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3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid

    • Product Name 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid
    • Alias Boc-Pip(NO2)-SH
    • Einecs 831-617-9
    • 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

    291009

    Chemical Name 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid
    Molecular Formula C20H19N3O7S2
    Appearance Solid
    Purity Typically >95%
    Cas Number NA
    Solubility Soluble in DMSO, DMF; slightly soluble in water
    Storage Temperature -20°C (recommended)
    Functional Groups Carboxylic acid, nitro, amide, thiol, carbamate
    Optical Activity Chiral (2S,4S configuration)
    Synonyms 4-Nitrobenzyloxycarbonyl-4-mercapto-L-prolyl-3-aminobenzoic acid
    Stability Sensitive to light and oxidation
    Usage Peptide and pharmaceutical intermediate
    Safety Handle with gloves and eye protection

    As an accredited 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 500 mg amber glass vial, sealed with a screw cap, labeled with product details and safety information.
    Shipping The chemical **3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)carbonyl-2-pyrrolidinyl]carbonyl]amino]benzoic acid** is shipped in a securely sealed container under ambient or refrigerated conditions, depending on stability requirements. Packaging complies with all relevant regulations for hazardous materials to ensure safe delivery and prevent degradation or contamination during transit.
    Storage Store 3-[[[(2S,4S)-4-Mercapto-1-(4-nitrobenzyloxy)carbonyl-2-pyrrolidinyl]carbonyl]amino]benzoic acid in a tightly sealed container, protected from light and moisture, at 2–8°C (refrigerator). Avoid exposure to strong oxidizing agents, acids, and bases. Store under an inert atmosphere (e.g., nitrogen or argon) to prevent oxidation of the thiol group. Handle with suitable personal protective equipment in a well-ventilated area.
    Application of 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid

    Applications of 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid in Industrial Manufacturing

    As a specialized manufacturer, we supply 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid (MNBCPBA) for advanced chemical synthesis in highly regulated sectors. Our product delivers precise functionality required for API intermediates, protected peptide synthesis, custom bioconjugates, and high-performance analytical tools. Below, we detail key industrial avenues where this compound integrates directly into manufacturing, with compliance, process, and formulation highlights from real-world production lines.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    MNBCPBA serves as a chiral peptidomimetic intermediate in regulated pharmaceutical settings for the synthesis of next-generation APIs, especially in the production of protease inhibitors and complex cyclic peptides. Its orthogonally protected amino- and thiol- functionalities allow for stepwise modular additions, enabling pharmaceutical manufacturers to assemble multifaceted drug candidates under controlled environment. This raw material enters multi-stage reaction sequences involving hydrogenation, deprotection, and cyclization while maintaining stereochemical integrity.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (FDA)
    • EU GMP EudraLex Volume 4, Annex 1/2
    • Ph. Eur. Monographs on intermediate purity and identity

    Typical usage ratio

    • 0.8—1.2 molar equivalents relative to adjacent peptide units, exact ratio fine-tuned by reaction scale and downstream cyclization yield requirements

    Downstream process integration

    • Introduced following Boc/Fmoc-based stepwise peptide assembly and prior to final macrocyclization or cleavage for API candidate formation

    Final product types

    • Antiviral and anticancer cyclic peptide APIs
    • Enzyme inhibitor drug substances
    • Diagnostic peptide intermediates for parenteral formulations

    2. Protected Peptide and Peptidomimetic Synthesis

    Process chemists use MNBCPBA in solid-phase peptide synthesis (SPPS) workflows, utilizing its sterically-differentiated protection groups to construct complex peptide backbones with site-specific cysteine modifications. This approach maintains specific reactivity for later disulfide or conjugate linkage, ideal for the construction of bioactive oligopeptides and peptide libraries used in pharmaceutical screening and therapeutic research.

    Industry compliance standards

    • USP General Chapter <1069> “Peptide Synthesis”
    • ISO 9001:2015 for custom peptide production
    • Ph. Eur. 2.2.46 Chromatographic purity standards
    • Applicable proprietary CMC documentation

    Typical usage ratio

    • 10–20% relative to resin-bound amino acid equivalents; process developers adjust for length of chain and side-chain protection strategy

    Downstream process integration

    • Added during resin-based automated or manual synthesis cycles; cleaved or retained as protecting group before final peptide release, as process demands

    Final product types

    • Protected peptide fragments for pharmaceutical R&D
    • Peptide standards for QC in biotechnology
    • Peptidomimetic lead compounds for screening libraries

    3. Bioconjugate Linker and Site-Specific Modification Agent

    Biotechnologists deploy MNBCPBA to install protected mercapto groups at strategic locations in protein or antibody conjugates, supporting site-selective drug payload attachment while reducing off-target reactivity. The stable linkage ensures that conjugates remain non-reactive during large-scale processing and only activate upon controlled downstream deprotection. This is essential in antibody-drug conjugate (ADC) manufacture and advanced protein labeling.

