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D-Glutamine

    • Product Name D-Glutamine
    • Alias 2-Aminoglutaramic acid
    • Einecs 210-483-1
    • 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

    101742

    Name D-Glutamine
    Molecular Formula C5H10N2O3
    Molar Mass 146.15 g/mol
    Cas Number 5959-95-5
    Appearance White crystalline powder
    Solubility In Water Soluble
    Melting Point 215-218°C (dec.)
    Ph Approximately 5.0–6.0 (10 g/L in water)
    Specific Rotation +6.3° (c=2 in 5N HCl)
    Storage Temperature 2-8°C
    Synonyms D-2-Aminoglutaramic acid
    Pubchem Cid 69327

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

    Packing & Storage
    Packing White, sealed plastic bottle labeled "D-Glutamine, 100g," featuring hazard symbols, batch number, and manufacturer information, tamper-evident cap included.
    Shipping D-Glutamine is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is typically transported at ambient temperature unless otherwise specified, and accompanied by appropriate labeling and documentation. Safety data sheets (SDS) are included for regulatory compliance and safe handling during transit. Handle with care to avoid spillage.
    Storage D-Glutamine should be stored in a tightly closed container, protected from light and moisture. Store at 2-8°C (refrigerator) for optimal stability. Keep away from incompatible substances and sources of ignition. Ensure proper labeling and avoid repeated freeze-thaw cycles. Follow local regulations for safe chemical storage and prevent contamination by handling with clean, dry equipment.
    Application of D-Glutamine

    Applications of D-Glutamine in Industrial Manufacturing

    D-Glutamine serves as a specialized ingredient in several established industrial sectors, where its functional properties meet rigorous regulatory and process requirements. As the direct manufacturer, we supply D-Glutamine for integration into differentiated production environments. Below, we detail the material’s practical roles in industrial-scale settings, precise incorporation points in manufacturing, applicable regulatory guidelines, common formulation concentrations, and specific end-use articles.

    1. Parenteral Nutrition Solutions

    Pharmaceutical manufacturers utilize D-Glutamine in parenteral nutrition formulations designed to support protein metabolism in clinical and hospital care settings. This amino acid functions as a conditionally essential nutrient in intravenous solutions, contributing to nitrogen balance for patients with increased metabolic needs, such as those in post-operative recovery or intensive care units. It is critical to control both the concentration and purity of D-Glutamine within infusion-grade blends according to regulatory and pharmacopeial requirements to prevent metabolic complications or adverse reactions during patient administration.

    Industry compliance standards

    • European Pharmacopoeia (EP) monographs for amino acids for injectable use
    • United States Pharmacopeia (USP) requirements for parenteral nutrition
    • Good Manufacturing Practice (GMP) for finished pharmaceutical production (21 CFR Part 211 / EU GMP)
    • Relevant hospital compounding guidelines (e.g., USP <797>)

    Typical usage ratio

    • 2–8 g/L in ready-to-use parenteral nutrition solutions, adjusted according to patient demand and safety assessments according to clinical use protocols

    Downstream process integration

    • Added during the amino acid solution compounding phase, followed by sterile filtration and aseptic filling into IV bags under controlled conditions

    Final product types

    • Intravenous parenteral nutrition bags
    • Ready-to-infuse hospital-use amino acid formulations
    • Pre-mixed multi-chamber parental infusion systems

    2. Cell Culture Media Production

    Bioprocess and biotechnology companies include D-Glutamine in cell culture media, supporting cell viability, proliferation, and specific protein expression in large-scale fermentation and cell-based biomanufacturing. Unlike L-glutamine, D-Glutamine provides select advantages in specialized cell metabolism research and certain hybridoma lines with defined metabolic needs. Accurate sourcing and batch-to-batch consistency are required for reproducible cell growth performance, with formulations often fine-tuned for research, diagnostic, or strict commercial bioprocessing.

    Industry compliance standards

    • ISO 13485 quality management for medical device and diagnostics raw materials
    • ICH Q7 guidelines for API/multi-use excipient traceability
    • US FDA cGMP for biologics production (21 CFR Parts 210 & 211)

    Typical usage ratio

    • 0.2–4 mM in final media formulations, optimized per cell line and bioprocess protocol

    Downstream process integration

    • Dosed during preparation of basal or serum-free media, followed by sterile filtration and bottling, or incorporated in upstream bioreactor charge for commercial fermentation runs

    Final product types

    • Custom and standard cell culture media powders and solutions
    • Cell-based therapeutic and research reagent kits
    • Large-scale cell proliferation feed solutions for industrial bioprocessing

    3. Medical Diagnostic Reagents

    Manufacturers of clinical and laboratory diagnostic kits may select D-Glutamine for specific colorimetric, enzymatic, or buffer systems where its unique isomeric configuration enables critical substrate or control reactions. Its stability and low background interference are essential where precision measurement is required, for example, in amino acid determination kits, specific enzyme activity assessment, or in the development of rare analyte detection protocols for certified laboratories or OEM diagnostic platforms.

