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(+)-Cis-2-Benzylaminocyclohexanemethanol

    • Product Name (+)-Cis-2-Benzylaminocyclohexanemethanol
    • Alias JKL-1051
    • Einecs 611-394-4
    • 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

    281032

    Chemical Name (+)-Cis-2-Benzylaminocyclohexanemethanol
    Molecular Formula C14H21NO
    Molecular Weight 219.32 g/mol
    Cas Number 142877-62-9
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Optical Activity Chiral, (+)-enantiomer
    Stereochemistry Cis isomer
    Smiles OC1CCC[C@H](NCC2=CC=CC=C2)C1
    Inchi InChI=1S/C14H21NO/c16-14-8-4-5-12(9-14)15-10-13-6-2-1-3-7-13/h1-3,6-7,12,14-16H,4-5,8-10H2
    Storage Conditions Store at -20°C in a tightly sealed container

    As an accredited (+)-Cis-2-Benzylaminocyclohexanemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of (+)-Cis-2-Benzylaminocyclohexanemethanol is packaged in a sealed amber glass bottle with tamper-evident cap.
    Shipping (+)-Cis-2-Benzylaminocyclohexanemethanol is shipped in secure, sealed containers compliant with chemical transport regulations. Packaging ensures product stability and prevents contamination or leakage. The shipment includes proper labeling, safety documentation (SDS), and conforms to international standards for hazardous materials, ensuring safe and efficient delivery to the designated destination.
    Storage Store (+)-Cis-2-Benzylaminocyclohexanemethanol in a tightly sealed container, away from moisture, light, and incompatible substances such as strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area at room temperature, preferably in a chemical storage cabinet. Ensure proper labeling and follow local safety regulations for handling and disposal. Use personal protective equipment when handling the compound.
    Application of (+)-Cis-2-Benzylaminocyclohexanemethanol

    Applications of (+)-Cis-2-Benzylaminocyclohexanemethanol in Industrial Manufacturing

    As a dedicated manufacturer, we supply (+)-Cis-2-Benzylaminocyclohexanemethanol to industries where precise chemical composition and manufacturing consistency are critical. Below, we detail the application landscape for this chiral intermediate based on current real-world downstream uses in specialty chemicals, pharmaceuticals, and advanced material synthesis. Each section highlights industry standards, recommended dosage ranges, process integration nodes, and final market products.

    1. Pharmaceutical Chiral Intermediate for Neuroactive Compounds

    Our material serves as a key chiral intermediate in the synthesis of select CNS-active pharmaceutical ingredients, where enantiopurity directly impacts downstream pharmacological profiles. Medicinal chemistry teams integrate this compound within asymmetric hydrogenation and reductive amination protocols to build complex frameworks for psychoactive agents and anti-depressant drug candidates. We maintain strict chiral integrity from batch to batch, supporting API manufacturers who require consistency for regulatory filings and GMP production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <795> and <797> for compounding quality
    • Ph. Eur. monographs for chiral intermediates
    • FDA 21 CFR Part 211 for finished pharmaceuticals traceability

    Typical usage ratio

    • Annualized process campaigns usually specify 1.1–1.5 molar equivalents per target API batch, with adjustment based on yield studies and chiral purity retention requirements.

    Downstream process integration

    • Introduced following Grignard addition to construct the cyclohexane scaffold.
    • Participates in multistep synthesis starting from the amidation or reductive amination stage, depending on route.
    • Chiral resolving agents or auxiliary components co-react in parallel for enantiopurity validation.
    • Aqueous workup, chromatography, and crystallization steps follow for final API isolation.

    Final product types

    • Chiral CNS-active pharmaceutical intermediates
    • Enantiomerically pure building blocks for anti-depressants
    • Specialty APIs for clinical development
    • Reference standards for pharmacological assays

    2. Intermediate for Piperidine-Based Fine Chemicals

    This compound functions as a synthetically valuable intermediate in constructing substituted piperidine rings, necessary for a range of fine chemicals, including performance additives and specialty flavor precursors. Chemists leverage the chiral center to introduce controlled stereochemistry, a requirement for downstream processes where regio- and stereo-selectivity affect final product functionality, especially in fragrance or specialty additive industries.

