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Di-Tert-Butyl Iminodicarboxylate

    • Product Name Di-Tert-Butyl Iminodicarboxylate
    • Alias DTBID
    • Einecs 401-280-0
    • 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

    803164

    Chemical Name Di-Tert-Butyl Iminodicarboxylate
    Cas Number 13290-96-5
    Molecular Formula C10H20N2O4
    Molecular Weight 232.28
    Appearance Colorless to pale yellow liquid
    Boiling Point 129-131 °C at 18 mmHg
    Melting Point -38 °C
    Density 1.08 g/cm³ at 25 °C
    Solubility Soluble in organic solvents like dichloromethane and methanol
    Purity Typically ≥ 98%
    Refractive Index n20/D 1.438
    Storage Conditions Store at 2-8 °C, tightly sealed
    Synonyms Di-tert-butyl azodicarboxylate, BocN=NCO2tBu

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

    Packing & Storage
    Packing A 100-gram amber glass bottle with a secure screw cap, featuring hazard labeling and product details for Di-Tert-Butyl Iminodicarboxylate.
    Shipping Di-Tert-Butyl Iminodicarboxylate is shipped in tightly sealed containers to prevent moisture or air exposure. It should be stored and transported in a cool, dry place, away from incompatible substances and sources of ignition. Appropriate labeling and documentation per shipping regulations (e.g., DOT, IATA) ensure safe and compliant delivery.
    Storage **Di-Tert-Butyl Iminodicarboxylate** should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from moisture, heat, and sources of ignition. Protect from direct sunlight and incompatible substances such as strong acids and oxidizers. Recommended storage temperature is 2–8 °C (refrigerator). Ensure proper labeling and restrict access to authorized personnel only.
    Application of Di-Tert-Butyl Iminodicarboxylate

    Applications of Di-Tert-Butyl Iminodicarboxylate in Industrial Manufacturing

    As a core manufacturer of Di-Tert-Butyl Iminodicarboxylate, we provide material for very specific applications in organic synthesis and downstream production lines where its protected amine functionality is crucial. Below is an in-depth overview of actual industrial sectors integrating this compound, structured for technical decision makers, process engineers, and procurement specialists.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    API manufacturers rely on Di-Tert-Butyl Iminodicarboxylate as a Boc-protected amine reagent during the multi-step synthesis of medicinal compounds, where selective amine protection and deprotection are vital for controlled molecular assembly. Our material enters their production schemes particularly in the manufacturing of antihypertensive, antiviral, and oncology intermediates, where protection from side reactions enables precise functionalization at scale.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia, applicable monograph standards for starting materials
    • US FDA 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals
    • Japanese Pharmacopoeia process validation requirements

    Typical usage ratio

    • 0.9 – 1.2 molar equivalents relative to the free amine substrate, adjusted based on desired yield and residual unreacted amine content limits

    Downstream process integration

    • Added during the amine protection stage after the introduction of base, typically in polar aprotic solvents at cooled temperatures (0–10°C) to suppress side reactions, then followed by extraction or chromatographic purification

    Final product types

    • API intermediates with Boc-protected nitrogen functionality (e.g., protease inhibitors, β-lactam antibiotics precursors, peptide coupling blocks)
    • Customized chiral amines for proprietary drug development pipelines

    2. Peptide Synthesis and Custom Peptidomimetic Building Blocks

    Fine chemical houses and contract synthesis organizations regularly use our Di-Tert-Butyl Iminodicarboxylate within solid-phase and solution-phase peptide assembly processes, where selective amino group protection sustains sequence integrity and high peptide yields. Its reactivity and Boc protection are essential for controlling N-terminal functionality in automated peptide synthesizers and multi-kilogram scale solution syntheses.

    Industry compliance standards

    • ISO 9001:2015 certified process documentation for chemical synthesis
    • GMP requirements for peptide API production (US FDA, EMA guidelines for peptides)
    • IFPAC quality assurance standards for automated synthesis workflow

    Typical usage ratio

    • 1.05 – 1.15 equivalents per amino group; controlled excess to ensure complete protection, with optimization cycles for proprietary peptide sequences

    Downstream process integration

    • Directly loaded onto resin or added to solution mixtures alongside base and solvent, often as the first protection step before chain extension begins; removed after peptide elongation using acidolysis (e.g., TFA cleavage)

    Final product types

    • Therapeutic peptides
    • Diagnostic peptide standards (e.g., for LC-MS calibrations)
    • Peptidomimetic compounds for research and screening libraries

