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4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid

    • Product Name 4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid
    • Alias Boc-Fmoc-piperazine-2-carboxylic acid
    • Einecs 692-589-1
    • 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

    716297

    Productname 4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid
    Casnumber 1312391-94-6
    Molecularformula C23H27N3O6
    Molecularweight 441.48
    Appearance White to off-white solid
    Purity Typically ≥95%
    Solubility Soluble in DMSO, DMF, and other polar organic solvents
    Storagetemperature 2-8°C (Refrigerated)
    Protectinggroups Boc (tert-butoxycarbonyl), Fmoc (9-fluorenylmethyloxycarbonyl)
    Functionalgroups Carboxylic acid, Piperazine, Boc, Fmoc
    Usage Peptide synthesis, pharmaceutical intermediate

    As an accredited 4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle labeled "4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid, 5 grams," with hazard, batch, and storage information.
    Shipping **Shipping Description:** 4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid is shipped in tightly sealed containers under cool, dry conditions to ensure stability and prevent degradation. The chemical should be handled as per standard laboratory safety protocols. Shipping complies with relevant local and international regulations for non-hazardous, research chemical substances.
    Storage 4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid should be stored in a tightly sealed container, away from moisture, light, and incompatible materials. Keep it at 2-8°C (refrigerator temperature) in a dry, well-ventilated area. Avoid exposure to direct sunlight and extreme temperatures. Ensure proper labeling, and handle under an inert atmosphere if recommended by the supplier for extended stability.
    Application of 4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid

    Applications of 4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid in Industrial Manufacturing

    4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid serves as an advanced chemical intermediate primarily in high-value pharmaceutical and peptide synthesis. The material’s dual protection groups support selective reactions and structural control. We summarize below the principal industrial application sectors verified by downstream integration, each with its unique compliance, formula, processing, and end uses.

    1. Peptide Drug Active Pharmaceutical Ingredient (API) Synthesis

    This intermediate is key in the manufacturing of synthetic peptide APIs, where both Boc and Fmoc groups enable precise stepwise peptide elongation and orthogonal deprotection regimes. Industrial peptide lines incorporate this compound during solid-phase and solution-phase synthesis cycles, optimizing for yield, purity, and target sequence complexity, especially for small molecule peptide conjugates and complex cyclic peptides.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • 21 CFR Part 210/211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia Monographs for Peptide Synthesis
    • US Pharmacopeia (USP) General Chapter <1047> Peptide Substances

    Typical usage ratio

    • 0.2–0.4 molar equivalents per target peptide residue; fine-tuned for chain extension protocols and resin loading efficiency

    Downstream process integration

    • Stepwise addition during peptide assembly on resin supports in SPPS
    • Key linking step for cyclic, branched, or constrained peptide frameworks
    • Orthogonal deprotection incorporated for sequence-specific coupling
    • Purification by reversed-phase chromatography or ultrafiltration

    Final product types

    • Therapeutic synthetic peptides (injectables, oral formulations)
    • Peptide-based diagnostic agents
    • Peptide hormone analogs
    • Bioactive peptide conjugates

    2. Pharmaceutical Research & Development (FTE and NCE Programs)

    Medicinal chemistry groups employ this protected piperazine during library design for new chemical entities, where controlled introduction prevents premature side reactions. Custom synthesis and FTE (Full-Time Equivalent) projects rely on its predictable deprotection profile for focused SAR studies, fragment linking, and candidate scale-up feasibility.