    Industry compliance standards

    • ICH Q6B “Specifications: Test Procedures and Acceptance Criteria for Biotechnological/Biological Products”
    • ISO 13485:2016 (medical device—bioconjugates for diagnostics and therapeutics)
    • USP <1047> “Gene Therapy Products” (bioconjugate extension)

    Typical usage ratio

    • 2–5% w/w relative to total protein/antibody mass, with stoichiometry tuned by target modification degree and scale of conjugation batch

    Downstream process integration

    • Reacted post-protein purification at the linker installation stage; removal or activation steps follow for site-specific drug or dye coupling

    Final product types

    • Antibody-drug conjugates (ADC)
    • Site-specifically labeled biotherapeutics
    • Protein, peptide, or enzyme-fluorophore conjugates for in-vitro diagnostics

    4. Analytical Reagent and Quality Control Reference Manufacturing

    Producers of analytical kits and reference materials use MNBCPBA in the multi-step synthesis of advanced derivatization agents. Its protected functionalities grant analysts precise control in developing reagents for HPLC, LC-MS, and immunoassays, which require consistency in both batch synthesis and reagent shelf-life. The compound sustains traceability required for characterization of impurities and validation standards in pharmaceutical and biotechnology QC labs.

    Industry compliance standards

    • ISO/IEC 17025:2017 “General requirements for the competence of testing and calibration laboratories”
    • USP <1224> “Transfer of Analytical Procedures”
    • FDA 21 CFR Part 11 (electronic records for analytical data)

    Typical usage ratio

    • 5–15% as a derivatization agent or reference material basis, with adjustments per analytical platform and matrix complexity

    Downstream process integration

    • Integrated after primary reagent synthesis or mixed into final kit solutions for standardization, ready for downstream QC release and customer validation

    Final product types

    • Certified reference standards for peptide and protein analysis
    • High-purity derivatization reagents for chromatographic applications
    • Pre-formulated analytical controls for regulated QC laboratories
    Free Quote

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    Certification & Compliance
    More Introduction

    3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid: Introducing a Precision-Driven Building Block

    Everyday Insights from the Factory Floor

    Watching each batch of 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid come together feels like charting out a roadmap for high-precision organic synthesis. Our technicians know this compound by the familiar tang in the air, the shimmering yellow-tinted powder that signals a reaction run under clean, controlled conditions. Walking through the plant gives you an appreciation for the layered chemistry involved and the specialized nature of the output.

    This product came about because our research partners and in-house scientists saw an unmet need in the peptide and small-molecule field. Getting this molecule to purity wasn’t just a matter of routine process steps and time on the reflux line—it meant hours spent optimizing the deprotection stages, selecting anhydrous conditions during coupling, and keeping rigorous checks on the formation of side products. It required skills honed over thousands of production runs, navigating pressure from both large-scale industrial demand and small-batch specialty requests.

    Meeting Modern Synthetic Challenges

    People underestimate how much modern chemistry hinges on tools at the building-block level. We see 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid playing an outsized role in pharmaceutical research because the S-protected pyrrolidine scaffold sets the molecule up for further derivatization. While many manufacturers try to cut corners with generic precursors, our focus on stereoselectivity and maintaining both the 2S,4S configuration and intact protecting groups makes all the difference in the downstream chemistry.

    This compound never leaves the plant before undergoing repeated HPLC and NMR checks. Our chemists have found that even a slight drop in enantiomeric purity introduces roadblocks for peptide coupling and can affect the yield of longer synthetic pipelines. Decades of attention to chromatographic behavior and crystal morphology allow us to guarantee that our finished product will behave consistently, whether in a medicinal chemistry platform or in early-stage drug development. This sort of rigor started as a practical matter—customers kept coming back with requests for better quality, less batch variation, and longer shelf stability.

