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Tert-Butyl N-(4-Aminobutyl)Carbamate

    • Product Name Tert-Butyl N-(4-Aminobutyl)Carbamate
    • Alias Boc-1,4-diaminobutane
    • Einecs 630-608-7
    • 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
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    Specifications

    HS Code

    496457

    Product Name Tert-Butyl N-(4-Aminobutyl)Carbamate
    Cas Number 18295-96-6
    Molecular Formula C9H20N2O2
    Molecular Weight 188.27 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 38-41°C
    Boiling Point 302.3°C at 760 mmHg
    Solubility Soluble in organic solvents such as ethanol, methanol, dichloromethane
    Storage Temperature 2-8°C
    Density 1.01 g/cm³
    Iupac Name tert-butyl N-(4-aminobutyl)carbamate
    Smiles CC(C)(C)OC(=O)NCCCCN
    Synonyms Boc-1,4-diaminobutane; Boc-Butane-1,4-diamine
    Refractive Index 1.464 (Predicted)

    As an accredited Tert-Butyl N-(4-Aminobutyl)Carbamate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle containing 25 grams of Tert-Butyl N-(4-Aminobutyl)carbamate, sealed with tamper-evident screw cap and labeled for laboratory use.
    Shipping Tert-Butyl N-(4-Aminobutyl)carbamate should be shipped in proper, tightly-sealed containers under ambient temperature conditions. Ensure it is securely packaged to prevent leaks and protected from moisture. Comply with all regulatory requirements and include appropriate labeling, Safety Data Sheet (SDS), and hazard documentation with the shipment to ensure safe handling and transport.
    Storage **Tert-Butyl N-(4-Aminobutyl)carbamate** should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible materials such as strong acids or oxidizing agents. Refrigeration (2–8°C) is often recommended to maintain stability. Always follow appropriate chemical storage and safety guidelines.
    Application of Tert-Butyl N-(4-Aminobutyl)Carbamate

    Applications of Tert-Butyl N-(4-Aminobutyl)Carbamate in Industrial Manufacturing

    As the original manufacturer of Tert-Butyl N-(4-Aminobutyl)Carbamate, we support advanced synthesis needs across highly specialized industrial verticals. This material features a protected amine functional group and defined chain length, meeting demanding formulation, regulatory, and purity requirements in each application area below.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical active ingredient producers integrate this carbamate during the multi-step synthesis of small molecule APIs, where the Boc-protected butylamine serves as a crucial intermediate. The protected amine function enables selective deprotection in late-stage coupling reactions, reducing risk of side reactions and streamlining impurity control. Formulators adjust loading based on stoichiometric demand within synthetic routes of various drug candidates, particularly in antineoplastic and CNS projects.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF, EP, JP monographs for related pharmaceutical substances
    • U.S. FDA 21 CFR Part 211 (cGMP for finished pharmaceuticals)
    • Traceability under ISO 9001:2015 and documented impurity profiling

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to core amine coupling step; precise input varies by synthesis pathway and scale, based on target API output.

    Downstream process integration

    • Added during intermediate protection phases in multi-step batch or flow synthesis, followed by selective deprotection and final coupling or cyclization.

    Final product types

    • Small molecule APIs for oncology, neurology, and antiviral formulations
    • Key intermediates used in custom pharmaceutical research
    • Peptide-based drug compounds requiring temporary protection

    2. Peptide Synthesis and Peptidomimetics Manufacturing

    Specialty peptide contract manufacturers include this Boc-butylamine derivative as a chain elongation reagent when assembling peptidomimetics or non-natural amino acid analogs. The Boc group offers controlled amine protection under acid-labile conditions, ensuring selective incorporation without premature loss in Fmoc/tBu strategies. Producers select usage levels by peptide chain design and desired side-chain accessibility, integrating QC checkpoints for residue integrity.

    Industry compliance standards

    • ICH Q11: Development and Manufacture of Drug Substances
    • ISO 13408: Aseptic Processing of Health Care Products
    • USP General Chapter <1055> “Peptide Substances”
    • Custom validation protocols as per client-specific regulatory submissions

    Typical usage ratio

    • 1.0–1.5 equivalents per coupling cycle; level adapted for each peptide’s sequence and target scale to minimize resin overhead and solution waste.

