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HS Code |
625838 |
| Product Name | D-Tert-Butylglycine |
| Cas Number | 13936-70-0 |
| Molecular Formula | C6H13NO2 |
| Molecular Weight | 131.17 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Chirality | D-configuration |
| Melting Point | 102-104°C |
| Solubility | Soluble in water |
| Boiling Point | N/A (decomposes before boiling) |
| Storage Conditions | Store at 2-8°C |
| Inchi Key | PXUUKTSEHYHELE-VKHMYHEASA-N |
| Smiles | CC(C)(C)[C@@H](N)C(=O)O |
As an accredited D-Tert-Butylglycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | D-Tert-Butylglycine is packaged in a sealed, amber glass bottle containing 25 grams, labeled with product details and safety information. |
| Shipping | D-Tert-Butylglycine is shipped in tightly sealed containers under ambient conditions. The packaging complies with standard chemical safety regulations to prevent contamination and moisture exposure. Shipping labels indicate the chemical’s identity and hazard status, ensuring safe handling during transit. All relevant documentation accompanies the shipment as per regulatory guidelines. |
| Storage | **D-Tert-Butylglycine** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the chemical away from moisture, acids, and incompatible materials. Store at room temperature or as recommended on the manufacturer's label. Ensure proper labeling and access for authorized personnel only. |
Applications of D-Tert-Butylglycine in Industrial ManufacturingD-Tert-Butylglycine serves as a highly specialized amino acid building block across several demanding industrial segments. With our advanced synthesis capabilities, we deliver reliably pure product for your specific downstream process needs. Below, we detail the principal sectors leveraging this material, each with distinct operational and regulatory requirements. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers use D-Tert-Butylglycine as a critical chiral auxiliary or protecting group precursor during multi-step synthesis of selected APIs, especially in the development of peptide-based drugs and beta-lactam antibiotics. It enters process schemes for asymmetric synthesis where chiral purity must meet registration standards. Application often involves incorporation in key intermediates, followed by removal or further chemical modification, contributing directly to regulated drug substance synthesis. Maintaining control over trace impurity content is essential for compliance in regulated environments. Industry compliance standards
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2. Peptide Therapeutics ManufacturingContract peptide manufacturers use D-Tert-Butylglycine as a non-proteinogenic amino acid in solid-phase peptide synthesis (SPPS) workflows. Its side chain properties offer improved bioavailability or enzymatic resistance in peptides. High purity material is required to avoid incorporation of byproducts, as product peptides must meet stringent pharmacopeial monograph requirements for clinical or commercial applications. Manufacturing protocol dictates precise amino acid sequence incorporation via automated synthesizers, with protective group strategies tailored for each custom sequence. Industry compliance standards
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3. Pharmaceutical Intermediate SupplySpecialty fine chemical manufacturers incorporate D-Tert-Butylglycine for the preparation of high-value intermediates supplied under contract to the pharmaceutical sector. It is instrumental in constructing complex, chiral intermediates featuring t-butyl and glycine moieties for further transformation in final drug substance synthesis. Downstream clients require tight batch-to-batch consistency for successful scale-up and regulatory verification during drug application filings. Industry compliance standards
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4. Chiral Catalyst and Ligand ProductionCatalyst manufacturers utilize D-Tert-Butylglycine as a starting material when synthesizing chiral ligands and organometallic catalyst components for enantioselective reactions on industrial scale. The rigid t-butyl and amino carboxylate functionalities contribute to ligand frameworks that drive selectivity in hydrogenation or cross-coupling processes. Precision in enantiomeric excess and heavy metal impurity control is mandatory for catalytic material destined for drug and fine chemical synthesis. Industry compliance standards
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5. Agrochemical Chiral Intermediate SynthesisAgrochemical producers employ D-Tert-Butylglycine in the synthesis of certain chiral agrochemical intermediates, notably where selective stereochemistry impacts bioactivity and environmental fate of crop protection agents. The glycine derivative functions as a base material for preparing non-natural amino acid analogs or as a chiral auxiliary during key synthetic steps. Production for agrochemical use must document compliance to international residue and impurity limit standards prior to downstream formulation. Industry compliance standards
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In the landscape of amino acid derivatives, D-Tert-Butylglycine has carved out a valuable place. From our vantage point as a chemical manufacturer, we see its real-world demand up close—contract manufacturers in pharmaceuticals, lab scientists, and R&D teams across the specialty chemicals sector have all come knocking for this molecule. With the CAS number 63113-19-7 and recognized as one of the more robust, sterically hindered derivatives, D-Tert-Butylglycine offers more than just a textbook pathway to peptides and other compounds. Our production scale runs from multi-kilo to several tons every year, driven by batch consistency and on-time delivery, which sets us apart from smaller and less experienced facilities.
