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4-Azidobenzoic Acid

    • Product Name 4-Azidobenzoic Acid
    • Alias 4-Carboxyphenyl azide
    • Einecs 210-010-0
    • 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
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    Specifications

    HS Code

    707466

    Product Name 4-Azidobenzoic Acid
    Cas Number 2997-18-4
    Molecular Formula C7H5N3O2
    Molecular Weight 163.13 g/mol
    Appearance Light yellow to beige powder
    Melting Point 147–151°C
    Solubility Slightly soluble in water
    Density 1.48 g/cm³
    Purity Typically ≥97%
    Structural Formula C6H4(N3)COOH
    Iupac Name 4-azidobenzoic acid

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

    Packing & Storage
    Packing 4-Azidobenzoic Acid, 5g, comes in a sealed amber glass bottle with hazard labels, screw cap, and tamper-evident seal.
    Shipping 4-Azidobenzoic Acid should be shipped in accordance with hazardous material regulations. It must be packed securely in airtight, chemically resistant containers, clearly labeled, and cushioned to prevent damage. The package should be handled by authorized carriers with proper documentation, and shipped with temperature control if required, to ensure safety and regulatory compliance.
    Storage 4-Azidobenzoic acid should be stored in a tightly sealed container, away from light, heat, and sources of ignition in a cool, dry, and well-ventilated area. It should be kept away from incompatible materials such as strong acids, bases, and reducing agents. Due to its azide group, handle with care and avoid mechanical shock or friction to prevent potential explosive decomposition.
    Application of 4-Azidobenzoic Acid

    Applications of 4-Azidobenzoic Acid in Industrial Manufacturing

    4-Azidobenzoic acid serves as a key intermediate in organic synthesis, polymer modification, and active pharmaceutical ingredient (API) production. As a direct manufacturer, we maintain material consistency and technical documentation to support precise formulations for regulated industrial applications.

    1. Pharmaceutical Intermediate Synthesis

    This compound enables the construction of complex heterocycles and modified aromatic structures in medicinal chemistry. Drug development pipelines employ it for preparing azide-functionalized building blocks, particularly in the production of experimental and targeted therapies using click chemistry approaches. Controlled additions during acylation or conjugation steps support high purity for downstream API synthesis, from laboratory scales up to GMP-compliant pilot runs.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • Ph. Eur. General Monographs for Pharmaceutical Substances
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (for clinical research ingredients in China)

    Typical usage ratio

    • 0.5–5 molar equivalent per coupling reaction, adjusted based on target molecular design and reaction pathway

    Downstream process integration

    • Reactant in copper(I)-catalyzed azide–alkyne cycloaddition
    • Intermediate in custom linker synthesis for antibody-drug conjugates (ADC) production
    • Introduced after primary amination or halogenation steps in multi-step API synthesis routes

    Final product types

    • Antitumor lead compounds
    • Pain management actives with triazole moieties
    • Click-chemistry pharmaceutical probes

    2. Surface-Modified Polymer Manufacturing

    The azide group enables chemical grafting onto polymer substrates for functional surface modification. Precise metering yields pre-activated polymers used in electronics, medical devices, and diagnostics. The compound enters melt blending or solution-phase modifications to introduce photo-reactive or bio-reactive sites, supporting downstream crosslinking and sensor integration.

    Industry compliance standards

    • ISO 10993 (Biological Evaluation of Medical Devices, for biomedical polymers)
    • RoHS Directive (EU Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • REACH Annex XVII (Substance restrictions for polymer additives)
    • UL 94 (Flammability requirements for plastic materials)

    Typical usage ratio

    • 0.1–2% by weight for polymer batches, determined by grafting density targets and downstream application specificity

    Downstream process integration

    • Post-polymerization functionalization through melt kneading or solvent swelling techniques
    • UV crosslinking after azide group installation
    • Covalent attachment of biomolecules or dyes in microfluidic chip assembly

    Final product types

    • Bioactive polymer films for biosensors
    • Photo-patternable resins for microelectronics
    • Drug-eluting stent coatings

    3. Photoreactive Crosslinking Agent for Specialty Coatings

    By exploiting the photolability of the azide functional group, specialty coatings manufacturers deploy this compound as a photo-crosslinker. Upon UV irradiation, the azide moiety releases nitrogen, generating reactive nitrene species that covalently bond with substrate surfaces or within polymer matrices. This method supports production of scratch-resistant and chemically stable coatings in electronics and industrial equipment sectors.