    Downstream process integration

    • Charged during protected amino acid coupling onto solid-phase peptide synthesis (SPPS) resin or in solution-phase chain elongation, followed by acidolytic Boc removal prior to final cleavage.

    Final product types

    • Pharmaceutical-grade synthetic peptides
    • Bioactive peptidomimetics for research and pilot clinical development
    • Modified peptides for diagnostics and in vitro assays

    3. Fine Chemical Building Block for Agrochemical Synthesis

    Major agrochemical manufacturers utilize this carbamate as a protected amine building block during the synthesis of advanced pesticide or herbicide intermediates. The tert-butyl group prevents undesired amine reactivity under chlorination, esterification, or alkylation conditions. Technical managers specify precise dosing to maintain balance between reaction yield and downstream purification efficiency, focused on compliance for environmental and safety audits.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals (EC 1907/2006) for manufacturing clearance
    • ISO 17025 for analytical testing/validation of intermediates
    • Local environmental safety directives and GHS labeling

    Typical usage ratio

    • 0.6–1.0 equivalents relative to the target heterocycle or aromatic substrate; adjusted for specific crop-protection synthesis route and impurity thresholds.

    Downstream process integration

    • Charged during initial amine introduction for protected synthesis steps, prior to selective deprotection and final functionalization into active pesticidal agents.

    Final product types

    • Herbicide intermediates with protected amine groups
    • Custom pesticide precursor blocks for in-house R&D
    • Select fungicide active compounds after final deprotection

    4. Custom Polymer Synthesis for Specialty Material Development

    Research-focused polymer producers rely on this Boc-protected butylamine for controlled chain extension and end-group modification during advanced polymerization methods. The carbamate group facilitates post-polymerization functionalization in block copolymer design or dendrimer synthesis, while protecting the amine until final chain-end transformation. Project teams calibrate input levels based on monomer conversion targets and tailored polymer property requirements.

    Industry compliance standards

    • ISO 9001:2015 quality management for specialty chemical manufacturing
    • ASTM D2769 for specialty polymer testing
    • RoHS compliance for electronics-enabling materials (where applicable)
    • REACH chemical safety assessment for European supply

    Typical usage ratio

    • 0.5–2.0 mol% relative to initiator or core monomer unit; input tuned for polymer backbone design, molecular weight targets, and end-use mechanical properties.

    Downstream process integration

    • Integrated as chain extender or reactive intermediate during step-growth and living radical polymerization, followed by thermal or acidolytic Boc removal for chain-end functionalization.

    Final product types

    • Functionalized specialty polymers and block copolymers
    • Dendritic macromolecules for electronic, biomedical, or nanotech use
    • Modified surface coatings requiring terminal amine groups post-deprotection

    5. Active Intermediate for Chemical Biology Research Reagents

    Suppliers to life sciences researchers leverage this compound in the multi-step synthesis of molecular probes, fluorescent tags, and bioconjugation reagents. The Boc group guards against undesirable amine modification during dye coupling, spacer addition, or click chemistry, with adjustment in loading by linker structure and research scale. Manufacturers document each batch with spectral and HPLC identity for reference in published research.

    Industry compliance standards

    • ISO 13485 for medical and diagnostic reagent manufacturing (if applicable)
    • OECD GLP (Good Laboratory Practice) for research chemical synthesis
    • ISO/IEC 17025:2017 for analytical method validation
    • RoHS/REACH certification for export and lab supply

    Typical usage ratio

    • 1.0 equivalent per linker or dye-conjugate coupling; modified for reagent structure and anticipated deprotection yield.

    Downstream process integration

    • Combined into multistep linker or probe assembly for temporary amine protection, with Boc cleavage scheduled before final labeling or conjugation to biomolecules.

    Final product types

    • Amine-reactive linkers for bioconjugates
    • Photoaffinity labels for proteomics research
    • Fluorescent tags and enzyme substrates for imaging/diagnostics

    6. Protected Amine Source for Fine Organic Synthesis Services

    Custom synthesis organizations apply this protected amine in the scalable production of high-value reference standards, impurity markers, and advanced intermediates for pharmaceutical and industrial clients. The Boc function ensures residue integrity across multi-step modifications with strong acids or bases, enhancing synthetic reliability. Loading scales with customer batch requirement and project-specific route design.