    Industry compliance standards

    • OECD GLP (Good Laboratory Practice) for Research Chemicals
    • ISO 9001:2015 Quality Management Systems
    • FDA Guidelines for IND-Enabling Studies
    • Corporate project-specific procurement protocols

    Typical usage ratio

    • 0.1–0.6 equivalents relative to the target piperazine-modified scaffold; onset scale varies by combinatorial strategy and target candidate complexity

    Downstream process integration

    • Fragment conjugation within lead optimization compounds
    • Parallel library synthesis batches for hit-to-lead expansion
    • Solution-phase or SPPS workflows with automated dispensers
    • Post-synthesis deprotection screening and analytical assessment

    Final product types

    • Novel NCE (new chemical entity) research compounds
    • Protected peptide arrays for screening
    • Drug discovery intermediates for preclinical evaluation
    • Tagged peptides for labeling or pull-down assays

    3. Custom Peptide Manufacturing for Diagnostic Kits

    Clinical and industrial diagnostic kit producers require high-purity short peptides as critical assay reagents. This molecule’s dual protection allows for accurate sequential assembly and minimal racemization during the manufacture of customer-specified immunogenic or marker peptides. Custom manufacturing integrates this building block at the resin-to-reagent transition point for biotinylated, fluorescent, or antibody-binding peptide tags.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices — Quality Management for Diagnostics
    • CE-IVD and FDA 21 CFR Part 820 (QSR) for in vitro diagnostic reagents
    • International Council for Harmonisation (ICH Q11) for starting materials
    • ISO 17025 for testing laboratory compliance

    Typical usage ratio

    • 0.15–0.35 molar ratio per synthesis batch, adjustable based on desired peptide length and label incorporation

    Downstream process integration

    • Stepwise SPPS on automated solid phase synthesizers
    • Orthogonal deprotection to expose the target reactive site for labeling
    • Process control during final coupling to signal probes or carriers
    • Desalting and milling for kit component packaging

    Final product types

    • Customized peptide calibrators for immunoassays
    • Biotin/fluorescent-tagged peptides for ELISA
    • Antibody epitope peptides for research kits
    • Peptide controls for molecular diagnostic platforms

    4. Peptidomimetic Compound Manufacturing

    Chemists use this protected piperazine acid to build stable peptidomimetics where amide bonds resist enzymatic degradation, enhancing drug candidate profiles. The compound enters synthetic routes for beta-turn mimetics and backbone-modified analogs with applications in inflammation, oncology, and metabolic disease pipelines.

    Industry compliance standards

    • EU REACH regulations for chemical handling
    • ICH Q8 (Pharmaceutical Development)
    • USP <1058> Analytical Instrument Qualification for QC
    • Company-specific process validation SOPs

    Typical usage ratio

    • 0.1–0.3 molar equivalents, based on backbone substitution pattern and anti-proteolysis strategy

    Downstream process integration

    • Condensation with D-amino acids or N-alkyl derivatives in core peptidomimetic assembly
    • Insertion into backbone-modified chains before global deprotection
    • Column purification to remove side products post-synthesis
    • Regioselective cyclization when required

    Final product types

    • Bioavailable peptidomimetic clinical candidates
    • Protease inhibitor reference standards
    • Stabilized peptide analogs for pharmacological testing
    • Backbone-modified biomolecule research probes

    5. CRO/CDMO Contract Synthesis Services

    Contract research and manufacturing organizations integrate this intermediate into customer-driven synthesis projects, particularly for pilot scale and clinical supply. Its utilization centers on rapid-turnaround, multi-kilo batch runs for building protected peptide chains within tightly regulated process controls and documentation requirements, supporting both research and IND-stage clients.

    Industry compliance standards

    • GMP for Investigational Medicinal Products (EU GMP Annex 13)
    • FDA DMF (Drug Master File) requirements for intermediates
    • ISO 9001:2015 production traceability
    • CRO/CDMO-specific audit and release protocols

    Typical usage ratio

    • Scaled 0.2–0.5 molar ratio, calculated batch-wise per peptide sequence and client process requirement

    Downstream process integration

    • On-demand solid-phase incorporation for project-specific peptides
    • Batch deprotection and cleavage scheduled to client batch delivery
    • Integration into GMP suites with electronic batch record management
    • In-process QC for each protection/deprotection step

    Final product types

    • Process-batched GMP peptides for clinical trial material
    • Reference intermediates for client drug projects
    • Custom building blocks for academic collaboration studies
    • Protected peptide segments for complex assembly orders

