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N-Boc-1,6-Diamino-Hexane Hydrochloride

    • Product Name N-Boc-1,6-Diamino-Hexane Hydrochloride
    • Alias Boc-1,6-diaminohexane hydrochloride
    • 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

    377935

    Product Name N-Boc-1,6-Diamino-Hexane Hydrochloride
    Cas Number 141253-07-0
    Molecular Formula C11H25ClN2O2
    Molecular Weight 252.78 g/mol
    Appearance White to off-white solid
    Purity >98%
    Melting Point 120-125°C
    Solubility Soluble in water and methanol
    Storage Temperature 2-8°C
    Ph 1 In Water 4.0 - 6.0
    Synonyms tert-Butyl (6-aminohexyl)carbamate hydrochloride
    Chemical Structure Boc-NH-(CH2)6-NH2·HCl
    Inchi Key QNMVRNBEVZPTAR-UHFFFAOYSA-N

    As an accredited N-Boc-1,6-Diamino-Hexane Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle containing 25g of N-Boc-1,6-Diamino-Hexane Hydrochloride, labeled with product name, quantity, and hazard symbols.
    Shipping N-Boc-1,6-Diamino-Hexane Hydrochloride is shipped in tightly sealed containers to protect it from moisture and contamination. The package is labeled according to chemical safety regulations and handled in accordance with standard policies for non-flammable, solid laboratory chemicals. Shipping complies with relevant transport regulations and includes appropriate documentation for safe delivery.
    Storage N-Boc-1,6-Diamino-Hexane Hydrochloride should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, well-ventilated area (2–8 °C recommended). Protect from heat, strong acids, and bases. Store under inert atmosphere if possible to prevent hydrolysis or degradation. Proper labeling and segregation from incompatible materials is essential for safety and chemical integrity.
    Application of N-Boc-1,6-Diamino-Hexane Hydrochloride

    Applications of N-Boc-1,6-Diamino-Hexane Hydrochloride in Industrial Manufacturing

    N-Boc-1,6-Diamino-Hexane Hydrochloride serves as a protected diamine intermediate widely adopted in the synthesis of high-value specialty chemicals for pharmaceuticals, biotechnologies, and advanced materials. Our manufacturing experience supports direct integration of this intermediate in rigorous downstream processes, ensuring conformity to regulated industry specifications and customer-specific requirements.

    1. Peptide API Intermediate Synthesis

    Major peptide-based pharmaceutical companies rely on this protected hexamethylene diamine for stepwise solid-phase peptide synthesis, where it acts as a spacer or linker to maintain precise chain structure. The selection of this intermediate minimizes side reactions in automated peptide assembly, supporting stable Boc deprotection and ensuring high product purity for regulated drug substances. Its compatibility with Fmoc/Boc strategies makes it a trusted choice for commercial-scale synthesis of peptide APIs under validated cGMP processes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices
    • United States Pharmacopeia (USP) In-Process Controls for Peptide APIs
    • European Pharmacopoeia (Ph. Eur.) monographs for peptide substances
    • FDA 21 CFR Part 211 Drug Manufacturing Regulations

    Typical usage ratio

    • 0.9–1.2 molar equivalents relative to protected amino acid per coupling step, adjusted by peptide sequence elongation requirements

    Downstream process integration

    • Charged after initial resin swelling, before chain assembly steps in solid-phase reactors
    • Removed after Boc deprotection cycles during chain elongation
    • Intermediate purified pre-API isolation in pilot and commercial scale

    Final product types

    • Peptide APIs for injectable and oral pharmaceuticals
    • Diagnostic peptide reagents
    • Therapeutic oligopeptides

    2. Antibody-Drug Conjugate (ADC) Linker Synthesis

    Manufacturers of targeted biologic therapies incorporate this diamine derivative during linker synthesis for Antibody-Drug Conjugates (ADCs). Its defined chain length and removable Boc protection provide essential control in bifunctional crosslinkers securing the antibody to cytotoxic payloads, offering selective cleavage profiles and predictable stability under physiological conditions. Precision during this stage underpins the performance and safety profile of final ADC formulations.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • Good Manufacturing Practice Guidelines for Biologics (WHO TRS 999, Annex 2)
    • USP General Chapter <1047.1> Design of Biologics
    • Guidance for Industry: Monoclonal Antibodies and Related Products (EMA)

