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N-Boc-Ethylenediamine

    • Product Name N-Boc-Ethylenediamine
    • Alias Boc-EDA
    • Einecs 680-422-9
    • 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

    973098

    Cas Number 74370-58-8
    Molecular Formula C7H16N2O2
    Molecular Weight 160.22 g/mol
    Iupac Name tert-butyl N-(2-aminoethyl)carbamate
    Appearance Colorless to pale yellow liquid or oil
    Purity Typically ≥98%
    Boiling Point 127-128 °C at 2 mmHg
    Density 1.014 g/mL at 25 °C
    Solubility Soluble in most organic solvents such as dichloromethane and methanol

    As an accredited N-Boc-Ethylenediamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing N-Boc-Ethylenediamine, 25g, is packaged in a sealed amber glass bottle with a screw cap, labeled with hazard and product information.
    Shipping N-Boc-Ethylenediamine is shipped in tightly sealed, chemically resistant containers to prevent moisture and air exposure. It is transported according to standard regulations for non-hazardous chemicals, with labeling for identification and handling instructions. The product should be stored in a cool, dry place away from incompatible materials during transit.
    Storage N-Boc-Ethylenediamine should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Avoid exposure to strong acids, bases, and oxidizing agents. Refrigeration (2–8°C) is recommended for long-term storage to maintain stability and prevent decomposition. Ensure proper labeling and follow all relevant chemical safety guidelines.
    Application of N-Boc-Ethylenediamine

    Applications of N-Boc-Ethylenediamine in Industrial Manufacturing

    Our N-Boc-Ethylenediamine supports critical steps in the synthesis of high-value molecules across the pharmaceutical, agrochemical, fine chemical, and specialty polymer sectors. As a manufacturer, we supply material conforming to demanding technical and regulatory parameters so industrial customers can maintain batch reproducibility and meet both internal and market compliance obligations. Below, we detail several established downstream application scenarios relevant to large-scale and specialty manufacturing.

    1. Pharmaceutical API Intermediate Synthesis

    Process chemists employ N-Boc-Ethylenediamine as a protected diamine during multi-step synthesis of small-molecule active pharmaceutical ingredients, where selective amine deprotection is necessary. The Boc protection minimizes side reactions, supporting high-yield transformations, especially in the construction or modification of beta-lactam rings, piperazine cores, or related heterocycles. Typical formulations leverage its solubility in organic solvents for seamless scale-up in GMP-compliant facilities, making it a cornerstone in the large-scale preparation of patented and generic APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.)
    • ChP (Chinese Pharmacopoeia) for excipient traceability

    Typical usage ratio

    • Applied at 0.85–1.15 molar equivalents relative to target amine sites; exact proportion depends on desired substitution pattern and process batch scale.

    Downstream process integration

    • Charged at intermediate condensation or protection/deprotection stages; Boc group cleavage occurs post-functionalization using standard acidolysis protocols (e.g., TFA/DCM).

    Final product types

    • Cephalosporin and penem antibiotics
    • Piperazine-based anticancer and neuroactive agents
    • Small-molecule antivirals utilizing protected diamine scaffolds

    2. Peptide Synthesis Building Block

    N-Boc-Ethylenediamine acts as a bifunctional synthon in solid-phase peptide synthesis and fragment coupling, especially for cyclic peptide and peptidomimetic drugs. The Boc-amine provides temporary protection, enabling highly selective chain elongation and cyclization reactions under controlled pH and solvent conditions without premature deprotection. Quality control teams routinely test for orthogonality to Fmoc- and Cbz-protected sequences during parallel synthesis campaigns, essential for regulatory submissions.

    Industry compliance standards

    • USP General Chapter <797> (sterile compounding)
    • European Pharmacopoeia 2.8.15 (Amino acid analysis)
    • GMP Part II for Active Substance manufacture
    • ISO 14644 cleanroom standards for peptide production

    Typical usage ratio

    • Used at 1.00–1.05 equivalents per desired branch or linker; excess minimized to lower downstream purification requirements.

    Downstream process integration

    • Incorporated into peptide elongation cycles as a protected diamino building unit; final deprotection and cyclization performed via acidolytic cleavage on resin or in solution.

