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3-Hydrazinobenzoic Acid

    • Product Name 3-Hydrazinobenzoic Acid
    • Alias 3-HBA
    • Einecs 237-701-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    107249

    Chemical Name 3-Hydrazinobenzoic Acid
    Cas Number 99-07-0
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Appearance White to off-white solid
    Melting Point 160-163 °C
    Solubility In Water Moderately soluble
    Pubchem Cid 7281
    Smiles C1=CC(=CC(=C1)C(=O)O)NN
    Inchi InChI=1S/C7H8N2O2/c8-9-6-3-1-2-5(4-6)7(10)11/h1-4,9H,8H2,(H,10,11)
    Storage Conditions Store at room temperature, protected from light

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

    Packing & Storage
    Packing 3-Hydrazinobenzoic Acid, 25g: Supplied in a sealed, amber glass bottle with a tamper-evident cap and detailed safety labeling.
    Shipping 3-Hydrazinobenzoic Acid is shipped in tightly sealed containers to prevent moisture and light exposure. Packages are labeled with appropriate hazard warnings, and transported according to regulations for chemicals, ensuring safety and integrity during transit. Avoid extreme temperatures. Shipping complies with relevant local, national, and international chemical transport guidelines.
    Storage 3-Hydrazinobenzoic acid should be stored in a tightly sealed container, away from light and moisture. Keep it in a cool, dry, well-ventilated area, preferably in a chemical refrigerator. Store separately from oxidizing agents and strong acids. Ensure appropriate labeling and follow institutional guidelines for hazardous chemicals to prevent exposure or accidental reactions.
    Application of 3-Hydrazinobenzoic Acid

    Applications of 3-Hydrazinobenzoic Acid in Industrial Manufacturing

    3-Hydrazinobenzoic Acid serves as a critical intermediate for several high-value industrial segments. Our manufacturing-grade material meets stringent requirements for pharmaceutical, agrochemical, dyestuff, and specialty chemical sectors. Below, we detail its integration into real production environments, including compliance, ratio ranges, plant processing, and typical end products developed by downstream clients.

    1. Pharmaceutical Intermediate for Antineoplastic Agents

    Leading pharmaceutical firms utilize 3-Hydrazinobenzoic Acid in the synthesis of active pharmaceutical ingredients, including kinase inhibitors and antitumor agents. Its structure enables efficient construction of hydrazide functional groups required in various cytostatic compound manufacturing. Our material’s purity, impurity profile, and trace metal controls consistently meet requirements for regulated drug synthesis. Process engineers introduce this intermediate during early-stage fragment coupling reactions, supporting controlled molecule assembly and purification steps for APIs with strict batch release criteria.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <795> for compounding
    • European Pharmacopoeia monograph for related intermediates
    • 21 CFR Part 211 (US FDA)

    Typical usage ratio

    • Batch load ratio varies from 0.85 to 1.1 molar equivalents per target hydrazide structure, optimized based on downstream yield and byproduct profile

    Downstream process integration

    • Charged during initial heterocycle formation or hydrazone condensation after primary aromatic ring synthesis
    • Reacted under inert atmosphere with chlorinated reagents or carboxylic acid derivatives
    • Purification follows with silica gel chromatography and controlled crystallization

    Final product types

    • Antineoplastic APIs, e.g., benzohydrazide-based kinase inhibitors
    • Pharma-grade hydrazone compounds
    • Research chemicals for advanced oncology formulations
    • Building blocks for nucleoside analogs

    2. Agrochemical Synthesis for Herbicidal Active Compounds

    Chemical formulators employ 3-Hydrazinobenzoic Acid as a key reactant for herbicidal products targeting resistant weed populations. Its core hydrazino functionality allows downstream manufacturers to construct selective active ingredients that interfere with specific plant metabolic pathways. Plant quality teams assess incoming raw material against defined GLP and GHS standards, ensuring fitment into large-volume synthesis campaigns for agricultural chemicals intended for global markets.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Ingredients (FAO/WHO)
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006
    • Globally Harmonized System (GHS) classification

