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Boc-Trans-4-Aminocyclohexanol

    • Product Name Boc-Trans-4-Aminocyclohexanol
    • Alias Boc-4-ACH
    • Einecs 682798-89-6
    • 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

    215036

    Product Name Boc-Trans-4-Aminocyclohexanol
    Synonyms tert-Butoxycarbonyl-trans-4-aminocyclohexanol
    Molecular Formula C11H21NO3
    Molecular Weight 215.29
    Cas Number 112674-42-3
    Appearance White to off-white solid
    Purity Typically ≥ 98%
    Melting Point 90-94°C
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Solubility Soluble in DMSO, Methanol, and partially in water
    Optical Activity Typically supplied as racemic (±) mixture
    Smiles CC(C)(C)OC(=O)N[C@@H]1CCC(CC1)O

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

    Packing & Storage
    Packing Boc-Trans-4-Aminocyclohexanol is packaged in a 25g amber glass bottle with a secure screw cap and clear labeling.
    Shipping **Shipping for Boc-Trans-4-Aminocyclohexanol:** This chemical is shipped in tightly sealed, inert containers to protect from moisture and contamination. It is typically transported under ambient conditions, but should be kept cool and dry. Ensure compliance with relevant chemical handling and shipping regulations; consult the Safety Data Sheet (SDS) for detailed guidance.
    Storage Boc-Trans-4-Aminocyclohexanol should be stored in a tightly sealed container, protected from moisture and light, at 2–8°C (refrigerator). Keep in a cool, dry, well-ventilated area, away from incompatible substances such as strong acids and oxidizing agents. Proper storage maintains compound stability and prevents degradation. Clearly label the container and handle with appropriate personal protective equipment (PPE).
    Application of Boc-Trans-4-Aminocyclohexanol

    Applications of Boc-Trans-4-Aminocyclohexanol in Industrial Manufacturing

    Boc-Trans-4-Aminocyclohexanol finds specialized use in advanced chemical synthesis, offering reliable functional group protection and structural versatility. As a manufacturer with significant process know-how, we support industries with high regulatory demands and documented process control. Below are real downstream segments where our production material proves essential, with detailed compliance, formulation, process, and product information for each application.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical companies use this compound as a key intermediate for synthesizing chiral piperidine and cyclohexanol-based APIs. The protected amino alcohol group ensures selectivity in multi-step syntheses, enabling precise regioisomeric control demanded in modern drug development. Facilities integrate our material at nucleophilic substitution or reductive amination stages, with real-time monitoring via HPLC and NMR to ensure purity according to batch release standards.

    Industry compliance standards

    • EU GMP (EudraLex Volume 4, Part I and II)
    • US FDA 21 CFR Part 210/211
    • ICH Q7 for API production
    • Relevant USP or Ph. Eur. monographs for intermediates

    Typical usage ratio

    • 30–50 mol% relative to the target core during key intermediate steps
    • Ratios adjusted based on chiral purity requirements and final API yield targets

    Downstream process integration

    • Integration at initial amination or protection steps in API synthesis
    • Removal of Boc group during late-stage deprotection prior to final ring closure or coupling reaction
    • Process guided by validated cleaning and in-process analytical protocols

    Final product types

    • Chiral antihypertensive agents (e.g., selective beta-blockers)
    • Antiviral drug intermediates
    • CNS-active pharmaceutical intermediates
    • Custom-developed clinical trial compounds

    2. Peptide Synthesis for Research and Therapeutics

    Peptide manufacturers utilize this amino alcohol for site-specific incorporation and modification in peptide chains. Its Boc-protection enhances orthogonal protection strategies, reducing byproduct formation during solid-phase peptide synthesis (SPPS). The crystalline structure allows for high solubility and low racemization risk, especially when combined with Fmoc chemistry protocols.