    Industry compliance standards

    • IVDD/IVDR (EU Regulation on in vitro diagnostic medical devices – EU 2017/746)
    • ISO 13485:2016 for medical device and reagent manufacturing
    • US FDA 21 CFR Part 820 Quality System Regulation for diagnostics

    Typical usage ratio

    • 0.01–1% (w/v) within reagent solutions or buffer compositions, depending on the specific assay and analytical sensitivity required

    Downstream process integration

    • Blended into targeted reagent/buffer master mixes prior to volumetric filling or lyophilization of single- or multi-component diagnostic kits

    Final product types

    • Clinical chemistry test kits targeting amino acids or related parameters
    • Custom reagent vials for OEM analyzers
    • Reference controls and calibration standards in certified laboratory packages

    4. Specialty Food Additive for Medical Nutrition

    Producers of medical nutrition and specialty diet foods incorporate D-Glutamine in certain clinical dietary products intended for hospital, enteral feeding, or convalescent uses. Its inclusion supports nitrogen provision and gut function maintenance, often in formulas targeting patient groups who cannot tolerate conventional proteins or require precision amino acid supplementation. All ingredient levels and processing steps must adhere to food safety and nutritionally justified guidelines, with hazard analysis and dedicated traceability throughout manufacturing and labeling.

    Industry compliance standards

    • Codex Alimentarius (CODEX STAN 180-1991 – Additives Permitted in Foods for Special Dietary Uses for Infants and Young Children)
    • EU Regulation (EU) No 609/2013 on Food for Specific Groups
    • US FDA 21 CFR 104.20 for nutritional quality of specialty foods
    • GMP and HACCP requirements for special medical purpose foods

    Typical usage ratio

    • 0.1–0.6% by weight, subject to specific patient dietary protocol and national regulatory limits on non-L amino acids in foods for special medical purposes

    Downstream process integration

    • Incorporated post-thermal treatment into liquid bulk blends; alternatively, dry-blended into enteral powder mixes prior to packaging to preserve amino acid integrity

    Final product types

    • Enteral tube-feeding medical nutrition solutions
    • Powdered or liquid foods for special medical purposes (FSMPs)
    • Hospital-grade meal replacement formulas
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    Competitive D-Glutamine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    D-Glutamine: Specialty Amino Acid for Advanced Formulations

    Pursuing Purity and Reliability in Amino Acid Manufacturing

    Every batch of D-Glutamine we produce comes from decades of process refinement and a commitment to consistent purity. Synthetic pathways have evolved alongside our industry experience, giving us a product that answers the technical needs of formulators who want both quality and reliable sourcing. D-Glutamine isn't a catch-all ingredient—it fills distinct functions for compounders targeting nutritional, pharmaceutical, or biochemical applications where interference from impurities or unwanted isomers must stay out of the way.

    Glutamine as an amino acid is found in food and in living tissue, but mass markets chase its L-form, since that's what biology selects for protein building. The D-form, in contrast, rarely comes up in nature and carries different behavior in both structure and reactivity. When a lab or formulation calls for D-Glutamine, specificity matters. You can't expect results from generic L-glutamine, and racemic mixtures don't deliver the same outcomes. We focus on isolating the D-isomer with a specification target of ≥99% purity, proven by batch HPLC. Moisture control in our standard grade keeps water content below 0.5%, favoring applications where flowability, storage, and downstream processing all benefit from minimal hydration.

    How D-Glutamine Stands Apart from L-Glutamine and DL-Glutamine

    Customers often ask why the D-form commands attention when the L-form dominates nutritional conversation. The answer sits at the intersection of research and formulation requirements. D-Glutamine's unique chirality changes its role in peptide synthesis, chiral catalysis, and as a configurational probe for enzyme studies. Unlike L-glutamine, which the human body absorbs and utilizes readily, D-Glutamine interacts differently in biological systems and tends to stay inert or act as a marker or blocker in biochemical work. For pure research, adulteration with L-Glutamine introduces confounding variables that can't be tolerated.

    DL-Glutamine—the racemic blend of both D- and L- forms—finds use in some basic chemical settings but can't support research protocols demanding rigorous control or regulated outputs. We have observed cases where customers who started with DL-formulations saw inconsistent results in enzyme inhibition studies, later traced to minor L-form reactions. Whenever the chirality of an amino acid affects cell metabolism, receptor targeting, or synthetic construction of non-canonical peptides, only single-isomer sourcing eliminates the risk of unexpected interactions. In manufacturing, even a fraction of cross-contamination can trigger downstream reprocessing, waste, and lost time.

