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Boc-3-Aminobenzoic Acid

    • Product Name Boc-3-Aminobenzoic Acid
    • Alias Boc-3-ABA
    • Einecs 697-729-9
    • 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

    571986

    Product Name Boc-3-Aminobenzoic Acid
    Cas Number 10374-49-7
    Molecular Formula C12H15NO4
    Molecular Weight 237.25
    Appearance White to off-white powder
    Purity Typically ≥98%
    Melting Point 140-144°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Temperature 2-8°C
    Inchi Key ZZZPUAHSQAHSJD-UHFFFAOYSA-N
    Synonyms tert-Butyl 3-aminobenzoate-1-carboxylate
    Smiles CC(C)(C)OC(=O)C1=CC(=CC=C1)N
    Usage Peptide synthesis intermediate

    As an accredited Boc-3-Aminobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-gram Boc-3-Aminobenzoic Acid is packaged in a sealed amber glass bottle with a screw cap and tamper-evident seal.
    Shipping Boc-3-Aminobenzoic Acid is shipped in tightly sealed containers to protect against moisture and contamination. It is typically transported at ambient temperature, unless otherwise specified, and should be kept away from incompatible substances. Packaging complies with safety regulations to ensure secure delivery and minimize the risk of spills or exposure during transit.
    Storage Boc-3-Aminobenzoic Acid should be stored in a tightly sealed container, protected from moisture and light, at a cool, dry place—preferably at 2-8°C (refrigerator temperature). Ensure good ventilation and avoid exposure to strong acids, bases, and oxidizing agents. Proper labeling and storage prevent degradation and contamination, maintaining the compound's stability and purity.
    Application of Boc-3-Aminobenzoic Acid

    Applications of Boc-3-Aminobenzoic Acid in Industrial Manufacturing

    As a manufacturer specializing in Boc-3-Aminobenzoic Acid, we supply this intermediate to key segments of the pharmaceutical and fine chemical industries. Our production and quality assurance processes are tuned to the technical requirements and compliance frameworks of each downstream application. The following sections detail practical integration and usage across major industrial manufacturing scenarios.

    1. Small-Molecule API Synthesis in Oncology Drug Development

    Pharmaceutical companies engaged in oncological therapeutics use our compound as a protected amino building block during multi-step organic synthesis of various anti-cancer drug candidates. The boc-protected functionality provides temporary amine protection in solid-phase and solution-phase peptide and heterocycle formation, allowing for precision in subsequent deprotection and coupling steps. The upstream addition occurs prior to key cyclization or amidation reactions, minimizing impurities and enabling efficient downstream purification processes in clinical and commercial API production.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) General Chapter <823>
    • European Pharmacopoeia Monograph requirements for amino acid derivatives
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 5–15% molar ratio relative to target amine group; precise proportion depends on synthesis pathway and stepwise protection requirements

    Downstream process integration

    • Charged into protection step reactors during initial amide or peptide synthesis
    • Deprotection executed post-chain elongation or ring closure for further derivatization
    • Removed under acidic treatment without compromising product integrity

    Final product types

    • API intermediates for antineoplastic agents (e.g., benzoic acid-derived pharmaceutical actives)
    • Protected peptide segments for targeted cancer therapies
    • Heterocyclic medicinal compounds used in clinical trials

    2. Peptide Synthesis for Diagnostic Reagents

    Producers of diagnostic kits and custom research reagents rely on Boc-3-aminobenzoic acid as a key Fmoc- or Boc-protected aromatic linker during solid-phase peptide synthesis (SPPS). The position and electronic character of this protected amino benzoic acid support precise attachment of fluorophores or enzyme labels, enhancing peptide probe functionality and stability required in immunoassays, ELISA reagents, and fluorescent tagging. Process engineers integrate our material at linker-loading or branching points in automated synthesizers, maintaining purity and yield standards for downstream labeling and conjugation.

