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L-Glutamic Acid 5-Cyclohexyl Ester

    • Product Name L-Glutamic Acid 5-Cyclohexyl Ester
    • Alias Ciglutaric acid
    • Einecs 629-835-7
    • 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

    670034

    Chemical Name L-Glutamic Acid 5-Cyclohexyl Ester
    Molecular Formula C11H19NO4
    Molecular Weight 229.28 g/mol
    Cas Number 80701-54-6
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Optical Activity L-isomer (specific rotation available upon request)
    Synonyms L-Glutamic acid 5-cyclohexyl ester; Cyclohexyl L-glutamate
    Usage Research, pharmaceutical intermediates

    As an accredited L-Glutamic Acid 5-Cyclohexyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing L-Glutamic Acid 5-Cyclohexyl Ester, 25g, is supplied in a sealed, amber glass bottle with tamper-evident cap and safety labeling.
    Shipping L-Glutamic Acid 5-Cyclohexyl Ester should be shipped in tightly sealed containers, protected from light and moisture. Transport under cool, dry conditions, using secondary containment to prevent leaks. Ensure compliance with all relevant chemical shipping regulations and provide appropriate hazard labeling and documentation. Handle with care to avoid breakage or spillage during transit.
    Storage L-Glutamic Acid 5-Cyclohexyl Ester should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible materials such as strong oxidizers. Protect from direct sunlight and sources of ignition. Recommended storage temperature is 2-8°C (refrigerated). Ensure that the storage area is clearly labeled and complies with appropriate chemical safety regulations.
    Application of L-Glutamic Acid 5-Cyclohexyl Ester

    Applications of L-Glutamic Acid 5-Cyclohexyl Ester in Industrial Manufacturing

    L-Glutamic Acid 5-Cyclohexyl Ester finds adoption in select industrial manufacturing processes where its unique structural properties support specialized chemical transformations or performance enhancement. As the original producer, we collaborate closely with downstream sectors to ensure compliant integration, consistent quality, and predictable outcomes. The following scenarios illustrate the core application domains currently sourcing this ester at scale.

    1. Chiral Intermediate Synthesis for Pharmaceutical APIs

    Leading pharmaceutical manufacturers utilize this compound as a chiral building block in the stereoselective synthesis of advanced intermediates. Its cyclohexyl-modified profile enables precise induction of desired spatial orientation during peptide coupling and heterocycle formation, forming an integral stage in development pipelines for certain CNS-active ingredients and next-generation peptide drugs. Integrating this ester in strategically designed reaction schemes allows direct advancement under GMP conditions.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP General Chapters for Chiral Purity Testing
    • EU EudraLex Volume 4 GMP Guidelines
    • FDA 21 CFR Part 211

    Typical usage ratio

    • Introduced at 1.8%–4.5% molar equivalent relative to the core amino acid sequence, optimized according to target chiral purity and downstream protection strategies

    Downstream process integration

    • Condensed into the synthetic sequence after initial amino acid activation, typically by carbodiimide coupling; enters main synthesis train early for efficient chiral center introduction; salt management and byproduct removal performed inline for high-yield output

    Final product types

    • Chiral pharmaceutical intermediates for CNS compounds
    • Peptide-based drug substance precursors
    • Amino acid derivatives for advanced research formulations

    2. Specialty Monomer Component in Functional Polyamide Production

    Chemical manufacturers leverage the cyclohexyl-functionalized glutamic acid ester as a modifier in advanced polyamide synthesis targeting high-performance engineering plastics. Its unique side-chain structure imparts altered crystallinity, mechanical flexibility, and thermal behaviour, supporting advances in electronic encapsulation, filtration membranes, and low-permeability packaging materials. Process control focuses on accurate dosing and validated reaction parameters to secure consistent chain distribution and property profiles in the resulting polymers.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for Manufacturing)
    • REACH Regulation (EC) No 1907/2006
    • ASTM D4066 (Polyamide Resin Classification)
    • RoHS Directive (EU 2015/863 for restricted substances in electronics)

