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4-Hydrazinobenzoic Acid

    • Product Name 4-Hydrazinobenzoic Acid
    • Alias PABA-Hydrazine
    • Einecs 219-019-8
    • 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

    689069

    Chemical Name 4-Hydrazinobenzoic Acid
    Cas Number 619-67-0
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Appearance Light yellow to beige solid
    Melting Point 206-210 °C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes
    Synonyms P-Hydrazinobenzoic Acid; 4-Carboxyphenylhydrazine
    Storage Conditions Store at 2-8°C, protected from light
    Pubchem Cid 12494
    Inchi Key YBXBUERUJXLUOQ-UHFFFAOYSA-N
    Structure Benzene ring with carboxylic acid at para-position to hydrazine
    Hazard Statements Irritant; may be harmful if swallowed or inhaled

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

    Packing & Storage
    Packing 4-Hydrazinobenzoic Acid is supplied in a 25g amber glass bottle with tamper-evident seal and chemical hazard labeling.
    Shipping 4-Hydrazinobenzoic Acid is shipped in tightly sealed containers to prevent moisture ingress and contamination. It is packed under cool, dry conditions, labeled according to hazardous material transport regulations. Appropriate documentation, such as Safety Data Sheets, accompanies each shipment to ensure safe handling during transit and upon delivery.
    Storage 4-Hydrazinobenzoic acid should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as oxidizers. It should be kept in a cool, dry, and well-ventilated area, ideally at room temperature. Handle under a fume hood to prevent inhalation, and use proper protective equipment to avoid contact and contamination.
    Application of 4-Hydrazinobenzoic Acid

    Applications of 4-Hydrazinobenzoic Acid in Industrial Manufacturing

    As an established chemical manufacturer, we supply 4-hydrazinobenzoic acid for specialized applications where its unique reactivity enables strict quality and performance criteria across several advanced production sectors. Below, we outline real industrial downstream scenarios demonstrating how formulators and processors integrate this compound, supported by authentic compliance frameworks, dosage guidance, and process insights.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Antituberculosis Intermediates

    Pharmaceutical plants employ this building block to synthesize key intermediates for antituberculosis drugs, particularly in routes preparing hydrazide-containing APIs. Pharma-grade quality and traceability are essential at every stage, from raw material input through strict process controls, to fulfill Good Manufacturing Practice requirements and ensure reliable batch-to-batch consistency for regulatory submissions and commercialization.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/EP/BP monographs for related compounds
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 0.8–1.2 molar equivalents per target intermediate, adjusted based on yield optimization and side reaction minimization during hydrazinolysis steps

    Downstream process integration

    • Inserted after upstream benzoic acid derivative activation; reacts with acyl chloride or ester to generate hydrazide intermediate via solution-phase or slurry-phase synthesis under controlled temperature and pH

    Final product types

    • First-line antituberculosis agents (e.g., Isoniazid intermediates)
    • Hydrazide-linker APIs for infectious disease treatments
    • Chemical reference standards for method validation laboratories
    • Pharmaceutical research intermediates

    2. Specialty Azo Dye Manufacturing

    Industrial organic dye manufacturers leverage this compound’s hydrazine group for diazotization, yielding highly stable azo chromophores for advanced textile and laser dye systems. The formulation process demands stringent color fastness and purity, supported by precise process analytics and effluent control measures, since downstream use frequently targets regulated consumer-facing goods.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for harmful substances in textiles)
    • REACH Annex XVII (restrictions on certain azo compounds)
    • GOTS (Global Organic Textile Standard) for input chemical screening
    • ISO 9001:2015 for dye manufacturing facilities

    Typical usage ratio

    • 0.5–1.0 wt.% of batch mass, tailored based on precursor purity and target absorption intensity in downstream coloration stages

    Downstream process integration

    • Introduced post-aryl amine derivatization; undergoes diazotization with nitrite source in acidic aqueous phase, then couples with aromatic partners to generate stable azo bonds for pigment precursor slurries

    Final product types

    • High-performance textile azo dyes
    • Laser printer colorants
    • Industrial inkjet pigments
    • Synthetic fiber masterbatches

    3. Corrosion Inhibitor Precursor for Water Treatment Chemicals

    Engineered water treatment solution producers select this hydrazine derivative to formulate high-activity intermediates that block electrochemical corrosion in industrial cooling and boiler systems. The compound is valued for its reactivity in chelation and surface film formation, supporting extended asset lifetimes and reduced metal leaching, especially in facilities bound by stringent water discharge permits.

