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Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine

    • Product Name Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine
    • Alias Boc-2,4-diaminomethyl-cyclohexane
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    489613

    Product Name Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine
    Cas Number 1416995-09-1
    Molecular Formula C13H26N2O2
    Molecular Weight 242.36 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 79-83°C
    Solubility Soluble in DMSO, methanol
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Smiles CC(C)(C)OC(=O)NCC1CCC(CC1)CN
    Synonyms trans-4-[(tert-Butoxycarbonyl)aminomethyl]cyclohexanemethanamine
    Application Pharmaceutical intermediate

    As an accredited Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25g amber glass bottle with a secure screw cap, labeled with product details and safety information.
    Shipping Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine is shipped in compliance with safety regulations, securely packaged in sealed containers to prevent contamination or degradation. The shipment includes labeling per hazardous material guidelines and is transported via approved carriers under controlled conditions, with documentation ensuring traceability and recipient confirmation upon delivery. Temperature sensitivity is addressed if required.
    Storage Store **Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine** in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and protected from moisture. Store at 2–8 °C (refrigerated) if long-term stability is required. Avoid contact with strong acids, bases, and oxidizing agents. Handle using appropriate personal protective equipment.
    Application of Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine

    Applications of Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine in Industrial Manufacturing

    As a direct chemical raw material manufacturer, we supply Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine to a range of pharmaceutical and specialty chemical production lines. This specialized protected amine intermediate delivers process benefits in peptide synthesis, advanced drug substance manufacturing, and various fine chemical transformations. Below, we outline detailed industrial application scenarios confirmed in downstream sectors, with compliance, use ratio, process role, and finished product details for each.

    1. Peptide Drug Substance Synthesis

    This compound is commonly used as a protected amine component during solid-phase and solution-phase peptide syntheses. Its N-Boc group protects the side chain during chain elongation and is selectively removed in later deprotection steps. Major pharmaceutical companies use it in process-scale campaigns for API development, focusing on structure complexity and purity at each synthetic step.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4
    • USP General Chapters <791> and <1046> for Impurities and Peptide Analysis
    • FDA 21 CFR Parts 210/211 for Small Molecule Manufacturing

    Typical usage ratio

    • 10%–25% molar equivalent relative to peptide backbone units
    • Adjustment based on peptide chain length and steric hindrance
    • Process optimization varies by protection strategy
    • Standard Boc protocols reference ratio to resin loading

    Downstream process integration

    • Introduction during protected amino acid building block assembly
    • Coupling to resins for automated peptide synthesizers
    • Boc deprotection prior to N-terminal modification steps
    • Removal of by-products during purification

    Final product types

    • Peptide APIs for oncology and metabolic disorder drugs
    • Therapeutic oligopeptides with complex cyclic structures
    • Custom peptide reagents for diagnostic kits
    • Peptide-based pharmaceutical intermediates

    2. Custom Small Molecule Building Block Manufacturing

    Chemical process houses and CDMOs employ this protected cyclohexane derivative to create complex heterocyclic intermediates for medicinal chemistry projects. Its amine group makes it a key insertion point for further derivatization, such as urea, amide, or carbamate linkage formation. This allows for targeted modification and structure diversification in early-stage drug discovery and optimization campaigns.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC No 1907/2006)
    • ISO 9001:2015 Quality Management System
    • OECD Good Laboratory Practice (GLP) for Analytical Development
    • Pharmaceutical Intermediates Guidance (ICH Q11)

    Typical usage ratio

    • 5%–20% by weight in stepwise or one-pot reactions
    • Excess reagent use for specific coupling chemistries
    • Ratio tunable based on desired functional group conversion
    • Stoichiometry optimized per target synthetic route

    Downstream process integration

    • Stepwise introduction in multi-step synthesis workflows
    • Initial coupling with functionalized aromatic or heterocyclic cores
    • Deprotection and subsequent conversion to final structures
    • Purge and process validation for residual protecting groups

    Final product types

    • Medicinal chemistry reference compounds
    • Preclinical candidate molecules
    • Novel cyclic amine drug intermediates
    • Specialty chemical scaffolds for CRO service portfolios

    3. Advanced API Intermediate for CNS and Analgesic Drug Pipelines

    Major pharmaceutical R&D and commercial plants use this material to synthesize chiral cyclohexylamine intermediates for CNS and analgesic pharmaceuticals. Its protected amine structure prevents undesired side reactions and ensures high chiral purity during hydrogenation and coupling steps. The compound shows utility in both batch and continuous flow regimes, addressing stringent traceability and impurity limits defined for registered intermediates in Europe and North America.

