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L-Glutamic Acid Alpha-Benzyl Ester

    • Product Name L-Glutamic Acid Alpha-Benzyl Ester
    • Alias benzyl α-aminoglutarate
    • Einecs 248-983-7
    • 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

    580710

    Chemical Name L-Glutamic Acid Alpha-Benzyl Ester
    Molecular Formula C12H15NO4
    Molecular Weight 237.25 g/mol
    Cas Number 40064-34-4
    Appearance White to off-white solid
    Melting Point Approximately 101-105°C
    Solubility Soluble in organic solvents like ethanol and methanol
    Storage Temperature 2-8°C (refrigerated)
    Purity Typically ≥98%
    Optical Rotation [α]20/D +13° (c=1, H2O)
    Synonyms Benzyl L-glutamate, L-Glutamic acid, 1-benzyl ester

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

    Packing & Storage
    Packing The L-Glutamic Acid Alpha-Benzyl Ester is packaged in a sealed 25g amber glass bottle with a secure screw cap.
    Shipping L-Glutamic Acid Alpha-Benzyl Ester is shipped in tightly sealed containers, protected from moisture and light. The package is clearly labeled as a chemical product and handled according to standard hazardous material procedures. It is transported at ambient temperature, with appropriate documentation and compliance to all relevant shipping and safety regulations.
    Storage L-Glutamic Acid Alpha-Benzyl Ester should be stored in a tightly sealed container, protected from light and moisture, and kept at room temperature (15–25°C). Avoid exposure to air and humidity to prevent degradation. Store in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Follow proper safety protocols as outlined in the chemical's MSDS for safe handling and storage.
    Application of L-Glutamic Acid Alpha-Benzyl Ester

    Applications of L-Glutamic Acid Alpha-Benzyl Ester in Industrial Manufacturing

    L-Glutamic Acid Alpha-Benzyl Ester plays a precise role as a specialty intermediate within several fine chemical, pharmaceutical, and peptide synthesis sectors. Our factory supplies this compound for established commercial and regulated synthesis workflows. The following industrial applications illustrate concrete use cases in real production environments.

    1. Peptide Synthesis: Protected Amino Acid Building Block

    This ester serves as a protected form of glutamic acid for solid-phase and solution-phase peptide synthesis. It introduces the glutamic acid residue while blocking the alpha-amino group, protecting the molecule during chain assembly. Production lines use this ester to control stepwise peptide elongation and minimize racemization, ensuring sequence accuracy required for API and research-grade peptides.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for protected amino acids
    • 21 CFR Part 210/211 cGMP regulations for pharmaceutical production in the US
    • US Pharmacopeia (USP) requirements for amino acid derivatives (research/clinical)

    Typical usage ratio

    • Commonly applied at 1 molar equivalent to the target peptide sequence site
    • Adjusted between 0.9–1.2 equivalents, depending on coupling efficiency and desired chain length

    Downstream process integration

    • Charged into peptide synthesizers or batch vessels after initial resin pre-swell and Fmoc deprotection steps
    • Coupling with base and activating agent (e.g., HATU, DIC) under controlled temperature and humidity

    Final product types

    • Synthetic therapeutic peptides
    • Diagnostic and research peptides
    • Peptide-based active pharmaceutical ingredients (APIs)
    • Precursor peptide fragments for further modification

    2. Chiral Pharmaceutical Intermediate for Active Compounds

    The alpha-benzyl ester derivative allows precise chiral introduction when preparing advanced pharmaceutical intermediates. It enters amidation or hydrolysis transformations during the synthesis of pharmaceuticals where the stereochemistry of the glutamate moiety is critical. Manufacturing plants rely on it to generate non-racemized glutamic acid fragments within complex small molecule APIs, establishing purity and regulatory compliance.

    Industry compliance standards

    • EDQM CEP and Certificate of Suitability for pharmaceutical intermediates
    • Japanese Pharmacopoeia (JP) specifications for amino acid derivatives used in APIs
    • ICH Q3A/B: Impurities in New Drug Substances/Products
    • GMP compliance under EudraLex Volume 4 guidance

    Typical usage ratio

    • Typically used at 1.0–1.2 molar equivalent per target chiral center
    • Excess may be applied for complete conversion in multi-step API synthesis, based on step yield and downstream purification constraints

    Downstream process integration

    • Introduced during stepwise amidation, ester hydrolysis, or as a quenching reagent following activation
    • Reaction monitored by HPLC to ensure selective incorporation and minimize epimerization

    Final product types

    • Chiral API intermediates (e.g., anticonvulsants, neuroprotectors)
    • Non-racemized N-alkyl glutamate derivatives
    • Pharmaceutical-grade fine chemicals containing glutamic acid structure
    • Advanced bulk intermediates for proprietary synthesis pipelines

    3. Specialty Fine Chemical for Agrochemical Synthesis

    Chemical factories use L-Glutamic Acid Alpha-Benzyl Ester as a precursor for the synthesis of amino acid–based chelating agents and plant growth regulators. Its role is essential in assembling agrochemical actives where biocompatibility and targeted delivery require protected amino acid scaffolds. The intermediary structure facilitates downstream modifications critical for the final activity spectrum in agrochemical formulations.