    Industry compliance standards

    • REACH (EC 1907/2006) registration for specialty chemical handling in Europe
    • ISO 9001:2015 for process quality assurance
    • IFRA Standards for fragrance intermediate purity
    • FEMA GRAS status for relevant flavor intermediates

    Typical usage ratio

    • Stoichiometric: Precise 1:1 molar input relative to ring-closing reactants; excess may be applied (up to 10%) in pilot scale to ensure complete conversion where selectivity is prioritized.

    Downstream process integration

    • Direct amination or cyclization after introduction to the base-catalyzed reaction;
    • Undergoes batch reactor input during piperidine core construction;
    • Intermediate purification steps including distillation and recrystallization to avoid racemization;
    • Final output proceeds to alkylation, acylation, or further modification depending on end-use.

    Final product types

    • Piperidine-based flavor and fragrance agents
    • Specialty pharmaceutical intermediates
    • Functional chemical additives for plastics or coatings
    • Custom intermediates for contract synthesis

    3. API Intermediate for Antihypertensive Drug Synthesis

    The raw material is routinely selected by large-volume pharmaceutical manufacturers working on high-purity intermediates for certain antihypertensive APIs based on its unique amino alcohol backbone. Technical teams rely on its stereochemical fidelity during step-growth synthesis, where improper isomer ratios can compromise downstream batch rejection rates. Intermediate processing involves multi-kilo reactors with real-time optical rotation and HPLC checks to maintain required chiral specifications during scale-up.

    Industry compliance standards

    • EU GMP Guidelines (EudraLex Vol 4 Part II) for API intermediates
    • ISO 13485:2016 for pharmaceutical quality systems (where applicable)
    • Chinese Pharmacopoeia API standard (ChP, current edition)
    • FDA DMF (Drug Master File) reference support

    Typical usage ratio

    • Process-controlled feed at 0.95–1.2 equivalents per batch, titrated depending on scale and target purity; adjusted for batch-to-batch yield consistency, monitored by in-process QC.

    Downstream process integration

    • Enters as an advanced intermediate after initial aromatic ring modifications;
    • Addition to reductive amination or chiral resolution setups;
    • Isolated via solvent extraction then submitted to carbonate or sulfonate derivatization, depending on the target NCEs (new chemical entities);
    • Subject to inline optical and chromatographic purity checks post-reaction.

    Final product types

    • Sartans and related antihypertensive APIs
    • Intermediate stock for generic drug libraries
    • Precursor for clinical and tox batch lots
    • Characterized samples for regulatory submission

    4. Building Block in Chiral Ligand Synthesis for Catalysis

    High-throughput screening labs and industrial catalyst producers specify this raw material in custom chiral ligand synthesis, focused on assembling new-generation asymmetric catalysts. Precision control of the cyclohexane scaffold and benzylamino functionalization directly dictates ligand folding and, ultimately, catalytic performance in enantioselective hydrogenation, C–C coupling, and transfer hydrogenation processes. The raw material's reproducible purity supports research-to-pilot translation without introducing additional enantiomer separation steps.

    Industry compliance standards

    • ISO 17025:2017 for process chemical purity verification
    • Responsible Care® for catalyst material handling and effluent management
    • OECD Good Laboratory Practice (GLP) for catalyst validation studies
    • Patent-specific documentation for research and scale-up

    Typical usage ratio

    • Typically charged at exactly 1.0 molar equivalent per ligand synthesis, modified only if parallel-arm structures are synthesized; custom ligand projects may increase ratio to accommodate side-reactions or imine formation efficiency studies.

    Downstream process integration

    • Input for the first condensation reaction with chiral acids or phosphines;
    • Sequential addition to multinuclear metal complexes during catalyst motif assembly;
    • Undergoes swing-purification followed by direct QC by NMR and mass spectrometry;
    • Supports direct formulation of new chiral catalyst batches for pilot or commercial manufacturing.

