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4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester

    • Product Name 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester
    • Alias Boc-AEP
    • Einecs 629-568-4
    • 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
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    Specifications

    HS Code

    531504

    Product Name 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester
    Cas Number 119878-10-5
    Molecular Formula C11H23N3O2
    Molecular Weight 229.32 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 60-65°C (approximate)
    Solubility Soluble in DMSO, methanol
    Storage Conditions Store at 2-8°C, tightly closed
    Smiles CC(C)(C)OC(=O)N1CCN(CCN)CC1
    Synonyms Tert-butyl 4-(2-aminoethyl)piperazine-1-carboxylate

    As an accredited 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, sealed with a screw cap, labeled with chemical name, formula, quantity, and hazard warnings.
    Shipping The chemical **4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester** is shipped in sealed, chemical-resistant containers. It should be protected from moisture and extreme temperatures. Packages are cushioned, clearly labeled according to relevant regulations, and shipped via certified couriers specializing in hazardous or sensitive materials, ensuring safe and compliant delivery.
    Storage 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester should be stored in a tightly sealed container, protected from moisture and light, at a cool temperature (2–8°C recommended). Ensure it is kept in a dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents, and clearly labeled to avoid accidental misuse or contamination.
    Application of 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester

    Applications of 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester in Industrial Manufacturing

    As the direct manufacturer, we support global bulk production for regulated industries that require advanced piperazine derivatives. Our facility delivers high-quality 4-(2-amino-ethyl)-piperazine-1-carboxylic acid tert-butyl ester, suitable for demanding downstream processes with strict regulatory, technical, and formulation needs. Below are verified industrial application sectors and their critical requirements.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical firms utilize this compound as a key intermediate in the multi-step synthesis of selective antihypertensive agents, CNS drug precursors, and certain urological APIs. Its protected amine and carboxylate groups offer essential selectivity and stability during amidation or reductive amination reactions. We deliver material supporting both pilot-scale and commercial production under cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs where applicable
    • FDA 21 CFR Part 210/211 cGMP for finished pharmaceuticals
    • APIC “Guidance on Quality Management for APIs”

    Typical usage ratio

    • Stoichiometric: 0.95–1.05 mol per targeted amide linkage
    • Process optimization may shift ratios ±5% based on downstream coupling reactants

    Downstream process integration

    • Direct input after raw crystallization or pre-dissolution in DMF
    • Applied during N-alkylation, subsequent deprotection, and cyclization steps
    • Integrated into reaction sequences ahead of final API API formation

    Final product types

    • Antihypertensive API (e.g. imidazoline derivatives)
    • CNS drug substance intermediates
    • Advanced piperazinyl urea compounds

    2. Custom Peptide Synthesis Protection Chemistry

    Contract peptide manufacturers deploy this tert-butyl piperazine derivative as a temporary side chain protecting group for amine functionalities during Fmoc/t-Boc solid phase peptide synthesis. It prevents side reactions under base-induced cleavage, improving peptide sequence fidelity, especially in long-chain analogues.

    Industry compliance standards

    • USP <1045> Bulk Peptides
    • ISO 9001:2015 for peptide synthesis production environments
    • Peptide Synthesis Good Practice (PSGP) from PeptideSociety

    Typical usage ratio

    • Equimolar to target functional group (1:1 relative to peptide couplings)
    • Excess up to 1.1–1.2 eq for challenging resin attachment stages

    Downstream process integration

    • Loaded onto solid-phase resin before primary chain elongation
    • Cleaved by acidolysis after desired sequence assembly
    • RC purification prior to final crude peptide isolation

    Final product types

    • Therapeutic research peptides (GLP-1, integrin ligands, etc.)
    • Peptide-based diagnostics
    • Custom peptide libraries for drug screening

    3. Macrocyclic Compound Precursor Manufacturing (Specialty Chemicals)

    Specialty intermediates suppliers use this piperazine ester to introduce tertiary amine and carboxylic acid masked functionalities into complex macrocyclic cores. The compound supports convergent strategies for building N-heterocyclic macrocycles, targeting advanced catalysis, polymerization, or chelation end uses.

    Industry compliance standards

    • REACH Registration (EC) No 1907/2006 for specialty amine chemicals
    • ISO 14001:2015 for environmental management in specialty synthesis
    • Responsible Care program participation

    Typical usage ratio

    • 0.9–1.1 eq per targeted heterocycle ring segment
    • Adjusted for fragment coupling efficiency

    Downstream process integration

    • Chemoselective assembly via SN2 or reductive amination steps
    • Post-deprotection introduction of macrocyclic side chains
    • Final macrocycle closure via heating or high-dilution conditions

    Final product types

    • Advanced macrocyclic ligands
    • Specialty chelation agents
    • Catalyst pre-ligands sold for organometallic or photoredox applications

    4. Bioconjugation & Diagnostics Intermediate

    Producers of site-specific protein modification reagents and conjugates use this intermediate for generating piperazine-functionalized linkers. The tert-butyl protected amine offers programmable orthogonal reactivity, supporting spacer-chain synthesis in bioconjugation kits and diagnostic labeling chemistry.