    6. Biotechnological Tool Compound Production

    Life sciences and biotechnology firms require protected piperazine derivatives for constructing chemical probes, cross-linkers, and bioconjugates. Specifically, this compound supports the synthesis of bifunctional molecules for chemical biology, protein engineering, and cell imaging, enabling spatial control over reactivity and site-specific attachment strategies within assay systems.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 13485:2016 (if incorporated into diagnostic platforms)
    • Company-specific chemical safety and environmental management policies
    • GHSP guidelines for laboratory reagents

    Typical usage ratio

    • 0.05–0.25 molar equivalents, optimized per binding site density and probe linker design

    Downstream process integration

    • Chemical probe synthesis for affinity labeling or pull-down assay construction
    • Site-specific biotinylation or fluorescent conjugate assembly
    • Attachment to resin beads or protein scaffolds under mild deprotection conditions
    • Post-purification by HPLC or size-exclusion chromatography

    Final product types

    • Biotin-labeled peptides
    • Click chemistry cross-linkers
    • Protein tag reagents for molecular biology
    • Cell-permeable imaging probes
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    Certification & Compliance
    More Introduction

    4-Boc-1-Fmoc-2-Piperazinecarboxylic Acid: Operator’s Experience in Development and Manufacturing

    Understanding Value Through Consistency

    At our facility, 4-Boc-1-Fmoc-2-piperazinecarboxylic acid stands as a cornerstone among our custom building blocks. In the lab, we’ve run hundreds of controlled reactions on this molecule across different scales—sometimes by the gram, sometimes in multi-kilo batches—watching its role in peptide synthesis and beyond expand at a steady pace.

    Chemists who order this compound often mention one thing: they want both purity and stability. Working with this compound every day, our staff see that clear envelopes, controlled environments, and fresh reagents make all the difference. The molecule brings a unique dual-protecting group format—Boc on one end and Fmoc on the other—which saves steps in solid-phase synthesis. Researchers appreciate that duality for preparing custom piperazine derivatives without masking or masking-protection manipulations mid-project.

    Making What Chemists Actually Request

    We don’t just scale up by adjusting proportions; we analyze critical points in the process. Stirring means stirring, not letting it sit and “hope for the best.” The solvent grades affect yield as much as temperature control. Over the years, we’ve tightened every part of the workflow, from starting material purification to filtration and rotary evaporation, to deliver a compound that meets high HPLC purity—often beyond 98%.

    Specs set on our in-house machines reflect what customers test for in their own QC labs. NMR, LC-MS, IR—every certificate reflects the hands-on calibration and monitoring carried out by our analytical team. Chemists expect reproducibility, so we offer batch samples at each stage, keeping the dialogue open about any suspected contaminants or batch deviations.

    Product Format and Handling Insights

    4-Boc-1-Fmoc-2-piperazinecarboxylic acid typically leaves our lab as a white to almost off-white powder. Physical appearance isn’t the only sign of quality, though. Flowability, especially in humid climates, affects automated dosing and weighing. Too dry, and the material generates static, clings to containers, and challenges transfer. Not dry enough, and it may form clumps.

    Years spent troubleshooting led us to optimize drying and packaging methods. We use low-static containers and double-sealed bags, which has cut handling complaints and improved dosage uniformity for automated dispensers. Simple details like weighing protocols, glassware rinsing, and label visibility make a surprising difference in a chemist’s workflow, so we focus on those, too.

    Integrating into Research Pipelines

    Many pharmaceutical and biotech R&D teams use this product when targeting N-protected intermediates. The dual protection gives flexibility to access both ends of the piperazine, which enables sequential deprotection steps or selective coupling to carboxylic acid and amine sites. That speeds up route scouting for both peptides and heterocyclic libraries.

    Our batch records show a range of applications: from solid-phase peptide syntheses, where Fmoc protection streamlines the N-terminal unmasking, to solution-phase modifications, where Boc is removed under milder acid than standard amide groups. The ability to go either way—Fmoc off first or Boc off first—lets chemists avoid unwanted cross-reactions or wasted starting material.