    Industry compliance standards

    • ANSI/AWWA B603 (Standard for Corrosion and Scale Inhibitors)
    • ISO 9001:2015 (Production quality management)
    • Local EPA/NPDES permits for industrial waste water effluents
    • OECD guidelines for biodegradability and aquatic toxicity testing

    Typical usage ratio

    • 0.02–0.08 wt.% relative to total inhibitor blend, modified by target metal types and system volume in commercial water cycles

    Downstream process integration

    • Reacted with carboxylic or phosphonic acid co-components at controlled pH in blending reactors, forming chelating complexes before liquid formulation or powder drying stages

    Final product types

    • Closed-cycle cooling water corrosion inhibitors
    • Boiler water conditioning additive blends
    • Premixed scale and corrosion control agents for HVAC systems
    • Specialty maintenance chemicals for industrial water loops

    4. Analytical Reagent Production: Detection of Reducing Sugars

    Producers of laboratory analytical reagents employ this compound to manufacture hydrazone-functionalized assay kits, especially for the colorimetric quantification of reducing sugars in food and pharmaceutical raw materials. The purity and batch reproducibility directly affect calibration accuracy, so manufacturers operate under ISO and traceability guidelines relevant for certified laboratory standards.

    Industry compliance standards

    • ISO 17034 (General requirements for reference material producers)
    • ISO 9001:2015 (Analytical reagent production)
    • AOAC Official Methods for sugar analysis
    • FDA guidelines for laboratory reagents in food testing

    Typical usage ratio

    • 0.1–0.3 wt.% in dry powder reagent kits, determined by the assay’s detection range and color development speed

    Downstream process integration

    • Introduced into mixing vessels with buffer salts and chromogenic additives; processed via dry blending or wet granulation before batch validation and packaging for end use in accredited laboratories

    Final product types

    • Reducing sugar quantification kits
    • Food industry analytical standards
    • Pharmaceutical quality control test kits
    • Reference solutions for instrument calibration

    5. Synthesis of Advanced Heterocyclic Compounds for Agrochemical Discovery

    Research-driven agrochemical developers utilize the reactivity of this compound’s hydrazine group for constructing pyrazole and other nitrogen-containing heterocycles, opening pathways to novel pesticide and herbicide candidates. High-grade consistency and trace impurity control are required to meet regulatory expectations and ensure reliable structure-activity relationship studies throughout crop protection chemical development pipelines.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 (R&D and production management)
    • FAO/WHO specifications for agricultural chemicals
    • REACH registration compliance for new agrochemical substances

    Typical usage ratio

    • 0.2–0.7 molar equivalents per cyclization reaction, modified to optimize product selectivity and minimize byproduct formation in research and pilot scale

    Downstream process integration

    • Added after aldehyde or β-diketone substrate activation in heterocycle formation, followed by condensation and cyclization under solvent-controlled, low-water conditions

    Final product types

    • Pyrazole derivative agrochemical leads
    • Herbicide active ingredient prototypes
    • Insecticide screening compounds
    • Pilot-scale research intermediates
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    Certification & Compliance
    More Introduction

    4-Hydrazinobenzoic Acid: A Specialty Intermediate Forged for Innovation

    Developed With Precision—Designed for Applied Chemistry

    Years of hands-on experience in organic synthesis have taught us that every functional group, every bond, and every impurity holds power over the final result. With 4-Hydrazinobenzoic Acid (CAS No. 619-67-0), our process starts on the level of molecular detail and ends in support for your most challenging research and production needs. Many have worked with common hydrazine derivatives, but our focus remains on the unique attributes of 4-Hydrazinobenzoic Acid: a compound that anchors specialty projects in pharmaceuticals, agrochemicals, dyes, and analytical chemistry. We’ve made and scaled this molecule for innovators because, over decades in the lab and in batch production, we’ve watched its structural qualities make all the difference between a project’s promise and its actual payoff.