    Industry compliance standards

    • ISO 13485:2016 for in vitro diagnostic reagent production
    • ISO 9001:2015 for custom bioconjugation chemicals
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.8–1.2 eq based on molar equivalents of active attachment points
    • Optimized depending on required linker density

    Downstream process integration

    • Employed in solution or solid phase linker assembly
    • Protective group removal triggers downstream coupling to biomolecules
    • Purified via preparative chromatography for end-use QC

    Final product types

    • Activated PEGylation linkers
    • Site-specific antibody–drug conjugate linkers
    • Diagnostic protein or peptide labels

    5. Polymer Additive Component for Antistatic and Antifouling Coatings

    Coating manufacturers incorporate the compound as an intermediate or masked amine functionality for synthesis of advanced polyimide, polyamide, or polyurethane additives. The piperazine-derived structure enhances antistatic, conductivity, and antifouling performance in finished coatings used in electronics and marine sectors.

    Industry compliance standards

    • ASTM D257 – Standard Test Methods for DC Resistance or Conductance of Insulating Materials
    • REACH-compliant formulation for non-toxic additives
    • ISO 9001:2015 for polymer additive manufacturing

    Typical usage ratio

    • 0.2–1.0% w/w as a reactant or additive in polymer premix
    • Ratio adjusted according to target antistatic or surface energy properties

    Downstream process integration

    • Added prior to pre-polymerization cycles or curing stages
    • Unmasked post-polymerization for functional group expression
    • Final QC on dispersion and reactivity in cured matrix

    Final product types

    • Antistatic polyimide films
    • Antifouling polyurethane marine paints
    • Conductive topcoats for electronics housings

    6. Fine Chemicals for High-Performance Surfactants

    Advanced surfactant production facilities use this material as a precursor for synthesizing custom amphiphilic piperazine derivatives. These novel surfactants meet tough performance needs in pharmaceutical wetting agents, oilfield chemical packages, and specialty dispersants requiring controlled hydrophile-lipophile balance.

    Industry compliance standards

    • OECD Guidelines for Testing Chemicals (biodegradability and eco-toxicity)
    • ISO 9001:2015 certified fine chemical site
    • REACH chemical registration for European distribution

    Typical usage ratio

    • 0.6–1.2 eq relative to hydrophobic chain inputs
    • Adjusted based on desired HLB value of final surfactant

    Downstream process integration

    • Intermediate stage of surfactant head group synthesis
    • Incorporated before final neutralization or alkylation
    • Allows block polymer or ionic surfactant generation

    Final product types

    • Water-miscible pharmaceutical wetting agents
    • Oil dispersant additives for energy sector
    • Functional surfactant blends for cleaning formulations
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    Certification & Compliance
    More Introduction

    Introducing 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester: A Perspective from the Producer’s Bench

    What This Molecule Brings to the Table

    Our team has been making 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester for years—long enough to see how subtle shifts in process and raw material selection influence the final product’s behavior. Chemists in various fields often come to us for materials that don’t just tick off a box on a spec sheet, but actually drive their processes the way they expect. This compound, known among chemists for its robust role in peptide synthesis, brings to the lab a combination of straightforward reactivity and meaningful protection for functional groups such as carboxyl and amine. The tert-butyl ester on this molecule keeps the carboxyl end safe during the choppy steps of synthesis, so it can be unmasked later—smoothly and predictably, which matters when yields, timelines, and reputation ride on the outcome.

    Our Approach: Fidelity and Function

    Manufacturing specialty intermediates like this doesn’t begin and end with reaction vessels. Years of trial and correction have taught us that the consistency of starting materials, temperature profiles, and the hands-on attention during workup make decisive contributions to product purity and stability. While many resellers focus only on purity percentages or moisture content, we aim deeper: reproducibility, shelf stability, and traceability. We can’t stress enough how much the control of microimpurities—sometimes only a fraction of a percent—can make or break long synthesis campaigns, especially for pharmaceutical work. This is why every batch sees scrutiny at every stage, from incoming raw amines to the final, packaged piperazine derivative.

    Differentiation: Not All Sources Give the Same Results

    Not all chemical products of the same name behave identically in practice. Speaking with researchers and production chemists, we find time and again that off-brand sources can introduce lurking issues: colored byproducts, unexpected reactivity, even strange solubility behaviors due to trace amounts of secondary amines or over-alkylation. Our process rejects these problems by integrating in-line analytical controls and batch-based feedback so that each lot stays close to an optimal structure, free of mischievous side-chains or hard-to-detect contaminants.