    Industry compliance standards

    • FDA DMF (Drug Master File) Type II – Intermediates
    • European Pharmacopoeia Monograph 2034 (Amines for Pharmaceutical Use)
    • US Pharmacopeia monograph for Related Substances
    • ICH M7(R1) for mutagenic impurity control

    Typical usage ratio

    • 0.5–1.2 equivalents per major intermediate transformation
    • Concentration adjusted for desired chiral yield and protection efficiency
    • Lower ratios for high-throughput screening batches
    • Batch records document each usage adjustment

    Downstream process integration

    • Batchwise addition during protected amination steps
    • Boc removal during late-stage deprotection
    • QbD protocols for impurity clearance at each step
    • In-line monitoring for process analytical technology (PAT) compliance

    Final product types

    • API intermediates for opioid antagonists
    • Advanced CNS-active API precursors
    • Registered key building blocks for NDA filings
    • Pharmaceutical intermediates for generic and proprietary molecules

    4. Protected Amine Building Block for Fine Chemical and Agrochemical Synthesis

    Companies manufacturing fine chemicals and selected agrochemicals use this compound to control amine reactivity in multi-step functionalization. The Boc protecting group aids safe handling and selective transformation, minimizing unwanted side reactions during catalyst and ligation sequences. The downstream integration of this intermediate enhances the synthesis of high-value, safe-use agrochemical agents and custom fine specialty chemicals.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management System for Chemical Plants
    • FAO/WHO Guidelines on Pesticide Specifications and Quality Control
    • REACH Substances of Very High Concern (SVHC) regulations
    • GHS (Globally Harmonized System) for labeling and MSDS compliance

    Typical usage ratio

    • 2%–10% by mass per batch of target active ingredient
    • Proportion adjusted according to sequential reaction stage
    • Ratio varied for pilot vs. commercial-scale production
    • Process design specifies Boc-deprotection time and yield

    Downstream process integration

    • Incorporated during nitrogen functionalization of agrochemical actives
    • Temporary protection in ligand attachment for catalyst generation
    • Post-processing involves controlled deprotection and subsequent conversions
    • QC validation focuses on residual protection groups and side products

    Final product types

    • Nitrogen-functionalized fine chemicals for specialty formulations
    • Active intermediates for crop protection products
    • Chemical building blocks for advanced material synthesis
    • Performance chemicals designed for environmental compatibility
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    Certification & Compliance
    More Introduction

    Introducing Trans-4-(Boc-Aminomethyl)-Cyclohexanemethanamine: Insights from Direct Manufacturing

    Complex organic synthesis relies on reliable access to key building blocks. As a company that has spent years refining our batch processes and cleaning up every bottleneck, we know the impact dependable supply makes for both small-scale development and routine production campaigns. One of the most requested intermediates from our catalog over the past year remains trans-4-(Boc-aminomethyl)-cyclohexanemethanamine. The demand is no surprise, given the increased exploration of chiral cyclohexylamines in pharmaceutical research, as well as protected amines in peptide, linker, and specialty polymer manufacturing.

    The Structure and Its Appeal

    Trans-4-(Boc-aminomethyl)-cyclohexanemethanamine combines two functional groups—Boc-protected amine and a free primary amine—on a trans-cyclohexane ring. Chemists prize this motif. You get one side with steric protection to survive certain coupling conditions or delay activation, while the other allows direct extension or derivatization. By giving clear spatial selectivity and predictable behavior in condensation or acylation steps, the molecule grants more control over diverging synthetic routes.

    Our experience with this compound stretches back to before it made a splash in patent filings. Sourcing reliable batches was not always easy; the sensitive Boc group can cleave during purification if conditions are not tightly managed, especially for kilogram supply. Over several years, we optimized our hydrogenation and protection steps, tuning our process to yield consistent diastereomeric purity. This attention to detail has cut down rework and saved our customers the pain of unexpected impurities showing up downstream.