    Typical usage ratio

    • 0.5–1.0 equivalent relative to activated carboxylic component, varied by payload–antibody ratio (PAR) design and analytical validation

    Downstream process integration

    • Serves in solution-phase linker formation prior to conjugation with antibody via NHS ester or maleimide activation
    • Used in linker-payload assembly under mild, aqueous-compatible reaction conditions

    Final product types

    • Commercial ADC drug substances
    • Clinical-stage bioconjugates for research and development
    • Stabilized linker molecules for diagnostic conjugates

    3. Polyamide and Polyurethane Chain Extension

    Producers of advanced polyamides and polyurethanes utilize this protected diamine in segmented polymer synthesis. The Boc protection ensures blocked reactivity during the pre-polymer step, only exposing the amine functionality during controlled deprotection and subsequent chain extension. This strategy provides unique physical properties and tailored molecular weight distributions for high-performance materials used in medical and engineering applications.

    Industry compliance standards

    • ISO 10993 Biological Evaluation (for medical polymers)
    • USP Class VI Plastic Material qualification (where applicable)
    • REACH Regulation (EC 1907/2006) for chemical safety
    • ISO 9001 Certified Polymer Quality Systems

    Typical usage ratio

    • 2-10% by monomer weight, dependent on desired segment length and final mechanical properties, verified by GPC and DSC analysis

    Downstream process integration

    • Incorporated at oligomer or pre-polymer stage as a chain extender or comonomer
    • Boc group removed thermally or chemically prior to final polycondensation/crosslinking

    Final product types

    • Medical-grade polyamide tubing
    • Segmented polyurethane elastomers
    • Specialty engineering polymers for bioprocessing equipment

    4. Small Molecule Drug Building Blocks

    Contract research and manufacturing organizations use this compound as a protected diamine scaffold for custom small molecule development. The Boc group enables orthogonally protected strategies key to synthesizing molecules with complex amine substitution, such as kinase inhibitors or CNS-active compounds. Researchers depend on its stability and traceable impurity profile throughout route scouting, scale-up, and GMP kilo-lab production, particularly for clinical trial material that requires strict documentation and batch traceability.

    Industry compliance standards

    • ICH Q3A/B Impurity Guidelines for New Drug Substances
    • FDA IND Enabling Manufacture Guidance
    • ISO 17025 Analytical Traceability
    • GMP-compliant Documentation and Change Control

    Typical usage ratio

    • 0.8–1.5 equivalents, depending on the stepwise requirements of the synthetic route, and adjusted by LC-MS monitored reaction completion

    Downstream process integration

    • Added at early to mid-stage during key coupling, reductive amination, or urea/thiourea formation
    • Boc group removed via controlled acidolysis ahead of final purification steps

    Final product types

    • Clinical trial API intermediates
    • Lead structure analogues for medicinal chemistry
    • Screening compounds for pharmaceutical research

    5. Crosslinker Manufacturing for Modified Proteins

    Specialty bioprocess contractors employ this Boc-protected diamine to produce advanced crosslinking agents designed for precise modification of proteins and enzymes. The intermediate structure allows staged functionalization, giving protein engineers flexibility for introducing specific reactive groups required in site-selective conjugation. These carefully engineered crosslinkers ensure functional retention and biocompatibility in downstream therapeutic or diagnostic protein products.

