    More Introduction

    Ethyl 3-Aminopropanoate Hydrochloride: Manufacturer’s Practical Perspective

    What We’re Making and Why It Matters

    Ethyl 3-Aminopropanoate Hydrochloride shows up on order sheets from labs and pharmaceutical plants who need to build molecules efficiently and dependably. In our plant, every raw drum, every filtration, every particle tells a story. This compound combines functional versatility with an approachable, manageable profile, making it a dependable workhorse in complex organic transformations. Over years of hands-on production, feedback from partners, and close observation of impurities during syntheses, we’ve seen exactly what makes this product more than just another catalogue line.

    Working at scale has taught us that freshly prepared Ethyl 3-Aminopropanoate Hydrochloride delivers crystal-clear advantages for researchers and production chemists. Some of the best pharmaceutical intermediates start with this molecule. It slots into peptide coupling steps, and forms the critical linkage in many biological building blocks. Our formulation focuses on solvent-free crystallization and precise hydrochloride conversion. Consistency matters, so we keep batch variation extremely tight—purity and moisture content are where reactions live or fail. We monitor water content and trace residue; no shortcuts here.

    How Production Experience Shapes Quality

    Raw material checks start with amino acids and esters, sampled, tested, and rejected if they don’t meet our in-house specs. Reactors run at well-calibrated temperatures, with semi-automated control—machines help, but human intuition guides most of it. Through years of process tweaks, we realized that moisture is the silent saboteur. Too dry, and crystallization becomes tricky. Too wet, impurities carry through. By doing all synthesis and purification in dedicated suites, we keep contamination from other amines or esters out of the equation.

    After crystallization, we lean on checked drying protocols to get residual solvents down while keeping the hydrochloride salt from caking. Analytical teams pick over every batch—no substitution for sharp eyes. Finished material runs through HPLC and titration, making sure amine content matches, ester group is unreacted, and chloride sits within range. For shipment, packages seal right after final QA, so product hits the client’s shelves as fresh as what left the dryer.

    Specifications that Make a Difference

    In our operation, the grade of Ethyl 3-Aminopropanoate Hydrochloride we supply serves several major R&D and production needs. Chemists in peptide research choose this compound for its reliable reactivity. Synthesis teams value low residual solvent—ethyl acetate, methanol, and even traces of hydrochloric acid get monitored batch-wise. We aim for assay values above 98%, with water under 0.5%. The white to off-white crystalline powder pours steadily and handles without the clumping found in less closely monitored lots.

    Some producers cut corners by mixing fractionated lots or failing to monitor airborne chlorides in aggressive seasons. We don’t have room for that. If a run strays, it becomes internal rework or landfill. By working from bulk scale, we avoid introducing fine impurities that appear after incomplete solvent handling in smaller processes. In essence, our process relies on repetition: stable temperatures, controlled addition rates, and experienced staff monitoring each step.

    Role Across Industries: Why End Users Come Back

    We serve customers who don’t have time for rework or batch failures. Academic groups and process chemists in pharmaceuticals, biomaterials research, and specialty intermediates return because our material gives them reliable yields and predictable side-product profiles. For instance, in certain peptide syntheses, inconsistent amine content can throw off downstream steps, doubling costs in both labor and solvents. We’ve seen cases where clients reported as much as 20% lower yield from off-brand lots versus our own. Cutting out variable purity and unclear residuals ensures chemists don’t have to reoptimize each time. It’s not just about purity on a datasheet—it’s about whether the intended reaction runs straight through or stalls unpredictably.

    Over time, we learned the most frequent feedback centers on physical form—how the powder flows, how easily it dissolves, and whether it gives consistent reactions without side-crystallization. Powder sticking on scale, or lots needing extensive grinding, slows work and brings avoidable headaches. Our engineering team put effort into controlling both moisture content and particle size distribution, so each bag behaves the same across shipments. If an overseas customer calls and says our latest lot clumps or arrives yellowed, we want to know, because it means a slip at one stage—from drying temperatures to packaging conditions—but it rarely happens due to our checks.