    Typical usage ratio

    • Reacts at 0.7 to 1.2 equivalents per final herbicidal scaffold, determined by process kinetics and crop residue limits

    Downstream process integration

    • Blended into condensation reaction sequence for hydrazone and semicarbazone formation with chlorinated benzoic acids
    • Intermediate purification by solvent extraction prior to final active ingredient isolation
    • In-process HPLC monitors conversion and impurity carry-through

    Final product types

    • Herbicidal actives for pre-emergence and post-emergence formulations
    • Custom hydrazone derivatives for agrochemical R&D
    • Bulk technical-grade pesticides for downstream formulation partners
    • Synergist intermediates used in multi-mode herbicide blends

    3. Synthesis of Specialty Azo Dyes

    Manufacturers in the dyestuff sector consume 3-Hydrazinobenzoic Acid for the production of high-performance azo dyes. Its ability to introduce hydrazide linkages provides access to unique colorimetric properties and enhances solubility profiles for use in textile, leather, and plastic coloration. Production sites implement continuous sampling to ensure lot-to-lot consistency, which is essential for achieving reproducible chromatic results in bulk dye synthesis under regulated environmental controls.

    Industry compliance standards

    • EN 71-3 (Safety of Toys: migration of certain elements) for textiles
    • OEKO-TEX® Standard 100 (textile processing)
    • REACH Annex XVII for azo dye restrictions
    • ISO 105 testing for color fastness

    Typical usage ratio

    • Advanced at 0.5 to 1.3 equivalents relative to diazonium coupling agents depending on desired chromophore density and end-use requirements

    Downstream process integration

    • Introduced into the diazotization stage with nitrosating agents
    • Subsequently coupled to aromatic amines or phenolic substrates
    • Final dye purification via salt precipitation and filtration

    Final product types

    • Reactive azo dyes for polyester and cotton fibers
    • High-stability colorants for synthetic polymers
    • Leather and inkjet textile dyes with improved lightfastness
    • Specialty pigments for technical coatings and plastics

    4. Precursor for Heterocyclic Fine Chemicals

    Advanced chemical synthesis plants rely on 3-Hydrazinobenzoic Acid to build complex heterocyclic molecules utilized in materials science and electronics sectors. Its hydrazino group acts as a versatile nucleophile during ring closure steps, enabling the rapid construction of benzo-fused heterocycles and related aromatic systems. QA and QC teams document chain-of-custody for all material movements, guaranteeing traceability in compliance with ISO and regional chemical control statutes.

    Industry compliance standards

    • ISO 9001 Quality Management System
    • Japan Chemical Industry Association JCIC Safety Data requirements
    • Toxic Substances Control Act (TSCA, USA)
    • China RoHS for electronic materials

    Typical usage ratio

    • Deployed at 1.0 to 1.5 equivalents in nucleophilic cyclization with diketone or polycyclic aromatic precursors, tuned according to product specificity and desired functionalization level

    Downstream process integration

    • Dosed to initial or mid-stage heterocyclization reactors
    • Condensed with carbonyl-containing intermediates for pyrazole and quinazoline scaffolds
    • Final fractions isolated by column chromatography and solvent recrystallization

    Final product types

    • Organic semiconductors for electronic devices
    • Specialty ligands for catalysis
    • Benzo-fused heterocyclic R&D compounds
    • Material science intermediates for OLEDs and displays
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    Certification & Compliance
    More Introduction

    3-Hydrazinobenzoic Acid: Our Perspective as the Manufacturer

    Understanding 3-Hydrazinobenzoic Acid from the Source

    After decades at the core of fine chemical manufacturing, we have had a front-row seat to witness the evolving value and utility of 3-Hydrazinobenzoic Acid (CAS No. 535-87-5). We do not just pack this compound off of a shelf—we produce, handle, and refine it in-house. This means our insights stem directly from the batch floor, from the QC bench, and from numerous discussions with R&D teams striving to move science forward. We know the challenges a researcher faces while searching for high-purity specialty intermediates, especially those involved in pharmaceutical syntheses, dye chemistry, and advanced materials. Every shipment reflects our ongoing commitment to reliability.