    Industry compliance standards

    • ISO 13485: Medical Devices Quality Management Systems (for diagnostic reagent kits)
    • Applicable CLSI (Clinical and Laboratory Standards Institute) protocols for reagent performance
    • European Directive 98/79/EC (In Vitro Diagnostic Medical Devices)

    Typical usage ratio

    • 3–10% weight/weight with respect to total amino acid pool; adjusted based on the peptide length and desired labeling density

    Downstream process integration

    • Loaded onto resin during initial synthesis as a protected branching or terminal residue
    • Enables stepwise elongation while safeguarding aromatic amino position
    • Deprotected after peptide chain assembly for coupling with label or dye

    Final product types

    • Immunodiagnostic peptide standards and controls
    • ELISA and lateral flow assay substrate conjugates
    • Fluorescent peptide probes for research use

    3. Advanced Material Modification for Polymer Synthesis

    Manufacturers of specialty polymers and functional materials use our product as a boc-protected aromatic acid monomer in the creation of high-performance polyamides and aromatic polyesters. By introducing Boc-3-aminobenzoic acid at the monomer stage, process chemists can precisely control polymer branching and introduce pendant amine functionalities after selective deprotection. This approach is critical for customizing polymer backbone architecture and preparing resins for high-temperature, chemical-resistant coatings or biocompatible implants.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • REACH Regulation (EC) No 1907/2006 for polymer intermediates
    • RoHS Directive 2011/65/EU (for electronic and medical-grade polymers)

    Typical usage ratio

    • 1–8% molar ratio in feedstock blend, dependent on target functional group density and resin formulation

    Downstream process integration

    • Fed into polycondensation or copolymerization reactors with diacids/diols
    • Deprotection performed after initial polymerization to reveal free amino groups
    • Post-functionalization executed for tailored surface chemistry

    Final product types

    • High-temperature resistant polyamides for automotive and aerospace
    • Biocompatible polyester scaffolds for medical devices
    • Functional polymer additives for specialty coatings

    4. Intermediate for Agrochemical Active Synthesis

    Agrochemical producers apply this boc-protected aromatic compound as an intermediate during multi-stage synthesis of selective herbicides and growth regulators with benzoic acid core structures. The Boc group preserves the amine function through demanding chlorination and acylation reactions, improving overall yield and target-specific activity. Our customers dose the compound at key protection steps, then perform a controlled deprotection immediately prior to final coupling or salt formation for enhanced biological activity and improved formulation stability.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 (for quality management in agrochemical intermediates)
    • REACH Regulation (EC) No 1907/2006 (chemical safety and registration)

    Typical usage ratio

    • 5–12% weight/weight relative to targeted intermediates, optimized for each synthetic sequence and based on desired protection-deprotection efficiency

    Downstream process integration

    • Added at the initial protection stage prior to aggressive electrophilic substitution
    • Maintains amine integrity through chlorination and coupling
    • Removed before final crystallization and granulation

    Final product types

    • Benzoic acid-based pre-emergent herbicides
    • Plant growth regulator intermediates
    • Active ingredients for selective weed management solutions
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    Certification & Compliance
    More Introduction

    Boc-3-Aminobenzoic Acid: Behind the Scenes in Chemical Manufacturing

    Everyday Insights from a Manufacturer’s Perspective

    You spend years in a plant, you start to see what chemicals really mean for research teams and industrial chemists. Boc-3-Aminobenzoic Acid, with CAS number 31142-56-0, earns quiet respect on our production lines. It’s not a big-volume commodity, and not a flash-in-the-pan specialty. This compound stands for consistency, dependability, and the kind of nuanced innovation that drives real results in peptide synthesis and analytical work. Peeling away the salesman jargon leaves room to talk openly about what it really offers, how we get it right, and what sets it apart when you put it side by side with similar products.

