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D-Tert-Butylglycine

    • Product Name D-Tert-Butylglycine
    • Alias DTBG
    • Einecs 661-969-2
    • 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

    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 & Storage
    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.
    Application of D-Tert-Butylglycine

    Applications of D-Tert-Butylglycine in Industrial Manufacturing

    D-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) Synthesis

    Pharmaceutical 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

    • ICH Q7 GMP Guidelines for active substances
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (EP) Monographs (Reference for amino acid derivatives in APIs)
    • USP General Chapters <1058> and <1085> for analytical quality and purity

    Typical usage ratio

    • Applied at 0.5–4.0 molar equivalents, depending on the target API route; stoichiometry adjusted by process step and yield optimization targets.

    Downstream process integration

    • Introduced during chiral auxiliary coupling or protection/deprotection cycles within stepwise organic synthesis of active intermediates.

    Final product types

    • Chiral pharmaceutical intermediates (e.g., key intermediates for beta-lactam antibiotics)
    • Peptide-derived drug substances
    • Custom synthetic APIs for clinical use

    2. Peptide Therapeutics Manufacturing

    Contract 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

    • ICH Q11 for API manufacture
    • ISO 9001:2015 for peptide production quality
    • US Pharmacopeia (USP) and EP Peptide Monographs
    • FDA 21 CFR Part 210/211 for therapeutic peptides

    Typical usage ratio

    • Incorporation as a single amino acid per target sequence, generally 1–2 residues per peptide chain; overall usage varies by batch size and target yield.

    Downstream process integration

    • Fed into peptide chain elongation cycles during automatic solid-phase peptide assembly, with monitored addition to resin-bound intermediates.

    Final product types

    • Therapeutic peptides for injectable formulations
    • Diagnostic peptides
    • Research-grade custom peptides

    3. Pharmaceutical Intermediate Supply

    Specialty 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

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 applicable for registration and use in EU
    • FDA DMF submission standards (where required for intermediates in US)
    • Good Distribution Practice (GDP) for intermediate handling and supply

    Typical usage ratio

    • Utilized at 5–30% weight basis relative to target intermediate, determined by synthetic conversion efficiency and impurity risk management.

    Downstream process integration

    • Reacted in solution phase synthesis with controlled temperature profiles, feeding into subsequent condensation or alkylation steps for intermediate build-out.

    Final product types

    • Contract-manufactured pharmaceutical intermediates
    • Key starting materials for synthetic APIs
    • Building blocks for high-value R&D compounds

    4. Chiral Catalyst and Ligand Production

    Catalyst 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

    • ISO 9001:2015 for catalyst manufacturing QA
    • REACH Regulation for EU market
    • Analytical purity standards per in-house catalyst manufacturer controls
    • Environmental, Health and Safety (EHS) company protocols for chemical handling

    Typical usage ratio

    • Routinely dosed at 1–2 molar equivalents for chiral ligand synthesis; proportion customized for specific ligand frameworks and catalyst batch size.

    Downstream process integration

    • Incorporated in ligand-forming reactions, such as amidation or esterification, then converted to active catalyst complexes by subsequent metalation or functionalization steps.

    Final product types

    • Chiral ligands (for asymmetric catalysis)
    • Organometallic catalysts for enantioselective synthesis
    • Research and industrial catalyst kits

    5. Agrochemical Chiral Intermediate Synthesis

    Agrochemical 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

    • Global GAP for agricultural input safety
    • OECD Guidelines for Testing of Chemicals
    • FAO/WHO JMPR residue limit guidelines
    • ISO 9001:2015 for chemical manufacturing

    Typical usage ratio

    • Added at 2–8% of total reaction substrate mass, depending on batch yield targets and stereochemical control requirements for intermediate synthesis.

    Downstream process integration

    • Integrated during early intermediate formation for selective synthesis of chiral building blocks, followed by conversion to the desired final agrochemical active or precursor.

    Final product types

    • Chiral intermediates for herbicides or pesticides
    • Agrochemical actives with tailored stereochemistry
    • Precursors for plant growth regulators
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    Certification & Compliance
    More Introduction

    D-Tert-Butylglycine: Reliable Solutions Straight from Our Production Floor

    Understanding D-Tert-Butylglycine’s Role in Modern Chemistry

    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.

    Our Model and Specifications—Quality Built on Principle

    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.

    Where D-Tert-Butylglycine Meets Real-World Needs

    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.

    Comparing to L-Tert-Butylglycine and Unprotected Glycines

    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.

    Let’s Talk Real-World Manufacturing Challenges

    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.

    About Real Traceability, Not Just Paperwork

    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.

    Addressing Critical Use Cases Out in the Field

    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.

    Green Chemistry and Safety In Manufacturing

    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.

    Direct Manufacturer Value Versus Third-Party Buying

    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.

    Adapting Processes as Customer Demands Change

    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.

    Regulatory Alignment and Global Standards

    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.

    Building Trust Through Consistent Performance

    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.

    Facing the Future with Real Product Leadership

    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.