    Key Attributes Developed Through Practice

    3-Hydrazinobenzoic Acid, with the formula C7H8N2O2, stands apart for both its chemical reactivity and functional versatility. Our years of optimizing its synthesis have resulted in a crystalline product that reliably meets or exceeds 98% purity by HPLC. Purity isn’t just a number. Even traces of metal contamination, solvent residues, or incomplete conversion show up quickly in downstream reactions. We run every batch through strict QC to maintain batch-to-batch consistency, because we see how low impurities shape the difference between reproducible experiments and frustrating troubleshooting. The targeted molecular weight of 152.15 g/mol holds firm in our process, and our melting range lands close to 225–229°C without broad smearing—an essential indicator of quality in hydrazine derivatives.

    Our staff learned long ago that minor process variations ripple out as unpredictable outcomes for customers. Subpar crystallization methods create issues with filtration and drying, and the color of the finished product—pure white or slightly off-white—tells us much about residual side-products or incomplete purification. Fresh batches always release a faint hydrazine odor; any deviation in aroma corresponds to non-standard impurities. These observations come from years of direct handling, not from abstract product summaries.

    Applications, Not Just in Theory

    Through direct conversations with top-tier pharma and specialized dye manufacturers, we see the spectrum of uses 3-Hydrazinobenzoic Acid supports. As a hydrazino-functionalized aromatic acid, this compound stands out for its ability to participate in diazotization, condensation, and ring-closure reactions without losing its character under moderately tough conditions.

    Customers pursuing synthesis of pyrazole, indazole, and triazole derivatives find it hard to source intermediates as adaptable as this molecule. The strongly nucleophilic hydrazino group attached to the benzoic acid gives an edge in constructing heterocycles and hydrazones that might otherwise demand multi-step routes or expensive reagents. In the pharma field, bioactive trials often hinge on reliable access to such intermediates, from initial medicinal chemistry hits to scale-up for animal testing. Delays caused by poor reactivity or unreliable supply can interrupt serious projects. We have witnessed more than one collaboration expand after teams realized our batches gave consistent yield and product fidelity.

    This compound’s value branches out further. Several pigment and dye innovators turn to our product to build azo compounds that must endure harsh processing, lightfastness testing, or textile application without decomposing. We have watched our product move from laboratory-scale synthetic experiments to pilot-scale production, eventually entering commercial colorant lines. Outside these main fields, academic materials chemists sometimes employ our batches to engineer molecular sensors or as building blocks for metal-organic frameworks, benefiting from the reactivity unlocked by both carboxylic acid and hydrazino groups in the same scaffold.

    Differentiation: Not All Intermediates Are Created Equal

    Direct production experience teaches lessons that specification sheets do not capture. 3-Hydrazinobenzoic Acid often gets compared with other common hydrazino aromatics, such as 4-hydrazinobenzoic acid or phthalic hydrazide. We see meaningful differences in practical reactivity, solubility, and safety. The meta-configuration of our material’s hydrazino and carboxylic acid groups changes both chemical and physical behavior. In our reactors, we observe that 3-derivatives frequently show different tautomeric preferences, affecting both yield and purity profiles in downstream coupling chemistry compared to the para isomer.

    From a handling standpoint, the 3-hydrazinobenzoic acid we manufacture displays slightly higher water solubility and a different thermal decomposition pattern relative to its counterparts. These subtle property shifts show themselves most clearly during chemical transformations that demand tight temperature control and product isolation. Synthesis of certain triazoles, for example, can run to completion with our 3-isomer more smoothly than with structurally similar competitors. We learned over time that attempted substitutions with 4-hydrazinobenzoic acid often force chemists to adapt their protocols, modify solvent systems, or add extra purification stages—ultimately costing time and budget.