    Understanding the Core: What Makes Boc-3-Aminobenzoic Acid Tick

    Chemists recognize the Boc (tert-butoxycarbonyl) group as one of the most reliable protecting strategies for amino groups. 3-Aminobenzoic Acid serves as a solid aromatic scaffold, sturdy enough to host multiple functional transformations without giving in to unwanted side reactions. When these two pieces come together in Boc-3-Aminobenzoic Acid, the resulting molecule brings exactly the kind of stability and reactivity profile that peptide chemists crave. The Boc group keeps the amine tucked away during steps that would otherwise trigger side reactions or ring closures. Once you’re ready, simple deprotection returns that amine to reactive duty.

    Manufacturers like us measure success in spectra, melting points, and narrow purity ranges. We see raw data every day—NMRs, HPLC runs, FTIR data—so we weigh every bit of a synthesis batch against not only patent specifications but also against what downstream users report in real-world use. Our typical batches land at a purity above 99%. Those couple tenths matter for assay reproducibility in peptide mapping or even in scale-ups for preclinical intermediates. We see requests, too, for different grades: some lines want a high-end, chromatography-validated, peptide-grade lot; others need cost-effective technical material for screening. Real demand flows from the way end-users—synthetic chemists, bioconjugation labs, and preparative chromatography groups—see actual performance, not just how a marketing page presents it.

    Why Purity—and What We Do to Make It Reliable

    Contaminants don’t play well in peptide synthesis. Trace amounts of unreacted amine or mis-protected precursor show up as impurities in target products, affecting yield, downstream purification, and even biological testing. We’ve wrestled with this—batch after batch, across different temperature profiles, using alternative protection/deprotection regimes. Real improvement comes down to process control. From reagent weighing to the choice of Boc anhydride, every minor change leaves a fingerprint on the final purity.

    Unlike many intermediates, Boc-3-Aminobenzoic Acid stays impressively stable when stored in cool, dry spaces, with no tendency to yellow or degrade under standard warehouse conditions. Our team tracks changes not just on paper or in data sheets, but through visual checks, sample pull-outs, and routine spot-testing throughout the year. Customers doing peptide coupling want peace of mind that five-, six-, even twelve-month-old batches behave the same as the first drum cracked open.

    Speaking as a Producer: Handling and Usability in Practice

    Chemists want to spend less time on rework or troubleshooting. The way Boc-3-Aminobenzoic Acid behaves under common lab conditions matters more than some might think. Clumping, hygroscopicity, or uncontrolled particle size slow down workflow, especially at pilot and kilo-lab scales. Each season teaches us to avoid excess moisture, static buildup, or container cross-contamination.

    We’ve worked closely with industrial users who run multi-kilogram synthesis campaigns. They report fewer issues with agglomeration or caking compared to certain other Boc-amino acids—credit goes not only to the molecule itself, but to process choices in drying and packaging. Some operators like the coarse crystalline form for easier weighing; others need powdery consistency for rapid solution dosing. Both are achievable with tight controls from crystallization to post-drying handling.

    Comparisons that Matter: What Sets Boc-3-Aminobenzoic Acid Apart?

    It may look like just another derivative in catalogs, but on the production floor differences appear fast. Take the position of the amine group. 3-Aminobenzoic Acid stands apart from its ortho- and para- isomers. The meta (3-) substitution pattern shapes not only overall reactivity but also solubility and compatibility in certain peptide or linker syntheses. Boc-protected ortho-aminobenzoic acids introduce ring strain and can misbehave under certain coupling conditions; para-substituted analogs show slightly different coupling efficiency. Our customers in solid-phase peptide synthesis, especially those fabricating drug conjugates or fluorescent labels, mention improved yields and cleaner purification profiles using the meta version for specific routes.