    Industry compliance standards

    • ISO 13485 Medical Devices Quality Management
    • USP General Chapter <1047.2> Bioprocess Materials
    • FDA Chemistry, Manufacturing, and Controls (CMC) for Biologics
    • EMA Guideline on Quality of Protein/Peptide Drug Substances

    Typical usage ratio

    • 5–25 mmol per mole protein, optimized based on desired modification level and protein mass

    Downstream process integration

    • Synthesized into bifunctional or heterobifunctional crosslinkers, then introduced into aqueous protein modification reactions post-purification
    • Boc group deprotected on completion of linker attachment, enabling direct protein coupling

    Final product types

    • Site-specifically modified enzymes
    • Diagnostic protein conjugates
    • Protein–polymer hybrid materials
    Free Quote

    Competitive N-Boc-1,6-Diamino-Hexane Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    N-Boc-1,6-Diamino-Hexane Hydrochloride: A Reliable Intermediate for Precision Synthesis

    Understanding the Role of N-Boc-1,6-Diamino-Hexane Hydrochloride in Modern Chemistry

    As the direct producer of N-Boc-1,6-Diamino-Hexane Hydrochloride, we have learned the product’s real-world value by tracking both internal quality results and extensive client feedback. This compound, catalogued as Model: NBH-101, bears the chemical formula C11H25ClN2O2 and a molecular weight of 252.78 g/mol. We focus on this molecule because it brings predictability and flexibility to a broad range of synthetic operations. Chemists know the challenges of scaling up reactions when intermediates show large lot-to-lot variations; our process emphasizes consistency so researchers and production teams can maintain workflow and hit their yield targets reliably.

    Most development chemists encounter hexamethylenediamine derivatives frequently, though the protected forms, particularly with Boc and hydrochloride functionalization, introduce distinct handling and performance characteristics. By securing the amine groups with tert-butoxycarbonyl (Boc) protection, the molecule enables selective deprotection protocols—something that simple diamines cannot guarantee without risking cross-reactions or competitive side processes. The hydrochloride form increases storage stability, prevents unwanted absorption of atmospheric water, and cuts down on amine odor during handling.

    Achieving Purity That Withstands Rigorous Demands

    It is not enough to offer just a named compound. Chemical manufacturers have a responsibility to back their products with reliable, verifiable purity records. Analytical records for our standard material show purity levels exceeding 98%. This benchmark holds across multiple kilograms and over many repeat batches. Scaling any intermediate exposes problems that small-scale practice can overlook. Our team tackles these by optimizing the workup, identifying side-product profiles downstream, and tuning our reaction parameters to squeeze out consistent, high-purity product. Engineers and operators perform NMR and HPLC analysis after each major batch, verifying that every shipment meets the exacting standards set by pharmaceutical, materials, and fine chemical partners.

    Some competitors offer similar-sounding diaminohexane products. The differences become clear after testing: many alternatives exhibit batch-to-batch inconsistency, off-spec coloration, or unwanted secondary amine contaminants. Poor control at the Boc-protection stage or during hydrochloride formation often leads to residual solvent or partial protection—this derails sensitive cross-coupling or protection/deprotection sequences that demand clean starting points. Years of client conversations have shown that even minor deviations force costly troubleshooting and can disrupt timelines. Our cumulative experience in large-scale manufacture means fewer last-minute issues and more predictable project workflows.

    From Intellectual Property Projects to Scalable Manufacturing

    Several years ago, we began supporting early-stage pharmaceutical development programs with N-Boc-1,6-Diamino-Hexane Hydrochloride. In these settings, the need shifts rapidly from gram-scale test runs to tens or even hundreds of kilograms. By controlling each variable—from raw material selection through packaging—we reduce surprises during scale-up. For example, degradation rates under various storage conditions can impact not only performance but also regulatory compliance. We invest in moisture-protected storage, nitrogen blanketing, and continuous climate control in our warehouse. These steps translate to higher shelf life and reduced variability when researchers move from bench scale to pilot or full-scale production.

    Our engagement does not end with delivery. End users often encounter planning bottlenecks if a material drifts off spec. Each batch ships with a complete analytical record, including HPLC, NMR, melting point, and water content. We answer technical requests directly and support troubleshooting, not just with paperwork but also with access to the chemists and engineers who know the process inside out. Most troubleshooting issues traced by external users—such as unusual salt formation, unexpected solubility, or off-target reactivity—link back to either upstream impurities or variable protection ratios in supplied intermediates. Our direct manufacturing approach addresses these risks in real time.