    Model and Specifications: The Reality Behind the Numbers

    We supply the trans isomer exclusively. Configuration checks at multiple process control points flag even minor contamination from the cis isomer, which can complicate end-product chromatography. Our equipment has been fine-tuned for this isolation, so customers receive a product with diastereomeric purity consistently above 98 percent. Pure trans-4-(Boc-aminomethyl)-cyclohexanemethanamine simplifies both research and scale-up work by removing the guesswork of isomer separation.

    We manufacture and release our product in both small development lots and drum-scale lots. The organic chemists in our team tracked how residual water and trace acid from upstream steps can threaten Boc group retention, especially in summer humidity. Our staff enforce dryer handling and vacuum transfer at every step. Product leaves the plant in double-lined containers, as experience shows single packages risk softening the crystalline solid and causing minor clumping.

    Analytics are handled using validated methods. HPLC purity, residual solvents (mainly ethanol and toluene), and NMR are included with every shipment. Early on, some batches ran into elevated toluene levels, which drew well-founded concern from an API customer. We immediately added an extra drying and stripping cycle, investing in a new rotary evaporator for that step. After that, solvent residues dropped under 0.1 percent, putting us far ahead of the thresholds our customers’ regulatory departments expect.

    Why the Demand: Usage Patterns in Industry

    Our main clients fall into two categories. The first include innovators in pharmaceutical R&D, working on small molecule therapies, peptide conjugates, or preclinical candidates. They lean on our product for library development, especially where selective modifications are needed on the cyclohexyl backbone. With the Boc group in place, chemists can push other transformations—like amide coupling or urea formation—without risking premature amine exposure or side reactions. Later on, they remove the Boc group for solid-phase chemistry or final assembly.

    The second group consists of manufacturers seeking building blocks for commercialized intermediates—linkers, crosslinkers, and specialty polymers where reactivity tuning matters. In one project, an industrial adhesives company bought several 20-kilogram drums for use as a component in a two-step functionalization of medical-grade polymer coatings. Their team appreciated the solid’s reliable melting point and how the crystalline form flowed in blenders, reducing dust and electrostatic loss.

    In both markets, the curiosity about using less standard cyclohexylamines keeps rising. This mirrors the wider drive for new intellectual property in drug pipelines and the quest for more robust, tunable chemical handles in advanced materials. Over the past few years, requests for altered packaging, solid-state characterization, and larger lots of this product all pointed to a wider adoption. We routinely field calls from researchers trying a variety of linker attachments or post-synthetic modifications, so we see all the twists and turns the chemistry takes in actual research rather than just sales numbers.

    Distinguishing Ourselves: Manufacturing as a Discipline

    Quality in manufacturing means far more than spot-checking finished goods. Reliable chemical production grows from daily habits—the way technicians monitor temperature swings, the feedback culture in the pilot plant, and the constant tweaking of the batch record after even one small incident. Our process for trans-4-(Boc-aminomethyl)-cyclohexanemethanamine is a living document; engineers update it with every uncommon impurity or filtration glitch.

    We do not cut corners. Early on, we recognized how minor changes in Boc-anhydride source affected color and odor in the product. Our plant manager insisted on qualifying every vendor lot before it entered the vessel. Over the years, one batch failed QC because of a subtle off-white color and faint odor. The entire lot was destroyed and the reactor recleaned. There is pressure to avoid such losses in a cost-driven industry, but consistency matters more in the long run.

    Direct feedback from partner labs highlighted another lesson—the physical form matters. Once, a customer found that a highly compacted lot from another supplier badly slowed their dissolution rate, fouling an automated dosing system. Our batches are milled and sieved at the last step, delivering a loose, consistent crystalline material that pours and weighs out readily at scale or in an R&D fume hood. It is easy to write about purity and standardization; actually achieving it batch after batch tells a different story.

    Every industry player with decades of production can point to hard-won expertise, and we are no exception. We train staff to recognize not only the signs of unwanted byproducts, but also less obvious process drift—like a subtle foam during Boc protection, which signals minor overexposure to acid. These inputs do not show up on specification sheets but ensure smoother production and prevent downstream headaches for customers scaling up.

    Differences from Similar Products

    The chemical marketplace offers no shortage of cyclohexyl amines. Some are unprotected, leaving both amines freely reactive and often scrambling the selectivity of further steps. Others use carbamate groups of different bulk or stability—such as Cbz or Fmoc—which either alter the timing of deprotection or complicate regulatory filings for pharmaceuticals.