    Unlike traders, we don’t resell or blend. Everything leaving with our name stems from continuous batches traceable to in-house production. We’ve waded through the residue data to optimize wash cycles, not just to pass an inspection but to keep out the kind of cross-contamination that plagues small-lot operations or resold warehouse goods. That commitment shows up when clients report months of smooth operation. Their teams rarely report outliers or odd reactivity, and we stay open about process changes—if a reaction tank gets relined, if a new dryer gets commissioned, clients know.

    Comparison with Other Related Products

    Ethyl 3-Aminopropanoate Hydrochloride isn’t the only aminopropanoate on the market, nor is it the easiest to handle. But its hydrochloride salt confers some real advantages for many users. In free base form, the amine is volatile, harder to store, and sensitive to ambient humidity and CO₂. We manufacture the hydrochloride version so it weighs and dissolves in water or solvents more predictably and holds up in transit—especially for exporters crossing hot or humid zones. Competing salts—such as the tosylate or acetate—offer less stability for certain syntheses, and users have described inconsistent formation of byproducts. Pure free base compounds tend to suffer oxidative decomposition, a problem we avoid entirely by sticking to the hydrochloride route.

    Other non-ester amino compounds can’t fill the same niche. The combination of an ethyl ester group with a primary amine makes Ethyl 3-Aminopropanoate Hydrochloride a versatile coupling partner. Cheaper analogs, with methyl esters or longer alkyl chains, turn out to have different reactivities. In the lab, we’ve seen methyl esters hydrolyze too quickly, and bulkier esters introduce extra steric drag that kills yields. Some customers tried switching to isopropyl or tert-butyl esters to shave costs, only to come back frustrated with solubility issues or inconsistent coupling. The ethyl group hits a sweet spot—economic and reactive enough for most downstream chemistry, without excessive volatility or reactivity.

    In certain bioconjugation efforts, the hydrochloride manifests another strength: it remains stable for longer periods, even in less than ideal storage. Custom peptide houses noted that product arriving from other sources tended to degrade, especially after shipment delays or port stays. Our material, regularly tested up to six months after packing, avoids these pitfalls due to tight pH and moisture controls. This quality consistency matters most for customers running multi-step syntheses; a degraded starting material ripples through every subsequent step, leading to costly failed batches and time-consuming troubleshooting.

    Trusted Handling and After-Sales Support

    Being a manufacturer adds a layer of responsibility—support doesn’t end at shipment. Our tech teams frequently field calls about product application or troubleshooting. Years of manufacturing have provided rich insight into the quirks and strengths of Ethyl 3-Aminopropanoate Hydrochloride. From resolving queries on solubility in mixed solvent systems to offering tips on long-term storage, we believe technical support is as important as the batch itself.

    Customers often ask about best mixing practices. Through bench and kilo-lab work, we’ve determined the optimal dissolution approaches—gentle heating can accelerate solvation, yet overheating leads to localized hydrolysis. For those scaling up processes, our advice draws on plant experience, not speculative theory. Sometimes, we suggest incremental additions to new reactors because we’ve seen issues arise from charging all at once—lumps can form, solvents can oversaturate, and certain byproducts can sneak in.

    Clients in regulated environments—pharma and biotech in particular—value documentation that tracks every step. Our QA team provides comprehensive reports tracing every raw input, all the way to finished batch output. These aren’t generic. Each certificate reflects real in-plant data, demonstrating commitment to transparency. In instances where a customer’s process throws up a problem, technical teams dig into batch records and, if needed, dispatch fresh samples drawn from retained stocks for onsite troubleshooting. Our approach cuts downtime and limits finger-pointing; solutions come from manufacturers who know how each shipment was produced.

    Market Trends and User Insights

    Ethyl 3-Aminopropanoate Hydrochloride continues to expand in use as new pharmaceuticals target ever more complex protein interactions or metabolic pathways. Trends in personalized medicine and biomolecule synthesis further raise demand for consistent, high-quality building blocks. Out in the field, we have witnessed leading researchers and scale-up teams migrate away from less consistent sources as regulatory scrutiny climbs. They cite less downtime and greater process robustness after switching to our supply—an outcome rooted in process discipline.

