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Glycyl-Dl-Valine

    • Product Name Glycyl-Dl-Valine
    • Alias H-Gly-DVal-OH
    • Einecs 257-354-7
    • 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
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    Specifications

    HS Code

    958071

    Name Glycyl-DL-Valine
    Molecular Formula C7H14N2O3
    Molecular Weight 174.2 g/mol
    Cas Number 3063-12-5
    Appearance White to off-white powder
    Solubility Soluble in water
    Melting Point 251-255 °C (dec.)
    Purity Typically ≥98%
    Storage Temperature 2-8 °C
    Synonyms Glycylvaline; Gly-Val

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

    Packing & Storage
    Packing Glycyl-Dl-Valine is packaged in a sealed, amber glass bottle containing 25 grams, labeled with product details and safety information.
    Shipping Glycyl-DL-Valine is shipped in tightly sealed containers, protected from moisture and light. It should be handled in compliance with safety data, using gloves and eye protection. The package is labeled as a non-hazardous chemical, compliant with international shipping regulations, and stored at room temperature unless specified otherwise by the supplier.
    Storage Glycyl-Dl-Valine should be stored in a tightly sealed container, protected from moisture and light. Keep the compound at a cool, dry place, ideally at 2-8°C (refrigerated), to maintain stability. Avoid exposure to strong oxidizing agents. Ensure proper labeling and store away from incompatible substances. Follow all relevant safety guidelines for chemical storage to prevent contamination or degradation.
    Application of Glycyl-Dl-Valine

    Applications of Glycyl-Dl-Valine in Industrial Manufacturing

    As a dedicated manufacturer of Glycyl-Dl-Valine, we deliver consistent, specification-controlled quality to support critical industrial applications. Our expertise ensures tight integration with regulated downstream sectors that demand high formulation predictability and traceability. Glycyl-Dl-Valine serves as a vital raw material in several specialized production environments, each governed by strict industry standards and process requirements. Below we present real-world downstream scenarios where our material is actively deployed.

    1. Peptide-Based Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers rely on Glycyl-Dl-Valine as a building block in the synthesis of complex peptide APIs, including research-stage oligopeptides and small-scale commercial actives. Its defined chirality and purity profile allow precise sequence assembly during solid-phase peptide synthesis (SPPS) and solution-phase batch operations. Selection of this dipeptide enables downstream process chemists to streamline protection/deprotection cycles within tightly monitored manufacturing workflows, supporting regulatory dossiers for human therapeutics.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.), relevant peptide monographs
    • U.S. FDA cGMP—21 CFR Parts 210/211
    • WHO TRS 957 Annex 2 peptide guidelines

    Typical usage ratio

    • Sequence-dependent; 0.5–5.0 molar equivalents per peptide batch step, adjusted by target peptide length and desired yield optimization

    Downstream process integration

    • Introduced during the elongation phase of SPPS via Fmoc/Boc methods, or in solution-phase fragment coupling as an intermediate dipeptide protecting group

    Final product types

    • Synthetic peptide APIs (e.g., generic hormone analogues, peptide drugs for chronic diseases)
    • Investigational new drug (IND) candidates for clinical trials
    • Reference standards for analytical QC labs

    2. Cell Culture Media Formulation for Bioprocessing

    Producers of tailored cell culture media include Glycyl-Dl-Valine to supply specialized dipeptide nutrition in animal and microbial cell propagation, particularly for high-density fermentation and high-titer monoclonal antibody production. It facilitates stable peptide-based nitrogen delivery, reducing risk of ammonia accumulation and allowing for controllable nutrient feed during growth and expression phases. This function is especially relevant for high-value biologics and vaccine manufacturing, where media consistency and component traceability are validated under bio-manufacturing standards.