    Anatomy of a Multi-Purpose Intermediate

    We chose to refine this molecule not because it fills a standard inventory gap but because it fits right where medicinal chemists meet practical manufacturing. Each delivery batch must maximize free thiol content after selective deprotection, keep the benzyloxycarbonyl group untouched, and retain the right configuration to allow for peptide extension or conjugation. Traditional alternatives, such as unprotected pyrrolidine analogs, fail to offer this trifecta; they often undergo oxidation or racemization, which leads researchers nowhere.

    Our process produces this compound as an off-white to faint yellow solid, with consistent particle size that allows straightforward handling in glovebox assembly or standard bench-top procedures. It’s easy to underestimate how much a dependable intermediate helps a synthetic team stay ahead of schedule. Bottlenecks caused by unreliable material quality waste weeks and money.

    At our plant, the push for higher-purity intermediates comes from lived experience—not from academic abstraction. Incorrect rotamer ratios once sent an entire multi-kilo batch for disposal. We now run extra DMF washes and careful crystallization steps because we know exactly where mistakes might lie and how quickly they spread through a research program. Delivering this benzoic acid derivative at >98% chemical purity gives customers peace of mind and predictable reaction setups, whether for early-phase SAR explorations or pilot-scale manufacturing.

    Specifying What Sets It Apart

    One thing we’ve learned in production is that there’s almost always a trade-off between speed and exactitude. Here, we draw a hard line at every critical control point, particularly in handling and storage. Our synthesis leverages both classical solid-phase peptide chemistry knowledge and tailored solution-phase couplings, keeping side reactions in check.

    Competitor materials sourced from intermediaries often arrive with mismatched certificates or insufficient detail on diastereomeric purity. We believe our in-house controls—tracking every input from batch to final drum, archiving spectral data in redundant labs, and maintaining hands-on staff—beat even high-end traders and third-party resellers. Our confidence doesn’t come from blind loyalty to our brand, but from years spent seeing what subpar material does to a customer’s workflow.

    Several researchers have commented on our product’s predictable performance during deprotection or coupling runs. In the early days, a client flagged subpar yields from a commercial supplier and traced them back to byproduct build-up during base treatment. The root cause proved to be incomplete removal of nitrobenzyloxycarbonyl protecting groups, which stemmed from vendor negligence during final crystallization. Since then, close attention to every protecting group has paid dividends—customers routinely report increased consistency in their custom peptide runs.

    Usage Driven By Research Demands

    Seeing our compound in the hands of a drug discovery team never stops being rewarding. Scientists working on peptide-mimetic inhibitors rely on crystal-clear starting materials, with tightly controlled protecting group strategies. Here, the mercapto group allows for flexible modifications—after mild deprotection, it delivers a reactive thiol amenable to linkage formation or cross-coupling reactions. Retaining both the carboxylic acid and amino connectivity at the right spatial orientation means the product plugs easily into established synthetic routes.

    We get feedback from labs running high-throughput screens that our product holds up under automated synthesis protocols—even through hundreds of cycles. Any single failure in the supply chain can throw an entire research timeline into disarray. By keeping rigorous documentation and ensuring our batches match their meticulous standards, we support teams working on urgent timelines, including those tackling fast-evolving health challenges.

    Beyond drug discovery, custom peptide houses and contract manufacturing firms source this intermediate to obtain specialty conjugates and proprietary peptidomimetics. The specific nitrobenzyloxycarbonyl protection allows for sequential deprotection, which helps in orthogonally assembling intricate molecular scaffolds. Direct feedback from manufacturing chemists, process engineers, and analytical teams helps us fine-tune even small process parameters, from moisture control to elimination of residual catalysts.

    Challenges In Real-World Manufacturing

    The journey from bench to industrial scale is rarely smooth. Each time we scale a reaction or tweak a temperature ramp, we risk shifting selectivity or throughput. Early process runs showed unexpected polymerization during acidolytic work-up; we reengineered solvent selection to solve the problem. While many marketers highlight theoretical yields, we rely on realized output—what leaves the reactor, passes QC, and fits directly into the customer’s existing workflow.

    We learned not to take shortcuts on analytical validation. Staff spend long hours cross-checking peak splitting in NMR, running duplicate HPLC columns, and seeking even the subtlest impurity signals. The discipline comes from knowing one false “clean” signal can, down the line, trigger investigation recalls, especially in regulated sectors like GMP production. Through these persistent commitments, we earn trust not just with paperwork, but with material reliability batch after batch.

