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2-Ethoxybenzhydrazide

    • Product Name 2-Ethoxybenzhydrazide
    • Alias 2-Ethoxybenzohydrazide
    • Einecs EINECS 235-351-3
    • 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

    351201

    Product Name 2-Ethoxybenzhydrazide
    Cas Number 13435-19-9
    Molecular Formula C9H12N2O2
    Molecular Weight 180.20 g/mol
    Appearance White to off-white solid
    Melting Point 116-118°C
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically >98%
    Smiles CCOc1ccccc1C(=O)NN
    Storage Temperature Store at room temperature

    As an accredited 2-Ethoxybenzhydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Ethoxybenzhydrazide is supplied in a 25g amber glass bottle with a secure screw cap, labeled with hazard and handling information.
    Shipping **2-Ethoxybenzhydrazide** should be shipped in tightly sealed containers, protected from moisture and physical damage. Handle as a chemical substance following standard hazardous material regulations. Ensure labeling in compliance with local and international shipping guidelines, including safety data documentation. Avoid exposure to incompatible substances during transit, and transport at ambient temperature unless specified otherwise.
    Storage 2-Ethoxybenzhydrazide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Ensure proper labeling and keep storage containers securely sealed when not in use. Use appropriate personal protective equipment when handling.
    Application of 2-Ethoxybenzhydrazide

    Applications of 2-Ethoxybenzhydrazide in Industrial Manufacturing

    2-Ethoxybenzhydrazide serves as a specialized intermediate within several advanced chemical production chains. Its integration supports the pursuit of higher purity and tighter product consistency demanded by regulated sectors. Below, we detail direct industrial deployment scenarios verified within our manufacturer network, touching on relevant compliance standards, incorporation rates, processing routes, and resulting end products.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies use 2-ethoxybenzhydrazide as a nucleus in the creation of hydrazide-containing drug intermediates, especially in the synthesis of anti-tubercular, anti-cancer, and antibacterial agents. It enters the process after primary condensation reactions, undergoing further cyclization or functional group modifications to craft complex molecules. Reliable bulk quality control and traceability ensure the downstream final APIs meet international safety and purity mandates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur. 11.0)
    • 21 CFR Parts 210 & 211 (FDA GMP for drugs)
    • China Pharmacopoeia (ChP 2020)

    Typical usage ratio

    • Applied at 0.5–1.2 molar equivalents relative to the target active intermediate; batch size and reaction yield determine adjustment.

    Downstream process integration

    • Charged during post-ketone or esterification stages, preceding hydrazide formation and cyclic condensation steps.

    Final product types

    • Isonicotinohydrazide derivatives (anti-tubercular drugs)
    • Triazole agents (antifungal pharmaceuticals)
    • Hydrazide-based kinase inhibitors
    • Intermediate components for targeted oncology compounds

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    Agrochemical formulators incorporate this raw material when engineering hydrazide scaffolds essential for selective herbicide or fungicide molecules. The molecule’s ethoxy substitution offers compatibility with substitution reaction schemes, leading to high-yield formation of biologically active carboxylic or aromatic derivatives. Application precision drives batch reproducibility essential for registered crop-protection agents.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 – European market registration
    • China Pesticide Registration Guidelines (ICAMA)

    Typical usage ratio

    • Used at 2–8% by weight in synthesis routes for downstream intermediates; concentration set by target molecule stoichiometry.

    Downstream process integration

    • Added post-aryl ester hydrolysis stage to facilitate nucleophilic substitution or cyclization reactions in active ingredient manufacturing.

    Final product types

    • Hydrazide-bearing herbicides (e.g., pyrazole or triazole derivatives)
    • Aromatic carboxylic acid fungicides
    • Precursor compounds for broadleaf weed control blends
    • Seed treatment formulation intermediates

    3. Organic Pigment and Dye Production

    Dye and pigment manufacturers employ the material in the construction of hydrazone and azo pigment classes, where the hydrazide group participates in coupling reactions delivering high color fastness and chromatic purity. Control over addition rate and reaction temperature permits tuning of particle size and dispersion, key for achieving the required performance in coatings, plastics, and printing inks.