    Industry compliance standards

    • ISO 9001:2015 Certified Custom Synthesis Facilities
    • Client-mandated analytical release criteria: HPLC purity, NMR identification
    • Confidentiality and traceability under cGMP-exempt protocols
    • Material safety compliance (SDS, GHS labeling)

    Typical usage ratio

    • Equimolar to targeted protected amine intermediates; process chemists fine-tune charge based on multi-step reaction stoichiometry and customer project scale.

    Downstream process integration

    • Fed alongside reaction partners for selective amine introduction and safeguarded manipulation; final Boc removal and product purification before release or scale-up.

    Final product types

    • Reference standards for impurity identification
    • Custom tailored functionalized intermediates
    • Niche organic compounds for future study or scale-up
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    Certification & Compliance
    More Introduction

    Tert-Butyl N-(4-Aminobutyl)Carbamate: Precision in Protective Chemistry

    Understanding Tert-Butyl N-(4-Aminobutyl)Carbamate from the Manufacturer’s Perspective

    Every professional working in protective-group chemistry eventually faces the task of selecting the right compound for amine protection. Our experience producing Tert-Butyl N-(4-Aminobutyl)Carbamate has taught us much about why researchers choose this molecule for their synthetic routes, what role its structure plays, and what practical results it offers compared to alternatives.

    Connection Between Product Structure and Synthetic Outcomes

    The structure of Tert-Butyl N-(4-Aminobutyl)Carbamate brings distinct consequences at the bench. Its tert-butoxycarbonyl (Boc) group, attached to the terminal amine, allows users to introduce or remove amine protection with mild conditions—often using standard acids or bases without risk of racemization or harsh degradation. In contrast, similar analogs can demand either stronger reagents, risk backbone cleavage, or complicate purification.

    We produce this product to meet the demands of those seeking clean N-Boc deprotection while leaving sensitive functional groups untouched. Streamlined purification after Boc-removal has saved countless hours of column time in laboratories relying on our batches, confirmed by numerous feedback cycles over years of manufacturing experience.

    Production Consistency: Our Experience and Its Benefits

    The journey from starting materials to finished Tert-Butyl N-(4-Aminobutyl)Carbamate involves several steps where trace metallic residues, solvent impurities, or intermediate instability can spoil the final material. Our production protocols depart from generic procedures, introducing multiple quality assurance checks at vulnerable stages such as N-alkylation and Boc installation.

    Through feedback from pilot batches, we recognized that moisture control during Boc protection must exceed standard Good Manufacturing Practice thresholds. Even trace water content can cause incomplete reactions or decomposition, particularly at scale. After upgrading reactor drying systems and validating every batch using NMR and HPLC, we achieve superior batch-to-batch reproducibility, which translates directly to more predictable customer results.

    Scale-up teaches lessons not always obvious at the bench. Larger reactors require vigilant monitoring of mixing and heat transfer, especially when volatile tert-butyl chloroformate is involved. We have addressed these issues by optimizing stirring blade design and stepwise addition rates, reducing the risk of localized overheating and guaranteeing consistent conversion.

    Specifications That Matter in Daily Lab Use

    Colleagues in formulation, peptide synthesis, or pharmaceutical research care about properties that affect yield, stability, and downstream processing. In our hands, the typical product presents as a free-flowing white crystal, easily soluble in polar aprotic solvents including DMF and DMSO, providing seamless transfer between steps. We have observed that its melting point range reliably signals product purity, with any deviation alerting to contamination or incomplete reactions.

    Practical handling experiences have proven that our product remains stable during standard storage conditions without caking or liquefying—a concern with lower-quality batches originating from less stringent drying. Customers working with moisture-sensitive routes regularly call out minimal clumping and superior dissolution among the most appreciated features.

    Usage in Complex Synthesis: Lessons from the Factory Floor

    In peptide synthesis, protection and deprotection must occur with precision. Feedback from users confirmed the high tolerance of our Tert-Butyl N-(4-Aminobutyl)Carbamate for common acidic and basic workups, even in multi-step routes with dense functionalization. One repeated observation is the straightforward removal of the Boc group, which occurs cleanly under conditions that spare benzyl or Fmoc groups—crucial in solid-phase applications.