    Final product types

    • Chiral ligands for industrial asymmetric catalysis
    • Specialty catalyst kits for pharmaceutical synthesis
    • Custom ligands for academic and industrial research
    • Catalyst libraries for HTE/Regulatory submission
    Free Quote

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    Certification & Compliance
    More Introduction

    (+)-Cis-2-Benzylaminocyclohexanemethanol: Leveraging Experience in Fine Chemical Production

    A manufacturer’s relationship with chemical products often starts with a problem to solve—pure, reliable intermediates that support drug discovery or advance new synthetic methods. In the world of chiral cyclohexane derivatives, (+)-Cis-2-Benzylaminocyclohexanemethanol stands out for hands-on reasons. Years spent building the synthesis, tweaking purification, and tracking what this molecule brings to downstream chemistry have taught us its value. Technical teams in our shop know its quirks as intimately as their own equipment; that makes a difference for researchers at the bench.

    Understanding the Model and Production Approach

    For (+)-Cis-2-Benzylaminocyclohexanemethanol, model numbers or codes serve as bookmarks in our records, linking to real batch histories. Crafting this compound starts with our experience managing stereoselective synthesis. A controlled, stepwise addition yields the cis-stereochemistry that chemists demand. Every purification batch provides a lesson: column loads, solvents, temperature fluctuations, and resolving power all leave fingerprints. A single deviation in enantiopurity or minor impurity affects the downstream reliability for customers. Reproducibility is not a luxury. It hinges on consistent raw materials, thorough in-process controls, and the team’s attention. Over the years, we dropped old catalysts in favor of ones that boost selectivity and save energy during work-up. Customers who need grams, multikilograms, or development batches have seen these optimizations make a difference in turnaround and quality.

    Why Chemists Return to This Building Block

    In practice, this cyclohexanemethanol derivative supports medicinal chemistry projects that need a chiral amine and secondary alcohol together in a rigid framework. Its benzylamino group positions it uniquely for further derivatization. Our clients use it to access custom pharmaceutical leads, probe structure–activity relationships, or craft designer catalysts. Running the synthesis ourselves means hearing regularly from users—sometimes with complaints, often with creative suggestions. Some folks struggled with off-odor or color in older lots; we solved those by polishing the crystallization solvent system, leading to a whiter, cleaner product with higher chemoselectivity for their next step.

    Reaction repeatability is critical. Throughout hundreds of batches, we’ve measured chiral purity and analyzed impurity profiles ourselves. The feedback loop from researchers’ analytics comes straight through our doors: an unexpected side-product, a faint off-ratio on an NMR, or a shift in melting point gets investigated right away. Chiral HPLC, optical rotation, and GC all play supporting roles—not just in meeting the release criteria but in signaling trends that help us refine upstream steps. Compared to similar products with looser tolerances, ours reduces the risk of sequence failure.

    Specifications Informed by Real-World Use

    Customers who depend on (+)-Cis-2-Benzylaminocyclohexanemethanol value reliability over paper specs. Physical form — a white to off-white crystalline solid in most lots — makes measuring straightforward and minimizes wasting precious stock. Moisture content, residual solvent, and chiral purity matter most to the next synthetic step. Working with drug innovators showed us how even small solvent residues can throw off downstream reactions or crystallizations, so we fine-tuned our drying cycles to beat standard thresholds.

    Long-term partners tell us fluctuations in assay or optical rotation influence their reaction set-ups. For this reason, every batch is made with strict adherence to a tolerance that matches the most demanding applications. We do not try to push arbitrary analytical numbers to inflate a specification sheet; instead, we focus on delivering real, batch-to-batch consistency that saves our clients resource-draining rework. Those who have worked with generic, unbranded sources in the past often tell us our product provides more confidence and fewer surprises.