    Industry compliance standards

    • USP Chapter <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • ISO 13485:2016 Medical Devices—Quality Management Systems
    • ICH Q5A(R1)—Viral Safety Evaluation of Biotechnology Products
    • 21 CFR 600–680 (biologics regulations)

    Typical usage ratio

    • Added at 0.05% to 0.5% w/v, fine-tuned based on cell line metabolic profiling and target culture density

    Downstream process integration

    • Blended into powdered or liquid basal media during upstream formulation, sterile-filtered into feed solutions, or dosed directly into bioreactors during fed-batch cell expansion

    Final product types

    • Custom cell culture media blends for CHO and HEK293 expression systems
    • Vaccine fermentation base media
    • Media supplements for bioproduction of therapeutic monoclonal antibodies and recombinant proteins

    3. Nutritional Fortification in Clinical and Medical Nutrition

    Manufacturers of clinical nutrition blends and specialty enteral products use Glycyl-Dl-Valine to enhance peptide-based protein sources for patients with compromised protein absorption. The dipeptide form permits rapid gastrointestinal uptake and reduces allergenicity compared to intact proteins, supporting formulation of easily digestible, hypoallergenic medical nutrition for both adult and pediatric populations undergoing metabolic stress or gastrointestinal recovery.

    Industry compliance standards

    • Codex Alimentarius STAN 180–1991 (Formula Foods for Special Medical Purposes)
    • EU Regulation (EU) No 609/2013 (Food Intended for Infants and Young Children)
    • ISO 22000:2018 (Food Safety Management Systems)
    • China GB 29922-2013 (General Rules for Clinical Nutrition Food)

    Typical usage ratio

    • Typically 0.1% to 1% by total protein mass in reconstituted finished nutrition formulas, optimized for target peptide profile

    Downstream process integration

    • Added into aqueous phase during pre-homogenization steps prior to spray drying or aseptic packaging of liquid diets

    Final product types

    • Clinical enteral tube feeding solutions
    • Specialized pediatric peptides drinks
    • Ready-to-feed medical nutrition for post-surgical or malnutrition patients

    4. Analytical Standards and Quality Control Reference Materials

    Certified standards producers and pharmaceutical QC laboratories incorporate Glycyl-Dl-Valine in the preparation of peptide reference mixtures necessary for chromatographic calibration, method development, and batch release testing. The structurally defined dipeptide supports precise method validation, trace residue analysis, and system suitability testing, particularly in reversed-phase HPLC and capillary electrophoresis platforms used for multi-component peptide formulations.

    Industry compliance standards

    • USP General Chapter <621> Chromatography
    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • Pharmacopeial requirements for reference standards (USP RS, EP CRS)
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation

    Typical usage ratio

    • Utilized at 0.01–0.5 mg/mL for reference solution preparation, with dosing dependent on analytical method sensitivity and target quantitation range

    Downstream process integration

    • Weighed and dissolved directly into calibration mixtures or standard stock solutions for analytical batch runs; included as a defined marker in multi-peptide purity assessments

    Final product types

    • Peptide calibration standards for HPLC, UPLC, and CE
    • Quality control kits for batch release testing
    • Analytical verification reference samples for peptide laboratories

    5. Precursor for Biocatalyst Development and Enzyme Screening

    Innovation-driven enzyme manufacturers and biotechnology labs adopt Glycyl-Dl-Valine as a model substrate for evaluating protease specificity, peptidase selectivity, and new biocatalyst libraries. It delivers a defined dipeptide structure for screening substrate recognition, kinetic characterization, and validation of enzyme engineering outcomes, particularly in high-throughput or automated screening platforms seeking to map substrate conversion profiles under bioprocessing-relevant conditions.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 (Quality Management in Laboratory Operations)
    • Sigma-Aldrich Analytical Quality Assurance Specifications
    • EU Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) where applicable

    Typical usage ratio

    • Used at 0.05 mM to 5 mM in screening assay mixtures; concentration adjusted according to enzyme turnover rates and substrate background requirements