    Typical usage ratio

    • Incorporated at 2%–6% w/w of total monomer load, proportion varies depending on targeted polyamide performance curves; adjusted in pilot scale trials to align with end-use durability and compliance requirements

    Downstream process integration

    • Dosed into melt-phase polymerization reactors immediately after feedstock pre-heating; degree of incorporation monitored in situ by NMR and melt viscosity tests; post-polymerization, the modified polyamide undergoes extrusion and pelletization for further fabrication

    Final product types

    • High-barrier polyamide films for food and industrial use
    • Dielectric encapsulation grades for electronic circuits
    • Structural engineering thermoplastics

    3. Peptide Coupling Auxiliary in Advanced Peptide Synthesis

    Contract peptide manufacturing and research labs use this chemical as a coupling auxiliary in the solid-phase synthesis of complex oligopeptides. It enhances selectivity and steric guidance during chain extension steps, particularly for introducing sterically hindered amino acids or cyclic side chain modifications. Precise feed control combined with analytical cycle monitoring ensures low racemization risk and consistent final sequence integrity for high-value custom peptides.

    Industry compliance standards

    • USP <797> (Pharmaceutical Compounding – Sterile Preparations)
    • ISO 13408 (Aseptic Processing of Health Care Products)
    • ICH Q11 (Development and Manufacture of Drug Substances)
    • Ph. Eur. Monograph 2034 (Peptide Active Substances)

    Typical usage ratio

    • Blended at 0.5%–2% relative to total amino acid content in the solid-phase reactor, with adjustments based on resin loading and targeted cycle efficiency

    Downstream process integration

    • Added at pre-coupling steps during Fmoc/t-Boc methodology; solvent compatibility and wash protocols validated for each batch; auxiliary residues eliminated during final cleavage and purification to prevent impurity carryover

    Final product types

    • Research grade oligopeptides
    • Pharmaceutical development peptides
    • Biologics building blocks

    4. Modifier in Biomedical Device Coatings

    Producers of specialized biomedical devices, such as implant coatings and tissue engineering scaffolds, incorporate this ester as a structural component in the modification of polymeric coatings for enhanced biocompatibility and tailored cellular response. The cyclic ester’s configuration supports controlled hydrolysis rates and cellular uptake modulation, relevant for medical environments where tissue integration and bio-inertness are strictly regulated. Strict production hygiene and traceability are mandatory throughout the process.

    Industry compliance standards

    • ISO 10993-1 (Biological Evaluation of Medical Devices)
    • ISO 13485:2016 (Medical Devices Quality Management)
    • US FDA 21 CFR 820 (Quality System Regulation for Devices)
    • USP Class VI Biological Reactivity Tests

    Typical usage ratio

    • Ranges from 1.2%–3% w/w in the total polymer blend, fine-tuned via in vitro testing to match targeted cell adhesion or growth profiles per device specification

    Downstream process integration

    • Integrated into polymeric coating baths pre-casting or pre-spray; in-line monitoring implemented for viscosity and homogeneity; applied by dip-coating, spray, or spin-coating depending on substrate geometry

    Final product types

    • Implant surface-modified components
    • Bioresorbable scaffold coatings
    • Hemocompatible stent surfaces

    5. Additive in Enzyme Stabilization Solutions

    Biotechnology and enzyme manufacturing facilities deploy this ester to enhance the stability and shelf-life of sensitive enzymes during liquid or lyophilized formulation. Its hydrophobic-cyclohexyl grouping reduces unwanted aggregation and provides a protective effect in complex protein mixtures used in diagnostics and industrial biotransformation. Adoption in this context involves tight quality metrics for purity, and formulation teams closely monitor storage performance.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • ICH Q6B (Specifications: Test Procedures and Acceptance Criteria for Biotechnological Products)
    • OECD Principles of Good Laboratory Practice
    • EP Monograph 1684 (Enzyme Preparations)

    Typical usage ratio

    • Added at 0.8%–2.5% in enzyme formulation buffers; optimized per enzyme class based on stability assays and long-term storage testing