    Academia and industry partners have shared case studies involving drug development, where the stable Boc-protected amine backbone helps construct linkers or side chains for small-molecule libraries. We've seen this product used to expand chemical diversity through late-stage modifications, where unprotected amines might otherwise trigger unwanted side reactions or polymerization.

    Our production staff note the product's resilience against oxidative degradation—an advantage highlighted by those synthesizing in open systems or during extended reaction times. This stability often translates to reduced loss and a lower need for reprocessing, an appreciated cost and time saving for large-scale operations.

    Differences from Competing Amine Protecting Agents

    The chemical supply chain offers several alternatives to Tert-Butyl N-(4-Aminobutyl)Carbamate, including Fmoc or Cbz-protected analogs. Years of production and direct customer questions have built a clear picture of why scientists continue returning to Boc as the preferred solution for primary amine protection.

    One of the most compelling differences we hear reported involves selectivity during deprotection. Boc groups release under acidic conditions, such as trifluoroacetic acid, with minimal by-product formation. Fmoc groups come off in base, often producing dibenzofulvene, which can complicate cleanup and cause adducts with nucleophilic building blocks. Our Boc-protected product remains predictable for removal, even when sensitive electrophiles or base-sensitive moieties occur further down the chain.

    We have also learned that solubility profiles can differ, and that matters in scale-up. Boc-protected compounds frequently dissolve in both organic solvents and, after acid activation, aqueous solutions. In our own plant, this aids in solvent exchange, purification, and crystallization. Direct comparison tests have shown that our product outperforms Cbz analogs in both stability and ease of handling, sparing users from repeated drying cycles or decomposition during shipment, particularly when global transport routes involve temperature shifts.

    Operational safety brings its own considerations. We manufacture Boc-protected amines under conditions that minimize exposure to hazardous gases or reactive halides. Other protecting agents often require high-pressure conditions, hazardous waste treatment, or use of noxious reagents that add downtime and cost. Our workflow avoids these problems, reducing the environmental footprint—something regularly raised by environmental compliance audits and procurement teams.

    Value Created Through Transparency and Technical Support

    Customers approach us with questions during both planning and troubleshooting phases of synthesis. Open dialogue gives us continuous feedback, and also helps users adjust to changing regulatory expectations or optimize their own production costs. We see value in sharing our manufacturing experience, including tips on safe handling, best storage practices, and shortcutting purification without loss.

    For example, chemists often want to know the precise origin of any trace impurities detected by microanalytical scans. We disclose process adjustments—such as in-process quenching of unreacted tert-butyl chloroformate or the use of certified anhydrous solvents—which explains not only the final assay but also the pathway to improvement in purity standards. This partnership creates trust, which goes a long way in regulated industries where batch recalls or out-of-spec events must stay rare.

    During customer site visits, our technical staff routinely advise on timing and order of addition—even going as far as recommending reactor modifications or glassware upgrades based on our own lessons from scale-up. These contributions often avoid known pitfalls such as foaming during deprotection or excessive hydrolysis in humid environments.

    Environmental and Safety Realities

    Manufacturing specialty carbamates at scale involves balancing chemical efficiency and environmental responsibility. Our facilities operate with onsite scrubbers and waste treatment units, and all batch records include reagent recovery steps. By optimizing yields through continuous process monitoring, we reduce the downstream load of waste and residual solvents—a point not lost on customers facing mounting regulatory oversight.

    Colleagues have pointed out that certain competing amine protecting groups produce higher volumes of toxic by-products or demand waste handling infrastructure not available in smaller labs. Our in-house data confirm that Boc processes generate largely benign tert-butyl variants and CO2, which can be managed with existing safety equipment rather than requiring custom hazard protocols.

    The hands-on experience shared by our operators has influenced how we label, package, and ship. For example, our packaging comes lined to prevent infiltration of moisture, and bulk shipments receive tracking to allow rapid intervention in the rare event of spillage or temperature deviation. Customers who have switched from generic suppliers reported fewer incidents of sticky, degraded material—a difference that traces back to tight control over every link in the chain from synthesis to delivery.