    Industry compliance standards

    • ICH Q11 for drug substance synthesis
    • ISO 9001:2015 certified QC protocols
    • GMP Annex 1 for peptide manufacturing
    • Synthetic peptide compendia requirements

    Typical usage ratio

    • 1 equivalent per protected residue site
    • Typical ranges: 0.9–1.2 equivalents, depending on sequence length and resin loading

    Downstream process integration

    • Boc-group addition in the initial protection phase for cyclic or branched peptide targets
    • Stepwise coupling and deprotection cycles under inert atmosphere conditions
    • Integrated with automated SPPS equipment and in-line mass spectrometry checks

    Final product types

    • Therapeutic peptides for metabolic diseases
    • Peptide-based drug candidates for oncology
    • Research-grade oligopeptides for academic institutions
    • Peptide APIs for clinical batch supply

    3. Custom Synthesis of Analytical Reference Standards

    Chemical analysis laboratories and standards manufacturers require high-purity reference compounds containing defined stereochemical centers. Here, the protected aminocyclohexanol supports precise configurational synthesis, allowing traceable production of calibration substances for regulatory or forensic labs. We provide lot-specific documentation and route-of-synthesis transparency, which are critical for regulatory submissions.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation
    • Ph. Eur. Chapter 5.12 for reference standards
    • US EPA protocols for environmental standards traceability
    • ISO Guide 34 for reference material producers

    Typical usage ratio

    • Stoichiometric to target analyte, typically 1:1
    • Mass adjusted according to analytical purity and reference requirements

    Downstream process integration

    • Introduction during the stereoselective synthesis step of reference compound assembly
    • Boc-protection maintained until purification is complete
    • Cleavage and final formulation under strict cleanroom and documentation conditions

    Final product types

    • Stereo-defined analytical standards for pharma QC labs
    • Certified reference materials for regulatory agencies
    • Traceable isotope standards for environmental analysis
    • Internal standards for forensic toxicology labs

    4. Chiral Ligand and Catalyst Synthesis in Fine Chemical Production

    Fine chemical producers implement this raw material as a building block to generate chiral ligands and catalysts for enantioselective hydrogenation or asymmetric synthesis. Its molecular structure enables robust covalent attachment to backbone scaffolds, resulting in high-yield ligand production after targeted deprotection and functionalization. Full batch records and origin traceability are provided to meet downstream audit requirements.

    Industry compliance standards

    • Responsible Care® chemical management principles
    • REACH registration for processing aids
    • ISO 14001 for environmental management in catalyst production
    • Internal quality audits aligned with OECD GLP for catalyst development

    Typical usage ratio

    • 5–20 mol% relative to main ligand scaffold
    • Tuning based on required enantioselectivity and downstream transformation efficiency

    Downstream process integration

    • Coupling during initial ligand assembly under anhydrous conditions
    • Boc removal following completion of backbone modifications
    • Ligand screening with transition metals using high-throughput reactors

    Final product types

    • Enantioselective hydrogenation catalysts
    • Custom chiral ligands for metal-catalyzed reactions
    • Process development tools for agrochemical production
    • Research grade catalysts for contract synthesis labs

    5. Synthesis of Protected Cyclohexanol Derivatives for Agrochemical R&D

    Agrochemical research groups employ protected aminocyclohexanol derivatives during early-stage synthesis and lead optimization of pesticide and herbicide candidates. The Boc group enables selective manipulation of secondary amine and hydroxyl positions before scaffold diversification, supporting high-throughput discovery under regulated pilot-scale conditions. Our material batches include detailed impurity profiles for downstream risk assessment.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO guidelines for agrochemical development
    • Chemical notification regulations (e.g., EU REACH, US TSCA)
    • ISO 9001:2015 process management systems

    Typical usage ratio

    • 10–30 mol% relative to target scaffold during model compound synthesis
    • Adjusted based on reaction scale and structural diversity goals