    Industry compliance standards

    • ISO 787 series (General methods of test for pigments and extenders)
    • EN 71-3:2019 (Safety of toys—Migration of certain elements—for pigments in toys)
    • China National Standard GB/T 5211 (Pigment quality inspection)
    • Oeko-Tex Standard 100 when used for textile applications

    Typical usage ratio

    • Introduced at 1–2.5% by total pigment mass; adjusted according to shade intensity and coupling agent reactivity.

    Downstream process integration

    • Integrated into diazotization and coupling stages during hydrazone dye and pigment synthesis, following pre-conditioning of substrate aromatic amines.

    Final product types

    • Yellow and red hydrazone organic pigments
    • High-color-strength textile dyes
    • Printing ink concentrates for industrial printheads
    • Polymer-compatible colorants for film and fiber coloration

    4. Analytical Reagent Manufacturing

    Analytical reagent producers capitalize on the reactivity of this compound for derivatization kits, particularly for the quantitative detection of carbonyl compounds in food, environmental, or pharmacological samples. Detailed formulation control and high-purity sourcing are vital, enabling supply of ready-to-use or customizable test reagents for laboratories adhering to international analytical protocols.

    Industry compliance standards

    • ISO 17025:2017 (General requirements for the competence of testing/calibration laboratories)
    • AOAC Official Methods of Analysis
    • USP <1225> Validation of Compendial Procedures (for analytical reagents used in pharma QC)
    • Chemical Society of Japan Standards for Analytical Reagents

    Typical usage ratio

    • Reconstituted at 0.01–0.05 mol/L in buffered solution formulations; precise concentration set based on target analyte and assay sensitivity requirements.

    Downstream process integration

    • Applied post-dissolution and filtration, entering as a labeling or derivatization agent in the final liquid or coated solid reagent formulations.

    Final product types

    • Ready-to-use carbonyl detection kits for HPLC/UV analysis
    • Derivatization reagents for air quality test cartridges
    • Standardized reagent sets for food additive verification
    • Environmental water and soil analysis assay materials
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    Certification & Compliance
    More Introduction

    Introducing 2-Ethoxybenzhydrazide: Purposeful Chemistry from the Source

    Producing 2-Ethoxybenzhydrazide in our facility means handling every step with care, from raw material selection to the moment it leaves our doors. Over years in the business of fine chemicals, we’ve learned that each molecule tells a story — not only of synthesis, but also of the priorities of our customers and the real-world tasks they face. This compound, recognized by its model name and CAS No. 939-88-0, reflects that approach. It belongs to the hydrazide family, a group familiar in research and industrial settings for specific reactivity and role in building more advanced molecules.

    Our batches of 2-Ethoxybenzhydrazide present as an off-white solid, with a stability pattern and handling profile consistent with established aromatic hydrazides. Its molecular structure supports selective transformations, making it a reliable partner in fields ranging from pharmaceutical R&D to specialty pigment synthesis. Over the years, requests for this particular hydrazide have grown as more researchers recognize its place in medicinal chemistry — especially as an intermediate feeding into complex heterocycle formation, or in custom coupling reactions where precision matters.

    Benchmarks and What Sets 2-Ethoxybenzhydrazide Apart

    Manufacturing 2-Ethoxybenzhydrazide at scale demands consistency — not just in appearance, but in reactivity, solubility, and trace impurity profile. Many chemists have shared frustration with unreliable supply or off-spec hydrazides. Having managed both small-lot and multi-hundred-kilogram runs, we pay close attention to solvent residues and purification, as even minor contamination can cause problems for downstream synthesis. Routine batch testing extends beyond basic melting point: we look for moisture levels, preservation of functional groups, and the kind of photostability that matters if you’re planning extended storage.