    Regulatory environments change fast. Our experience in pre-audit checks and compliance inspections means we maintain product standards above the minimum. This reduces risk if requirements shift upwards—customers rely on us to pass not just for today’s needs but for the inevitable tightening of industry norms. Longevity in markets comes from delivering standard lots batch after batch, not from attempting shortcuts or chasing today’s lowest price.

    Pricing pressures remain ever-present, especially in commodity chemical sectors. We choose not to compete as the cheapest player. Instead, experience shows that failing batches or inconsistent deliveries create hidden operational costs for end users that far outstrip a unit price. Our partners point out that the overall cost-of-ownership for chemicals goes beyond invoice price: downtime, batch rejections, and increased compliance labor easily offset any notional savings from lower-quality imports. Keeping this in mind shapes every process tweak or improvement—our focus lands on cost avoidance through quality, not just up-front price.

    Solutions From Direct Manufacturing Experience

    We’ve learned that problems in production and application rarely stay abstract. When a specific lot of Ethyl 3-Aminopropanoate Hydrochloride performs below par, it’s not just a production hiccup—it affects real projects, from clinical trials to pilot campaigns. With direct manufacturing comes more tools for real solutions. If a client runs into solubility issues, we provide recommendations for solvent choices based on both public literature and our own lab records. For product stability, insights come from time-in-motion studies and stress tests on real packed samples. After observing a few shipments degrade in high humidity, we adjusted packaging and drying cycles—feedback loops between lab, plant, and customer keep processes robust.

    Pure speculation doesn’t help anyone when things go sideways. In the rare cases where a client finds downstream reactivity fluctuations, our chemists bring out archived batch samples and align QA data to the reported result, narrowing the issue faster than a multi-layer distribution chain ever could. Problems once traced to specific lot anomalies—unexpected yellowing, minor odor shifts, or simply higher than expected melting points—often tracked back to a relaxation in process control. Addressing these means reinforcing standards, sharing lessons with every operator, and, where needed, retraining staff to spot edge cases.

    Long-term, our customers don’t just want a one-off fix. They want robust, predictable flow from raw compound to finished target molecule. Experience running these lines taught us to invest not only in hardware but also in continuous documentation and up-to-date analysis methods. In plant improvements, like closed transfer systems for handling hydrochloric acid, started out as incremental changes and ended up being standard procedures after proving their worth in product consistency.

    Commitment to Growth and Technical Leadership

    Science doesn’t stand still, and neither does chemical manufacturing. As pharmaceutical and life science sectors push boundaries, they bring new requirements for starting materials—requirements that only experienced, adaptive manufacturers handle consistently. Ethyl 3-Aminopropanoate Hydrochloride may seem straightforward, but shifts in applications, purity demands, and regulatory environments mean every cycle offers room for betterment. We review field reports, listen closely to what works and what frustrates, and turn that input into new projects aimed at process, stability, or handling improvements.

    Recent improvements have focused on enhanced particle size control and bulk packaging integrity. By changing the way we handle slurry concentration ahead of final drying, we make product that resists caking, pours more reliably, and dissolves faster. Handling scale-up runs for pilot launch customers, we adopted quick-change filters and transport bins, slashing the risk of cross-lot contamination without ballooning costs. It’s direct, on-floor feedback and a willingness to fix what’s needed that keeps both us and our customers competitive.

    A lot of chemical suppliers can promise the same specification on paper. What we’ve learned is the real difference comes in the moments that aren’t written—how you react to the odd outlier, whether you pick up the call at midnight, and if you care as much about the next batch as you do about the first. In our plant, Ethyl 3-Aminopropanoate Hydrochloride doesn’t just pass through unexamined. Every kilo processed is another step toward better, more reliable science, on the line and in the world’s labs.