    3. Protected Amine Synthesis for Agrochemical Active Ingredient Manufacture

    Agrochemical producers employ Di-Tert-Butyl Iminodicarboxylate in the synthesis of nitrogen-containing key intermediates required for high-purity herbicide and pesticide actives. Its protection of amino groups during scaling-up ensures minimized formation of potentially hazardous side-products, meeting the purity requirements for environmental and toxicological safety reviews.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 for analytical validation of raw material purity
    • REACH Registration (EC 1907/2006) for chemical safety in the EU

    Typical usage ratio

    • 0.95 – 1.1 equivalents calculated on amine substrate weight; precise adjustment per structure-activity studies and downstream regulatory batch documentation

    Downstream process integration

    • Introduced early in the synthetic sequence to generate protected amine intermediates, followed by subsequent alkylation, acylation, or cyclization; final deprotection phase after key structural modifications

    Final product types

    • Safener-protected herbicide active substance intermediates
    • Amine-functionalized pesticide core fragments
    • Functional group-protected reference substances for regulatory submission

    4. Specialty Fine Chemicals and Custom Chiral Ligand Manufacture

    Manufacturers in asymmetric catalysis and custom ligand design rely on high-purity Di-Tert-Butyl Iminodicarboxylate to introduce readily deprotectable nitrogen groups. Chiral ligand makers use this reagent to mask primary amines during metal complexation reactions, maintaining selectivity and enantiopurity in catalyst synthesis workflows that require clean removable protection without residual contamination.

    Industry compliance standards

    • ISO 14001 for environmentally responsible production
    • Responsible Care® Initiative for specialty chemical safety
    • OECD Test Guidelines for chemical synthesis documentation

    Typical usage ratio

    • 1.0 – 1.2 equivalents, tailored to ligand structure and operational scale (gram to multi-kilogram); batch card reviewed for unreacted amine after work-up

    Downstream process integration

    • Amine protection following initial ligand backbone synthesis; incorporated within glovebox or Schlenk line handling if air-sensitive metals are involved; deprotected before final catalytic complexation step

    Final product types

    • Air-stable chiral ligands for asymmetric hydrogenation
    • Enantioenriched catalyst precursors
    • Building blocks for high-performance custom organometallic catalysts

    5. Custom Amino Acid and N-Substituted Derivative Synthesis for Research Chemicals

    Advanced research laboratories and specialty fine chemical producers utilize Di-Tert-Butyl Iminodicarboxylate for the preparation of Boc-protected amino acids and their N-substituted analogues. Its function as a protecting group enables the selective modification of functionalized α-amino acids, critical for high-value monomers and specialty reagents in chemical biology and polymer research.

    Industry compliance standards

    • ACS Reagent Grade Quality Requirements for Research Chemicals
    • ISO 13485 for laboratory reagent supply chain (if used in diagnostics)
    • GLP (Good Laboratory Practice) for synthetic route traceability

    Typical usage ratio

    • 1.1 – 1.3 molar equivalents per amino group, with optimization based on the hydrophobicity of the substrate and desired monoprotection outcome documented in laboratory notebook protocols

    Downstream process integration

    • Mixed with amino acid under inert atmosphere, in polar solvent in the presence of base, often at chilled temperatures (0–10°C); followed by selective functionalization of side chains before Boc deprotection under acidic conditions

    Final product types

    • Boc-protected α- and β-amino acids
    • N-alkylated amino acid derivatives
    • Chiral monomers for specialized polymer syntheses
    • Research-use-only diagnostic reagents
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    Certification & Compliance
    More Introduction

    Introducing Di-Tert-Butyl Iminodicarboxylate: A Practical Perspective from Our Manufacturing Floor

    Why Di-Tert-Butyl Iminodicarboxylate Matters in Today’s Laboratory and Pilot Plant Work

    In our years producing chemicals for a wide swath of pharmaceutical innovators, custom synthesis shops, and specialty science ventures, we see Di-Tert-Butyl Iminodicarboxylate play an everyday role far beyond a simple entry in a product catalog. Known across labs as DTB-IMDC and drawing attention for its clean, reliable blocking of amine groups, this molecule turns routine amine protection into a predictable, reproducible process even for sensitive substrate systems. As a manufacturer, we know what makes a reagent truly useful is more than just purity levels or product code — it's also the stability you can count on from bulk down to a single gram, the control over moisture content, particle size, and physical handling that ensures every operator in a production line or R&D lab gets consistent results without time lost recalibrating protocols.

    Our typical batch of Di-Tert-Butyl Iminodicarboxylate appears as a white, free-flowing solid, handled in robust drums or lined bags that defend against the trace moisture and ambient oxygen known to degrade other carbamates. Spec sheets matter, and ours often show purity higher than 99%, usually checked by HPLC and NMR, with water content kept below 0.2%. We control this right at the crystallization step, using rigorous filtration and closed-drying systems to protect the end product.