    Downstream process integration

    • Boc-group incorporation at initial protection stage to prevent side-reactions
    • Subsequent ring modification and functionalization for compound library expansion
    • Pilot-scale validation with parallel purification and analytical testing

    Final product types

    • Lead candidates for crop protection agents
    • Model compounds for herbicide screening
    • Reference substances for registration dossiers
    • Protected intermediates for downstream agrochemical synthesis
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    Certification & Compliance
    More Introduction

    Boc-Trans-4-Aminocyclohexanol: A Closer Look from the Manufacturer’s Viewpoint

    Meeting the Demands of Modern Synthesis

    Manufacturing Boc-Trans-4-Aminocyclohexanol every day gives a unique perspective on its value in research and production settings. Familiarity comes not just from handling large batches, but from seeing how consistently it delivers in rigorous laboratory and industrial processes. With ongoing demand from pharmaceutical synthesis and custom chemical projects, our focus remains on reliable consistency, high purity, and tight control over byproducts.

    Chemists rely on this molecule for its role as a building block in peptide chemistry, small-molecule drug design, and bespoke intermediates. The presence of both the tert-butyloxycarbonyl (Boc) protecting group and the trans-4-amino-cyclohexanol core structure allows it to slot efficiently into multi-step processes. Different research teams have their preferences for specific stereochemistry or protecting groups, but the trans configuration paired with Boc offers an unusual blend of stability and reactivity. There’s never a shortage of requests for this product in both R&D and scale-up environments.

    Specifications and Manufacturing Practices

    From the manufacturer's bench, purity rates dominate internal discussions far more than abstract numbers on a data sheet. Our typical batches exceed 98 percent purity, judged by HPLC and NMR, because even minor contamination affects downstream reactions. The most common model we produce falls in the 25kg lot size, targeting the needs of mid-scale pharmaceutical development, but smaller and larger requests come in as scientists move between benchwork and pilot-plant regimes.

    Moisture content and residual solvent monitoring become routine checkpoints. Tight control on solvents, whether ethanol or ethyl acetate, prevents complications in both crystallization and purification steps. Our dedicated isolation areas, monitored for cross-contamination, reflect lessons learned years ago—small changes in humidity and storage temperature can alter stability and shelf-life. We never ignore seemingly ‘small’ variables, knowing their direct impact on reproducibility for our customers.

    Role in Peptide Chemistry and Intermediate Synthesis

    Feedback from our partners reveals that Boc-Trans-4-Aminocyclohexanol shines in the protection of amino groups during solid-phase peptide synthesis. Its tert-butyl carbamate shield withstands the conditions commonly used during chain elongation, and gentle removal at the right phase helps chemists avoid racemization or byproduct formation. Across dozens of runs observed in our facility, we’ve noticed it offers cleaner deprotection profiles than more volatile alternatives. For manufacturers, this means fewer purification headaches and faster cycle times.

    Companies synthesizing chiral intermediates for active pharmaceutical ingredients point out the importance of reliable trans configuration every shipment. The stereochemistry impacts bioactivity, so strict controls on optical purity are non-negotiable. Our experience with chromatography, solid-phase extraction, and crystallization optimization produces an enantiomerically enriched material every batch. Continuous improvement often comes from real feedback — catching small shifts in rotatory power or identifying unexpected side products well before the molecule lands in a customer’s flask.

    Comparing Boc-Trans-4-Aminocyclohexanol with Related Compounds

    Chemists often debate the merits of Boc, Fmoc, or Cbz protection. We manufacture alternatives alongside Boc-Trans-4-Aminocyclohexanol, so we see firsthand how switching between these changes handling, storage, and yield. Boc groups stand up to basic conditions, resisting cleavage until exposed to strong acid or specialized reagents, unlike Fmoc-protected analogues that often fall apart under UV or mild base. Cbz options avoid some impurity issues, but usually require harsher deprotection, upping risks for sensitive intermediates. For trans-4-aminocyclohexanol derivatives, Boc protection gives a balance between safeguarding against side reactions and releasing under controlled acidic cleavage.