    Real-World Application: Why Synthetic Planning Benefits from Boc Protection

    Protecting groups might seem like textbook organic chemistry, but in industrial environments, the selection of a protection strategy can determine the success or failure of an entire process. N-Boc-1,6-Diamino-Hexane Hydrochloride stands out because the Boc group is robust under a wide range of conditions, including aqueous workups and many oxidative protocols. Deprotection typically proceeds under acidic conditions without scrambling sensitive motifs elsewhere in the molecule. Chemists gain tight control over which end of the molecule they activate at each step. This capability simplifies multi-step synthesis, particularly when developing peptides, specialty monomers, or bridging units in macrocycles.

    In our experience, some teams prefer unprotected 1,6-hexanediamine or mono-protected derivatives, hoping to cut a step. Down the line, many encounter selectivity issues that cause low yields and product contamination. The Boc-protected version, especially as the hydrochloride salt, avoids these headaches by stabilizing both ends and making purification straightforward. This approach smooths regulatory interactions, especially for active pharmaceutical ingredient (API) projects where documentation and reproducible process controls carry extra scrutiny.

    Comparing with Other Aminohexane-Based Building Blocks

    Reflecting on customer projects over the years, clear operational differences emerge between N-Boc-1,6-Diamino-Hexane Hydrochloride and other related intermediates. For example, mono-Boc-protected hexanediamines often lead to confusing mixtures during peptide coupling or when used to bridge motifs in specialty polymer synthesis. By fully Boc-protecting both ends, the molecule delivers clear, single-product reactivity patterns. This helps drive up final yields and reduce side project remediation.

    Other suppliers sometimes offer freebase forms or mixed protection technologies. These may seem more convenient but usually result in unpredictable storage stabilities and inconsistent solubilities. For research teams operating in tightly regulated environments, every deviation can trigger compliance reviews or failed production runs. By offering only the hydrochloride salt, we maintain batch integrity and reduce the risk of absorption of trace acids or water, which can undermine sensitive synthetic sequences.

    Field experience reveals that packaging also shapes success rates. Direct users report frustration with static-prone powders or poorly sealed primary containers. Our operations shifted years ago to custom-sealed, low-static poly bottles inside multi-layer barrier wrap with clear exterior labeling and tamper evidence. This level of QA/packaging reduces human error risk during material withdrawal and weighs out in both the analytical and prep lab settings.

    Meeting Project Demands: Specification You Can Trust

    Before any shipment, users ask about melting point behavior, particle size spread, and residual solvent content. We respond based on direct manufacturing knowledge, not just stock specs scraped from catalogs. The melting point typically falls in the 115–123°C range, confirming both the correct Boc protection and hydrochloride state; analysis via NMR confirms chemical identity and rules out ring-closure or decomposition products.

    Particle size remains a practical consideration for bench chemists and kilo-scale operators. Finer materials may clump or cake more easily, forcing extra drying or grinding steps. Our drying and sieving line assures controlled flow properties without risking major fines or dusting. Water content (Karl Fischer, validated method) consistently tracks below 0.5%, supporting dry weight accuracy for precise stoichiometric planning.

    Trace residual solvents frequently cause headaches in high-performance synthesis, particularly as regulatory environments tighten. We commit to strictly monitored solvent removal at scale, backed by gas chromatography analysis on every lot. If specifications shift for customer applications—for example, for inhalation-grade projects or high-tier API projects—we offer tailored solutions, guided by our in-house chemists rather than off-the-shelf options.

    Upstream Security: Sourcing and Traceability

    Competent manufacturing goes beyond the reactor vessel. We dedicate significant resources to qualifying suppliers, from the alkyl diamines through the Boc anhydride down to the hydrochloride. Good supply security prevents batch failures and keeps projects on schedule. All raw materials are fully traceable; our purchasing teams conduct annual audits and cross-lab verification to avoid off-grade stock reaching the main synthesis step. As global supply chains show increasing volatility, this high-touch approach pays dividends in project reliability.