    One early large-scale project with a major research group highlighted the effect of trace metal scavenging. Boc-3-Aminobenzoic Acid, if purified with an optimized process that minimizes residual metal, delivers consistently high-quality product—even in sensitive bioanalytical workflows. We invested in process tweaks—alternative crystallization solvents, advanced filtration, multiple rinses—to keep trace levels low enough for LC-MS labs. Over years, this meant less batch rejection, fewer headaches, and more trust from recurrent customers.

    Why Real Control Is All about Process, Not Marketing

    A reliable supplier isn’t just the company in the catalog. It’s the team standing behind every lot—chemists, operators, managers, quality folks—whose years of troubleshooting build a body of knowledge. Delivering Boc-3-Aminobenzoic Acid to spec isn’t a given. In the real world, raw materials fluctuate, but customers still want the same sharp melting range and the same easy dispersion in solvents, batch after batch, year in and year out.

    Overhead lighting and ventilators in a plant won’t compensate for poorly monitored reactors. We run full audits not only post-process but at each step. Early detection tools—portable FTIR, regular spot-checks with handheld NIR—reduce the chance of batch deviation. Only through that routine do you get repeatability that end-users notice. Experience has taught our team that even a minor pH drift near neutralization, or a slightly extended stirring period in Boc protection, can shade the result. Feedback from customers often leads to tweaks in our process, tightening specs further and bringing practical value rather than just ticking regulatory boxes.

    Application in the Real World: Chemistry Gets Practical

    Peer-reviewed papers often mention Boc-3-Aminobenzoic Acid, but the literature rarely covers everyday workflow. We hear about its use from discovery chemistry up to pilot-scale production. The product enters the picture early—often as a protected intermediate that helps stitch together building blocks while keeping the amine out of trouble. Benefits go beyond academic curiosity: pharmaceutical companies rely on it as a backbone for modified peptides, linker units in antibody-drug conjugates, and fluorescent-tagged probes for diagnostics.

    Researchers value what lasts through long-term storage, ships safely across continents, and arrives as white, crystalline material time after time. We field requests for technical support not only on reactivity profiles, but on solvent compatibility, coupling methods (EDC, DCC, HATU) and deprotection options (TFA, HCl gas, etc). Our technical team compiles application notes after repeated customer engagement—tips that turn into updated SOPs both inside our factory and out in the field.

    Switching from Boc-3-Aminobenzoic Acid to other protected benzoic acids isn’t a formality. NMR shifts, solubility, and coupling efficiencies all influence synthetic outcomes. End-users chasing better yields often discover only after a few runs that the meta-isomer delivers distinct behavior, especially for sequence-specific modifications. Every feedback cycle—whether praise or complaint—flows right back into how we refine batch controls and customer guidance.

    Practical Considerations: Storage, Packaging, and Transport

    Shipping grams to kilograms across long distances isn’t just a matter of containers and labels. The physical stability of Boc-3-Aminobenzoic Acid helps us sleep at night: well-packaged, it resists atmospheric moisture, rarely cakes up during seasonal changes, and shows robust shelf life. We keep standard stocks in food-grade polyethylene drums for bulk users and smaller amber bottles for research volumes. Some customers with automated dispensaries ask for anti-static liners, while older labs simply focus on well-sealed bags to avoid air ingress. Both approaches suit this compound well.

    We monitor transit conditions closely—temperature-controlled trucks for large volumes, along with robust secondary packaging for overseas cargo. Reports from the field confirm that our batches arrive undamaged, with color, texture, and purity maintained even after two weeks in customs or long-haul transits. Every lot keeps a retained sample for reference, both for customer quality queries and for in-house trend tracking.

    Differences from Similar Products: Subtle but Significant

    Standing next to Boc-4-Aminobenzoic Acid, differences begin with the chemistry. The meta arrangement introduces changes in coupling efficiency and opens up unique synthetic applications, especially in the creation of non-natural linkers, altered pharmacophores, and probe design. Ortho-protected alternatives sometimes hinder downstream reactivity, thanks to hydrogen bonding or ring strain near functional groups. The meta variant—Boc-3—proves more forgiving in diverse reaction conditions.