    Industry compliance standards

    • ISO 9001:2015 (Quality management requirements for production lines)
    • ASTM D3359 (Measurement of adhesion by tape test)
    • EN 13523-11 (UV resistance standards for coil coatings)
    • GADSL (Global Automotive Declarable Substance List, for electronics coatings)

    Typical usage ratio

    • 1–10 parts per hundred resin (phr), adjusted with respect to coating thickness and UV exposure parameters

    Downstream process integration

    • Dispersed in acrylic or polyurethane resins prior to coating application
    • UV treatment step activates crosslinking directly on substrate
    • Final curing under inert atmosphere to maximize bond formation and uniformity

    Final product types

    • Display panel hardcoat layers
    • Anti-fingerprint coatings for touchscreens
    • Protective finishes on industrial printing plates

    4. Bioconjugation Reagent for Diagnostic Kit Manufacturing

    Lab-grade preparations use 4-azidobenzoic acid for site-specific labeling and immobilization of biomolecules in in vitro diagnostics (IVD). Introducing azide groups via carboxyl activation enables covalent coupling with alkyne-functionalized antibody or protein partners, creating stable conjugates for lateral flow assays, microarrays, and ELISA substrates. This supports high batch-to-batch reproducibility vital to diagnostic device manufacturers.

    Industry compliance standards

    • ISO 13485 (Quality management for medical device production)
    • IVDR (EU In Vitro Diagnostic Regulation 2017/746)
    • US FDA 21 CFR 820 (Quality System Regulation for medical devices)
    • CLSI EP17 (Protocols for analytical performance of IVD reagents)

    Typical usage ratio

    • 0.01–0.1 mg per mg protein, tuned according to molecular weight and desired conjugation density

    Downstream process integration

    • Amide bond formation post carbodiimide activation
    • Protein labeling prior to lyophilization and assembly into test kits
    • Surface coupling on polystyrene or nitrocellulose membranes under controlled conditions

    Final product types

    • ELISA diagnostic plates
    • Rapid lateral flow immunoassay strips
    • Fluorescence-tagged molecular probes
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    Competitive 4-Azidobenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Azidobenzoic Acid: A Manufacturer’s Perspective on Production, Purity, and Applicability

    Introducing 4-Azidobenzoic Acid

    Working daily on the production floor, I’ve watched many organic intermediates flow through our reactors, but 4-Azidobenzoic Acid stands out for its reliability as a building block in modern synthetic chemistry. Known by its molecular formula C7H5N3O2, this substance carries an azido group at the para position to the carboxylic acid on a benzene ring, which opens the door to a unique array of chemical transformations. For teams focusing on active pharmaceutical ingredients, photoreactive polymers, or conjugation applications, this particular benzoic acid derivative often solves specific synthetic hurdles that other functionalized benzoic acids do not.

    Characteristics Stemming from In-House Synthesis

    Our expertise in producing 4-Azidobenzoic Acid isn’t built on guesswork. Over years of refining reaction conditions for azidation and carboxylation, our operators have seen the difference it makes to maintain reaction temperatures in the optimal window, minimize side product formation, and handle diazotization steps with precision. 4-Azidobenzoic Acid tends to decompose if mishandled, particularly under high heat or when exposed to strong acids, so strict process controls lead to fewer impurities and a consistent, off-white crystalline powder.

    We achieve typical purity levels above 98% using high-performance liquid chromatography, because any trace by-products or residual reactants can hamper downstream reactivity. This is not an idle boast – research customers who have struggled with unreliable lots from indirect suppliers have brought contaminated material to us for reprocessing. Poorly synthesized 4-Azidobenzoic Acid can introduce nitroso or amino side groups that stall coupling reactions. By taking full responsibility for our chemistry, we save our partners days or weeks of troubleshooting in their own labs.

    The Role of Safety and Handling Knowledge

    Longevity in manufacturing teaches that specialty azides call for trained hands. Despite its manageable hazard profile compared to more volatile azides, 4-Azidobenzoic Acid deserves care during both synthesis and shipment. Factory teams wear antistatic gear and maintain nitrogen atmospheres during bottling to prevent dust cloud ignition. Customers benefit from this diligence since the product’s integrity partly relies on how gently it’s handled after crystallization and drying. Each batch gets packed in moisture-proof containers, never left to atmospheric exposure, because the azido group reacts with water over time and sensitivity grows.