    Industry compliance standards

    • ISO 9001:2015 certified production management for chemical intermediates
    • FAO/WHO specification guidelines for agricultural active substances
    • European Union Regulation (EC) No 1107/2009 for plant protection products
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for import/distribution in the EU

    Typical usage ratio

    • 1.0–1.5 molar equivalent relative to targeted chelating or signaling moiety
    • Adjusted for specific downstream conversion efficiency and purity requirements of the agrochemical formulation

    Downstream process integration

    • Added in batch synthesis reactors post-initial alkylation or acylation step
    • Participates in condensation or esterification with micronutrient complexes or signaling peptides

    Final product types

    • Amino acid chelated micronutrient fertilizers
    • Plant growth-regulating peptides and oligopeptides
    • Specialty crop-protection intermediates
    • Seed treatment enhancers based on amino acid backbones

    4. Advanced Chemical Synthesis for Functional Materials

    This raw material enables the production of customized polyamides and copolymers requiring specifically protected amino acid monomers. Factories incorporate it during polymerization runs to modulate molecular weight, branching, and backbone chirality. Each batch uses a defined ratio to target properties like biocompatibility, mechanical strength, or solubility in high-value applications, such as hydrogels, membrane materials, or biomedical carriers.

    Industry compliance standards

    • ISO 13485:2016 for materials intended for medical device manufacturing
    • FDA 21 CFR 177 for safety of indirect food additive polymers (where applicable)
    • ISO/TS 80004-2:2015 for engineered nanomaterials in advanced materials sector
    • Quality management according to GMP or equivalent process controls

    Typical usage ratio

    • 0.5–3 mol% of total monomer feed in copolymerization reactions, adjusted to achieve target architecture and polymer functionality
    • Ratios based on performance endpoint testing, such as mechanical analysis or degradation rates

    Downstream process integration

    • Fed into polymerization reaction with other diacid, diamine, or diol monomers
    • Pre-functionalized before chain extension or block assembly steps for specialty materials

    Final product types

    • Bio-based polyamide fibers and films
    • Hydrogel matrices for wound care and drug delivery
    • Specialty membranes with engineered permeability
    • Scaffold materials for tissue engineering applications
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    Certification & Compliance
    More Introduction

    L-Glutamic Acid Alpha-Benzyl Ester: A Manufacturer’s Perspective

    Our Experience with L-Glutamic Acid Alpha-Benzyl Ester

    In our chemical facility, the story of L-Glutamic Acid Alpha-Benzyl Ester reads like a case study in refined synthesis work and real-world application. Among the portfolio of building blocks we produce for the pharmaceutical and fine chemical industry, this molecule stands out for its reliable behavior and unique value in both research and industrial settings.

    We prepare L-Glutamic Acid Alpha-Benzyl Ester in batches that meet exacting quality standards, and each lot rises from carefully sourced raw materials. The process, involving esterification, protection, and purification, demands tight environment control at every stage. Staff skill and a disciplined schedule drive our results; safeguards keep the end product consistent in appearance, purity, and solubility time after time.

    Colleagues in the lab often remark on how the freshly isolated product carries a specific mild aroma due to the benzyl residue. The crystalline solid forms in a batchwise process. Finished material consistently tests above 99% purity, as determined by HPLC and NMR verification. We monitor for benzyl ester hydrolysis and control all parameters closely. Just one year ago, a customer sent back third-party lab data confirming that our product performed above their synthetic expectations—and outperformed other market offerings in terms of reactivity and recovery.

    Why L-Glutamic Acid Alpha-Benzyl Ester Matters

    Chemical manufacturers who look beyond commodity manufacturing know that certain protected amino acids act as keystones in the assembly of more complex molecules. L-Glutamic Acid Alpha-Benzyl Ester fills this niche. It provides a carboxyl group shielded by a benzyl ester—the right touch for peptide synthesis and specialty chemical projects.

    Lab teams favor alpha-benzyl esters since they protect against side reactions not just during classic peptide coupling, but in more demanding asymmetric synthesis operations. Whenever working chemists must introduce protected glutamic acid into a peptide chain by solid-phase or solution-phase methods, they appreciate an ester group that offers solid stability under most coupling conditions, yet deprotects efficiently later by hydrogenolysis. This flexibility comes from the benzyl group, and its performance sets the product apart from straight methyl or ethyl esters.