    Downstream process integration

    • Prepared as a substrate in buffer solutions and delivered to robotic screening decks or batch reactors for enzyme performance measurement

    Final product types

    • Enzyme activity screening panels
    • Custom biocatalyst assay kits
    • Substrate libraries for synthetic biology tool development
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    Certification & Compliance
    More Introduction

    Glycyl-Dl-Valine: Our Commitment to Precision Peptide Synthesis

    Understanding Glycyl-Dl-Valine in the Landscape of Peptides

    As a manufacturer, we have watched the field of peptide synthesis evolve steadily over decades. Glycyl-Dl-Valine, a dipeptide combining glycine and the racemic form of valine, reflects careful attention to purity, practical production, and compatibility with demanding biochemical applications. Our experience preparing this compound draws on troubleshooting reactor conditions, refining purification steps, and ensuring batch-to-batch reproducibility. Working hands-on with Glycyl-Dl-Valine requires respect for its chemistry, especially given the challenges presented by racemates in both synthesis and downstream processing.

    Our Process: Honing Consistency and Quality

    Developing Glycyl-Dl-Valine demanded investment in robust, scalable production steps. The reaction relies on precise control of condensation between protected amino acid derivatives followed by strategic deprotection. Our years on the factory floor taught us how small fluctuations in pH, reaction time, or moisture can throw off yields or result in side products that complicate purification. It takes more than textbook knowledge; it means running columns late into the night, analyzing fractions one after another, and continuously revisiting the process protocols until results meet our standards every time.

    We supply Glycyl-Dl-Valine in bulk with a molecular formula of C7H14N2O3, presenting as a white to off-white crystalline powder. Analytical results confirm high purity using HPLC and NMR, not just at the bench but on production-scale batches. Maintaining strict limits on residual solvents and related substances, we use validated drying and packaging workflows that minimize contamination and moisture uptake. The packed material leaves our lines only after passing these checkpoints. Years of handling dipeptides have taught us how sensitive customer applications can be to minor impurities.

    Why Users Choose Racemic Forms Like Glycyl-Dl-Valine

    Most technical end-users approach us looking for both convenience and versatility. The DL-form of valine in this dipeptide gives broader compatibility in experimental setups because it reflects a mixture of stereoisomers, letting users model natural peptide variations or study enzyme selectivity without sourcing costly optically pure materials. Synthesizing the racemate, however, is no shortcut; controlling stereochemistry in production and verifying the racemic ratio each lot is critical for consistent biological results. Some labs need the racemic form for enzyme screens; others use it as a building block in more complex methods that do not require chirality at this stage. Both have given us feedback over the years that it matters deeply to have traceable, QC-verified material.

    Comparison with Single-Isomer Dipeptides and Free Amino Acids

    Our seasoned production technicians recognize the critical distinctions between Glycyl-Dl-Valine and analogous compounds. The dipeptide features a peptide bond linking glycine to valine, setting it apart from simple amino acid mixtures in terms of both chemical stability and reactivity. Compared to Glycyl-L-Valine or Glycyl-D-Valine, the DL-form provides a balance for applications that do not call for chiral specificity, simplifying procurement without introducing potential for isomeric impurity confusion seen in other supply chains. Single-isomer dipeptides are essential where enzyme or receptor interactions are strictly stereospecific. Conversely, racemic dipeptides give researchers a flexible, cost-efficient option for broader screening or scale-up.

    Working in manufacturing, we notice that some users mistakenly substitute free amino acids dissolved together in place of a dipeptide. Our teams clarify where the risk lies: only a formed peptide bond grants the biochemical linkage necessary for many peptide-uptake tests, cell culture studies, or pharmacokinetic models. Without this linkage, the compounds behave entirely differently in solution and in vivo. Packaged Glycyl-Dl-Valine from our plant bears the assurance that the product matches its intended specification, preventing suboptimal outcomes in experiments or formulations.