    Key Differences: Our Product vs. Alternatives

    Comparing 4-Azidobenzoic Acid to its closest analogs like 2-Azidobenzoic Acid or 3-Azidobenzoic Acid, chemists recognize its superior stability and predictable reactivity. The para-positioned azido group resists unwanted rearrangement and side reactions, giving cleaner conversion rates in click chemistry and Staudinger ligation. In practice, researchers see higher yields with our material due to careful control over isomeric purity. Some third-party traders do not distinguish between meta- and para- substitution, sending mixed shipments that confound analytical or synthesis efforts. Our QA team performs NMR on each batch to verify structure before labeling, so surprises are rare.

    Looking at more standard benzoic acids or even nitrobenzoic acid derivatives, 4-Azidobenzoic Acid’s azido group unlocks bioorthogonal chemistry that nitro, amino, or carboxyl alone cannot support. For photolabeling and surface modification, the azide functional group brings unique opportunity – it’s easily converted to reactive nitrenes with UV exposure. Our customers in materials science describe using our material to graft photoactive groups onto polymeric surfaces, and the difference between pure, well-preserved azide and degraded or impure product shows up directly in their spectral data and efficiency tests.

    Applications in Practical Synthesis and Research

    From our view inside the plant, the range of real-world uses keeps expanding. Pharmaceutical process chemists regularly request our 4-Azidobenzoic Acid for making target molecules via copper-catalyzed azide-alkyne cycloaddition reactions – the classic “click reaction.” Here, batch consistency pays off in reliable yield and minimal byproducts, streamlining scale-up. We’ve watched bench scientists study drug intermediates, bioconjugates, and sensors. The clean azide signal in spectroscopy makes peptide and nucleic acid coupling straightforward, with less need for time-consuming purification.

    In material science, university groups count on our product for crosslinking or adding functional handles to custom polymers. The integrity of the azido group matters because partial degradation means incomplete attachment or defective photopatterning. More than once, a polymer researcher has told us directly that our azide sources outperformed what they got from secondary suppliers, enabling more reproducible surface functionalization at pilot scale.

    Process Innovations That Make the Difference

    Over years of fine-tuning, we moved away from older routes that left too much inorganic salt and incomplete conversion. The original Sandmeyer reaction conditions, for instance, left occasional halide impurities that complicated purification. Now our operators use continuous-flow azidation for better heat control and safer gas handling. This cut down worker exposure while supporting larger lot sizes without sacrificing quality. Close monitoring of diazotization pH helped reduce diazene side product formation, and mechanical filtration replaced batchwise recrystallization to shorten cycle time.

    By keeping eyes on kilogram-scale runs, chemists on our team spot subtleties missed in academic-scale processes. Slight darkening during workup, for example, flags excessive nitroso impurity. High purity comes not from software-driven quality control, but from operators who know their process by heart. Small things like strict batch coding and hands-on transfer to drying lines keep shipments consistent and traceable. Clients mention this traceability as a reason for choosing factory-direct sources rather than middlemen, because they have specific questions that only actual producers can answer with confidence.

    Meet the Specifications That Matter

    We standardize our batches for researchers and industrial users alike. Most shipments offer 4-Azidobenzoic Acid as fine, off-white to yellow crystalline powder with a melting point in the 155–158°C range. Water content measures below 0.5% as determined by Karl Fischer titration. Chloride and sulfate are kept below 0.1%, and iron is routinely less than 5 ppm according to our ICP-OES scans. In-house NMR and FTIR characterize each lot for possible aromatic impurities, and stringent limits on residual solvents ensure compliance with both REACH and ICH Q3C solvent guidance.

    No two runs are exactly the same, but our technicians manage batch-to-batch variation through strict raw material approval and end-to-end lot documentation. Each batch comes with an individualized certificate and full spectra when requested. We invite visiting QA teams for audits to see for themselves how our operators control for cross-contamination and batch integrity at every step. This habit of transparency has led to long-term relationships with several advanced R&D partners.

    Troubleshooting Common Issues in Downstream Use

    Some partners in drug discovery have faced setbacks originating from unstable azides supplied by less experienced vendors. Instability often traces back to microscopic side-products, excessive moisture uptake, or contamination from inappropriate storage or shipping. An overlooked issue involves packing azides in inadequately sealed containers that allow slow hydrolysis. This risk disappears when we use our multi-layered, humidity-proof drums with integrated desiccant packs. Stable, dry 4-Azidobenzoic Acid is less prone to nitrogen off-gassing and decomposition, which means better batch reproducibility in chemical conjugations or polymer surface modifications.