    Production Focus and Analytical Controls

    We manufacture D-Glutamine in facilities dedicated to amino acid synthesis, using enantioselective resolution and purification methodologies. The backbone synthetic process starts from protected glutamic acid derivatives and moves through controlled chemical transformations, all tracked under cGMP and ISO principles. Analytical confirmations by HPLC and chiral column GC provide the confidence that scientists and compounders expect. Each drum or small pack goes out with a certificate including analysis numbers on isomeric composition, heavy metals, and microbial counts.

    Moisture and solubility impact service life and blending utility for powders. During drying steps, we control vacuum and temperature to minimize degradation, especially since D-Glutamine shows hydrolytic sensitivity near neutral pH. Our specifications reflect what development scientists have told us: low moisture ensures predictable handling, while the fine crystalline texture supports smooth dispersion in solution or solid-state mixes.

    Applications Moving Forward: Research, Synthesis, and Specialized Health

    D-Glutamine’s impact appears quiet but significant in R&D labs. Researchers use it for peptide sequence design, probing enzymatic selectivity, and as a control substance where its inert role compared to the L-form answers critical experimental questions. Enzyme mechanisms often depend on chirality—using the D-form as a substrate or reference helps untangle pathway details that otherwise remain hidden when only working with conventional L-glutamine. Chiral specificity also contributes to the development of advanced small molecule drug candidates, as some antagonists and diagnostic agents derive their selectivity from the presence of a D-amino acid scaffold.

    Nutritional supplement formulators rarely use D-Glutamine itself. Instead, they value its inclusion for studies into metabolic balance and its rare appearance as a biomarker for certain medical conditions. In clinical diagnostics, the D-isomer’s resistant metabolism allows trace monitoring in samples even after extended storage. Production at scale of high-purity D-form opens doors for research into gut microbiome interactions, as some gut bacteria show selective responses or even unique metabolic pathways for D-Glutamine, not shared by L-glutamine-consuming species.

    Another application anchors around regulatory standards in pharma ingredient development. Impurities in chiral molecules often reflect the limitations of a supplier’s synthesis. Regulatory paths for drug filings demand robust evidence, so D-Glutamine from a single-isomer facility with controlled documentation gives regulatory and quality teams proof of a tightly managed input. We’ve responded to audit requests from overseas clients requiring complete traceability back to our raw materials.

    What Sets Our D-Glutamine Apart

    Clients look for more than high-purity labels. They return because process control at a manufacturing level means supply continuity and batch-to-batch consistency. Decades of scale-up experience tell us that small changes in reaction parameters can show up as trace contaminants down the line. Our staff watch not just for specification numbers but also for trends from past production to predict and prevent fluctuation.

    Packaging is another point of difference. Standard 25 kg drums support industrial users, but we maintain filling rooms for custom-pack sizes, down to 100 grams for research and pre-clinical work. Every order comes from a single lot fill; no relabeling from pooled sources or inventory blending. Labs see the same solubility profile and crystal habit, whether ordering a kilogram or a truckload.

    We have developed technical bulletins based on real feedback from pharmaceutical and biopharma partners, highlighting best practices for dissolution, pH adjustment, and storage. Beyond documents, we offer direct access to our technical support staff, many of whom have spent years in amino acid process development before moving to customer-facing roles. Their guidance helps troubleshoot challenges such as precipitation during formulation or unexpected color formation under high-energy light.

    Waste, Sustainability, and Future Perspectives

    Making specialty D-amino acids at scale often means grappling with yield losses, solvent recycling, and waste minimization. In the early days, large solvent footprints and inefficient chiral resolutions led to cost overruns and sustainability problems. We now use closed-loop solvent recovery and re-use strategies, reducing virgin solvent demand and lessening environmental impact. Solid waste is tracked and processed according to local and international environmental standards, with audits and disclosures available to enterprise customers on request. Increasingly, our clients want to know about lifecycle impacts for inputs in their own ESG calculations. With process improvement, we’ve shrunk per-kilo waste volumes by over 40% compared to five years ago.

    Continuous monitoring for trace residuals—especially for metals or process solvents—means customers don’t face regulatory surprises. We have invested in better analytical instrumentation and in regular staff training to avoid operational drift or shortcutting protocol. As sustainability expectations rise, we are deploying additional process analytical technology to spot opportunities for recapture and reuse of intermediates previously lost during purification.

    Challenges Facing D-Glutamine Production and Solutions

    Not every barrier comes from the technical side. Demand for D-Glutamine remains lower than for its L-counterpart, which impacts supply chain economics. Keeping production plants on line for lower-volume D-isomer production relies not on volume play, but on relationships with specialist users who depend on regular, forecasted shipments.