    We also handle requests for similar hydrazine acids with alternate substitution patterns, but our experience points to distinct performance differences during scale-up: the 3-isomer’s propensity toward more straightforward crystallization, easier filtration, and reduced sensitivity to ambient air during storage. Not every hydrazino compound can boast such practical processing advantages. This is feedback echoed not simply from our own teams but from long-term customers who have switched back after encountering complications with other products.

    Standards and Responsibility: What Production Really Means

    True manufacturing carries a burden of certainty. Our production line uses kilograms of starting materials under conditions monitored around the clock. Maintaining clean, well-calibrated reactors means avoiding contamination before it happens rather than relying on end-stage testing to catch problems. Over the years, we’ve had to respond quickly to issues—such as a batch with higher than expected chloride content or a shift in pH after crystallization—because we realize these issues multiply downstream. Quality doesn’t come from wishful thinking or paperwork; sustained performance comes from continuous in-process monitoring, solvent stock management, and personnel training.

    Not every supplier gets their hands dirty in quite the same way. Our site runs routine elemental analysis, verifies structure using NMR and FTIR, and regularly benchmarks HPLC profiles against international standards. From raw material sourcing—checking every drum for genuine assay and origin—to final product isolation, we accept nothing less than full traceability. When users call us to discuss unexpected reactivity on their benches, we pull archived records and look for lot-specific data, instead of giving rehearsed textbook answers. This hands-on discipline ensures that every process, from hydrazine addition to washing, filtration, and drying, has a real person accountable at each stage.

    Seeing Usage Through the Eyes of the End-User

    Our conversations with scientists reveal recurring bottlenecks. The stubborn residue in a flask, a barely perceptible yellow tinge in a presumably white product, crystal formation that refuses to cooperate—all affect time-to-result more than standard paperwork ever could. We have responded by adjusting solvent choices, filtration speeds, and drying cycles based on real-world success and customer feedback. Moisture content, for example, goes far beyond a number in a table: a single-digit percentage may still trigger caking, and this frustrates bench chemists trying to weigh the compound with precision.

    We routinely receive reports from researchers troubleshooting synthetic routes. Too many intermediates sourced through opaque supply chains exhibit inconsistent batch-to-batch quality, leading to failed coupling or unexpected NMR shifts. We have committed to open discussion and technical support, sharing spectral data and comparative performance notes from both internal trials and collaborating labs. Our facility absorbs such learning into process refinement, ensuring persistent improvement.

    Some users inquire about shelf life or storage. Our product, stored in air-tight containers under clean, dry conditions, stays stable in pure form for extended periods. The hydrazino group, while reactive, does not decompose rapidly at room temperature when the substance is packed properly. We always stress that real-world handling impacts purity: excessive humidity or exposure to acidic fumes can gradually yellow the product, signaling slow onset decomposition or contamination.

    Beyond Quality: Safety and Environmental Accountability

    We produce 3-Hydrazinobenzoic Acid under strict adherence to both domestic and international safety standards. Hydrazine chemistry brings its own set of hazards—sensitization, potential carcinogenicity, and reactivity toward strong oxidizers. Our facility engineers process flows to minimize operator exposure, and we maintain rapid shutdown protocols in all synthesis lines handling hydrazino compounds. Regular air monitoring and operator health programs run on-site to safeguard our people. We do not take shortcuts with personal protective equipment or waste treatment.

    We acknowledge the growing push for greener, more responsible manufacturing. In recent years, we’ve mapped our waste streams and reengineered stages to reduce organic solvent use wherever possible. Washing and recovery systems ensure minimal hydrazine and solvent residuals enter effluent. Our energy consumption and emissions benchmarks are published transparently. By recapturing and recycling key solvents—especially during carbon-activated purification—we shrink both overhead and footprint.