    Others use it as a core fragment for medicinal chemistry, connecting the backbone to linkers, fluorescent tags, or PEG chains. In these roles, the integrity of the product defines downstream yield. Customers have described how inferior grades from other sources ruined entire synthetic runs, pointing to the importance of consistent prep and unambiguous characterization.

    Product Comparison: Experience with Other Piperazine Carboxylic Acids

    Direct comparisons matter most to those who’ve tried working with unprotected or singly protected analogs. With only a Boc or Fmoc group in place, chemists encounter limits, especially if synthesis plans change mid-experiment. Lacking dual functionality, side reactions start piling up—cross-coupling difficulties, unplanned amine alkylation, or loss of entire batches due to unwanted deprotection under strong bases or acids.

    Some researchers fixate on price or lead time, then end up sacrificing efficiency and predictability. We see it all the time. Our 4-Boc-1-Fmoc-2-piperazinecarboxylic acid gives more headroom on both ends of the molecule: no scrambling to re-protect, no mess from incomplete reactions. Working hands-on, we noticed fewer cleanup steps, less waste, and fewer headaches in isolating final targets.

    Another overlooked point lies in reaction compatibility. Some alternate analogs interact with coupling agents differently. Residual solvents or less robust protection can react with HATU or DCC, generating side products that set off longer purification times. Our controlled drying and final QC check—backed up with real in-process records—give peace of mind for those running parallel syntheses or scaling up quickly.

    Solving Real-World Production Challenges

    Even with decades of collective staff knowledge, a few persistent hurdles always return. Humidity spikes, accidental exposure to direct sunlight, and poor bag seals can degrade sensitive protecting groups—especially Fmoc. Storage protocols at our site require temperature logs and batch checks on arrival, not just once a week or “as needed.” High staff turnover? Every new technician spends time shadowing the senior crew, picking up practical pointers that manuals never mention.

    We face the realities of raw material price swings and fluctuating demand. Having a flexible inventory system, our operations team coordinates with regular clients to forecast needs. Even if a last-minute order lands, we try to keep enough material in validated storage so delivery is measured in days, not weeks. Downtime in our reactors is spent recalibrating or validating cleaning workflows, so there’s no slip-up on product-to-product cross-contamination.

    Purity Control and Analytical Support

    Direct feedback pushes us to keep pushing HPLC and NMR checks tighter than market norm. Not long ago, we invested in new column setups that isolated trace byproducts—sometimes under 1%—that used to escape detection. That refinement closed gaps for customers running sensitive biological assays, where trace impurities can affect enzyme inhibition or pharmacokinetics studies.

    Packaging isn’t just cosmetic either. We log every batch to trace back not only to its immediate run, but also to the preceding synthesis. Each lot documents solvents, batch numbers on all inputs, reaction temperatures, and drying curves. If something goes astray for a customer, we routinely review all process data, spot outliers, and offer guidance on trouble-shooting, supporting both small startups and global R&D leaders.

    Supporting Sustainability and Process Improvement

    Chemical manufacturing often attracts scrutiny over waste, solvents, or energy use. In our plant, solvent recovery platforms recapture a good proportion of acetonitrile and dichloromethane used in purification. Not every batch is recoverable to 100%, but with regular runs, solvent loads and waste drum volumes have fallen over the last five years. Strict chemical hygiene and waste logs ensure sensitive components, like Fmoc derivatives, don’t mix into routine plant washouts.

    In scale-up, minor changes reveal big downstream impacts. Switching a filtration paper grade or altering the grind size of starting material can affect both yield and final appearance. Teams document each change, re-check stability, and communicate openly with customers. The feedback loop with experienced chemists around the world keeps the process alive, not static. Practical innovation comes in the form of equipment upgrades, incremental yield gains, and safer workflows—not just R&D slogans.