    What Sets Our Material Apart

    Some buyers make decisions based on catalog copy, chasing the cheapest price or fastest turnaround. We didn’t build our product line around speed or discounts. Instead, we doubled down on close collaboration and batch-by-batch process verification. Unlike materials from anonymous brokers or poorly tracked imports, every lot comes with full traceability and in-house documentation. Our operators personally review and sign off on each shipment—the difference shows up in the small details, such as more predictable response in pilot scale reactions.

    Key differences separate our (+)-Cis-2-Benzylaminocyclohexanemethanol from generic alternatives: we control chirality at each stage, avoid contamination from catalysts or foreign residues, and work closely with customers’ technical staff to address their needs. Over the years, we’ve fielded questions about off-target isomer formation or how to recover yield after handling errors—the fact is, our technical support comes backed by direct process knowledge, not reading off a data sheet. This hands-on approach tightens the user experience. When new analytical requirements emerge, such as strict nitrosamine scrutiny, we adapt our controls and processes to keep ahead of emerging standards.

    Applications Seen in Real Projects

    The world of fine chemicals rarely stands still. Customers bring our (+)-Cis-2-Benzylaminocyclohexanemethanol into the lab for many reasons: starting-point for chiral ligands, preparing analogues for neurological research, exploring asymmetric catalysis, or feeding into patented synthesis routes. It spares them the headaches of isomeric confusion that crop up with loosely controlled precursors. Where one researcher uses it as a key chiral pool for an oxazolidinone, another might elaborate it into a new antiviral lead. We’ve collected many field reports of successful routes that depend on batch purity and physical consistency.

    Several biotechs and formulation labs mentioned the hassle of chromatography clean-up diminishing when switching to our product—less struggle with unwanted by-products, better integration with automated liquid handlers, more repeatable downstream transformations. This feedback shaped our internal criteria and batch release strategy. We see a lively give-and-take between innovation in user labs and process refinement in our own facilities.

    The Role of Consistency in Advanced Synthesis

    Chemical manufacturing is sometimes seen as simple repetition, but anyone troubleshooting a failed synthesis knows small differences in intermediate purity or solvent profile derail projects. Lab notebooks in our facility bear the history of changes: batches where concentrations drifted, lots where reaction times shifted, days when glassware or air exposure left a trace. Learning these lessons led to robust scale-up protocols and cleaner, more reliable finished product.

    Consistency pays off most in longer synthetic routes, where the wrong isomer load in a critical step means worthless product ten or twelve transformations later. Our clients express relief when their analytics bear out lot-to-lot reliability over years. Some have asked us to retain reference samples from specific lots, allowing them to revisit a successful screening hit months later and confirm root causes of changes—this continuity would be hard to guarantee with a pure distribution house or recataloged imports.

    Supporting Regulatory Pathways and Documentation

    Drug development teams and regulatory groups have special needs around chemical building blocks. We have written support for known impurity profiles, complete disclosure of synthetic routes, and documented audit trails going back well over a decade. Sometimes, long conversations with quality assurance specialists lead to subtle tweaks in batch labelling, secondary verification, or reserve sample protocols. Our background in supporting INDs and NDA filings means the paperwork is in place for pharmaceutical clients, but we do not rely on generic assurances or boilerplate texts.

    Being the actual producer, not a distributor, enables precise recall capability and rapid documentation delivery. Over the years, sponsors have appreciated having prompt access to historical batch analytics or clear, annotated chromatograms to support a regulatory query or CMC update. Leaning into transparency helped earn trust during inspections and technical audits, especially as international standards shift. For advanced materials like this, deep process visibility is not just a selling point—it’s the price of entry to the next generation of research.

    Problems Solved by Direct Manufacturer Involvement

    Having run into plenty of technical roadblocks ourselves, we know many ways intermediates can go wrong: batch-to-batch drift, accidental contamination, improper storage, transit heat spikes, even container leaching. Handling these variables calls for hands-on process engineering and continuous learning. In early years of manufacturing (+)-Cis-2-Benzylaminocyclohexanemethanol, storage temperature and container compatibility made a substantial difference; we have since moved to higher barrier packaging and track warehouse conditions down to the pallet.