    Traditional benzhydrazides have their place, but replacing hydrogen with an ethoxy group at the ortho position changes the reactivity pattern. The oxygen atom introduces electronic effects, influencing both nucleophilicity and the character of subsequent acylations or cyclocondensations. That shift makes this compound valuable when building substituted pyrazoles, isatin analogs, or hydrazone linkages that won’t behave with a plainer hydrazide backbone. From conversations with synthetic chemists, this distinction often marks the difference between yields that are routine and those that unlock a previously tough transformation. As a manufacturer running full QC/QA in-house, the enhanced selectivity in our material saves users troubleshooting time and helps them focus on scaling up or pushing forward with discovery.

    Practical Experience Driving Quality Choices

    Formulating 2-Ethoxybenzhydrazide starts with sourcing high-purity ethoxybenzoic acid, followed by carefully controlled hydrazinolysis. If the starting acid carries micro-levels of oxidized side products, problems compound during synthesis, increasing color or instability in the end-product. Our chemists set up analytical checkpoints before each stage proceeds. Handling hydrazine demands strict protocol, not just for safety but also for maintaining the hydrazide’s spectrum: unchecked conditions yield by-products that complicate workups or cause headaches downstream in chromatographic purification.

    Laboratory techs often ask about moisture absorption. Years of trial have shown that 2-Ethoxybenzhydrazide survives typical atmosphere and retains form if properly sealed. Overexposure, particularly in humid environments, does invite minor hydrolysis at the amide site, so we emphasize low-impact packaging — not flashy, just effective: sealed foil inside HDPE. Every lot runs through HPLC and NMR to confirm identity, since visual inspection alone misses isomeric shifts and dimers. Research clients appreciate rapid sample turnaround, but scale-up partners rely on prior consistency. Small differences in oven-drying or solvent changeovers introduce batch-to-batch variability; these are avoidable if you never cut corners, regardless of volume.

    Purity, Profiling, and Real-World Troubleshooting

    In the early days, lab-scale production sometimes brought us face-to-face with hard, slow-to-filter intermediates. Scale-up looked easy on paper, but overnight standing caused unpredictable crystallization profiles, affecting yield. Over time, we adjusted cooling rates and agitation, settling on a protocol that promotes formation of large, easily isolable crystals, not fine powders that waste product or complicate washing. This experience, shared across years and projects, built habits for good documentation and open dialogue with process engineers.

    Practicality shapes every choice: targeting residual solvents at less than 0.5% (by gas chromatography) always pays off for downstream users. Hydrazides seldom cause trouble if processed right, but excess solvent or entrained water opens the door for slow decomposition, yellowing, or inconsistent assay. Typical purity for this product reaches above 98% by area, with remaining minor components always identified in the certificate of analysis. On rare occasions, batches require a second recrystallization, rather than hasty release, to avoid later rework. This level of detail isn’t arbitrary — it grew out of direct requests from teams facing publication deadlines or preparing regulatory submissions where every variance can prompt questions.

    Comparisons with related hydrazides show why the ethoxy group at the 2-position makes a difference. Standard benzhydrazide features are there: ability to react with isocyanates, aldehydes, ketones, acid chlorides — but as routine test runs demonstrate, the substitution pattern of 2-Ethoxybenzhydrazide enables unique cyclizations and unlocks safer routes to functionalized pyrazoles. In one project, switching from plain benzhydrazide to the ethoxy derivative provided access to regioselective functionalization, reducing by-product load and cutting post-reaction purification time almost in half.

    Application Experience — Answers Beyond the Data Sheet

    Many of the scientists we work with aren’t just repeating textbook syntheses. Often, they’re trying to push a known reaction to suit a new target, or they’re optimizing steps for scale. 2-Ethoxybenzhydrazide finds its home in the stepwise buildout of pharmaceutical candidates, especially where controlling electronic effects and steric profiles can mean the difference between successful optimization and dead-end side products. It performs well in the formation of hydrazones — consistently clean conversion with common aldehydes and ketones, yielding crystalline materials easy to handle. Time and again, users report that our product’s purity profile directly supports these clean, high-yield hydrazone formations, which serve as stable intermediates for further modification.