    Downstream process integration

    • Included in blending tanks post-enzyme purification but prior to packaging; compatibility tested for each enzyme type; filtration employed to remove any insoluble aggregates prior to filling

    Final product types

    • Stabilized enzyme reagents for diagnostics
    • Industrial biocatalysts
    • Biotech process enzyme kits
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    Certification & Compliance
    More Introduction

    L-Glutamic Acid 5-Cyclohexyl Ester: Experience at the Source

    If you spend decades developing and refining amino acid derivatives, certain compounds naturally become part of daily conversations on the plant floor and in customer meetings. L-Glutamic Acid 5-Cyclohexyl Ester is one of those products that has steadily carved out its own space thanks to chemistry, customer push, and changing applications in both established and emerging industries.

    Understanding the Product from the Floor Up

    You can smell the difference in the plant. L-Glutamic Acid 5-Cyclohexyl Ester begins as high-purity L-glutamic acid reacting with cyclohexanol under precise controlled conditions. The esterification route we use creates a material with reliable structure, consistent reactivity, and little in the way of batch-to-batch drift. This specific compound goes by several shorthand models across markets, but we follow the structure C11H19NO4—each lot backed by actual chromatographic purity, DSC thermal data, and moisture verification at dispatch.

    Production quality relies as much on equipment as it does on the team. Skilled operators manage the pH, temperature, and catalyst load, guarding against side reactions with regular process controls, not just after-the-fact testing. Chemical fingerprints matter. So do small variations in solvent grade that outside descriptions gloss over. It's not magic, it's chemistry carried out by people who care about the result every single shift.

    Specs That Grow Out of Real Use Cases

    Early on, most partners in pharma and fine chemical operations expected to see narrow specs. We started at over 99% HPLC purity, water below 0.25%, and targeted a nearly colorless powder. Over the years, a few process tweaks let customers request material with especially low heavy metals or a particular enantiomeric excess. Sometimes we run custom drying to ensure less than 0.05% residual moisture—every measure coming from either feedback by real users downstream or from troubleshooting contamination risks together in multi-shift run-offs. That responsiveness pushes for tighter homogeneity. QC testing doesn’t end up on a worksheet; it shapes how we plan and execute.

    We don't churn out generic ester. Batches of L-Glutamic Acid 5-Cyclohexyl Ester get tailored for the application in mind: from specialty pharmaceutical intermediates to advanced polymerizations. It's the customer, not a specification sheet, who shows us the practical range needed. With decades of supply to both domestic and international manufacturers, specifications have matured alongside compliance demands—think ICH Q7, full traceability reports, and impurity mapping. Standard batches average between 10–100 kg to balance freshness and reduce need for storage that leads to hydrolysis or picking up odors from longer-worn containers.

    Where L-Glutamic Acid 5-Cyclohexyl Ester Works in the Real World

    This ester occupies a unique position between common glutamic acid derivatives and more niche protected amino acid compounds. Chemists began using it as a chiral synthon in solid-phase peptide synthesis, and its role has expanded as peptide and oligonucleotide work has reached new frontiers. The cyclohexyl ester protects the glutamate functionality during complex steps, offering a robust balance between hydrolytic stability and eventual ease of removal. Research groups say they appreciate that it resists base-catalyzed hydrolysis better than methyl or ethyl esters, but still deprotects under milder acidic or hydrogenation conditions. Those who scale up API intermediates in pharma tend to focus on high volume lot stability—supply gaps cause headaches, so synchronization between our plant schedule and their campaigns makes a real difference.

    Outside pharma, coatings and specialty polymer producers hunt for unique polyamides and as building blocks in hybrid resins. L-Glutamic Acid 5-Cyclohexyl Ester imparts the backbone with certain physical properties unavailable using smaller alkyl esters. Demand picks up whenever a customer needs glass transition temperatures dialed in without sacrificing processability. Research chemists credit this ester for pushing the limits of biodegradable plastics and advanced composites: stable enough for processing, reactive enough for downstream functionalization.