    Molecular Essentials

    Chasing purity in chemical manufacture is more than a set of standards—it’s a shared goal for the chemists who trust in our material. The raw formula (C7H8N2O2) forms the foundation of 4-hydrazinobenzoic acid, but getting there consistently at scale takes more than a recipe. We synthesize, isolate, and purify this compound as a dry white-to-off-white crystalline powder. Rigorous control over particle size and minimal impurities is not a matter of blanket claims but of daily routines, confirmed by HPLC and GC-MS with each generated lot. Our experience confirms that when hydrazine content shifts, or when residual solvents stray above acceptable limits, batch-to-batch consistency breaks down—and so does your research or production run. We’ve fine-tuned each stage, from reagent selection to final vacuum drying, because every chemist deserves predictable results and minimized troubleshooting.

    Product Model and Form

    Chemistry is only as reliable as the tools and feedstocks available. We build 4-Hydrazinobenzoic Acid to deliver consistency at laboratory and industrial scales. Our standard product model comes as a crystalline solid, typically with assay values above 98 percent, confirmed by multiple in-house and third-party analyses. Moisture and inorganic residues are tightly controlled. These are not just selling points; they’re habits shaped by customer feedback and our own troubleshooting. We never lose sight of the role user experience plays in process chemistry. If a colleague downstream can avoid filter clogging or unwanted byproduct formation, that reflects both pride and pragmatism in manufacturing.

    The Role of 4-Hydrazinobenzoic Acid in Synthesis Pathways

    We recognize that 4-Hydrazinobenzoic Acid rarely serves as an end product. More often, it enters complex syntheses, typically forming hydrazones, azo dyes, pharmaceuticals, or functionalized benzoic acids. Lab notebooks, scale-up reports, and direct feedback from industrial chemists all highlight a pattern: This acid’s hydrazine group, anchored at the para position of an aromatic ring, creates opportunities for selective coupling, substitution, and condensation reactions. Its carboxylic acid group remains reactive enough for amidation while preserving unique compatibility with various solvents and reagents. When working with antitubercular agents, certain nonsteroidal anti-inflammatory drug synthesis, and families of dyes and pigments, colleagues seek out this intermediate for the kind of chemistry that opens new routes or higher yields.

    Key Applications: Pharmaceutical Research

    Custom drug discovery seldom rests on the shoulders of mainstream raw materials. In pharmaceutical research, demand for versatile intermediates sits at an all-time high. Our records reflect frequent requests for 4-Hydrazinobenzoic Acid as a key building block in the development of new hydrazone-based drugs. Medicinal chemists appreciate the balance between reactivity and stability inherent to this compound. It withstands standard storage and shipping, and yet, under the correct conditions, reliably forms hydrazones and related structures vital in bioactive molecules. Several research groups, including partners working in both bioconjugation and radiopharmaceutical labeling, acknowledge its efficient handling in aqueous or polar solvents—a small but actionable advantage in lead optimization or process scale-up.

    Making the Difference in Dye and Pigment Manufacturing

    Decades of pigment and dye work in our own facilities highlighted a constant challenge: achieving bright, stable colors without compromising production speed or cost. 4-Hydrazinobenzoic Acid stepped forward as a workhorse. Its structure works exceptionally well as a coupling agent, particularly in azo dye synthesis, driving cleaner reactions and minimizing undesired byproduct formation. This clarity translates to sharper hues and better batch-to-batch consistency in the finished product. Manufacturers who’ve switched to this intermediate have cut waste and improved color purity—a lesson learned again each time an alternative fails to meet quality or regulatory benchmarks.

    Versatility in Agrochemical Synthesis

    Agricultural chemistry often calls for innovation under the weight of regulatory standards and cost control. We’ve supplied 4-Hydrazinobenzoic Acid to partners chasing more selective herbicides and fungicides. The ease of derivatization—thanks largely to its reactive hydrazine group—opens options for synthesizing protected intermediates or fine-tuning biocidal activity. A robust acid group ensures predictable modification by amidation, esterification, or salt formation. Our collective experience affirms that introducing this intermediate early in discovery discussions saves headaches in late-stage route improvements or impurity profiling. Over multiple projects, it emerged as the flexible lever to unlock new biological activity without introducing exotic or unreliable raw materials.

    Analytical and Diagnostic Uses

    Not every practical application ends in a bottle of product shipped to a plant. Much of modern analytical chemistry leans on unique functional groups for developing probes, sensors, and labeling tools. Our clients in diagnostics lean on the hydrazine group to form stable conjugates with aldehyde-containing biomolecules—often under mild conditions that preserve protein integrity. In both in-house and customer studies, 4-Hydrazinobenzoic Acid outperformed bulkier or less-reactive analogues by delivering predictable, single-adduct conjugation—a necessary feature for quantifiable analytical readouts. We watched in real time as method developers swapped out alternative hydrazines for our product and immediately watched noise decrease and signal increase in their assays.