    Differences don’t stop at protecting groups. We also handle cis-isomers—these differ in reactivity, solubility, and downstream compatibility. Our teams routinely compare crystallization behavior and solvent affinity for each isomer, looking for tweaks in cooling profiles and storage conditions. The trans form’s popularity derives not just from chemical theory, but from actual experience in column loading, chromatographic separation, and scale-up crystallization. Companies running multi-kilo campaigns highlight faster throughput and lower solvent consumption with the trans Boc derivative versus cis analogues. That means real cost reductions, fewer batch failures, and happier project managers.

    Addressing Real-World Manufacturing Challenges

    Every manufacturer faces surprises—a tendency for Boc deprotection to give off-colors, or the annoyance of birefringent contaminants hiding in a batch. Over the years, we’ve invested in inline monitoring, LC-MS for spot-checking, and continual operator training to catch these moments before they reach the customer. Attention to these setbacks leads directly to process improvements, fewer customer complaints, and a tighter operation overall.

    Raw material sourcing remains one of the more daunting hurdles. Global supply chains, as witnessed in recent years, swing in both price and availability. Reliable sourcing of cyclohexanol, isobutylene, and phosgene substitutes for carbamate formation requires constant vigilance. We make it a routine to audit suppliers, cross-examine certificates of analysis, and run random in-house verifications. If a lot enters our plant out of spec, rework or outright rejection happens immediately, because an impure starting material always comes back to haunt the final product’s stability and downstream compatibility.

    Ongoing Responsibility: Worker Safety and Environmental Impact

    Growth brings with it fresh responsibility—more workers in contact with reagents, and more chemical waste to manage. Our teams never compromise on personal protective equipment, ventilation, and spill response, especially during bulk Boc protection reactions where exothermic surges can surprise even experienced hands. Proper glove selection, downtime for fume hood maintenance, and rapid access to MSDS information remain standard here, not ‘best practices’ relegated to company slogans.

    Solvent recycling takes priority not just for cost, but for environmental stewardship. Our in-house systems capture, purify, and re-use solvents, reducing the draw from new supplies while keeping emissions in check. Regular audits confirm effluent streams meet or beat local regulations. These steps became standard after much trial and error—leak events, stack emission spikes, and near-misses all left hard lessons. Our practical approach comes from seeing what’s at stake, both for our staff and for the world outside the factory.

    Customer Partnerships and Collaborative Improvements

    Many of our best process upgrades originated from customer labs, not internal brainstorming. One pharmaceutical group’s insight on improved solvent mixes for recrystallization led us to test their method on larger scales—yield jumped, purity climbed, labor hours fell. Back-and-forth conversations about shipment packaging (vacuum-sealed, light-blocking materials, and smaller drummed lots) allowed our product to slot more seamlessly into automated dispensing systems at contract research organizations. We hone our approach not in isolation, but by keeping phones open to the people handling our compounds every day.

    Several research partners pointed out discrepancies in physical form—one year our crystals skewed toward a denser, less free-flowing habit, which slowed their dispensing robot. We responded by refining cooling profiles, altering seeding regimes, and standardizing particle size targets. Results showed up in fewer caking complaints and easier unloading. Direct, honest feedback from knowledgeable end-users drives more product improvement than any amount of form-filling or theoretical debate.

    Documentation and Transparency in Quality Assurance

    Quality control hinges not just on equipment or procedures, but on recordkeeping and transparency. Our practice has evolved to include robust tracking of every batch—raw materials, process notes, operator sign-offs, and rigour in final certificate of analysis generation. Day-to-day, we pull sample vials from previous lots for spot retesting, ensuring issues do not stay hidden in old paperwork.