    Applications from Biochemical Research to Nutrition Science

    Daily, we field requests from research and development groups seeking Glycyl-Dl-Valine for assay calibration, structure–activity studies, and active pharmaceutical ingredient intermediates. In biochemical research, this compound acts as a substrate for peptidase activity assays, offering a reliable tool for profiling enzyme selectivity. Our collaborations with academic groups have highlighted how consistency in dipeptide quality underpins scientific reproducibility—results that simply do not hold up when starting with impure or degraded material.

    Outside of pure research, Glycyl-Dl-Valine supports functional testing in nutrition science. Nutrient transport and absorption models often call for synthetic dipeptides to mimic dietary protein breakdown. A controlled supply of Glycyl-Dl-Valine lets nutrition scientists examine uptake kinetics, metabolic fate, and contribution to functional foods. We appreciate the difference between supplying a general lab chemical and supplying a reference-grade ingredient that directly influences study outcomes or formulation performance.

    Shipping to both large manufacturers and university labs, we get to see feedback from a range of users. From these conversations, we notice how important it becomes to maintain a diverse inventory—since some customers prefer smaller packaging for R&D or pilot batches, while others draw from ton-scale orders destined for pharma intermediates or specialized feed applications.

    Quality Assurance Driven by Direct Experience

    The emphasis on reliability at our facility stems from hard-earned trust. Years ago, we learned that variances in input amino acid quality could undermine downstream yields even when the analytical certificate passed basic checks. Part of our improvement came from setting stricter vendor requirements and documenting every lot’s traceability. We hold retention samples, review batch chromatograms, and check for repeatability between production cycles. Internal reviews after customer complaints—rare but informative—have often driven us to recalibrate equipment, deepen troubleshooting, and refine our workforce training.

    Our technical managers oversee ongoing method validation for both wet chemical and instrumental assays. By integrating newer techniques in LC-MS and TOC screening, we stay ahead of regulatory expectations and catch minor deviations quickly. Product management sometimes means admitting when a batch just does not meet standards and holding it back, even at a short-term cost. These decisions are rooted in years of seeing what happens when specification-cutting compounds reach sensitive downstream processes.

    Sustainability and Responsible Manufacturing

    Sustainability guides our process modifications. We operate in a regulatory landscape that gets stricter each year. Energy and solvent consumption drives not only operational cost but also environmental impact, so we invested early in recycling units for solvent recovery and stricter emission controls on all reactors. Training staff to spot waste points, run reactions at lower temperatures where possible, and fine-tune distillation procedures has reduced our water use and hazardous waste output substantially.

    Sourcing glycine and valine, we screen for suppliers with credible records on chemical safety and resource management. A few years back, a raw material shipment flagged during incoming inspection led us to realize how crucial robust supply chain management is for both quality and ethical operation. Now, audits and supplier retraining are regular features of our purchasing program, minimizing risk from contamination or unethical sourcing. These steps matter not simply for compliance but for the long-term viability of our industry.

    Addressing Challenges Unique to Dipeptide Synthesis

    Synthesizing dipeptides like Glycyl-Dl-Valine presents technical challenges different from large-scale amino acid production. Peptide bond formation creates risks of racemization, incomplete coupling, and side-chain modification. We learned early that industrial-scale reactions amplify these risks: what works in a flask can quickly become a headache in a 500-liter reactor. The racemic mixture requires extra care since separation or conversion of isomers post-synthesis is usually neither practical nor cost-effective. Process engineers in our team emphasize transitions between small- and large-scale that can introduce yield drops or impurity spikes, so pilot runs and close analytical support follow any process tweak.

    Another persistent challenge comes from ensuring stable shelf life. Glycyl-Dl-Valine is hygroscopic, demanding climate-controlled storage and rapid, sealed packing to maintain quality. Our staff monitors warehouse conditions, checks delivered product routinely, and continually reviews customer storage feedback. These practical steps keep the product free-flowing and chemically intact, supporting reliability across the full supply chain.