    Use in Peptide Synthesis: The Experience Behind the Hype

    Peptide chemistry isn’t just a numbers game—lab time and budgets ride on whether each coupling step actually delivers. The tert-butyl ester function in our 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid derivative shields the acid group, allowing chemists to direct reactivity elsewhere during chain elaboration. Labs using our material see predictable cleavage of the protecting group downstream—avoiding the kind of degradation or persistent side-products that can haunt less careful syntheses. This isn’t simply about having a protective group attached; it’s about ensuring its removal is clean and doesn’t leave residues that complicate purification or change the character of the target molecule. Our own purification staff verifies this through both classical techniques and LC-MS follow-up, ensuring end users avoid last-minute surprises.

    Working with This Piperazine Ester: Beyond the Certificate of Analysis

    Taking a batch from reaction to finish means more than hitting a purity metric. Our formulation process involves tight control over temperature and humidity, since the tert-butyl ester moiety can be sensitive to acidic or moisture-rich conditions. We store and ship each lot under nitrogen until it leaves the plant, ensuring minimal hydrolysis or darkening—a practice born out of harsh lessons from earlier days. The physical form—powder or crystals—results directly from careful control of crystallization and drying, not just from whatever happens in the reactor.

    As a producer, we’ve invested in analytical equipment that goes beyond traditional TLC or low-field NMR. High-resolution mass spectrometry and quantitative NMR confirm that the protecting group is in place and that trace impurities stay within strict boundaries. We find that for downstream users, this level of care means consistency not only in one reaction but across long production campaigns—a difference that matters when scale increases from milligrams to multi-kilogram runs. Several clients from pharmaceutical development have confirmed that less effort spends on purification and troubleshooting, leaving more time for advancing their actual research goals.

    Specification Details: Not Just a List, But a Practice

    Listing off “purity greater than 98%” or “moisture below 0.5%” only tells part of the story. We use dry solvents and freshly distilled starting materials wherever feasible, because piperazine derivatives—even with a bulky tert-butyl ester—can pick up trace water or byproducts if corners get cut. Our staff runs each batch through quantitative Karl Fischer titrations and verifies the active group by NMR integration. More than once, control chemists have rejected a batch that met nominal specifications but showed subtle baseline anomalies on HPLC—our policy is always to investigate rather than ship and hope. This attention prevents trouble from landing in end users’ labs, which keeps projects on track and relationships healthy.

    Field Feedback: How Real Users Describe the Difference

    Every producer likes to believe their product outshines others, but the truest feedback comes from the chemists using our 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester in real applications. Peptide synthesis faculty, development chemists, and process engineers have told us that the difference isn’t just in the wet-chemistry numbers. They report that solutions mix uniformly, with little evidence of “gumming” or residual color—a sign of cleanliness in the preparation. During deprotection, the tert-butyl group comes off clean, reducing the side reactions normally seen with harsher conditions. That predictability means fewer headaches chasing ghost peaks or unexpected isomers, keeping projects viable and competitive.

    Furthermore, scale-up departments give us feedback that, as batch size increases, our material avoids the lot-to-lot variation that can throw off pilot plant or production campaigns. This comes back to small but real investments in process control and the choice to overinvest in analytical checkpoints. It’s not only about chemistry, but about real-world project economics and timetables.

    Comparing with Other Protecting Groups and Esters

    Some may wonder why chemists would select a tert-butyl ester over methyl or ethyl alternatives. From our direct experience, methyl esters often require more aggressive conditions for cleavage, with a bigger risk of damaging acid-sensitive groups elsewhere in the molecule. The tert-butyl ester, by contrast, can usually be removed under gentler acidic conditions (commonly trifluoroacetic acid), minimizing risk to more delicate moieties in the peptide sequence. We tested various lots ourselves, watching the fate of side chains and protecting groups during deprotection. The tert-butyl group stands out for reliability, especially in multi-step syntheses where one misstep could mean weeks of lost labor.

    It’s also true that this piperazine derivative aligns well with solid-phase peptide synthesis protocols, because it maintains its structure under the base- or acid-switching cycles typical in automated systems. Peptides with unwelcome backbone cleavage or loss of side-chain protection cost real time and material. Selecting the tert-butyl ester helps avoid downstream headaches, giving chemists an edge in both manual and automated approaches.

    Supply, Scale, and Real-World Challenges

    Supplying this intermediate isn’t only a matter of making a chemical and putting it in a drum. Global raw material supply chains can change overnight. Our buyers track fluctuations in cost and availability of protected piperazines and amino alkyl intermediates, updating syntheses so a hiccup in one country doesn’t hold up work worldwide. We’ve learned to keep a buffer of raw reagents and carved out connections with specialty suppliers, keeping our reactors running when competitors scramble. This willingness to plan ahead—born from late-night troubleshooting sessions and lessons from plant shutdowns—makes the material flow more predictably to our clients.