    A few flavors and food additive groups explored this ester, but stringent food regulatory barriers keep the main thrust in technical and scientific applications. Our experience confirms trace impurities impact flavor more in these systems than almost any other. We walk customers through GC-MS data, illustrating even minor byproducts that could taint sensitive end products. This level of technical engagement beats simply sending a product sheet—it’s direct, solution-driven chemical partnership.

    Practical Differences from Standard Glutamic Acid Esters

    To the untrained eye, a cyclohexyl ester and a methyl ester might look like minor variations. The truth runs deeper. As a manufacturer, you see it during synthesis, storage, and customer use. The cyclohexyl group increases steric hindrance. Chemically, this means the ester stands up to harsher pH swings before breaking apart, giving a wider margin during synthetic procedures. A methyl or ethyl ester hydrolyzes if storage temperatures spike or if residual moisture creeps up, but the cyclohexyl ester resists this kind of degradation, making inventory planning less nerve-wracking for end-users running multi-week campaigns.

    Operations teams who handle daily warehousing notice another point: less volatility and fewer odors. Methyl and ethyl esters often give off sharper smells, and those with sensitive lungs find cyclohexyl esters more comfortable to work around, especially in closed rooms. We took feedback from partners with older HVAC systems and optimized packaging to minimize fugitive emissions. The cyclohexyl ring’s bulk and weight limits volatility, a detail we tracked not by speculation but by repeated stickiness and residue patches on old warehouse shelves. Cleaning labor costs go down, not a line-item on many accounting sheets but a real-world benefit plant managers appreciate.

    Another key factor: solubility. Cyclohexyl esters bring altered polarity and bulk compared to smaller alkyl analogs. This skew affects choice of solvents. Experienced chemists take advantage of the selective solubility for targeted extractions and purifications—polar protic solvents grab methyl esters much quicker, while cyclohexyl esters favor less polar media. We get regular calls from PhD students puzzled by an extraction failure, only to resolve it quickly with a pragmatic solvent switch. Our lab staff document these tweaks and pass them along, forming a real knowledge base that beats website tables of numbers.

    We’ve seen pharmaceutical customers make the switch after noticing fewer side-products in downstream hydrogenolysis steps. Some thioester impurities that challenge methyl esters simply don’t form with the cyclohexyl variant, reducing the need for repeated reprocessing. That’s less solvent waste, lower costs, and tighter production schedules—all priorities better controlled with the right choice of starting material. This isn’t simply a desk-level insight; it emerges from real batch campaign data, week after week.

    Reliability and Knowledge: The Manufacturer’s Edge

    Market supply hiccups ripple through the industry with every new compliance update or force majeure. Factor in container shortages or regulatory bottlenecks, and customers want the security of provenance. As the manufacturer, we offer more than just consistent product: full traceability, direct access to the chemists behind the batches, and immediate technical support. Whenever a customer’s QA team faces a new regulatory change—REACH, updated SARA, or a new country-specific monograph—our regulatory staff provide real-time documentation, not forms sourced from a middleman. Data doesn’t get diluted by traders. If an impurity level crops up above an agreed threshold, we troubleshoot and address root causes within our own supply chain. Decades of regulatory audits, onsite inspections, and customer visits go into every kilo shipped out the door. We know which raw material sources held up best under Covid supply crunches, and which partners deliver on time, every time.

    Direct manufacturing experience helps us anticipate wear points. Our teams track equipment maintenance, downtime, and even utility performance, all factors that predict and prevent batch interruptions. This kind of vigilance matters, particularly for customers with tight delivery windows and zero tolerance for off-spec intermediates. The relationship doesn’t end at the shipping dock—ongoing technical feedback from clients feeds back into process improvements and training for future runs. We’re not just monitoring raw material costs or new market entries; we’re tweaking reactor parameters, reviewing chromatographic profiles, and running simulations to stay ahead of production headaches.