    Real-World Performance: Feedback from Downstream Users

    Many years of supplying Tert-Butyl N-(4-Aminobutyl)Carbamate to R&D teams, CROs, and pharma manufacturers have produced a steady stream of technical insights about what works and what falls short. Repeated stories highlight the direct link between protecting group quality and larger outcomes, such as peptide yield, purity after preparative chromatography, and even the stability of sterile drug product formulations.

    One partner in oncology research detailed how elimination of minute amounts of side-product in our carbamate lots averted downstream impurities during conjugation steps. Synthetic teams working up kilogram lots supplied field confirmations that solid batch consistency eliminated delays in process validation, while avoiding failures seen with lesser purity materials sourced elsewhere.

    In the context of process R&D, our clients confirm that predictable removal of the Boc group unlocks more flexible process changes and late-stage functionalizations. These advantages add up—particularly in projects that scale from grams to tens of kilograms, where each interruption or equipment flush introduces non-trivial costs.

    Adaptability Across Diverse Applications

    Boc-protected amines occupy a critical role in combinatorial chemistry, where high purity and low cross-contamination rates matter as much as scale. During in-house collaborations, our teams have used Tert-Butyl N-(4-Aminobutyl)Carbamate to enable rapid synthesis of peptide-mimetic libraries, all while minimizing side-reactions in subsequent coupling steps. This flexibility often lets our partners introduce several iterative changes to their synthetic plan—something not always possible using other protecting groups where removal conditions overlap with cleavage of side-chain groups or sensitive moieties.

    We have also observed increased interest from teams engaged in biomolecule modification, such as oligonucleotide or antibody-drug conjugate production. In these areas, stability through automated liquid-handling cycles has attracted new users who appreciate the robust solubility and recovery provided by our batches. Direct comparisons to acyl or sulfonyl protecting groups show our product outlasts and outperforms when exposed to the full gamut of common reagents, including oxidants, reductants, and cyclic anhydrides.

    Predictability and Customization: Insights Earned Through Manufacturing

    Years spent refining our process—alongside dialogue with scientists—have demonstrated the need for customization in scale or purity. Some clients request material at a higher assay, demanding extra drying stages and analytics; others select screened particle sizes for specific applications in solid-phase synthesis or chromatography. We remain committed to flexibility without sacrificing quality, and our records show a direct correlation between tailored production and user success rates.

    Data gathered over numerous validation runs highlight several critical factors: fine control of pH during neutralization, fresh preparation of reagents, and exclusion of trace metal contamination. Each step, from initial charge to final isolation, benefits from the cumulative lessons of previous batches. Our ongoing investments in analytical instrumentation supply the certainty and documentation needed for even the most demanding regulatory submissions.

    Our Approach to Responsible Manufacturing

    Continuous improvement stands as a core value in our manufacturing practice. We invest not just in chemistry, but also in the tools and processes that make reliability possible. Digital batch records, continuous training for process operators, and rigorous third-party verification build a foundation that users can depend on. Human oversight and intervention, paired with automation where it grants true advantage, keep quality front and center, and not just as a slogan.

    We remain deeply aware that Tert-Butyl N-(4-Aminobutyl)Carbamate represents more than a chemical intermediate. In real-world terms, it's a building block whose predictability can make or break whole series of reactions in a development pipeline. That awareness shapes how we plan, how we produce, and how we engage with scientists seeking solutions to real problems every day.

    Conclusion: Lessons Learned and Shared

    After years of close work with partners on both sides of the laboratory and plant floor, we understand the impact that well-made Tert-Butyl N-(4-Aminobutyl)Carbamate offers. Our promise remains rooted in transparency, technical rigor, and an openness to challenge our own practices. In every batch, each adjustment, and all customer conversations, we apply what we have learned so that scientists can focus on innovation rather than troubleshooting their starting materials.

    Anyone considering this product—or debating which amine protecting group suits their needs—benefits from both proven data and lived manufacturing experience. We remain committed to supporting research, development, and industrial production with chemistry that stands up to real scrutiny, delivers in practice, and reflects the knowledge earned through every single run.