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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 | 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. |
Applications of Glycyl-Dl-Valine in Industrial ManufacturingAs 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) SynthesisPharmaceutical 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
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2. Cell Culture Media Formulation for BioprocessingProducers 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
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3. Nutritional Fortification in Clinical and Medical NutritionManufacturers 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
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4. Analytical Standards and Quality Control Reference MaterialsCertified 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
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5. Precursor for Biocatalyst Development and Enzyme ScreeningInnovation-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
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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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.