    Pricing stability always comes up with global raw material fluctuation. We have learned to hedge long-lead time chemicals and build raw stockpiles so price shocks in petroleum-based feedstocks, or commodity-grade intermediates, don’t force us into expensive spot markets. In years when sorbitol or protected glutamic acid supplies lagged, our advance contracting with upstream suppliers kept line staff running rather than idling out of material. Planning like this results in a steadier product flow, and, more importantly, fulfillment timelines customers trust.

    Another challenge is technical: scaling lab-developed synthesis to industrial scale without introducing new impurities or losing chiral selectivity. Cross-contamination controls and dedicated vessels play a role, but so does continuous operator training and process walk-throughs. Every staff member gets regular hands-on sessions with both new equipment and established processes, as gaps in documentation sometimes reveal themselves only through practical observation. Frontline teams have agency to stop batches or raise escalation when something feels off, preventing small deviations from snowballing into non-conforming product runs.

    Industry Feedback and Commitment to Research

    A consistent message has come back from our pharmaceutical partners: data transparency and responsiveness make a difference. Past recalls in the market, sometimes from vendors selling relabeled intermediates, have made our customers wary. We answer with test data and a history of repeatable, audit-ready documentation.

    We routinely work with academic labs pursuing new applications of D-Glutamine, supplementing our supply agreements with shared technical insight. Studies on stereochemistry, metabolic pathways in unusual bacterial species, and use as a probe for cells with non-standard metabolism often call for smaller, highly characterized lots. Our support in these collaborations helps push the boundaries of scientific understanding, while the practical feedback from these partners loops back into continuous manufacturing improvement.

    Looking Forward: Meeting Growing Precision Demands

    Future demand for single-isomer amino acids tracks the increasing specialization of biochemistry and drug development. As more therapies and materials science applications require highly selective building blocks, the value of precise, consistent D-Glutamine only rises. We keep adding analytical capabilities—NMR, advanced chiral HPLC, mass spectrometry—to stay ahead of both regulatory expectations and customer R&D requests.

    Automation and digitalization aren’t buzzwords for us—they translate to better record-keeping, less batch-to-batch variation, and improved traceability. Automated systems also catch deviations faster, ensuring process continuity even as staff rotate on holiday or shift work. In our view, the combination of human expertise and digital control delivers safety both for workers and for clients who rely on every fill.

    Dependable Sourcing, Supply Chain Stability, and Partnership

    D-Glutamine won’t show up on ingredient lists for everyday consumer goods, but its role in specialty science and manufacturing keeps it relevant for those working at the cutting edge. We shape our business around these customers, aligning resources, setting predictable delivery schedules, and using flexible manufacturing routes. Domestic and overseas shipping use high-grade, moisture-proof lining compatible with our strict parameters, helping customers avoid sudden uptake or material changes during long transits.

    We engage directly with users to develop mutual forecasts and stay ahead of planned scale-ups. Technical discussions between our QC and their R&D teams close feedback loops quickly, supporting custom specs—not just in terms of purity, but in form (particle size, solubility characteristics) or documentation needs. Clients in regulated markets depend on us for fast batch re-analysis and on-the-spot troubleshooting, and our sales and technical contacts stay with accounts for years, not turnover cycles.

    Informed Use and Safe Handling

    From our vantage point in manufacturing, safe sourcing and transparent supply chains matter as much as pure technical data. D-Glutamine is not a broad-use dietary ingredient: it waits for careful application in research labs or advanced manufacturing. We direct all of our documentation to the real risks and handling conditions found in practice—ensuring technical buyers understand both the properties of the chemical, and the practicalities of receipt, storage, and reuse.

    Shipping partners receive clear guidance on temperature guidelines, stacking limits, and moisture control, while our onsite handling follows extensive SOPs reflecting both chemical safety regs and the day-to-day experience of safe bulk management. For researchers, we supply technical notes tailored from in-house trials—dissolving D-Glutamine in specific solvents, avoiding rapid pH swings, and preventing photodegradation in bench-top storage.

    Trust, Expertise, and a Focus on Science

    Being the manufacturer gives us a perspective traders or resellers never see. We deal with the raw challenges in process variation, regulatory change, and batch-release anxiety. Clients turn to us when they need straight answers about supply, composition, or what’s really going on behind a certificate of analysis. Long-term relationships based on openness, responsible process management, and readiness to answer questions sustain our business year over year—even as market needs shift, new applications emerge, and regulatory pressure intensifies.

    Our people make the difference, from lab techs to process chemists through to customer-facing scientists. Technology and analytical platforms keep evolving, but field knowledge, experience troubleshooting production problems, and an investment in hands-on training define safe, reliable D-Glutamine manufacturing more than any buzzword or marketing slogan. We invite current and prospective partners to connect with us: whether the need is for a research lot, a kilogram for pilot-scale synthesis, or a full-scale manufacturing campaign, our doors are always open for honest conversation and proven technical support.