    One chronic challenge lies in logistics: the tert-butyl ester group, while durable in the lab, suffers degradation from long exposure to heat and humidity during transport. Our experience suggests shipping in climate-controlled containers, or at the very least well-sealed, nitrogen-flushed packaging, pays dividends in long-term product performance. Years ago, we reviewed returns from a hot, humid summer and traced imprecision in analytical results to storage conditions—not chemistry. This lesson changed our packaging forever, leading to better stability for everyone downstream.

    Key Choices in Manufacturing and Their Impact

    Making large batches for commercial customers presents risks, especially when scaling up from bench synthesis. The exotherm during the acylation step, for example, must be managed tightly, as uncontrolled reaction rates create caramel-colored impurities that are hard to remove. Our process engineers run simulated pilots before any new scale, ensuring heat transfer matches what junior chemists see during bench work. We insist on slow addition and precise stirring, accepting the increased labor so the material comes out clean and free of burnt notes. Those who have switched from less persistent suppliers notice fewer filtration steps in purification—detail that matters in real-world throughput, not just on a certificate.

    We also keep detailed records of every parameter, with lots backed up by raw data so clients can trace batch genealogy if needed. Our plant doesn’t rely solely on automation—experienced technicians walk the reactors, observing, noting, and recording so subtle anomalies are caught early. In our experience, machines catch most errors, but real improvement comes from hands with years of repetition.

    Compliance, Traceability, and Transparency

    Pharmaceutical developers and process chemists rely not just on chemistry but on trust in their suppliers’ transparency and regulatory compliance. We engage with third-party audits, welcome customer inspections, and offer full traceability from incoming raw amines to the outgoing protected intermediate. We use barcoding and lot tracking to avoid commingling and to connect every analytical record to its lot. Experience teaches us that this transparency reduces disputes, prevents expensive recalls, and reassures clients managing high-value projects.

    Our QA procedures address every stage of production, with regular proficiency testing for analytical staff and routine calibration of all equipment. We make sure findings match between technicians and across labs, eliminating subjectivity. Documentation includes not just pass/fail records but supporting chromatograms, full NMR spectra, and water content graphs. This level of record keeping, which takes extra effort, translates to fewer surprises and faster answers for everyone involved.

    Practical Applications Beyond Peptides

    Though most demand centers on peptide research, other laboratories leverage this protected piperazine for preparing novel intermediates, crosslinkers, or ligands in medicinal and materials chemistry. For example, the well-shielded carboxylic acid can serve as a handle for further modification—either for attaching to polymer backbones or for building more complex molecular architectures. Several groups have reported that the tert-butyl protection aids in site-specificity, supporting approaches where selective deprotection delivers cleaner final products. From our own sales records and technical support calls, we see use cases spanning drug conjugation, dendrimer assembly, and even specialty sensor development.

    Clients tackling early-phase drug discovery or materials innovation may run through hundreds of test reactions before a structure qualifies for scale-up. Providing a reliable, consistent intermediate means that time, money, and energy aren’t spent tracking down sources of side-reactions. Our own technical support staff have guided many users through tricky steps, sometimes catching issues that stem not from the product itself but from small changes in reagent quality or handling. Such collaboration shapes both our manufacturing practice and our understanding of what laboratories actually need.

    Continuous Improvement: Listening, Adjusting, Delivering

    Our culture of open feedback helps us spot and correct deviations in process, analytical standards, or documentation. Customers often suggest tweaks, whether for finer powder sizing or tighter packaging protocols to minimize static buildup. We listen, then adapt—sometimes refining our drying processes, sometimes improving analytical technique. Long-term, these incremental improvements let us maintain a high bar for reproducibility, even as clients’ requirements evolve.

    Each campaign, large or small, teaches something new about this ester and the myriad ways it fits into research pipelines. Regular reviews with technical users and in-house R&D staff keep our production dynamic and attuned to subtle shifts in chemistry practice.

    Final Thoughts from the Shop Floor

    Making 4-(2-Amino-Ethyl)-Piperazine-1-Carboxylic Acid Tert-Butyl Ester may look routine from the outside, yet every batch makes the lab team, process engineers, and quality analysts focus on the same goal: giving chemists an intermediate that advances their work in real, practical ways. Instead of just delivering numbers on a sheet, we pride ourselves on offering insights, reliability, and a willingness to solve problems before they reach the user. Years spent refining synthesis, packaging, and technical service mean that this product supports not only a single reaction but also builds momentum in whole research programs. We remain committed to the craft, listening to feedback and bringing new improvements with each lot—because, as our partners remind us, chemistry in the real world leaves little room for shortcuts.