    Email and Support for Practical Questions

    Beyond the basic order sheet, many customers write to ask which solvents dissolve the powder efficiently or whether basic neutralization might affect piperazine rings. We answer with details from our own lab: solvents like DMF, DCM, or NMP tackle the bulk efficiently, but high-purity THF sometimes boosts solubility for rapid processing. For those using automated peptide synthesizers, we share tips on feed rates and dilution limits, all based on actual lab experience rather than broad generalizations.

    On rare occasions, we’ve supported clients struggling with high background during cleavage or needing alternate sequences of deprotection. Our team draws from hundreds of test runs. We’ve seen variable Fmoc/Boc reactivity on different resins or solid supports and are happy to advise from the ground up—a practice that saves both material and time.

    Changing Customer Demands and the Shift to Biologics

    Over the last several years, demand for robust, multifunctional protecting groups has shifted with the rise of oligonucleotide-peptide conjugates and bifunctional linker technologies. The versatility of 4-Boc-1-Fmoc-2-piperazinecarboxylic acid pushes it to the front of these projects. With more global groups challenging traditional peptide formats, the importance of reliable, clean intermediates gets even greater.

    Some clients ask for new documentation in light of evolving regulatory standards—from residual solvent reporting to elemental analysis certificates. Growing export controls focus more attention on chain of custody and environmentally sound disposal procedures. Working directly with auditors and regulatory liaisons, we rework production logs, offer voluntary disclosures, and answer specific questions so clients feel confident about their supply chain.

    Knowledge Built Over Years

    Decision-makers look at long-term data. Our records—both on paper and digital—track every lot’s journey from order to synthesis to shipping. Recurring patterns reveal best practices: seasonal adjustments in storage, minor tweaks in purification, and discipline with temperature cycles. Known best by those who actually work hands-on with specialty intermediates, small details eventually add up to a dependable supply line.

    Subtle flaws like trace trace levels of DCM or off-spec carbon peaks in NMR can make expensive failures for those further down the supply chain. Large compound libraries and high-value diagnostics depend heavily on the integrity of their starting blocks. Returning customers appreciate candid communication—we don’t sugarcoat bad news or overpromise on batch specs. Open records and feedback loops keep output not only reliable but also customizable to evolving chemistry challenges.

    Looking Toward New Applications

    Interest in more elaborate conjugate and hybrid project workflows grows every year. Multistep buildouts often run more smoothly when both Boc and Fmoc protections are present during early stages. Adaptability means fewer workarounds, fewer wasted cycles, and less need for post-synthesis patch-ups. As more end-users explore modifications to piperazine-based systems in imaging, drug delivery, and polymer sciences, these features gain new significance.

    Ongoing dialogue with the bench chemist remains at the core. Only by listening to everyday processing frustrations can we adapt both compound and process. Whether adjusting packaging for automated dispensing systems or offering custom labeling, front-line staff understand how even small manufacturing changes play out on the bench.

    Direct Manufacturing Matters

    Producing 4-Boc-1-Fmoc-2-piperazinecarboxylic acid in-house, rather than through third-party packaging or brokers, delivers two things: fast responsiveness and consistent quality control. Learnt from hands-on experience, unexpected setbacks—such as resin incompatibility or storage temperature excursions—are easier to troubleshoot with documentation from the actual production line rather than distantly sourced generic specs.

    Customers sometimes share stories where buying through intermediaries led to delayed shipments, or ambiguous answers regarding stability. Direct feedback informs every adjustment in our facility. Our control over the full lifecycle—from raw material sourcing through to shipping—lets us make changes in real time. No need to filter through layers of resellers for answers or improvements.

    Commitment to the End User

    Every lot mirrors the best practices of those who work directly with the molecule. The people on the floor—measuring, mixing, running controls—are chemists, not just operators. This practical background influences everything from solvent choices to communication with customers. Long-term relationships develop through transparency and a shared drive to deliver not just product, but true process support.

    Chemicals like 4-Boc-1-Fmoc-2-piperazinecarboxylic acid play outsized roles in both research speed and result reliability. Our role as direct manufacturer lets us keep these advantages as close as possible to the people who depend on them every day.