    We have encountered raw material variability—some lots of starting amines or Boc-anhydride contain unacceptable levels of trace impurities. These can lead to colored byproducts or, worse, subtly altered reactivity in downstream steps. Our chemists deal with these problems in-house, screening lots and rejecting those that underperform, avoiding delays for our clients. This tight control builds real value for multidisciplinary teams looking to minimize surprises in sensitive synthetic programs.

    Storage, Handling, and Laboratory Workflow

    Every bench or process chemist thinks about practical handling challenges before placing bulk orders. The hydrochloride salt of N-Boc-1,6-Diamino-Hexane addresses typical pitfalls. It flows freely and resists atmospheric uptake, avoiding the stickiness and caking sometimes found with the free amine or even with the carbonate salt forms. Labs equipped with standard climate control remain the ideal environment; for long-term bulk storage, we advise keeping the product away from direct light and sources of strong acid or base, as with most protected diamines.

    On the production line, teams want to avoid static discharge, sample contamination, and bottle-to-bottle transfer loss. Our QA staff regularly inspects and tests packaged shipments, ensuring labels remain clear, batch numbers stay traceable, and containers hold their seals. Staff training in advanced packaging protocols pays off in shipping reliability—no batch leaves the plant without confirmed seal integrity, labeled dating, and technical permission from our analytical manager.

    Environmental Impact and Waste Minimization

    Industry shifts toward greener chemistry force all chemical producers to rethink both process and product impact. Boc chemistry sometimes raises concerns about solvent and auxiliary waste, particularly in large-scale operations. Over the last decade, we have updated our protocols to recycle spent Boc anhydride and media wherever possible. In some runs, we reduced auxiliary material use by 10-15% without dropping purity or yield. Our plant maintains solvent capture and recycling systems, cutting raw material procurement and waste disposal costs year-on-year.

    Downstream, most users handle hydrochloride salts with relative ease, but safe disposal and laboratory hygiene cannot be neglected. Clear documentation on waste codes, safe acid handling, and neutralization protocols ship with each large order. We routinely check in with frequent users to confirm that laboratory practices align with regulatory and safety norms, aiming to mitigate risks and report near misses that could affect future handling guidelines.

    Future Outlook: Anticipating Tomorrow’s Demands

    As protected diamine markets evolve, needs shift from standard building blocks to bespoke intermediates customized for specific routes, chiral selectors, or complex macromolecular targets. We participate in cooperative research with several clients and academic teams, iterating on next-generation protection strategies and downstream applications. As more regulatory scrutiny lands on pharmaceutical and electronic material supply chains, our investment in documentation—batch records, analytical reports, stability studies—delivers real security to program managers and regulatory auditors.

    We also track regulatory changes around amine and Boc-protected intermediates, engaging with trade associations and standard-setting bodies to anticipate changes that may impact project timelines. Our technical, regulatory, and QA teams stay updated, conducting risk analyses and training workshops. By staying connected to the evolving technical landscape, we deliver what projects need now and adapt to what clients may ask for next.

    Supporting Innovation Without Compromise

    Our entire product line, including N-Boc-1,6-Diamino-Hexane Hydrochloride, grew out of feedback from real-world users who need trustworthy materials for high-complexity synthesis. As direct producers, we bring both institutional experience and hands-on technical feedback to every batch, adapting processes based on both macro-scale trends and single-customer feedback. By avoiding shortcuts and delivering only on spec, we help research and production teams focus on innovation, not troubleshooting.

    Teams building novel peptide drugs, specialty monomers, or advanced materials require intermediates with proven reproducibility, clear analytical tracking, and ongoing technical support. Each batch reflects a commitment to this vision, shaped by persistent quality improvement and tight integration between production and analytical staff. N-Boc-1,6-Diamino-Hexane Hydrochloride may appear as a small cog in a larger system, but in practice, every successful project relies on the reliability and transparency we provide—from first inquiry through scale-up and on to routine delivery.