    Processing errors rarely escape an expert’s attention. Our team keeps detailed notes when deviations arise, such as mild color changes or delayed crystallization during final workup. Under these conditions, we isolate suspect sublots, conduct further analytical checks, and communicate findings directly to downstream users. Instead of quietly blending off-spec material or sending uncertainties down the line, we prioritize transparency. This approach heads off reactivity issues like click chemistry side reactions, where even a few percent of impurity will compromise isolation of final bioactive conjugates. Our clients in sensitive areas such as radio-ligand synthesis or bio-photolithography depend on this vigilance for confidence in their own protocols.

    Why Users Choose Factory-Direct Over Third-Party Sources

    Direct connection between manufacturer and researcher creates distinct advantages. We see it in feedback from labs scaling up from milligram to multi-gram reactions, or large-volume intermediates. In bulk shipments, minor supplier substitutions can result in compounded error, as slippage in isomer purity or moisture content adds up in process chemistry. Our partners keep their pipelines secure and predictable by returning to us for repeat orders, bypassing fragmented distribution networks. Having witnessed failures in multi-step syntheses due to contaminated raw material, we remain convinced that traceable, single-source procurement saves more than just paperwork headaches. It preserves data integrity and ensures timely delivery.

    Lab teams sometimes work under intense publication timelines, where an unreliable raw material interrupts not just chemistry, but careers. Several research groups have invited us to review failed syntheses, sometimes sending us their remnants for NMR analysis. In those cases, we frequently detect swapped isomers, hydrolysis products, or unexpected residuals that third-party suppliers overlooked. Direct engagement fosters that essential back-and-forth; every batch we ship includes batch records our customers can trace directly. On two occasions, researchers contacted us at the method development stage, asking which solvent washes or drying conditions to use for optimum results. That hands-on discussion cannot be matched by companies removed from actual production.

    Sustainability Efforts in Production

    Environmental responsibility matters to us as active chemical manufacturers. Older methods for synthesizing azidated aromatics required immense water and caustic usage, generating large volumes of brine and acidic waste. We now reclaim sodium azide in closed-loop systems, capture process water for on-site treatment, and minimize solvent burden through continuous distillation lines. Since azide intermediates must be handled as potential explosive precursors, managed waste handling isn’t just about compliance – it preserves both worker health and broader community safety. Regulatory inspections recognize these improvements, and we regularly share our learnings with downstream partners committed to green chemistry principles.

    Facility investments in process intensification have reduced energy consumption per kilogram of product. For every batch, operators log utility use and monitor emissions to meet ISO 14001 goals. By optimizing every stage, we not only cut cost but also limit atmospheric nitrogen oxides and runoff. Modern environmental compliance no longer feels like an afterthought in specialty manufacturing; it’s an active, day-to-day practice shaping decisions in real time. Our personnel receive yearly hazard and sustainability training that reinforces why these measures matter at the bench and in the surrounding community. Clients aiming for sustainable supply chains take this into account when selecting our azide intermediates, recognizing their own commitments are more likely to be met with us than with less transparent sources.

    Adaptability for Analytic and Process Chemists

    Supplying 4-Azidobenzoic Acid directly from our production facilities means we can customize specifications. Beyond default lots, we can provide size-graded crystals for easy dissolution or dust-free application, freeze-dried azides for extra moisture sensitivity, and micro-filtered grades for high-performance liquid chromatography users. This adaptability responds to feedback from advanced process labs, not generic catalog listings.

    For projects developing radiolabeled or isotopically enriched intermediates, our hands-on approach means we can integrate user-furnished isotopic labels directly during synthesis, minimizing recalibration or need for low-yield post-synthetic modification. Researchers told us this option let them maintain isotopic purity in radiotracer development, saving months of set-up. Other suppliers offering only standard catalog items can’t flex processes as easily, since they lack the underlying chemistry control and plant access necessary for custom runs. By contrast, onsite synthetic teams and responsive scheduling mean special projects proceed without needless bottlenecks.

    Links to Downstream Drug and Diagnostic Development

    Pharmaceutical and diagnostics companies approach us for 4-Azidobenzoic Acid as a starting material for small-molecule drugs, antibody conjugates, or radiolabel diagnostics. Every gram of azide can represent weeks of R&D extension if it arrives pure and on time. Recently, one customer shared results showing improved tumor targeting in vivo after switching to high-purity, factory-linked azide for their linker technology. Their team had previously relied on secondary suppliers with unclear batch provenance and saw inconsistent biological activity. Direct sourcing clarified batch integrity, and authorization labs could correlate every experiment back to a single, controlled lot.