    Customer audits pose stress tests for these systems. Requests for backup data, spectral traces, or more granular impurity breakdowns have become regular. A refusal to fudge figures or gloss over batch anomalies wins more trust than desperation to please on a single order. We notice that customers with their own rigid compliance regimes sense this difference—returns and disputes dwindle, repeat business climbs, and we earn more room to innovate on the next process tweak.

    Trends and Industry Evolution

    The push for greener chemistry and streamlined synthetic routes reverberates through our daily work. Late-stage functionalizations, hydrogen borrowing techniques, or use of alternative protecting groups push us to rethink traditional processes. Offering Boc-Trans-4-Aminocyclohexanol at scale means ongoing development in catalyst recovery, solvent selection, and waste minimization. We step carefully, since the market’s appreciation of sustainability comes with stricter documentation expectations.

    With regulations growing tighter year on year—both for chemical safety and environmental reporting—our attention doubles on maintaining compliance. REACH, TSCA, Japanese CSCL, and related frameworks guide our internal policies. Updates affect sourcing (especially for minor impurities or reagent carryover), shipping, and labeling. Experience shows a prepared, proactive response works better than reacting to a compliance warning after the fact.

    Responding to Supply Chain Disruptions

    Disruptions ripple across the industry, whether from logistics bottlenecks, geopolitical stress, transportation mishaps, or sudden demand swings. Our longstanding relationships with suppliers offer a certain buffer, but we place redundancy at the core of procurement. Alternative sources for common feedstocks, backup storage of critical intermediates, and advance engagement with shipping partners all come directly from lessons learned in past crunches. We have lived through enough price spikes and customs hold-ups to know preparation is the only safety net that matters.

    Finished product logistics now receives as much attention as synthesis itself. Stability during transit—temperature swings, vibration, and time in customs warehouses—prompts us to invest in climate-controlled storage, continuous data loggers, and tracking. Our technical team coordinates directly with freight forwarders on every large shipment, sharing information about special temperature sensitivities or time-sensitive orders. This hands-on attention cuts down loss due to spoilage and allows us to deliver what chemists expect at their own benches.

    Research Support and Application Guidance

    As demand for Boc-Trans-4-Aminocyclohexanol widens, we increasingly field requests for application guidance—solubility data in obscure solvents, compatibility with novel coupling reagents, or custom impurity profiling. Our technical team draws on years in the lab. Practical knowledge of how the compound behaves in water, DCM, DMF, or ether—what temperatures promote crystallization, which acids remove the Boc cleanly—anchors our technical support. Application notes and tailored support reach not only large multinational pharmas, but smaller, agile startups looking to get a new drug candidate advanced quickly.

    Specific questions come up frequently—does your Boc-Trans-4-Aminocyclohexanol tolerate hydrogenation catalysts, can it withstand specific peptide coupling conditions, or how does storage at sub-zero temperatures affect its shelf life? Our answers improve with each new challenge. Direct feedback and data sharing between customer labs and our technical team drive cumulative improvements, with each successful project refining our information pool—and occasionally suggesting a tweak for our own internal SOPs.

    Continuous Improvement and Looking Ahead

    Every year brings requests for new variants—novel protecting groups, altered stereochemistry, or higher purity thresholds. These challenges keep our production team sharp and our R&D chemists creative. Meeting stringent rez requirements for parenteral excipients or adapting to new synthetic methodologies doesn’t happen by reusing last year’s recipe. It calls for adaptability, quick learning, and a willingness to shake up standard routines.

    We know expectations will keep climbing: faster delivery, tighter specifications, cleaner documentation, and lower environmental impact. We welcome this direction, since every improvement on our line translates directly to fewer failures and bottlenecks in our partners’ discovery or production chains. Boc-Trans-4-Aminocyclohexanol earned its place in the toolkit through decades of feedback, hands-on refinement, and respect for the challenges our users face. The next evolution, whatever direction it takes, will be built by those who use it daily—guided by our willingness to listen, adapt, and deliver.