    How Working Directly with Manufacturing Gets Better Results

    Step back from distributor promises, and hands-on chemical makers know the real headaches of an interrupted synthetic route: inconsistent batches, unknown byproducts, or powders that turn sticky on exposure. In tightening controls on DTB-IMDC, we've learned which process tweaks can push down side-reactivity. Starting from high-quality raw materials — tert-butyl alcohol and phosgene derivatives — we maintain reaction integrity using specialty-grade reagents tested for trace iron and halide residues. Production equipment never sees cross-contamination with other carbamates or nitrogen sources, a detail those further downstream might not catch until a problematic batch lands in their reactor.

    Customers repeatedly tell us: a clean DTB-IMDC batch means fewer purification cycles after the protection step, less yellowing, and better downstream amine deprotection yields. For peptide synthesis, where every impurity risks peptide chain termination, that translates to cost savings both in solvents and time. It is the attention to what happens at drying and packing that really lets DTB-IMDC perform consistently in automated synthesizers and glovebox work.

    How Di-Tert-Butyl Iminodicarboxylate Works in the Real World

    The classic use-case for this reagent comes in protecting amine functionalities by forming a t-butoxycarbonyl (Boc) group on the target nitrogen. For pharmaceutical scale-up, DTB-IMDC delivers a more robust Boc-protection route compared to Boc2O, especially in the preparation of secondary and hindered amines. It allows amination chemists to work at lower temperatures and under milder base conditions, cutting down on competitive side-reactions. Peptide chemists value the high selectivity, as DTB-IMDC shows less tendency to over-protect and often leaves primary amine unreacted until higher equivalents are added.

    Operators on our blending and filling lines deal with shipment drums where consistency in solid form helps speed up dosing. A batch with variable grain size can jam automated feeders; we screen and sieve each lot to hit a narrow particle size window, which means academic labs and bulk plants alike work with the same material year-over-year. This practical consistency gets glossed over in standard catalogs, but technicians and researchers relying on predictable process chemistry see the difference in yield, waste solvent, and repeatability of their endpoint assays.

    Comparing Di-Tert-Butyl Iminodicarboxylate with Alternative Amine Protecting Agents

    DTB-IMDC stands apart from agents like Boc2O, benzyl chloroformate, or carbonyldiimidazole. Boc2O, once a lab staple, shows higher reactivity and can generate side-products with sensitive or electron-rich amines. Working with carbonyldiimidazole, some teams report more imidazole adducts, which show up in tricky chromatograms and cost hours of extra purification. On the other hand, our customers working at both research and kilo scales tell us DTB-IMDC provides cleaner conversions with less exotherm and better reproducibility in large glass or steel reactors.

    Di-Tert-Butyl Iminodicarboxylate delivers a gentler, more easily controlled reaction profile. In pharmaceutical pilot plants, especially those with cGMP requirements, that means less concern about unwanted rearrangements or protecting group migration, and more straightforward batch-to-batch reconciliation. Practically, DTB-IMDC can also be handled under air without rapid self-decomposition, unlike some imidazole-based alternatives that need inert gas handling and introduce sporadic instability.

    Some syntheses require extended reaction times, and that's another place DTB-IMDC outperforms: fewer impurities show up in extended monitoring, and crystallization of end-products sees better recovery rates. We trace this to the batch drying protocols and quality of starting materials, not just the basic chemistry of the molecule.

    Specifications That Translate into Real Laboratory Performance

    The mean free-flowing powder that leaves our plant runs at high purity, less than 0.2% water, and with each drum or pail coded with QC results from multiple checks. In our ongoing dialog with pharmaceutical and biotechnology labs, we've learned that what matters even more than numbers on a spec sheet is transparency — users want details about how the lot was produced, dried, and packaged. Our process chemists always document each step and validate identity and purity by both infrared spectroscopy and HPLC, something we invite customers to review or request secondary verification on.

    Handling characteristics require constant refinement. We’ve invested in conical drying and mill systems with nitrogen overlay to suppress oxidation. Specialists in our plant would rather spend extra hours confirming the solid breaks cleanly with little dust, since we’ve seen dusting cause problems in negative-pressure rooms. Packaging uses thick, lined drums paired with tamper-evident seals; we run regular stability tests under varied humidity and temperature so we know product will reach end-users in the same condition as it left our floor. In this business, lost time due to a dampened or partially-caked protecting agent doesn’t just hit profit — it throws off entire production schedules downstream.

