Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Glycylglycine

    • Product Name Glycylglycine
    • Alias 2-glycylaminoacetic acid
    • Einecs 217-608-7
    • 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

    288590

    Chemicalname Glycylglycine
    Casnumber 556-50-3
    Molecularformula C4H8N2O3
    Molecularweight 132.12 g/mol
    Appearance White crystalline powder
    Solubilityinwater Very soluble
    Ph 5.0-7.0 (1% solution)
    Meltingpoint 190-192°C (decomposes)
    Iupacname 2-(2-aminoacetamido)acetic acid
    Storagetemperature 2-8°C
    Synonyms Diglycine

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

    Packing & Storage
    Packing Glycylglycine is packaged in a sealed 500g white plastic bottle with a screw cap, labeled with product name and safety information.
    Shipping Glycylglycine is typically shipped as a stable, non-hazardous solid in tightly sealed containers to prevent moisture absorption. It should be kept in a cool, dry, and well-ventilated area during transport. Ensure compliance with local, national, and international regulations regarding chemical shipping and labeling. No special hazardous material handling is required.
    Storage Glycylglycine should be stored in a tightly closed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Store away from incompatible substances such as strong oxidizing agents. Ensure proper labeling and maintain according to safety guidelines to prevent contamination and degradation.
    Application of Glycylglycine

    Applications of Glycylglycine in Industrial Manufacturing

    Glycylglycine plays distinct functional roles in several specialized industrial production lines. As a manufacturer, we supply this material to quality-focused downstream clients who integrate it into process-specific formulations, adhering to regulatory requirements and product performance targets. Our application experience spans biotechnology, diagnostics, pharmaceuticals, specialty food additives, and surface treatment industries.

    1. Biological Buffers for Enzyme Manufacturing

    Enzyme production facilities use glycylglycine as a zwitterionic buffer within fermentation and purification stages where accurate pH stabilization directly impacts enzyme activity retention. Its low metal-binding profile and minimal UV absorbance make it ideal for sensitive biocatalysts in recombinant protein or bulk enzyme preparations. Operators dissolve it in precise weight concentrations adjusted during bioreactor scale-up and chromatography wash cycles, ensuring process repeatability batch-to-batch.

    Industry compliance standards

    • USP-NF (United States Pharmacopeia – National Formulary) for excipients
    • ISO 9001:2015 Quality Management Systems
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients

    Typical usage ratio

    • Commonly 10–50 mM in buffer solutions (0.75–3.7 g/L), adjusted by enzyme system and desired buffering capacity

    Downstream process integration

    • Dispersion into aqueous media for pH control in cell culture or enzyme recovery buffers; critical during both batch and continuous fermentation

    Final product types

    • Bulk industrial enzymes (proteases, amylases, lipases)
    • Recombinant therapeutic proteins
    • Diagnostic enzyme preparations for IVD kits

    2. Electrophoresis Buffer Component for Molecular Biology Reagents

    Molecular diagnostics and life science companies incorporate glycylglycine into polyacrylamide gel electrophoresis buffers for DNA, RNA, and protein separation workflows. Its stable buffering at near-neutral pH supports consistent resolution in SDS-PAGE and native PAGE applications required in biobanks and analytical laboratories. Lot traceability and purity are strictly controlled in process audits and QC release tests.

    Industry compliance standards

    • ISO 13485:2016 for medical device reagents manufacturing
    • REACH Regulation (EC) No 1907/2006 (for supply into Europe)
    • cGMP for reagent-grade chemicals used in diagnostics

    Typical usage ratio

    • 10–40 mM as the primary buffer ingredient in loading and running buffers, with concentration adjusted per separation protocol

    Downstream process integration

    • Direct mixing into standardized Tricine or Tris-Glycine buffers; formulated as liquid or dry buffer packs for end-user preparation

    Final product types

    • SDS-PAGE and native PAGE kits for protein/DNA analysis
    • Ready-to-use electrophoresis buffer solutions
    • Analytical reagent kits for laboratory and clinical use

    3. Raw Material for Parenteral Pharmaceutical Formulation

    Parenteral drug and infusion solution manufacturers select glycylglycine as a buffering agent in injectable formulations requiring controlled pH and low impurity risk. Its non-toxic, non-interfering nature is especially valued in products for intravenous use, such as peptide or protein drugs. Full compliance with pharmacopeial limits ensures safety and batch uniformity, verified through documented incoming goods inspections and validated production lines.