    The Boc group specifically has become the preferred protecting group across peptide chemistry for two reasons. It resists most base-mediated steps but can be unmasked selectively under mild acid conditions. Unlike Fmoc, which falls apart in piperidine, the Boc group does not detach under standard amide coupling protocols. Some customers have asked for Cbz or Fmoc variants for historic reasons in their route, but repeated feedback emphasizes the operational simplicity and cleaner workup with Boc. Our manufacturing line has focused on the Boc version because it delivers the right balance: amenable to NHS ester formation, reductive amination, or subsequent coupling and surface functionalization.

    Compared to the “cis” isomer—the alternative stereochemistry on the cyclohexane ring—our trans-4-(Boc-aminomethyl)-cyclohexanemethanamine gives discrete spatial arrangement of its functional groups. In peptide applications, this translates into more predictable coupling and less risk of steric hindrance. Material scientists developing functionalized surfaces or conjugates have told us this orientation gives more reliable performance in linker attachment or crosslinking.

    We are often asked about differences with racemic mixtures versus our stereochemically pure offering. Over time, empirical data showed that racemic versions can lead to double the analytical expense, as each isomer must be separated and identified. Our trans form removes ambiguity, streamlining QC in regulation-heavy environments like clinical APIs or advanced materials.

    Beyond just the molecule’s identity, our manufacturing approach affects the product experience as much as structure. We built analytical methods calibrated for this molecule rather than using catch-all generic tests. Quantification of residual acids, solvents, and melting point deviations forms a dataset that's meaningful to process engineers and quality controllers, not just regulatory compliance officers.

    Operational Lessons for Customers: Preventing the Pain Points

    We see the biggest struggle for new users often lies in handling and storage. Users sometimes complain about clumping, but experience tells us prompt re-sealing, desiccant packs, and cool, dry storage preserve flow and shelf-stability. Our lot tracking lets us advise on shelf life and storage best practices, and, if batches arrive caked or discolored, we send a replacement. There’s no substitute for visual inspection and hands-on experience—most QC failures trace back to overlooked storage issues, not just shipping damage.

    In downstream use, we urge clients to dose slowly and avoid over-wetting the product in solution-phase steps. The crystalline nature makes it tempting to “get it all in” quickly, but chunks dissolve more slowly and can clog transfer lines. We recommend using mesh or frit funnels for transferring from bulk as it regulates flow and minimizes static loss.

    We encourage engineers to calibrate their own methods for Boc cleavage. Overly aggressive acid can not only strip the Boc but also start reducing the cyclohexane ring itself, especially under heat. We’ve seen cleaner results from slow titration at controlled temperature, and some industrial users pre-test small aliquots before scaling up for the first time on a campaign.

    Every lot ships with complete supporting documentation. Our approach is based on using every comment and complaint, not hiding it. Transparency not only limits surprises in scale-up and validation, but builds trust—customers know which risks are real and which have been engineered out by experience.

    Our Promise: Consistency Born from Direct Experience

    The ultimate value of trans-4-(Boc-aminomethyl)-cyclohexanemethanamine rests not just on molecular design but on the supplier’s discipline and history. Every drum and bottle we ship is the result of learned lessons in handling, filtering, packaging, and, above all, listening to real chemists and engineers at the bench. We know this molecule finds its way into sophisticated drug candidates as well as large-scale performance material applications—the uses are always evolving.

    By focusing narrowly on reliable isomer control, minimizing solvent residues, and tuning granulation and packaging for end-use ease, our operation has transformed this building block from an unpredictable specialty item into a dependable, always-available staple. With the pace of medicinal chemistry and new materials research, that is what matters most.

    Supply chain stability has become even more critical as research cycles shrink and manufacturing windows tighten. We watch closely for incoming feedstock disruptions and re-test key reagents between shipments. Foresight from previous shortages has pushed us to stock up to 12 months’ worth of protected amine intermediates, shielding our customers against the ripple effects of market volatility.

    We encourage open dialog from anyone considering trans-4-(Boc-aminomethyl)-cyclohexanemethanamine for their chemistry. Engineers, project leaders, and process gurus don’t just want a product—they want insight, reliability, and hands-on support. Our team remains ready to share practical knowledge from the manufacturing trenches, so each partnership gets the foundation it deserves.