Producing D-Tert-Butylglycine, we focus rigidly on purity, chiral integrity, and batch traceability. Chemical purity (≥99%) only starts the conversation. We've invested in chiral HPLC analysis and stereo-specific synthesis approaches that ensure our material matches the D-enantiomer standard on every lot—never a guess, always verified. Moisture content holds below 0.5% as measured by Karl Fischer titration. We provide the free acid form—an off-white crystal powder—packaged in moisture-proof, food-grade drums, or smaller packs customized according to real customer demand, not just a catalog menu.
Our product doesn’t just fill space in a warehouse. It moves quickly out to biopharma labs, contract synthesis workshops, and academic institutions. D-Tert-Butylglycine’s unique side-chain structure allows for bulky protection in peptide synthesis. In non-racemic synthetic routes, our material blocks unwanted side-reactions, serving as a safe bet for researchers seeking high-yield coupling. Application extends to API intermediates, chiral building blocks, asymmetric catalysis, and even some agrochemical seed research pipelines.
Over the years, we’ve seen our product used to improve peptide and oligonucleotide drug development. Peptide engineers value the tert-butyl group for its steric profile, providing selective protection and easy deprotection under mild acidic conditions. This “built-in selectivity” reduces the need for repeated purification runs, which any peptide chemist will tell you, saves weeks in a GMP lab. For asymmetric synthesis experts, the D-configuration—a function of our fine-tuned fermentation and chemical transformation steps—drives selectivity for downstream reactions, limiting waste and side-products.
Questions about differences from similar products come up routinely. We manufacture both D- and L-configurations, but the D-enantiomer answers a distinct set of needs in syntheses where chirality controls bioactivity and pharmacokinetic outcomes. Pharmaceutical teams rely on this specific form for research and production of drugs that demand right-handed amino frameworks. Unlike standard glycine, which provides only minimal steric hindrance, tert-butyl substitution increases molecular bulk and decreases unwanted reaction sites. The real difference shows up in reaction yields and downstream purification: processes run smoother, less is lost, equipment runs cleaner.
Customers sometimes confuse tert-butyl-protected glycine esters with our free acid version. They aren’t interchangeable. Our product’s form—the acid, not an ester or salt—fits better into most solid-phase peptide synthesis pipelines. It offers cleaner removal of the protecting group and causes fewer chromatographic headaches.
Looking back, producing D-Tert-Butylglycine at scale required better than average technical solutions. Traditional glycine derivatives often suffer from cross-contamination during synthesis, but we invested early in self-contained reactors and tandem distillation lines. Our facility maintains humidity levels below 30% during the packaging phase, avoiding clumping and hydrolysis that can degrade sensitive amino acids.
Every batch starts with rigorous incoming raw material examination. We source tert-butyl bromide and glycine from pre-qualified vendors with track records. Once the intermediate forms, we rely on controlled pH monitoring during the workup—small pH swings can cause racemization, and nobody wants a mixed isomeric batch. Granulation nitpicking pays off when customers report yields in the high 90th percentile, instead of needing to troubleshoot downstream.
Chiral amino acids attract close scrutiny, especially in regulated sectors. As manufacturers, we back up every sales certificate with hard lab work: FTIR, NMR, mass spectrometry, and detailed chiral purity profiles—all run on each lot before it leaves our loading docks. In the rare case of customer complaint, we can trace a gram of powder back through each step, reactor, and even the staff who monitored the process. We’re not interested in generic batch records. Our internal digital platform stores every purity report, raw material invoice, and environmental monitoring log.
With more end users asking how “clean” their supply chain is, transparency counts. We participate in regular GMP and ISO audits, hosting auditors from outside and managing electronic batch records, not just binders on a shelf. Consistent documentation means faster market access for our customers—clinical trial suppliers need regulatory comfort from the start.
Our experience working closely with pharma customers tells us that not all D-Tert-Butylglycine comes out equal. Big pharma projects ask for stability data going back two years. We built out stability chambers for real-time and accelerated tests—five and 25 degree Celsius, plus high humidity. In one project for a leading peptide manufacturer, our early feedback tailored their entire synthesis flow, pushing them ahead of a crowded field.
Not every customer has deep technical teams. We routinely provide counsel on storage, dispensing, and waste disposal. Some small startups, fresh to handling chiral raw materials, found value in our tutorials and quick troubleshooting. More seasoned QC teams like to review our full impurity profile—narrative data, not just summary certificates. Our staff know the fine points of how D-Tert-Butylglycine behaves with different solvents and coupling reagents because we run our own synthesis trials, not just follow literature instructions.