    Industry compliance standards

    • USP, EP, and JP monographs for pharmaceutical excipients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice)
    • GMP Certificate of Suitability (CEP) for European market entry

    Typical usage ratio

    • Buffered at 10–20 mM (0.75–1.5 g/L) in final injectable products; ratio subject to solubility and product pH drift profile

    Downstream process integration

    • Added to compounding vessels under aseptic conditions; blending and in-process QC confirm solubility and pH prior to sterile filtration and filling

    Final product types

    • IV peptide and protein drug formulations
    • Biologic injectables requiring isotonic buffered solutions
    • Critical care premixed infusion bags

    4. Ingredient for Food Processing and Nutritional Supplements

    Food and nutraceutical processors utilize glycylglycine as a safe amino acid derivative for pH adjustment and as a protein stabilization agent in functional food formulations. It is applied in processes that demand low flavor impact and minimal allergen risk, such as ready-to-mix beverages, sports nutrition, and infant formula fortification. Our product meets food-grade purity specifications and undergoes rigorous batch testing to satisfy direct food additive regulations.

    Industry compliance standards

    • FCC (Food Chemicals Codex) specifications
    • GB 2760 (China National Food Safety Standard - Food Additives)
    • HACCP and ISO 22000 Food Safety Management Systems

    Typical usage ratio

    • Added at 0.01–0.1% w/w in food formulations; exact dosage based on protein content, flavor tolerance, and regulatory maximums

    Downstream process integration

    • Blending into powder or liquid ingredient batches during final mixing; product stability checks through shelf-life simulations

    Final product types

    • Fortified clinical nutrition beverages
    • Infant formulas and protein-enhanced drinks
    • Ready-to-eat food supplements

    5. Metal Surface Treatment and Plating Baths

    Chemical processing and metal finishing plants rely on glycylglycine as a complexing agent and stabilizer in advanced electroplating baths, notably in nickel and copper electrodeposition. It controls metal ion availability and improves deposit smoothness without introducing contaminants or accelerating bath breakdown, supporting even coating with high-purity outputs. Plant QA teams monitor residuals and bath performance in line with strict finished part specifications for high-value electronics and precision components.

    Industry compliance standards

    • ISO 9001:2015 for quality management in manufacturing
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electronics)
    • IECQ QC 080000:2017 (Hazardous Substance Process Management)

    Typical usage ratio

    • Applied at 5–20 g/L in plating bath formulations; optimal dosage determined by target deposit characteristics and operating temperature

    Downstream process integration

    • Direct addition to electrolyte tanks during bath make-up and maintenance cycles; online monitoring guides replenishment frequency

    Final product types

    • Fine electronic circuitry (printed circuit boards)
    • Industrial electroplated fasteners and connectors
    • Specialty coated metal parts for automotive and aerospace sectors
    Free Quote

    Competitive Glycylglycine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Glycylglycine: Product Experience From a Chemical Manufacturer

    Walking Through Decades With Glycylglycine

    Over years in fine chemical production, certain peptides come up time and again. Glycylglycine stands out. This simple dipeptide, with the formula C4H8N2O3, brings reliability to countless processes. The industry sometimes calls it glycyl-glycine or diglycine. Chemists appreciate its clean structure—two glycine residues linked by a single peptide bond. There’s no need for big, involved functional groups or hidden complexities. You receive a product that carries efficiency and predictability batch after batch, which matters at scale.

    Glycylglycine powder, white and free-flowing, flows easily in reactors and mixes smoothly during formulation. Precision holds significance to us. Our customers run precise assays—buffer preparations, peptide mapping, sometimes enzyme stability tests. We maintain a strict lot-testing protocol for such uses, confirming identity by melting point, purity with HPLC, and moisture with Karl Fischer titration. High transparency in quality control brings trust. I watch every bag packed with a minefield of real-world applications in mind, not just tick boxes on certifications.

    Specifications That Matter in Practice

    Most Glycylglycine models we manufacture follow specifications above 99% purity. Impurities—sometimes amino acid byproducts, sometimes trace metals—can sabotage experimental controls or chromatography consistency. For buffer preparation in molecular biology, customers cannot tolerate signal noise from rogue contaminants. Our typical batches register LOD (Loss On Drying) below 0.5% and heavy metal content at less than 10 ppm, suiting sensitive applications.