    Feedback on pigment development highlights another strength. In production of specialty dyes and pigments, not all hydrazides deliver the stability or color integrity required for high-performance outputs. Trial batches with 2-Ethoxybenzhydrazide demonstrated sharper endpoint signals and minimized off-shade formation compared to plainer derivatives. This reflects our priority in batch profiling: customers in demanding applications expect more than just a base compound — they want results that stay consistent once scaled.

    Not every use case can be predicted. We field regular inquiries from agrochemical innovators exploring novel pyrazole-building strategies or seeking improved selectivity for active ingredients. Our technical support sees frequent requests for solubility and compatibility data. Here, hands-on synthesis in our own labs has informed the guidance we offer, such as suggesting suitable solvents (DMF, DMSO, or acetonitrile for preparative runs), or flagging incompatibilities with strong oxidizers. Real situations demand knowledge honed by repetition, not just reference to published tables.

    Reliable Delivery, Every Batch

    Supply hiccups remain a recurring complaint in fine chemicals: sudden specification changes, long lead times, or ambiguous batch histories. Our approach cuts through that. Every order, whether for a few grams for research or larger industrial-scale lots, draws from a continuous production record. There are no mysteries about where a sample originated or whether tomorrow’s shipment will match today’s. All packaging runs under dry, inert conditions inside clean-room environments. Shipment includes lot-specific analytics: NMR, HPLC, melting point range, and, if requested, full spectral data.

    Transparency makes a difference. We’ve seen it smooth customs clearances, reduce QC rechecks, and help multiple labs tackle audit or grant deadlines without scrambling for documentation. Feedback loops among customers, our synthesis team, and the QC lab fine-tune every production run; process improvements don’t stay theoretical, but make their way into actual batch protocols next time out. This active listening stems from an old lesson: success in fine chemicals comes not through secrecy but through clear processes and shared know-how.

    What We’ve Learned and How That Shapes the Product

    Tech improvements never stand still. Ten years ago, hydrazide synthesis relied on pretty basic reflux gear — now, we use jacketed reactors with modular control over temperature and stirring, alongside automated sampling for in-process HPLC runs. These tools help spot endpoint drift before it affects product, preventing the kinds of trace impurities that frustrated early customers or forced project restarts. After installation of in-line moisture traps and late-stage microfiltration, complaint calls about suspended solids or turbid filtrates dropped sharply.

    Purification offers its own obstacles. Small variations matter: switching from ethanol to isopropanol in antisolvent steps shifts crystal morphology. Scaling from flask to reactor also means gravitational and heat transfer issues come into play, pushing us to revisit agitation speeds and cooling ramps. Skipping such details can mean lower yields, trickier filtrations, or compromised shelf-life downstream. By building knowledge across multiple product campaigns, we map those pain points and revisit procedures regularly. This approach keeps the product up to the demands of changing market requirements, not just yesterday’s standards.

    Safety and Environmental Responsibility Built In

    Producing hydrazide compounds calls for more than just reliable output. Hydrazines are challenging: exposure risk for staff, proper waste neutralization, VOC abatement, and disposal protocols for mother liquors all matter. We’ve updated our workflow to close off vapor paths, use scrubbers on fume lines, and treat effluent in line with local guidelines. Cross-training operators isn’t just regulatory — it secures every shift from slip-ups and passes that experience forward to tomorrow’s new hires.

    Demand for compliance documentation often grows as buyers move toward international registration or supply chains serving regulated end-users. Our due diligence builds from process to paperwork: MSDS, RoHS and REACH statements, and full traceability from incoming acid through finished packaging. Moving away from outdated legacy syntheses reduced our overall consumption of hazardous solvents and cut emissions, strengthening both internal safety culture and the wider community’s relationship with chemical manufacturing.