    Final product types

    • Biologically active cyclic peptides
    • Branched peptide therapeutics
    • Peptide-based diagnostic probes

    3. Agrochemical Active Ingredient Synthesis

    Production teams in agrochemical companies select N-Boc-Ethylenediamine for use as a nucleophilic intermediate when constructing diamine-linked ureas, carbamates, and heterocyclic pesticides. Its reactivity supports multi-step operations for complex herbicide or insecticide actives, where site-specific protection streamlines impurity removal and facilitates robust scale-up in plant conditions. Typical QC monitoring covers both residual Boc impurities and amine assay for regulatory compliance.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for active synthesis data
    • FAO/WHO pesticide formulation and identity criteria
    • REACH (EU) for substance registration and safety data sheets
    • ISO 9001:2015 Quality Management in agrochemical production

    Typical usage ratio

    • Added at 1.1–1.3 equivalents to target functional groups, with adjustments based on reaction selectivity and desired conversion rates in commercial reactors.

    Downstream process integration

    • Utilized during nucleophilic substitution or carbamate coupling; Boc removal occurs prior to final crystallization or formulation blending of the active ingredient.

    Final product types

    • Systemic herbicide active ingredients
    • Diamine-containing fungicidal agents
    • Insecticidal intermediates targeted for further derivatization

    4. Specialty Polymer and Crosslinker Manufacturing

    Materials developers introduce N-Boc-Ethylenediamine during the synthesis of functionalized polyamides, polyurethanes, and epoxy curing agents. The Boc group offers temporal protection of secondary amines while backbone modifications or grafting reactions proceed, ensuring precise control of crosslink density and molecular architecture. Process engineers monitor Boc deprotection kinetics to synchronize the crosslinker activation with polymer chain extension, influencing final mechanical and chemical resistance properties.

    Industry compliance standards

    • REACH Annex XVII for monomer and additive restrictions
    • ISO 9001:2015 (Quality management for polymer manufacturing)
    • FDA 21 CFR §177 (Indirect food additives: polymers) for food-contact applications
    • RoHS directive (if electronic encapsulation polymers)

    Typical usage ratio

    • Employed at 0.5–2.0% by weight for crosslinker precursors; optimized per batch through stoichiometric modeling and in-process validation.

    Downstream process integration

    • Introduced in pre-polymer blending tanks or during intermediate synthesis steps before chain extension; Boc group cleaved thermally or with acid catalysts prior to final curing.

    Final product types

    • High-performance polyamide resins
    • Branched polyurethane elastomers
    • Epoxy-hardener masterbatches for high-durability coatings

    5. Fine Chemical and Chelating Agent Production

    Chemical processors leverage N-Boc-Ethylenediamine for selective amine protection in the stepwise synthesis of chelating ligands and specialty fine chemicals. The protected diamine ensures high regioselectivity during alkylation or acylation, allowing for the generation of customized ligand frameworks used in analytical, water treatment, or catalysis sectors. Downstream, the Boc group can be efficiently removed without degrading sensitive chelating structures, ensuring product functionality and batch homogeneity.

    Industry compliance standards

    • ISO 9001:2015 (Quality Systems for Fine Chemicals)
    • EFfCI GMP for Cosmetic Ingredients (if applicable)
    • REACH registration for new chemical entities
    • GHS for proper labeling and handling

    Typical usage ratio

    • Applied at 1.0–1.2 equivalents to primary amine sites; fine-tuned per batch based on the core ligand structure and final purification protocol.

    Downstream process integration

    • Added in the alkylation or acylation phase for selective functionalization; Boc deprotection scheduled as a terminal step before isolation and quality assessment.

    Final product types

    • Custom chelating agents for metal ion sequestration
    • Ligands for homogeneous catalysis
    • Analytical standards and specialty reagents
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    Certification & Compliance
    More Introduction

    N-Boc-Ethylenediamine: A Manufacturer’s Perspective on Quality, Consistency, and Application

    Our Experience with N-Boc-Ethylenediamine Production

    N-Boc-Ethylenediamine, known in the trade as N-Boc-EDA, carries a special position in our line of specialty organic chemicals. With years spent optimizing batch synthesis and scaling up to meet customer demand, we’ve learned that this intermediate is a linchpin for peptide and pharmaceutical research. Sourcing quality N-Boc-EDA isn’t simply about purity on a certificate of analysis; the real gains come from eliminating batch variability, side reactions, and unpredictable reactivity in downstream processing.