    What Sets 4-Hydrazinobenzoic Acid Apart?

    Lab shelves and catalogues are full of hydrazine derivatives and substituted benzoic acids. Our ongoing comparison testing, and feedback from practicing chemists, consistently give 4-Hydrazinobenzoic Acid a unique edge for projects demanding both reactivity and a handle for further functionalization. Unlike generic hydrazine or simple substituted benzoic acids, this compound unites the nucleophilic flexibility of hydrazines with the coupling and ionic capabilities of a carboxylic acid. Most alternative hydrazines, including unsubstituted varieties or those with ortho/para methyl groups, either deliver lower yields, unpredictable byproducts, or storage hazards. Analogous benzoic acids lacking the hydrazine group cannot participate in hydrazone or azo coupling chemistry, cutting off entire branches of synthetic versatility. On the bench, and in production, our teams have seen how switching to this molecule sharpens the separation between targeted products and unwanted side streams—a critical point for chemists under pressure to clean up processes or submit cleaner patent filings.

    Production Challenges and Solutions

    Our journey with 4-Hydrazinobenzoic Acid began over a decade ago, not in a scaled-up reactor, but at bench-scale as a test for process robustness. Scaling up hydrazine-based chemistry poses real hazards—hydrazines demand careful containment, and managing exotherms becomes a round-the-clock task. Every batch goes through staged addition of hydrazine reagents under active temperature control, with real-time monitoring for runaway potential. Solvent selection matters a great deal. Over years trialing aqueous, polar aprotic, and hybrid solvent systems, our crew settled on a process that balances yield and operator safety. Controlling crystallization controls purity. Filtering, washing, drying: each is tracked with in-process control points governed by years of batch records, not marketing slides.

    Our approach to impurity control reflects lived experience. Early runs showed the presence of hydrazone and isonicotinate impurities, both of which penalized pharmaceutical customers. In response, purification routes evolved: We shifted to multi-stage crystallization, adopted solvent-wash protocols suggested by process chemists on the ground, and invested in replacing glassware and certain gaskets to avoid trace catalytic contamination. Feedback loops ran between the quality lab and the plant floor, with both groups measuring HPLC traces until tailing peaks disappeared. This is what drives long-term trust between a manufacturer and a chemist who counts on more than just a certificate of analysis.

    Focus on Stability and Storage

    Run enough batches of 4-Hydrazinobenzoic Acid, and certain truths surface about its handling in the real world. Cool, dry storage preserves crystal integrity and keeps degradation at bay, yet lessons from heat-stressed or humid plant environments show that exposure compromises both reactivity and solubility. We track both product age and the quality of packaging—shifting to high-barrier liners and desiccant packets made a marked difference in off-site studies, where hot climates and longer shipping lanes would otherwise erode product value. The choice came from practical trial, not theory: Stability studies conducted alongside our partners established that small investments in packaging technology cut losses and improved end-use satisfaction. There is no substitution for learning these lessons batch-to-batch and year-over-year.

    The Environmental and Regulatory Footprint

    The chemical world never stands still, and neither do the rules governing hazardous materials. Safety around hydrazine derivatives, in particular, drives genuine concern for environmental exposure, worker health, and regulatory compliance. We’ve navigated the evolving landscape by constant training, best-practice sharing, and performing disposal procedures that honor both international guidance and local law. Each lot comes from a plant where VOC abatement, hydrazine containment, and personal protection do more than fill checkboxes—they keep our operations sustainable, and our workers safe. Adoption of closed-transfer systems, investment in proper firefighting measures, and creation of redundant containment all grew from real world needs and audits, not from a concern for optics.

    Some regulatory bodies scrutinize hydrazine derivatives far more than innocuous organic acids. Consistent documentation, transparent SOPs, and having chemists signed onto each batch record all built the long-term trust that lets customers or inspectors visit unannounced. Each customer gets access to full traceability—not because it’s requested, but because, as a manufacturer, nothing reduces uncertainty like honest documentation. This investment extends to support for REACH registration and local regulatory dossiers, as partners demand and as markets shift. Only constant vigilance, real tracking, and willingness to open doors to visitors, regulators, and customers make a difference in long-term supply relationships.