    Working alongside scale-up chemists helps close the gap between pilot and production, letting us intervene rapidly when unexpected crystallization behavior or polymorph appearance emerges. Customers know exactly whom to reach for troubleshooting—they are not routed through anonymous call centers or sales reps with only PDF fact sheets. Dialogue with life science teams turned up points we had overlooked, such as optimal grind size for solid dispensing robots or the impact of microimpurities on diagnostic test stability. Each feedback loop brings process improvements we carry forward into each lot.

    Learning from User Challenges and Collaborations

    Honest mistakes, successful scale-ups, and twists of fate in synthetic campaigns all feed back into our operations. A recent case involved a customer attempting a hydrogenation step that repeatedly failed until they realized a trace metal content from an earlier batch had built up over time. Reverse engineering the culprit with their organic team, we tightened metal controls, adjusted internal cleaning protocols, and solved their bottleneck. Experiences like this keep us grounded in the daily realities chemists face.

    Every so often, a pharmaceutical customer approaches with a modified use scenario—solid-phase synthesis, for example, or a need for extra documentation to pass muster with new international guidelines. These conversations have expanded our understanding and improved our flexibility and documentation rigor. Custom batch sizing, specialized packaging, and expanded analytical panels came straight from genuine field needs.

    What We Hear from Users in the Lab

    Open channels with research chemists, process scale-up teams, and pilot plant managers have shaped our manufacturing philosophy. Users report fewer purification headaches and better batch recoveries compared to bulk-sourced material. Some commented that early-stage drug discovery projects run better with consistent chiral purity—especially under harsh or time-pressured deadlines. Scientists in crowded start-ups and university labs have remarked on easier project hand-offs, thanks to knowing the next shipment will meet the same tight specs as last time.

    Process engineers and purification teams noticed a reduction in baseline drift during LC-MS and cleaner baselines on NMR. These gains seem small, but for multi-step synthesis, time saved distinguishing genuine signal from impurity pays big dividends. As labs shift more toward automation and digital recordkeeping, traceable, reproducible intermediates become even more valuable. Our call logs show customer satisfaction improves when hands-on support comes directly from the folks who manufactured the lot, not a third-party warehouse with no process record.

    Staying Ready for the Next Challenge

    The market for advanced chiral amines and alcohols keeps evolving. Real-world synthesis routines do not always match textbook chemistry. Clients encounter new hurdles in purification, equipment breakdowns mid-run, or regulatory requirements surfacing faster than the papers are published. Our direct involvement in every stage, from raw material sourcing to final shipment, positions us to adapt quickly. When a new regulatory flag appears—like emerging restrictions on potentially genotoxic impurities—we implement screening at the manufacturer level rather than waiting for third-party requests.

    In-house investment in purification equipment produces dividends when tight physical form controls or customized sizes matter. We are not immune to supply chain shocks or global logistics snarls, but direct production means greater flexibility in switching to alternative feedstocks, ramping up capacity, or bridging technical gaps that traders often cannot manage. Customers who stick with us through several cycles learn to expect this attention to detail, and it has developed into long-term loyalty measured in repeat projects and referrals, not just single batch sales.

    Walking the Path with Innovators

    We draw on decades of production learning and user feedback with (+)-Cis-2-Benzylaminocyclohexanemethanol, supporting hands-on research, scale-up work, and regulatory filings. Every shipment represents decisions made about synthesis, handling, testing, and packaging. Feedback from scientists and engineers in the field directly upgrades our approach—lessons about shelf life, reaction selectivity, and ease of use. Over time, this practical focus shapes the product in ways that standard catalog chemicals do not match.

    Whether batches flow into new medicinal chemistry scaffolds or support regulatory-compliant manufacturing, we keep our priorities tuned to laboratory results and industrial scale realities. Differences between vendors fade in the face of clean analytics, clear documentation, reliable process support, and human relationships. Real-world chemistry rarely follows a script, so direct manufacturer involvement pays off again and again—solving actual problems, not just checking boxes on a list.