    Our production follows a carefully controlled synthesis route. We use only high-purity di-tert-butyl dicarbonate (Boc2O) as the protecting agent and freshly distilled ethylenediamine. Our final product, N-Boc-Ethylenediamine, comes as a colorless to pale yellow liquid or solid, depending on storage and ambient temperature. The molecular formula is C6H14N2O2, and CAS number 75092-66-7 is referenced for identification, but the performance of each batch draws more attention from the researchers who rely on it. Every synthesis step gets monitored for unreacted starting material, low-level contaminants, and potential overalkylation. Only lots that meet our established thresholds are released.

    Maintaining stability during shipping and storage takes more than a sealed bottle and a “keep cool” sticker. We package N-Boc-EDA in amber glass or HDPE containers, using nitrogen blanketing to slow degradation. Every customer receives a batch report that includes not only standard specifications such as GC-MS and NMR but also the specific generation conditions, which have helped us trace and reduce rare impurities years before most competitors adopted similar systems. These practices come not from following regulations but from hard-won lessons in minimizing risk for long-running pharmaceutical syntheses.

    Understanding What Sets N-Boc-Ethylenediamine Apart

    Many laboratories treat protecting groups as generic, but our experience shows that N-Boc-Ethylenediamine stands apart from related compounds like Fmoc-ethylenediamine or Cbz-ethylenediamine. The Boc (tert-butoxycarbonyl) protection offers a particular balance: easy enough to remove under mild acidic conditions but stable enough to survive most peptide coupling procedures and alkylations. Simple deprotection minimizes formation of side products, reduces loss during workup, and helps prevent clogging in process lines.

    Some alternatives use Fmoc or Cbz to protect ethylenediamine, but these come with different deprotection chemistry. Fmoc removal requires strong bases, while Cbz requires hydrogenation. Both require additional process controls and equipment, and not all customers have access to safe and reliable sources of these regents. Boc offers a broadly compatible compromise, which is why most of our pharmaceutical and peptide chemistry clients stick with this structure.

    Batch uniformity in N-Boc-EDA reduces purification steps downstream. We’ve invested in high-throughput analytical equipment, so we can calibrate process controls in real time. Sometimes, researchers spot subtle differences in reactivity when swapping lots; we welcome this feedback, since it helps us refine purification and drying routines. A little dialogue has paid off by cutting out residual either byproducts, which can affect coupling yields in solid-phase synthesis.

    Key Specifications: What We Measure, Why It Matters

    We monitor every lot of N-Boc-Ethylenediamine for purity, residual solvents, water content, and specific structure confirmation. HPLC and GC-MS play a role in confirming both content and absence of common impurities. We pay special attention to moisture, since even minor levels of water can lead to premature Boc removal or formation of diamine side products during extended storage.

    Impurity profiling for this compound extends beyond the usual suspects. We go after trace tert-butanol, unprotected ethylenediamine, and Boc dimer impurities. Deviations in synthesis—reflux time, solvent quality, neutralization efficiency—leave unmistakable fingerprints. As a manufacturer, catching these before the product reaches users reflects more devotion to the chemistry than any third-party checklist. Our product specs settle at 99% purity by both HPLC and NMR, but we take pride in providing the supporting spectra, so end users can review for themselves.

    Some years ago, a large-scale project demanded kilogram quantities with consistently low amine chloride levels. Through in-process phase separation and additional pre-neutralization, we learned how to keep salt contamination well under the limits that peptide coupling chemistry tolerates. That technical insight now gets baked into our standard process. In this way, the specifications on paper reflect more than a marketing claim—they come from requests and feedback from researchers who have run into real problems in the lab.

    Applications and the Reality in the Lab

    Chemists often use N-Boc-Ethylenediamine as a building block for peptide, urea, and carbamate linkers, along with other fine organic intermediates. Its most frequent use comes as a protected amine for solid-phase synthesis. We see the reality daily: a company needs to scale up a process, and a deviation in protecting group deprotection can derail the whole campaign. A robust, reproducible source of N-Boc-EDA can save weeks on projects by avoiding the guesswork of re-optimization.

    N-Boc-EDA provides a valuable route to protected amine intermediates. The other end of the molecule, the unprotected primary amine, gives flexibility for selective functionalization. For example, medicinal chemists use it to create linkers where only one amine participates in the next reaction. The Boc group, standing sentinel, waits until the chemistry is complete and then disappears with a short treatment of TFA or HCl in dioxane.