    We’ve scaled production up over the years. Standard packages often come in 25 kg fiber drums. Stability at ambient conditions counts, though we recommend a cool, dry place for longer term storage. True chemical manufacturers know packaging involves more than following a guideline—internal liners, lot numbering, desiccants—every detail preserves product integrity en route. The work doesn’t end at synthesis; maintaining quality through transport completes the chain.

    Real-World Usage Drives How We Produce Glycylglycine

    Laboratories in biotechnology, food analysis, and clinical research look for consistent buffer systems. Glycylglycine buffer, with a pKa around 8.2, offers a reliable range for enzyme kinetics or electrophoresis. Pharmaceutical preparatory processes draw on its stabilizing properties—where reaction conditions demand mild, non-interfering agents. That’s what steers our production targets. The end use experience shapes everything, from choosing raw materials to fine-tuning filtration and crystallization.

    Our clients use Glycylglycine for protein crystallization screens, where unpredictable backgrounds derail expensive efforts in structural biology. Hospitals and diagnostic labs regularly require batch-tested peptides for calibration standards. Glycylglycine’s role rarely makes headlines, but it holds together plenty of behind-the-scenes operations, from liquid chromatography to cell culture support.

    How We See Glycylglycine Compared to Other Peptides

    Unlike longer peptide chains, Glycylglycine doesn’t introduce multiple reactive sites into a reaction. Free from steric hindrance, it features just the minimal peptide backbone with both amine and carboxyl groups exposed. This boosts solubility in water and simplifies downstream recovery. Peptides with side chains—say, aspartic acid or lysine—bring added charge and reactivity, which helps in specialty synthesis but complicates situations where only buffering is required.

    Performance under heat and pH stress also distinguishes Glycylglycine from tripeptides or higher homologues. Shorter chains break down less readily, delivering longer shelf stability and repeat batch performance. We’ve noticed customers in bulk enzymology or formulation work prefer its robustness for just this reason. While some might prefer using simple glycine in place of Glycylglycine for certain low-cost jobs, our direct manufacturing experience says otherwise—the buffering window broadens and holds better, results repeat more tightly, and artifacts remain low.

    Comparing with other buffers, like Tris or HEPES, Glycylglycine stands with appealing biological neutrality. No interference with cell lines. No notorious baseline drift in chromatograms. We produce Tris too, but customers often pick Glycylglycine for more complicated biological readouts, especially when they watch for metabolic byproducts.

    Why Heavy Investment in Quality Processes Pays Off

    We run in-house microbial and endotoxin checks. Contaminants, even at parts-per-million, can throw off assays in basic research or pharmaceutical production. Over the years, continuous investment in purification—column steps, recrystallization, fine filtering—pays off. Years ago, slight changes in process water or equipment cleaning showed up as trace signals in HPLC reads from customers. Solving those incidents required not only tighter filtration, but operator training and internal audits.

    External audits from regulatory bodies keep us sharp, but our experience says direct conversations with researchers and technicians sharpen us more. Their feedback retools our manufacturing, packaging, and documentation. For example, when a research group highlighted batch-to-batch variance in a comparative stability test, we pulled production logs, ran real-time investigations, and restructured our internal tracking. Sharing those findings with other partners created a network effect—raising standards far beyond what any paperwork alone could have done.

    Challenges in the Glycylglycine Market

    Raw material price swings test any manufacturer. Glycine and ammonia derivatives historically move in sync with agriculture and pharmaceutical intermediates. Process efficiency, yield optimization, and raw input forecasting—these take longer to master but shore up resilience. A heavy production schedule won’t compensate for an unreliable supply chain. Some years, supply disruptions threatened to slow output. Switching to back-up suppliers and qualifying multiple raw materials kept customers’ lines running.

    Quality expectations escalate every year. Bioscience applications grow more sensitive, new detection technologies emerge, and documentation loads increase. Staying ahead means tracking industry changes closely—talking with instrument manufacturers, regulatory authorities, and application scientists. A strong feedback loop with end users avoids mismatches in declared values and on-the-ground needs.