    We also see less concern about byproduct formation during deprotection: TFA, commonly used for Boc removal, produces cleaner products and fewer complications in subsequent purifications. Researchers in bioconjugation and peptide mapping remark that columns last longer and analyses run more smoothly using metaposition derivatives, with fewer co-eluting impurities. Raw feedback from customers doing process development shows slightly better scalability and fewer dead-ends or bottlenecks when scaling from grams to multi-kilo batches.

    On the analytical side, spectral data come up cleaner, with less baseline disturbance, which simplifies both quantitation and impurity tracking. As a manufacturer, our own QA labs have seen smoother batch approvals and fewer requisite retests, which means more steady supply to long-term partners. Those who initially tried switching to “equivalent” products from other vendors often return after finding that batch-to-batch reproducibility lags behind, especially in high-precision synthesis lines.

    Addressing Challenges and Driving Continuous Improvement

    Supplying Boc-3-Aminobenzoic Acid at scale brings its challenges. Sourcing consistent starting materials, managing waste streams from Boc protection reactions, and keeping up with shifting regulatory demands keep us on our toes. Most issues arise not from the chemical itself, but from supply chain disruptions—delayed shipments of reagents, variable quality of solvents, or global regulatory shifts influencing precursor sourcing.

    We’ve developed alternative sourcing strategies for critical reagents, built up local partnerships, and increased on-site testing capability to respond faster to quality swings. This attention extends to environmental controls: continuous investment in waste stream management, solvent recycling, and safer process conditions pays dividends both for the environment and for our own operating costs. Customers—even those focused only on price or delivery—ultimately benefit from a more stable, resilient supply chain.

    Working with the Real End Users—Direct Feedback Loops

    Customers shape the product as much as process chemistry does. Regular calls with peptide research groups, pharmaceutical process teams, and diagnostic kit manufacturers create a living feedback loop. We’ve learned to adapt not only to specification demands, but also to evolving application needs—tighter particle size distributions for automated weighing, higher assay purity for novel drug candidates, and lot-to-lot tracking for regulatory submissions.

    Transparency builds trust. End users ask to review lot records, traceability documents, and impurity profiles. We respond openly: every specification comes with attached real-world batch reports, not just generic paperwork. Our lab team always stands ready to troubleshoot challenges, rerun analyses, and iterate to meet new project needs.

    Knowledge Sharing for Smarter Chemistry

    Reliable manufacturing isn’t just about selling material. We take pride in sharing knowledge accrued over decades—helping new chemists ramp up, supporting process troubleshooting, and adapting to never-ending shifts in synthetic approaches. Working with consortiums, academic groups, and contract manufacturers sharpens our focus and raises industry standards for Boc-3-Aminobenzoic Acid.

    Regularly reviewing published synthesis routes, updated analytical protocols, or customer innovation helps fine-tune our control strategies. Whether a question comes from a seasoned process chemist or a grad student setting up a coupling for the first time, we answer from experience, not from a generic script. Open dialogue drives improvement, not just in specs but also in reliability, shipment speeds, and trouble-free usage down the line.

    Looking Ahead: Reliable Supply, Reliable Chemistry

    Supplying Boc-3-Aminobenzoic Acid remains a day-to-day commitment to quality, safety, and open communication. The job isn’t finished when the drums leave the warehouse; we keep working to ensure every batch meets expectations on benches and in process plants around the world. Consistency, traceability, and responsiveness aren’t just buzzwords—they are part of how real manufacturing partners support scientific progress.

    Our longer view sees this molecule not as a finished product, but as a contributor in a chain of creativity that extends through research, drug discovery, diagnostics, and advanced materials. Staying flexible—while holding tight to the standards that matter—will keep Boc-3-Aminobenzoic Acid a trusted tool in the hands of researchers and industry practitioners for years to come.