    Supplying the World—Working With Chemists, Not Just for Them

    Manufacturers do not operate in isolation. We hear reports from academic groups discovering hydrazinobenzoic derivatives as latent antibiotics. Process chemistry teams facing stuck reactions call on us for tweaks to impurity profiles or customized particle sizes. Diagnostic assay developers reach out for rapid analysis tools, requesting batch retention samples to lock down their method validation. The drive to accommodate these shifting, often unstandardized requests means our operation bends as needed—whether the need is for increased documentation, a modified drying step, or pre-blended intermediates. Real problems are solved through dialogue, and we learn as much from those on the other end of our supply chain as from our own lab benches.

    Challenges of Scale-Up and Customization

    Every request to supply this acid at increased scale or in tailored forms introduced obstacles that had no ready-made fix. Handling requirements for drum lots of hydrazine derivative drew concern from shipping departments and regulatory watchdogs alike. We revised packaging methods, implemented GPS and temperature tracking for sensitive loads, and adopted plant-to-plant communication protocols so everyone in the handling chain received the details—well before material left our site.

    Large-scale synthesis taught us that flexibility in manufacturing sometimes outpaces paperwork. Requests for specific particle size ranges, increased solubility, or modified salt forms were common. In each case, we looped directly with application chemists to weigh trade-offs: Stability versus reactivity, cost versus consistency, and purity versus throughput. Such conversations helped guide investments, whether that meant a new drying oven, upgraded filtration units, or additional staff training. Adding a customized purification or blending step never arises from formality alone; it comes from real users who describe how material quality can make or break their development timelines.

    Comparisons and Cautions: Not All Hydrazine Components are Created Equal

    It’s tempting to believe close alternatives can substitute for 4-Hydrazinobenzoic Acid. This impression seldom endures through hands-on use. Laboratory and industrial reports recount how switching to generic hydrazines raises headaches: increased toxicity, greater volatility, and product contamination that undermines both research and consumer safety. We’ve watched companies turn to simpler benzoic acids to bypass regulatory scrutiny, only to find that synthetic utility falters: Color yield drops. The new molecule won’t functionalize as planned. Pharmaceutical intermediates fail at the critical step. Case studies from our partners affirm a pattern—when the right functional architecture isn’t present, process chemistry grinds to a halt, and the projected economic advantage evaporates.

    Each molecule carves out its own synthetic niche. Unsubstituted hydrazine sacrifices selectivity; safer benzoic acids never allow hydrazone or azo formation. By contrast, our 4-Hydrazinobenzoic Acid bridges these extremes, giving both synthetic flexibility and reliable handling. We build this not on generic tables, but by testing alternatives ourselves and sharing outcomes with every new scale, sector, and formulation.

    Practical Lessons Learned and Next Steps for the Onward Supplier

    Smart manufacturing improves not because of top-down mandates, but because of hands-on troubleshooting. A team that listens to feedback, tracks batch behavior, and piles up small improvements long enough sees outcomes shift. Through hundreds of production runs, stability tests, contaminant profiles, and customer site visits, our chemists and operators found that every point of control pays off. Documentation builds confidence; impurity knockdown sharpens performance; tailored drying and careful packaging diminish hazard and waste.

    Longstanding relationships with researchers and multinationals alike reinforce the value of repeated investment in staff education, process optimization, and transparency. Such commitments go well past just making the molecule—they extend to calibration protocols, disposal planning, and long-term recordkeeping. With each new run, new partner, or new geographic requirement comes opportunity to further tune 4-Hydrazinobenzoic Acid for its targeted uses and tackle its ongoing challenges.

    A Final Word—Making Tomorrow’s Chemistry Possible

    Our work with 4-Hydrazinobenzoic Acid stands as both a testament to the daily discipline in fine chemical manufacture and a launching ground for innovation. From pharmaceutical breakthroughs to efficient dyes, advanced agrochemicals to diagnostic tools: Each application relies on the sum of lessons forged in real-world production, not abstract spec sheets. Customers and collaborators shape our approach as much as regulations or internal guidelines. In staying attentive to every variable—raw materials, environment, documentation, and feedback—we aim to deliver a product and a partnership that advances both science and industry. Quality compounds do not come from assumptions; they’re built from transparent, adaptive, and thoroughly practiced manufacture.