    Researchers who value yield rarely want to risk racemization or accidental hydrolysis. Our quality checks—optical rotation, melting point consistency, infrared scan—mean developers can trust the stereochemistry of their intermediates. Over the last decade, improved equipment and a sharper focus on trace impurities have lifted product reliability. Customers in Europe and the Americas, after directly testing material from several sources, come back for repeat orders. Their process chemists report higher throughput and lower cleanup requirements with our specification.

    Model and Specifications in Context

    We produce the acid alpha-benzyl ester matching the parameters used by most leading biotech and pharma operations. The product comes as the hydrochloride or free base form, each with a narrow moisture content window. Our syntheses run at the multi-kilo scale, but the batch size flexes by project. Typical melting points register close to published literature values. Chiral purity ranks above 99%; specific rotation and residue on ignition comply with every major monograph.

    Data from our last five production runs show that alpha impurity levels remain below 0.2%. We avoid persistent residual solvents and validate using both GC and LC methods. Customers deploying the material in solid-phase synthesis say our crystalline ester handles better than comparable products, with steady dissolution and improved filtration times.

    There’s often debate in the industry about the need for alternative protection for the gamma-carboxyl instead of the alpha. In practice, we see recurring customer requests for the alpha-benzyl derivative because it serves as the precursor for side-chain modifications downstream, offering greater synthetic maneuverability. Fewer steps means faster turnaround and cheaper campaigns for custom peptide work.

    Where Customers Use Alpha-Benzyl Ester

    The primary application for our product remains peptide synthesis—both solid-phase and solution-phase. Since peptides play critical roles in medicine, diagnostics, and research, scientists rarely compromise on the chemical integrity of their protected amino acids. By relying on our alpha-benzyl ester, these groups gain an entry point for protected glutamic acid—one that resists standard acidic and basic conditions during peptide elongation, yet comes off cleanly under hydrogenation.

    In drug development, customers who develop new small molecules and peptidomimetics use our L-Glutamic Acid Alpha-Benzyl Ester in routes where an unprotected carboxyl group would otherwise lower overall yield or introduce byproducts. The benzyl ester excludes interference from other amino acid side chains, making it a clear choice for target-oriented syntheses.

    Recently, we followed a client's work as they advanced a novel oncology peptide therapeutic. They needed robust selectivity at their N-terminal step without risking backbone hydrolysis. Our product granted them a much smoother workflow. Improved deprotection rates meant they spent less time on purification and more time validating their biological data.

    Comparing with Other Esterified Glutamic Acid Derivatives

    Many manufacturers offer methyl, ethyl, or tert-butyl esters of L-glutamic acid. These products perform well for certain protected peptide protocols or as intermediates in basic organic synthesis. Here, the benzyl ester displays notable differences. Customers who switch from methyl to benzyl derivatives report fewer side processes during hydrogenolysis and no lingering catalyst poisons.

    In practical terms, alpha-methyl and alpha-ethyl esters remove under acidic or basic hydrolysis, but they often require harsher conditions, which may threaten delicate peptide sequences or stereochemistry further down the chain. In contrast, the benzyl-protected ester removes rapidly via hydrogenation, preserving functional group integrity elsewhere. For complex peptides featuring base-labile groups, this trait matters the most. Peptide chemists have told us that their yields stay higher and their reaction temperatures remain in safer bands with the benzyl ester in use.

    Comparing against gamma-benzyl esters, the alpha-benzyl form we supply matches more tightly with the needs of linear elongation and N-terminal sequence formation. In side-chain modification or for protected intermediates used in drugs targeting the nervous system, the difference between gamma- and alpha-protection shapes the downstream approach. Our long-term customers, many of which run pilot lines for pharma launches, discovered that process changes favor the alpha configuration due to its predictable deprotection and higher chemical stability under standard coupling conditions.

    Addressing Production and Quality Challenges

    We faced several technical challenges during the early scale-up phase. Specific details like moisture management during crystallization and efficient filtration determined the overall yield more than any single reagent choice. Operators learned that water traces impact both the formation and stability of the benzyl ester—small process improvements paid large dividends.

    Analytical work, particularly with ultra-high-performance liquid chromatography, uncovered a trend: periods of high humidity boosted trace levels of unreacted glutamic acid or over-benzylated byproducts. We countered this by upgrading our air handling and crystallization equipment. Today, batch-to-batch reproducibility gives customers confidence and reduces uncertainty in their internal validation runs.