    Working directly at the manufacturing level, the commitment to safe, low-waste production isn’t a catchphrase; it’s woven into weekly operations meetings, incident tracking, and resource allocation. We know every liter of water or kilogram of starting material not only carries sourcing and disposal costs, but also represents a chance to do better for workers, the environment, and the community surrounding our plant.

    Future-Proofing Our Production—Staying a Step Ahead

    Ongoing changes in regulatory expectations, customer quality control, and competitive pressure keep us pushing for continual improvement. Several years ago, we faced a surge in demand from pharma companies increasing high-throughput screening libraries. Meeting this surge meant scaling up without sacrificing purity. We invested in reactor automation and in-line analytics so that process upsets were identified and corrected before batches completed, not after. This hands-on process surveillance now sits at the heart of our operational philosophy.

    Frequent customer audits and on-site QC reviews keep our team alert. We treat each audit not as an interference, but as a valuable channel for uncovering hidden variabilities or improvement opportunities. Partnering with universities and research consortia introduces us to new application areas—such as advanced organic electronics—where demands for trace impurity removal reach new levels.

    Feedback from advanced R&D labs led us to develop finer particle size options and batch-specific documentation. We now support customers fine-tuning solid-state transformations or optimizing surface exposures. Our lab teams investigate next-generation crystallization techniques, seeking both productivity gains and incremental boosts in purity.

    Why Vertical Integration Delivers Value

    Our stake in both producing and supporting advanced aromatic hydrazines goes beyond transactional exchange. We experience fully the stress of raw material price fluctuations, the technical headaches of dealing with batch failures, and the satisfaction when customer feedback affirms our approach. When downstream users express doubts about moving forward with a new synthetic target over concerns of intermediate quality, we share our own lab data along with best practices for handling, solution preparation, and storage.

    Homegrown manufacturing also means rapid response. Should a customer require a specific batch requalification, alternate grade, or tailored formatting, we adapt within the same supply chain infrastructure—no relaying to offshore unknowns or chain-of-custody gaps. Institutions conducting quality-by-design studies and method validations receive immediate, traceable batch data direct from the origin point.

    Challenges and Realities in Hydrazine Handling

    Not everything about handling or delivering 3-Hydrazinobenzoic Acid flows smoothly every time. Equipment maintenance, sourcing pure hydrazine hydrate, maintaining reagent stocks, and balancing emergency readiness with throughput targets all form part of the package. Managing real-time safety data and cross-training new staff takes dedication and resources. We face the same logistical headaches as anyone—shipping timelines, customs documentation, regulatory registrations—yet our experience running operations in tough regulatory environments has taught us the necessity of contingency planning.

    In our experience, risk mitigation emerges not from grand slogans, but from granular, habitual discipline. Every batch run or new customer requirement nudges us to record, reflect, and reboot any process steps that trend toward nonconformance. Inclusion of additional purification steps, extending multi-point analytical control, and pre-emptively updating documentation in response to shifting regulatory frameworks comprise how we stay current.

    What Sets Us Apart

    Many sources sell 3-Hydrazinobenzoic Acid, yet few see the full picture from molecular design, to process optimization, to boots-on-the-ground production. Having produced, isolated, and refined this compound year after year, we bring practical clarity: problems are caught earlier, applications are supported with more than just certificates, and improvements track real user demand. Whether scale-up triggers a new impurity, or a research team requests nonstandard packaging to avoid contamination, our feedback loop remains open.

    We believe that genuine value for users of advanced chemical intermediates—be they in pharma, dye, or material science sectors—comes from upstream expertise, continuous QC rigor, and honest dialogue about expectations and limitations. Everything we deliver reflects lessons learned the “hard way”—from clogged filters, sticky batch residues, off-color product, or unplanned rework. Our product portfolio, especially 3-Hydrazinobenzoic Acid, features the strengths and reliability that only full-scope, original manufacturing brings to the table.