    Industrial-scale customers highlight different needs: stability, repeatability, and packaging fit for automation lines. Every time we load drums destined for a continuous synthesizer or automated peptide reactor, we tighten up our process to meet their demands. Fine-tuning stability, predicting shelf life, and reducing moisture uptake have come from seeing missteps in projects where overlooked storage led to costly batch failures. It’s a reminder that laboratory protocols don’t always translate to plant conditions—so we treat each request as fresh, tuning our material handling accordingly.

    Lessons from Industry: Avoiding Hidden Traps

    Over the years, the feedback loops between ourselves as producers and our buyers in pharma, biotech, and academia have shaped our understanding of N-Boc-Ethylenediamine. Sometimes, labs reported unexpected byproducts because low-level hydrolysis occurred before the opening of the container, or impurities in bulk shipments caused significant downstream contamination. We cheerfully address these practical issues, typically by customizing delivery modes or refining our own inert handling protocols. Just this year, we introduced improved labeling and tamper-evident seals after a client’s observations alerted us to a potential source of confusion between similar-looking amines in the storeroom.

    N-Boc-EDA can hydrolyze or lose Boc protection if exposed too long to air or humidity. We now stress the value of prompt weighing and resealing, sharing real-time data on shelf life when conditions push the limit. A technical note we send with each batch details storage best practices: cool, dry, tightly closed—drawn from our own benchmark studies, not duplicating what a textbook declares. Most of our regular clients know to snap up just enough for a few days’ work, leaving the rest protected, but these patterns only emerged after working out failures together in pilot programs.

    Differentiating N-Boc-Ethylenediamine from related products proved instructive. Users sometimes substitute N-Cbz- or N-Fmoc-ethylenediamine for convenience or availability. These swap-ins bring surprises: raised basicity, new byproducts during coupling reactions, or cumbersome deprotection that self-propagates into the next step. We recommend pilot trials and, as manufacturers, lend sample quantities to validate that our specific route’s product fits the target process. The real advantage of our method is its minimization of side products—once the supply chain locks in consistent material, process reproducibility improves and technical headaches reduce.

    Supporting Sustainable and Safe Manufacturing

    Attention to sustainability shapes how we handle both raw materials and waste streams. Boc chemistry produces CO2 and tert-butanol during deprotection, by the very nature of the route. In scale, these aren’t just minor emissions—they require capture and neutralization, and we established recovery loops for both. Our waste solvent treatment employs a closed system, with in-house distillation for recycling solvents back into production.

    Safety features in our plant design include continuous monitoring of temperature and pH during synthesis, not just for quality assurance but to preempt runaway reactions. Training our operators on the proper use of PPE and accident response forms another layer in keeping both staff and product safe. Our approach goes beyond regulatory boxes; we’ve found that direct feedback from those at the bench catches edge cases written standards can’t predict. As examples, we keep a roster of lessons learned—how to spot subtle signs of Boc deprotection or routine tweaks for purging critical lines before switching from N-Boc-EDA to other aliphatic diamines.

    An ongoing dialogue with customers, regulators, and our in-house chemists keeps us honest about our environmental and safety record. We share, transparently, our spill histories (fortunately rare), energy usage benchmarks, and solvent discharge reports with partners looking to audit their chemical footprints.

    Why Product Consistency Drives Research Success

    Every year, our regular customers in materials and medicinal chemistry come back with a list of pain points from comparable suppliers: variability in color, inconsistency in deprotection efficiency, residues that turn up as ghost peaks in LCMS. We understand that research, especially at the scale of combinatorial chemistry or early-stage drug synthesis, doesn’t have time or resources to troubleshoot mysterious differences between batches. That responsibility lies on us, not the downstream user.

    The most reliable discoveries emerge when the upstream building blocks behave as predicted and keep their side reactions in check. Our process for making N-Boc-Ethylenediamine evolved by repeating experiments to chase any outlier signature in chromatography down to its source. Sometimes, it meant cleaning up the glassware inventory, switching supplier lots of Boc2O, or running mock processing tests to simulate worst-case scenarios. Our investments in quality control labs pay off not only in more robust N-Boc-EDA but in less time spent fielding support calls and error reports.

    For academic labs, where turnover in personnel and changing grants can mean inconsistent storage or handling, we share bulletins on best practices. We have seen more than a few projects rescued by following our guidelines on splitting and dating working stocks—a tweak that came not from us, but from a creative technician in a peptide lab who couldn’t afford lost time.