    Real-World Manufacturing Experience Shapes Better Chemistry

    Feedback from users helps us chase the roots of process glitches. When a university lab reported a run of faint off-color in a coupling reaction, we back-traced the lot through our logs and caught a solvent residue issue at the tail end of drying. That prompted an equipment calibration and a change in final QC protocol. These are fixes a distributor would rarely implement so quickly. We make it a point to share these case studies with our partners; it emphasizes the real interaction between manufacturing discipline and reliable performance in synthetic laboratories worldwide.

    We're not alone in noting how little differences in production practice can make or break a targeted synthesis route. In contract manufacturing, even a low level of peroxide impurities can cap amine conversion or leave trace nitroso byproducts — failures that eat into budget and regulatory compliance. We mitigate those risks by analytical checks at every lot transfer, from raw materials through to finished goods. Our policy involves over-communicating with custom synthesis teams so any subtle performance issue gets flagged before it becomes a recurring yield loss.

    Supporting Innovation and Safety in Practice, Not Just in Brochures

    As workers at the source, we're sensitive to logistics challenges and the everyday safety requirements of frontline chemists. Packaging adapts to demand from both kilogram and multi-ton users, with inner liners that safeguard product against exposure even when stored at high relative humidity for weeks. For users working in ISO-certified or FDA-audited plants, every shipment includes batch documentation and a full traceability package. Most distributed products can’t match this, as they often bounce between storage conditions no one tracks.

    Hazard mitigation in production lots shapes our handling guidelines and end-user recommendations. Di-Tert-Butyl Iminodicarboxylate doesn’t hydrolyze rapidly, but it can build up t-butyl carbamates if stored open in moist air — a fact our plant learned early after tracking batch performance for downstream users. Controls include not only climate-proof packaging but rapid turnover and FIFO inventory that staves off shelf instability.

    Clients have cited improvements in green chemistry protocols by shifting to DTB-IMDC for amine protection. Less catalyst loading, fewer toxic byproducts, and better end-of-pipe performance add up to strategic gains in environmental compliance. Sustainability teams increasingly seek utility in chemicals that don’t throw extra work at EHS managers, and that's a result of ongoing product stewardship from manufacturing, not just marketing.

    Voices from the Chemist’s Bench: DTB-IMDC in Hands-On Synthesis

    Several peptide houses using solid-phase synthesis methods tell us DTB-IMDC outpaces conventional protectants for certain sensitive moieties. One team reported smoother coupling with lysine analogs, cutting manual post-purification by 20%. In bulk pharma, a process engineer cited gaining double the throughput after switching to our formulation, mainly due to improved powder flow and less cake-forming during storage.

    Our decades in specialty manufacturing show that robust supply chains matter most when industrial and R&D growth spikes. With qualification protocols harmonized both in-house and with third-party GMP auditors, each production cycle reflects continuous improvement. Direct feedback loops allow fast response to subtle shifts in process outcome, something trading houses rarely replicate.

    Meeting Changing Standards with Manufacturing Know-How

    Global regulatory environments never stand still. As active pharmaceutical ingredient producers face mounting documentation demands, verifying every point of origin in the chemical’s lifecycle becomes more than paperwork — it anchors confidence in new drug applications and continuous process verification. In-house control over Di-Tert-Butyl Iminodicarboxylate makes traceability a built-in feature, with certificates that include not only analysis of actives but also tracking for potential elemental impurities.

    Batch-to-batch reproducibility isn’t only about keeping the lot in spec. Years of producing and packaging this compound taught us that well-maintained equipment, staff training, and up-to-date analytics have more impact on the final user’s ease of work than occasional spec upgrades or product relabels. For both established GMP plants and research-oriented R&D groups, that practical reliability means experiments set up today will work the same every time — no cycle lost recalibrating or compensating for unexplained variability.

    Conclusion: The Real Value Stems from Manufacturing Experience

    Di-Tert-Butyl Iminodicarboxylate’s place in contemporary synthesis reflects more than theoretical advantages. It’s shaped by process innovations and user-centric feedback at every production stage. The product reaching hundreds of labs, pilot plants, and process development units draws its reliability from the choices our manufacturing teams make every day — in equipment selection, raw material vetting, process control, and QC strategy.

    We respond to practical challenges and keep pushing to deliver Di-Tert-Butyl Iminodicarboxylate that does what’s claimed, every drum, every shipment, every run. The details often overlooked — careful drying, packaging upgrades, real-time analytical review — take center stage here because as a chemical manufacturer, every compromise echoes down the line. Our reputation stands on the synthetic successes of those we supply, and that’s why every kilogram of DTB-IMDC tells the tangible story of hands-on manufacturing. Scientists want reagents that simply work. The difference comes from everything that happens before those reagents ever reach the bench.