    Competing facilities in different regions may rush the process, prompting occasional offers from buyers seeking lower prices with vague provenance. Our chemists recall instances where poor imitations devastated a project’s timelines, caused product recalls, or undermined regulatory trust. For a company like ours, reputation grows from the inside: each person who packs, checks, or ships this compound understands the stakes.

    Differences From Other Product Options

    Our take on this benzoic acid derivative centers on balancing functionality and purity. Some market alternatives arrive with purity just under typical research thresholds or lack annotation of stereochemistry. We run parallel verification—matching spectral fingerprints with archival standards and consulting both organic synthesis specialists and end-users. Our labs avoid common pitfalls by not swapping raw material vendors merely for price advantages.

    Differences from substitutes go beyond documentation. Most similar molecules feature less robust protection for the mercapto group, risking unwanted reactions during multi-step synthesis. Our product holds up through reagents needed for peptide chain extension, with the benzyloxycarbonyl group resisting attack until the researcher actively deprotects under planned conditions. Attempts to use less-pure or racemic alternatives often generate downstream purification headaches, lost time, and scale-up failures.

    We field direct reports from clients describing the difficulty of achieving high enantiomeric excess with generic pyrrolidinyl intermediates. Our solution stems from deliberate process control—temperature stabilization, precise pH adjustment, and experienced staff intervention during critical stages. Whether it’s large pharmaceutical research or a startup biotech, users want a reagent that avoids introducing unnecessary risk.

    Staying Ahead Through Responsive Innovation

    No chemical stays useful if it can’t keep up with shifting research goals. We continually refine synthetic steps based on emerging feedback. Beyond polishing for purity, we monitor for environmental compliance and handling safety to match evolving regulatory and end-market requirements. Each lot’s documentation, including stability and shelf-life data, gets archived and reviewed whenever we alter production—no batch escapes without complete traceability.

    The science never stands still: as research projects move from discovery through to pre-clinical work, the industry demands higher throughput, lower impurity levels, and expanded documentation. We respond with ongoing investment in upgraded reactors, stronger process analytics, and on-the-ground chemist training. We invite chemists to visit, watch their actual product being made, verify every batch point in person—not to show off, but to underline the seriousness of quality control.

    Data-driven process upgrades come from everyday reality. Last year, we expanded process analytics by adding tandem mass spectrometry mapping to routine QA, reducing missed byproducts by over half. Installation of more robust nitrogen blanketing cut down on batch-to-batch discoloration, which initially confused new customers until we unraveled the link between ambient oxygen and impurity buildup.

    A Living Commitment to Quality

    Factories face pressure from every direction: clients seeking faster turnaround times, procurement pressing for lower costs, regulatory agencies adding layer upon layer of compliance. Only real commitment to detail keeps a product like 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid among the most respected tools in advanced synthesis.

    That means updating staff training programs to focus on new hazard analysis, investing in closed-system equipment for safer thiol handling, and developing long-term relationships with vetted feedstock providers. No batch leaves the plant until experienced eyes inspect every stage. If issues crop up—whether in shipment, customs, or application—our technical support steps in, often working late to ensure researchers receive actionable advice.

    The reputation of a chemical manufacturer grows batch by batch—through silent mornings in QC labs, slow careful runs on preparative HPLC, and the handoff from raw precursor to finished container. Success doesn't rest on marketing claims, but on unwavering delivery of what scientists expect: consistent, clean, reliable input each time.

    Looking Forward: Building Trust, One Batch at a Time

    Tomorrow’s chemical solutions won’t look like yesterday’s. Advanced compounds such as our 3-[[[(2S,4S)-4-Mercapto-1-(4-Nitrobenzyloxy)Carbonyl-2-Pyrrolidinyl]Carbonyl]Amino]Benzoic Acid build on decades of learning and daily handling finesse. Every gram we ship has a story—of challenge, adaptation, and customer-focused improvement. Chemists working at the vanguard of research demand reliable tools, clear documentation, and stable supply lines.

    We believe our ongoing responsibility lies not just in one-time delivery, but in transparent process reporting, ongoing technical advice, and a willingness to adapt. As researchers stretch boundaries in molecular design, disease intervention, and industrial biochemistry, we respond not with generic sales talk but with the measurable, lived reliability and expertise that only a dedicated manufacturer can bring. Through each lot and every shipment, our job remains as clear as ever: support science as it is practiced, by real people in real labs, every day.