    Shifting Production Standards With New Technology

    Automation makes subtle changes possible in process control. Continuous monitoring of pH, temperature, and crystallization ensures our manual checks confirm data, not replace it. Overall timelines shrink, error rates drop, and product consistency increases. Machine-assisted packing cuts cross-contamination risks. Process transparency goes up—giving us faster interventions if something skews.

    It’s worth saying, human experience still matters. Enzyme residue from previous batches gets flagged by advanced sensors, but often, it’s skilled eyes and practiced hands that spot patterns before machines confirm them. Training new operators on the production floor—not just with manuals but through hands-on troubleshooting—keeps future lots as consistent as today’s.

    Sustainability and Environmental Responsibility

    Every chemical output has an environmental footprint. Wastewater and off-gas controls in Glycylglycine manufacturing run stricter every year. Closed-loop systems recycle water. Spent mother liquor gets processed with lower-energy distillation or passed to certified waste handlers. Facility energy use, once secondary, now gets regular audits for lowering carbon impact.

    We re-evaluate sourcing routes for raw glycine and related chemicals—picking suppliers with traceable, sustainable production whenever real. Pressure from global regulations plus market demand means more customers ask for documented compliance. We keep up-to-date with REACH and other regional frameworks to ensure uninterrupted export to international users. Team members take part in quarterly training covering not just compliance, but innovations that lighten environmental weight. Investment returns show over years: safer sites, less loss, and strong local relationships.

    Traceability in Every Drum: Building Customer Confidence

    No finished product leaves our site without a full traceability log. Raw material origin, batch processing times, operator shifts, test results—every step feeds into a master database. If a customer flags a concern or requests supporting analysis for regulatory filings, we retrieve and share full batch profiles. This system doesn’t grow overnight; it evolves with experience and customer collaboration.

    Recalls or deviations, even rare ones, teach more than easy runs. Our team investigates, documents corrective actions, and follows up with partners to confirm issues won’t repeat. Regular customer audits in our facility add an extra set of eyes. This level of transparency builds long-term partnerships. Many R&D teams who began with small orders years ago now source all routine peptide batches from us due to the depth of support and clear information.

    Collaborating With Real End Users: From Bench to Bulk

    Manufacturing in isolation brings little value. Information from university labs, regulatory authorities, and technical managers in diagnostic companies filters back to our plant—the cycle never ends. New applications sometimes call for minor process tweaks: customized sieving grades, specified particle size ranges, or unique packaging for automated pipetting. We adapt even for short runs, knowing it helps both sides grow market share and reputation.

    With Glycylglycine, feedback often highlights tolerances for endotoxin, batch color, and solubility. Working with a customer developing a next-generation chromatography column once drove us to eliminate trace cross-contamination with other amino acids. Tweaking cleaning regimens, auditing every pump line, and even swapping out gaskets on old tanks made sure every specification was real—not just a number on a sheet.

    What Differentiates Our Glycylglycine Manufacturing Approach

    Plenty of traders and resellers move Glycylglycine between borders. Our experience puts synthesis, purification, and packaging under one roof—no outsourcing to invisible parties. The facility design, raw material supplier selection, documentation, and batch release process remain visible and consistent. Every operator can trace a bag on the shipping dock back to a mixing kettle and supply vessel.

    In practice, this means strong reactivity toward customer feedback, and fast problem-solving if something unexpected shows up—a moisture spike, trace discoloration, or storage request. Solutions come from knowing every upstream and downstream angle, not waiting for slow third-party answers. We invest in ongoing staff training, participate in peer technical exchanges, and watch for incremental improvements in both batch consistency and safety.

    The Road Ahead for Glycylglycine and Beyond

    Biotechnology and specialty chemical sectors continue to demand higher reliability in every building block. Glycylglycine holds an established place as both a research tool and a production aid. Market trends point to ever tighter standards for contaminants, stricter environmental compliance, and a broader range of end uses in clinical and food analyses.

    We monitor industry guidance, work directly with analytical scientists, and maintain responsive support teams for faster troubleshooting. In return, we sustain the reputation of Glycylglycine as a reliable, clean, and flexible compound ready for evolving industrial needs. Every improvement in process, quality, or ethical supply increases our customers’ confidence that every drum of Glycylglycine strengthens their operations. As new challenges and technologies arrive in the field, we hold to the view that active partnership and deep technical roots make for products ready to back up vital analytical and manufacturing work without compromise.