Modern chemical manufacturing demands more than just cheap output. D-Tert-Butylglycine requires reagents that can be hazardous when mishandled—tert-butyl sources and strong bases. Instead of chasing yield at the cost of safety, we engineered closed material delivery systems and solvent recycling lines. Our scrapyard sees less than 5% of raw input head out as waste. Team members train on spill management, and we direct off-gasses through activated carbon before release.
Energy savings formed a major part of our update cycle last year. New reactor insulation brought thermal losses down significantly, cutting our energy consumption per kilogram produced. Customers who need supply chain sustainability documentation can see the reduction themselves, as our plant emissions data is available upon request.
There’s a marked difference between buying D-Tert-Butylglycine directly from the production source and from layers of intermediaries. Traders and brokers often don’t grasp the nuances of production schedules, impurity management, and customized packing. We’ve partnered on projects needing overnight dispatch of research-scale grams while preparing tonnage for validated supply chains.
Lead time contracts don’t come from thin air. We run multi-week rolling production plans, letting key partners book exact batch lots tied to their product codes, not just “next available” stock. Real-time delivery coordination with client logistics teams ensures better temperature monitoring during shipment—important for avoiding any degradation or double-handling. Customers get exactly what matches their internal formulation protocols—discussed and reviewed upfront.
R&D priorities keep shifting in specialty chemical areas, so our process development team keeps close tabs on requests for new derivatives. Some years, peptide drug researchers ask for multi-gram analytical samples. Next quarter may see a pivot, with bulk requirements for process validation. Project managers on our side assess lab pilot data and move quickly to scale up without sacrificing purity or yield. We maintain direct communication with end users—the people pipetting and weighing in real labs—so features like easier solubility, faster in-process checks, and simplified validation tests become built-in process values, not afterthoughts.
A real-world example stands out: a biopharma customer running early-phase process validation hit an issue with moisture. The off-the-shelf supplies from other sources exceeded 1% water content, stalling their lyophilization. Our technical group worked around the clock to re-run drying and deliver fresh D-Tert-Butylglycine—problem solved, production kept moving, and future orders landed with confidence. This level of direct engagement keeps us sharp and helps us see trends even before sales requests change.
D-Tert-Butylglycine has entered regulated pipelines, especially in advanced pharma applications. The shift from local markets to international clinical studies means more responsibility at the manufacturer’s end. We stay ahead of shifting legislation. Our facility follows ICH and local FDA guidance—not just GMP on paper, but in each controlled process. We test for residual solvents and provide full impurity lists.
We hold on-site regulatory and analytical chemists together, creating a feedback loop from production floor to compliance documentation. As regulations tighten for chiral precursors, we adapt—updating documentation, enhancing final lot analytics, and responding directly to client technical files for submission to health authorities. Customers engage in side-by-side reviews of our audit and validation files. It’s not abstract paperwork—it’s a working relationship grounded in shared accountability.
In global markets, trust comes from proven delivery, predictable batch quality, and open communication. D-Tert-Butylglycine is only as reliable as the systems supporting it. Industry partners from Switzerland, Japan, Germany, and North America have evaluated our performance through blind sample runs and follow up with extended supply contracts. We invite hands-on technical audits, share our error logs, and recover quickly from occasional setbacks with root-cause reports shared directly.
Working as the direct manufacturer, we learn early what customers value—and what pain points keep them up. Questions are answered directly, not filtered or delayed through third parties. Modifications, special packing requests, or process troubleshooting all run faster. Decades of chemical synthesis, sample shipment, and process support let us stand behind statements, not hide behind boilerplate. Our reputation grows with every batch shipped—one lot, one partnership at a time.
D-Tert-Butylglycine holds a firm place in the modern chemist’s toolkit. From small-molecule drug developers to specialty polymer startups, this molecule plays to its strengths where other amino acid derivatives fall short. Every gram we ship leaves our plant with tracked analysis, handled by teams who know both the science and the stakes.
As manufacturing economies and regulatory regimes evolve, chemical suppliers must rise above “commodity” thinking. The pressure to cut costs will never outweigh the risks of quality failures or inconsistent batches. Our journey as a direct manufacturer is measured in the trust returned by our partners—some spanning a decade or more. For scientists and engineers looking for D-Tert-Butylglycine, the real difference starts on the shop floor and ends with projects delivered ahead of schedule and to exacting specifications.