    Challenges and Honest Solutions

    No chemical line escapes challenges. L-Glutamic Acid 5-Cyclohexyl Ester brings its own. The cyclohexyl ring’s bulk drives up synthesis time and reagent cost compared to lower molecular weight esters. The reaction takes longer to reach full conversion, sometimes leaving trace unreacted acid if purification isn’t perfect. We’ve met these challenges by optimizing catalyst systems, moving towards higher selectivity, and investing in more robust purification protocols. Customers with highly sensitive downstream steps ship us feedback samples for additional LC-MS profiling, informing our ongoing improvements. Any observed drift in melting range or chromatogram impurity triggers a root-cause session across QC, production, and purchasing—everyone at the table speaks up. Each problem gets chewed on, and frequently, process changes result. In a field where some treat manufacturing like a simple rinse-and-repeat, we’re not afraid to revise after hard-won lessons.

    Packaging, a seemingly minor issue, revealed itself as a repeated trouble spot. In older drums, long-term storage produced micro-leaks and contamination risk, particularly in humid seasons. We made the shift to sealed PE-lined fiber drums, followed by inert gas flushing for international orders. Customers with large volume needs asked about returnable totes. After several pilot runs and customer feedback, we kept flexibility on packaging formats, weighing cost, risk, and ease of handling. The result? Less waste, better shelf life, easier transfer into production reactors, and, critically, confidence during inventory audits.

    Environmental questions come up every year—concerns about residual catalyst, energy input, and post-reaction waste streams. Long before ESG became a boardroom talking point, we started analyzing wastewater profiles and evolving scrubber technology to meet stricter local environmental controls. We partner with waste treatment specialists to ensure our effluent streams meet local and international benchmarks. Not every solution scales or pays back immediately. But as chemical manufacturers, the pressure to deliver clean, safe, and sustainable operations hits close to home. Any improvement in yield, purification, or material recycling means lower emissions and, ultimately, a more resilient operation. Clients notice. Some have shifted more of their purchasing to us after seeing documented progress in waste minimization reports, reinforced by third-party audits.

    Building Trust on Real Chemical Know-How

    Customers rely on more than technical specs. Success depends on the depth of chemical understanding backing each sale. Engaging with R&D and production leads, we lay out possible synthetic pathways, not just for L-Glutamic Acid 5-Cyclohexyl Ester but also for novel amino acid esters with custom protection profiles. We collaborate on drug discovery projects, process development, and troubleshooting campaigns, often discussing real-life failures in the search for a better workflow. Our teams share case studies—where tighter process controls improved impurity profiles or where an alternate purification avoided a common bottleneck.

    We host technical workshops, lab tours, and remote troubleshooting sessions, listening to feedback from plant engineers and analytical team leads. Over the years, this approach fostered lasting relationships, spurred cross-company innovation, and kept us responsive to changing customer priorities. Industry partners, whether seasoned process chemists or sourcing managers, see the difference in consistent communication, the transparency with which we address roadblocks, and the way we handle unexpected spikes in demand. Each batch shipped out the door carries this legacy of care, technical rigor, and commitment to progress.

    Why L-Glutamic Acid 5-Cyclohexyl Ester Remains in Demand

    Complexity in pharma, polymers, and advanced materials keeps growing. L-Glutamic Acid 5-Cyclohexyl Ester’s combination of stability, processability, and tunable reactivity enables new routes for APIs and high-performance materials. Downstream applications push manufacturers to tighten specs further—to reduce contaminants, to offer consistent supply, and to anticipate future regulatory requirements. We track these trends not from afar but from ongoing, on-the-ground discussions with users investing in competitive process chemistry. The ester’s low hydrolysis profile, strong selectivity, and favorable storage profile continue to add value in a market where risk reduction and reproducibility drive every decision.

    Customers don’t want surprises in their supply chain. That means fewer off-spec lots, technical support that responds fast, and a real relationship with the people managing the raw material end-to-end. With L-Glutamic Acid 5-Cyclohexyl Ester, our process knowledge shapes every batch. Across multiple industries—whether chasing a new generics launch or fine-tuning a specialty monomer—this hands-on experience guides our daily work and delivers consistent value for every order, every time.