    Economic pressure in drug manufacturing has sharpened attention to supplier reliability. Missed delivery windows or unreported material changes can delay clinical trials and binder registration. We built scheduling and reporting structures around these requirements, enabling regular communication with scientists working through toxicology or formulation hurdles. In a recent project, a clinical-stage company avoided several weeks of formulation troubleshooting because our technical team could clarify a minor solvent residue flagged in their analysis, referencing in-house records for batch provenance. Such interactions occur because factory teams develop relationships that extend beyond order fulfillment, supporting the broader goals of innovation and patient care.

    Pushing Technical Boundaries in Azide Chemistry

    Being rooted in manufacturing keeps us close to the latest synthetic demands. Advances in bioorthogonal chemistry, photolithography, and sensor development continually challenge us to refine 4-Azidobenzoic Acid’s performance and safety profile. This past year, we received requests for triply recrystallized, ultra-high-purity azide for sensitive photoreactive labeling. To meet these specifications, our synthesis line managers redesigned the final purification train and adjusted solvent stripping protocols, demonstrating that deep product familiarity enables us to evolve with changing user needs. These adjustments bring value not just to the requesting lab, but to everyone who relies on the enhanced protocols in subsequent orders.

    We regularly evaluate advances in green solvents and process catalysts. A switch from mineral acids to buffered systems has reduced raw material corrosion and improved downstream waste recovery. For large-volume users, we’ve piloted continuous-flow technology with inline monitoring, which both shortens reaction time and immediately flags unwanted side products to operators on the plant floor. These technical advances create higher consistency in the finished material, as confirmed by repeatable chromatographic and spectroscopic records batch after batch.

    Quality Assurance Through Relational Knowledge

    Textbook quality control covers the basics – appearance, melting point, spectroscopy – but factory veterans know that high quality comes from process intimacy. Being directly responsible for each batch hones attention to residual solvents, trace metals, and isomer purity in ways that outsourced suppliers often gloss over. Technicians carefully examine dried product for subtle hue changes and bulk density shifts that could signal impurity formation or inappropriate drying temperature. This habit, grown over dozens of cycles, has led to faster identification and correction of potential issues compared to distant QA checks in third-party chains.

    Users looking for low impurity load in bioconjugate or pharmaceutical work value this detail orientation. Our protocol for tracing every starting material through the synthesis chain to the final product label creates peace of mind. In contrast, product arriving via multiple offices or repackagers can lose critical information. Researchers returning for additional lots often remark on the confidence this breeds, simplifying regulatory filings, and reducing time lost to repeat characterization. By consistently closing the loop between batch production, analytics, and user feedback, we create a kind of organic quality system that evolves with every order.

    Continuous Learning From Real-World Application

    Direct feedback from the bench to the plant floor shapes improvements more quickly than any formal hearing. Users often describe how actual 4-Azidobenzoic Acid interacts with downstream enzymes, surface substrates, or photo initiators. We learned to fine-tune particle size range for better suspension in aqueous systems because a graduate student described filtration issues during protein labeling. By adapting granulation protocols, we improved material performance in dozens of unrelated labs. Factory teams read journal articles, join virtual seminars, and speak directly with end-users to keep pace with the global research community.

    Occasionally, entirely new applications prompt reevaluation of our own controls. Multistep radiolabel synthesis, for example, brought to light a subtle volatility issue under microwave irradiation. To solve this, we modified both filtration and final drying procedures, drawing on our direct knowledge of product thermodynamics. The ability to tune these variables on a short timeline comes from years of collective experience and a commitment to problem-solving that links producer and user as partners rather than as faceless supplier and buyer. Sustaining these relationships generates more than sales; it expands technical knowledge base across multiple industries.

    Summary: Why 4-Azidobenzoic Acid From Us Matters

    Manufacturing and supplying 4-Azidobenzoic Acid means taking every batch personally, attending to the difference only true producers can control – whether that’s eliminating excess moisture, hitting the right isomeric ratio, or supporting analytical questions long after delivery. This compound’s chemistry requires expert attention from synthesis to application, and only factory-based teams can deliver the trust, reliability, and product performance demanded by today’s pharmaceutical, materials, and research leaders. Every lesson learned in production carries forward into each order, closing the feedback loop and powering new discoveries with steadier hands and clearer knowledge.