    Quality assurance measures run deep. Every drum leaves the facility with a full panel of tests—chemical purity, chiral analysis, solvent content, and moisture balance. Years in the chemical manufacturing sector convinced us that documentation alone does not ensure quality. Only through solvent management and line cleaning does one achieve the purity our customers require, especially for food and pharma uses.

    We also opened clear communication channels with advanced users, so even rare performance concerns get addressed fast. One case saw blocking of our crystalline material during automated charging in a customer’s reactor. Our technical team visited, diagnosed storage temperature as the cause, and offered a modified drying package that solved the problem. Feedback of this type, direct and honest, strengthens both our product and the customer’s results.

    Environmental Considerations and Safety Experience

    Handling benzyl-protected amino acids always prompts thoughtful discussion about environmental controls and worker safety. In our facility, vapors from both reagents and solvents call for reliable capture and neutralization systems. We enforce strict enclosure policies wherever benzyl chloride or hydrogenation steps enter the process, preventing stray exposure and protecting both operators and the environment.

    Waste minimization drew our focus. Production teams worked to reclaim and recycle solvents, cut hazardous emissions, and maximize recovery of valuable intermediates. On the hydrogenation lines, engineers equipped vessels with real-time monitoring sensors for pressure and off-gas, responding to even slight changes in order to sidestep emissions accidents. These investments lowered both risk and operational cost.

    Our team holds regular safety audits, not just during annual certification but as a routine check. We reward operators who spot any potential for cross-contamination or identify odd trends in the process analytics. The culture in our plant makes clear that only through active vigilance and investment in equipment updates does true product quality persist.

    Field Learnings: Improving with Every Batch

    As direct manufacturers, we gather both routine quality metrics and real-world performance feedback. Over the years, customer insights shaped our practices. In one example, process chemists conducting multistep syntheses noted that our L-Glutamic Acid Alpha-Benzyl Ester performed better in extended shelf-life studies than other sources. Additional drying and packaging in inert atmospheres resulted in a product that maintained integrity even under lengthy transport or storage.

    Pharmaceutical clients became partners in method improvement. Their process development teams gave input on trace catalyst residues and fine-tuned our filtration approach for ultra-low metal content. These refinements enabled approval for use in regulated environments and satisfied the critical requirements of regulatory submissions. Laboratory managers, seeking to reduce deviation in peptide synthesis, consistently opt for material that exceeds compendial standards.

    Feedback also drove changes in labeling and documentation. As regulatory frameworks changed, our documentation adapted—not by adding generic statements, but via clear lot-level reporting. Every outgoing shipment carries robust batch history, so scale-up operations at customer sites progress without delay.

    Embracing the Role of Manufacturer in the Chemical Supply Chain

    Manufacturing at scale brings new pressures every season. Unforeseen raw material supply chain disruptions and dramatic shifts in global freight rates challenge every chemical producer. Despite these outside factors, our direct manufacturing controls make it possible to guarantee uninterrupted delivery of L-Glutamic Acid Alpha-Benzyl Ester. We maintain buffer stocks, regularly audit suppliers, and continually analyze the market for developing price trends.

    Customers value predictability. For example, a peptide facility once switched to our product after their old supplier ran into back orders due to upstream benzyl alcohol shortages. Our practice of dual-sourcing benzyl chloride and glutamic acid ensures that repeat orders fulfill on schedule. Long-standing relationships with logistics firms keep customs clearance and documentation moving.

    This experience, accumulated over decades, shapes our daily mindset. Engineers and QA personnel work in tandem to catch inconsistencies before they leave the site. Beyond process improvements, this hands-on approach puts the needs of peptide and fine chemical manufacturers at the heart of each production run. Direct dialogue with formulation scientists and operations managers prompts quicker innovation and smarter process improvements.

    Moving Forward with L-Glutamic Acid Alpha-Benzyl Ester

    Demand for protected amino acids continues to climb, as new clinical trials for peptides and biologics expand. Manufacturers must keep pace with shifts in synthesis trends—one year, solid-phase dominates; the next, solution-phase increases in popularity. Each segment needs reliable starting materials and precise chemical control.

    From our view, the future will likely require further tightening of impurity profiles, improved documentation, and even greener manufacturing routes. Already, teams are exploring biobased solvents and integrated recovery systems to minimize both environmental load and cost. Together with customers, we’re examining alternative deprotection strategies and catalyst options to match the evolution of both regulatory requirements and synthetic methodology.

    The journey of L-Glutamic Acid Alpha-Benzyl Ester is far from over. Its key position in advanced chemical and peptide synthesis assures continued innovation and attention. By staying focused on daily manufacturing discipline, close partnerships with users, and rigorous quality standards, our facility remains the preferred source for those who measure their progress in both yield and scientific contribution.