    Serving a Global Marketplace

    Over the years, exporting Glycyl-Dl-Valine has brought new insights into regulatory and logistical differences across regions. Each country brings its own expectations regarding documentation, test data, and traceability. Our in-house export team prepares full shipment records, ensuring each consignment includes the required analytical reports, safety information, and full chain-of-custody documentation. More than once we have had to rework a batch’s paperwork to match client import scrutiny or update our labeling standards following a market expansion.

    Direct feedback from international partners often leads us to tailor not just documentation but also aspects of the manufacturing and packaging process. One region may require tamper-evident seals; another, smaller pack sizes for ease of trial batches. We invest time in listening and responding because that is where our knowledge as producers makes a genuine difference. Years of shipping sensitive chemical products helped us anticipate transit delays, customs holds, and the variety of handling standards our product faces before reaching its end user.

    Building Trust through Transparency

    Being directly accountable means we publish our product data willingly and invite customers to audit our production process. On occasion, clients visit our site to witness first-hand the synthesis, purification, filling, and QA steps behind Glycyl-Dl-Valine. Staff members from R&D, production, and quality assurance discuss the process openly, answering technical queries and sharing troubleshooting stories from the floor. This level of openness creates the trust needed for long-term supply agreements, especially in markets where complex peptide precursors are critical.

    Feedback loops between production and customer service shape how we improve. Where clients point out analytics mismatch or application-specific issues, our technical team investigates both process and documentation until a solution becomes clear. We have adjusted our HPLC gradient for certain lots after repeated detection of late-eluting peaks; in another case, complaints about packing density prompted us to reengineer the filling line for smoother product handling. Our experience tells us: consistency counts, but so does the willingness to adapt based on practical reality.

    Ethics and Responsibility in the Chemical Industry

    Manufacturing specialty chemicals brings responsibility. We run routine safety and ethics training for every shift, not just to comply with external rules but because lives depend on responsible handling. Materials like Glycyl-Dl-Valine demand careful management in storage and dispatch. Our warehouse staff undergo hazard identification exercises and emergency procedure drills. Over time, this culture of vigilance protects both employees and customers. In practice, investing in workplace safekeeping and best-practice handling pays off by avoiding incidents that could erode both trust and operational continuity.

    Product traceability forms another core of ethical responsibility. We keep detailed logs tracing each component and work process, ensuring all Glycyl-Dl-Valine shipped can be tracked back to its lot origin. This level of control insulates downstream users against the unknowns of contamination and supports rigorous recall protocols should a supply chain issue arise—a scenario, thankfully, we have not had to enact due to our diligence.

    Anticipating Future Needs in Peptide Manufacturing

    The demand for well-characterized dipeptides grows each year as research, food technology, and pharmaceutical applications expand. As a manufacturer, we stay ready to scale to new batch sizes and accommodate tailored quality requests. Our process improvement team regularly invests in new reactor technology, enhanced control systems, and analytics that help us deliver faster and more reliably. We learn from both positive and negative experiences, sharing knowledge across shifts and mentoring the next generation of process chemists.

    Looking ahead, we see opportunities in more sustainable production methods, broader supply chain digitization, and extended technical support for application-specific formulations. Meeting both current and future demand relies on hard-earned expertise, constant improvement, and a hands-on mentality that never loses sight of the real-world needs of our customers.

    Why Manufacturers Make the Difference in Chemical Supply

    End-users depend on relationships with real producers. Every drum and bottle of Glycyl-Dl-Valine reflects our commitment—formed not in distant offices but on the production line itself. In contrast to secondary traders, our team answers for each production step, test result, and specification. We navigate the complexities of industrial chemistry daily, learning with each batch, collaborating with end-users, and investing in the community of scientific discovery and safe, responsible production. Our story is written in every shipment, every process tweak, and every challenge met through experience, integrity, and a drive to keep raising the standard for peptide manufacturing.