    Understanding the Demand: Research and Industry Drivers

    Academic groups continue pushing the envelope — new scaffolds for pharmaceuticals, custom dyes, or probe molecules. 2-Ethoxybenzhydrazide stands out in these circles for its clean conversion in condensation reactions and its unique pattern of reactivity, both under classic reflux and milder microwave or flow conditions. High-profile DFT studies and patent filings reflect repeat mention of ortho-ethoxy substitution offering differentiated electronic character, not just another basic hydrazide.

    Biotech and materials science benefit too. Researchers searching for stability in combinatorial libraries, or precise polarity in linker groups, rely on this molecular footprint. Applications keep expanding: one group reported use as a precursor for building metal-organic frameworks, citing the ethoxy group as pivotal for compatibility with their chosen ligands. Pigment developers, too, cite batch-to-batch color stability and reproducibility as key, often unattainable from off-the-shelf sources or routine importers unfamiliar with true process control.

    Whether supplying trial kilos for a pharmaceutical screen or stocking a recurring pigment manufacture run, we see foundational trends: users prefer direct access to technically capable partners able to discuss synthesis nuance, impurity thresholds, or changes in raw material sourcing. Working as both manufacturer and technical point-of-contact closes the loop, offering sector-specific feedback with every consignment.

    Differences from Other Hydrazides

    Face-to-face with new challenges, chemists in R&D or process scale-up environments seldom choose hydrazides solely based on cost or nameplate purity. Practicality, selectivity, and reactivity explain why 2-Ethoxybenzhydrazide sees renewed demand even as more generic derivatives crowd the catalogues. The ethoxy group, right at position two, tunes both reaction rates and product mix, minimizing unwanted cyclizations or uncontrolled branching that sidetrack time-sensitive projects. Most other benzhydrazides lack this balance of electron-donating power and steric bulk, which often makes all the difference in laboratory-scale optimization and industrial process control.

    The story goes beyond the bench. In pigment and dye synthesis, ordinary benzhydrazides can introduce batch color drift because of unwanted oxidations or side-reactions. 2-Ethoxybenzhydrazide’s structure holds color performance tighter. In pharmaceutical chemistry, analog development with standard hydrazides may stall when facile substitution or modification proves elusive; the ethoxy substitution turns possible dead-ends into tractable intermediates.

    True process differences between our product and basic competitors’ offerings persist through every stage. Our product doesn’t just match established analytic benchmarks; it reflects a culture of hands-on synthesis, feedback, and respect for the unknown. Fielding unexpected questions from frontline scientists changes practices: more frequent sterility testing for biochemistry clients, tighter packaging seals after lessons learned during monsoon season logistics runs, or offering micro-aliquots for trial since breakdown rates differ depending on climate and storage. All of that becomes part of the product’s real value by the time it reaches your door.

    What the Future Brings

    Chemistry never stands still. Growing demand for more task-specific intermediates, with fewer batch failures or unknown contaminants, keeps the pressure on us to avoid routine and stay responsive. Upcoming regulatory and technical changes only intensify the need for documentation, real synthesis expertise, and rapid sample turnaround. We don’t compete on lowest-possible price, but on making sure you get the 2-Ethoxybenzhydrazide you order — with all the behind-the-scenes work ensuring it performs as it should, whether for research, scale-up, or specialty pigment manufacture.

    From early-morning batch weighing to late-night troubleshooting, manufacturing this hydrazide brings new insights and reminders that every lot and every inquiry reflects a connected chemical community. Our knowledge base grows with every batch, supported by decades in the field and shaped by collaborations with those who look beyond catalog data and toward solutions in real practice. This remains the baseline for our continued investment — in equipment, in documentation, in training, and in supporting discovery, one compound at a time.