    Peptide Synthesis: Reliability Over Marketing

    N-Boc-Ethylenediamine has its most loyal user base among peptide chemists. Here, the difference between a good and great intermediate turns on more than price or purity; it comes down to how long the chemist spends clearing up side products at purification. In peptide coupling, amine purity is central. If a building block contains even trace free Boc2O or decomposed diamine, side reactions accumulate: capped chains, deleted sequences, or hard-to-predict mass shifts in LC-MS data.

    Our facilities dedicate complete lines to N-Boc-EDA, eliminating risk of cross-contamination from unrelated amines, halides, or acids. Routine customer feedback led us to screen for previously undetected inhibitors—small things, like a 0.05% methyl tert-butyl ether leftover, that can balloon during scale-up. A process operator flagged this after smelling residual ether in a late-night loading; days later, our analytical team refined the solvent swap. This underscores our approach: listen to those who use and those who make, and adjust accordingly.

    The product's physical form—liquid or low-melting solid—can influence reaction setup. Some customers need the liquid for rapid dispensing in automated systems, while others find a low-melting solid easier to weigh on analytical balances. We take note, configuring our storage and shipping for the preferred form, giving advance guidance about expected melting points under various temperature and humidity conditions.

    Why Real Dialogue with Customers Matters

    As manufacturers, we occupy both sides of the chemical supplier-customer relationship. We receive direct input from users who hit roadblocks, and we see which process variables trigger headaches in scale-up. The most productive improvements have come from conversations with development teams who detail their failure points, rather than from generic specification checklists.

    We invite on-site audits and supply QC samples wherever possible, encouraging feedback not just on numbers but on workflow effects—dissolution rate, ease of transfer, and clarity of deprotection. For some pilot projects, we’ve sent three consecutive lots with supporting analytical data, so customers can match their own benchmarks before moving to larger purchases. Our own chemists conduct field visits, sometimes observing step-by-step workflows to catch bottlenecks that wouldn’t show up on a datasheet. This has enabled us to shave minutes off process steps, pinpointing small changes that matter on the production floor.

    Feedback from a customer one year saved a week for another: a challenging peptide sequence failed because of a trace base impurity in the N-Boc-Ethylenediamine. That prompted an overhaul of our cleaning regime, introduction of inline acid scrubs, and tighter packing. Moments like this remind us that the chemistry and the process are inseparable—the reliability of the building block is mirrored in the downstream project timelines, budgets, and ultimately, discoveries.

    Looking Forward: Challenges and Opportunities

    Demand for N-Boc-Ethylenediamine remains strong, with new applications appearing in biomaterials, custom linkers for antibody-drug conjugates, and specialty monomer synthesis. Challenges are inevitable—raw material pricing, regulatory changes, and the growing emphasis on sustainable chemistry make this landscape a moving target. We invest regularly in process trials to source greener solvents, look for lower-carbon synthesis routes, and test packaging that suits both small-scale and industrial users.

    Improving shelf life is a work in progress. We collaborate with packaging experts to identify seals and liners that keep N-Boc-EDA dry even during long overseas journeys. By automating more of our batch monitoring and QC sampling, we reduce risk of unnoticed drift in product properties, saving clients time on incoming inspections. Our view is simple: the value added by tight process control upstream frees the end user to focus on research and production, not troubleshooting.

    As new end uses take shape—in diagnostics, surface coatings, and custom resin synthesis—we keep early-stage dialogue open with innovators who break new ground. These partnerships spawn fresh technical requirements: reduced bioburden for clinical trial intermediates, new analytical standards for trace metals, or unique packaging for robotic dispensing systems. We treat these as learning opportunities, using N-Boc-Ethylenediamine as a platform for process improvement across our entire product line.

    Conclusion: Experience Begets Reliability

    From the vantage point of a dedicated producer, N-Boc-Ethylenediamine is more than a line item on a reagent list. Every batch distills a mass of practical knowledge—how to synthesize, purify, protect, analyze, and deliver a building block that stays consistent across time and use cases. We hold ourselves to not only making pure N-Boc-EDA, but to fielding every real-world question and challenge, translating customer feedback into refined process steps. In this way, the reliability of N-Boc-Ethylenediamine stands not only as a matter of technical skill, but also as the sum of experience, accountability, and genuine partnership in scientific progress.