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3-Hydroxybenzylhydrazine Dihydrochloride

    • Product Name 3-Hydroxybenzylhydrazine Dihydrochloride
    • Alias 3-Hydroxybenzylhydrazine dihydrochloride, NSC 341868
    • Einecs NA
    • 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

    516748

    Product Name 3-Hydroxybenzylhydrazine Dihydrochloride
    Cas Number 101748-82-7
    Molecular Formula C7H11Cl2N2O
    Molecular Weight 211.08
    Appearance White to off-white powder
    Solubility Soluble in water
    Melting Point 218-221°C (dec.)
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Synonyms m-Hydroxybenzylhydrazine dihydrochloride
    Chemical Structure Hydrazine substituted benzene ring with a hydroxyl group at position 3
    Inchi Key ZGONEZABKNMQOH-UHFFFAOYSA-N

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

    Packing & Storage
    Packing The 10g vial of 3-Hydroxybenzylhydrazine Dihydrochloride is securely sealed in a labeled amber glass bottle for protection.
    Shipping 3-Hydroxybenzylhydrazine Dihydrochloride is shipped in tightly sealed, chemical-resistant containers, clearly labeled for laboratory use. The package is cushioned to prevent breakage and complies with all regulatory guidelines for handling hazardous chemicals. Shipping is typically via ground or air, subject to local and international chemical transport regulations.
    Storage 3-Hydroxybenzylhydrazine Dihydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep it at 2–8°C (refrigerated conditions). Ensure proper labeling and store away from incompatible substances, such as strong oxidizers. Use in a well-ventilated area or chemical fume hood, and handle with appropriate personal protective equipment to avoid contact and contamination.
    Application of 3-Hydroxybenzylhydrazine Dihydrochloride

    Applications of 3-Hydroxybenzylhydrazine Dihydrochloride in Industrial Manufacturing

    3-Hydroxybenzylhydrazine Dihydrochloride is a niche raw material valued in several specialized industrial and scientific domains. Its unique structure, high purity levels, and reliable reactivity make it essential for controlled synthesis and advanced formulation tasks across multiple downstream manufacturing sectors. Below we detail sector-specific applications, industry compliance, usage ratios, process integration, and end products based on current industry adoption.

    1. Pharmaceutical API Intermediate Production (Antineoplastic Agents)

    This compound functions as a key intermediate in the multi-step synthesis of certain hydrazine-based chemotherapy drug substances. Leading pharmaceutical manufacturers use it during the condensation and derivatization stages, enabling precise molecular modifications that produce active structures targeting oncological indications. The raw material quality and trace metal content must meet strict thresholds to avoid interfering with downstream API crystallization and GMP batch consistency. Production processes require secure closed systems to control for hydrazine-specific hazards and batch-to-batch contamination.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <797> and EP 2.2.46 Purity Specifications
    • 21 CFR Part 211 cGMP for Finished Pharmaceuticals
    • ICH Q3D Guideline on Elemental Impurities

    Typical usage ratio

    • 0.5–1.1 mol equivalent relative to primary precursor; ratio adjusted based on step yield and target compound molecular weight

    Downstream process integration

    • Added during Stage 2 or 3 of multi-step API synthesis; reacts with aromatic or aliphatic aldehydes under strictly controlled pH and temperature

    Final product types

    • Aromatic hydrazine-derived chemotherapeutic API cores
    • Final injectable or oral oncology medicines

    2. Agrochemical Research & Seed Treatment Synthesis

    The chemical serves as an intermediate in the synthesis of novel hydrazone-based agrochemicals, including select seed treatment agents and growth regulation products. R&D and pilot-scale production labs utilize it in the construction of target lead structures where potency and residual properties depend on precise benzylhydrazine integration. Stability and impurity control are essential during inclusion to protect subsequent bioactivity testing and field performance. Processing teams optimize its input based on desired seed coat penetration and downstream environmental impact.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides (FAO Plant Production and Protection Paper)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (for EU market development only)

    Typical usage ratio

    • 1–3% by weight per formulation batch; exact ratio based on seed variety, expected reactive site population, and crop safety protocol

    Downstream process integration

    • Introduced following initial solvent extraction; reacts with core seed protectant agents under rotating batch reactor conditions

    Final product types

    • Novel seed treatment solutions with systemic or contact activity
    • Prototype agrochemical actives for further biological evaluation

    3. Analytical Derivatization for Aldehyde Quantification in Food Safety Labs

    Many accredited analytical labs use this compound as a derivatization reagent for enhancing the detectability of trace aldehyde contaminants in food matrices. Reaction selectivity and hydrazone formation kinetics allow for standardized sample prep when coupled with advanced HPLC or GC/MS protocols. Highly sensitive methods require the raw material to be free of interfering secondary amines and residual solvents. Technicians calibrate addition levels to maximize chromatographic response without excessive background noise during validation and routine batch runs.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Accreditation Standards
    • Chemical Analysis Methods as per Official Methods of Analysis (AOAC International)
    • US FDA 21 CFR Part 130.9 Food Additive Analytical Methodology

    Typical usage ratio

    • 0.1–0.5 mmol per 10 mL sample; adjusted according to sample matrix complexity and targeted detection limit

    Downstream process integration

    • Direct addition to food extract samples during primary preparation; derivatization occurs prior to instrumental analysis step

    Final product types

    • Chromatographic derivatized aldehyde adducts for quantitative food safety reporting
    • Official certificate of analysis for regulatory release

    4. Specialty Dye and Pigment Synthesis

    In fine chemicals and specialty pigment operations, this hydrazine derivative supports development of novel dye intermediates with specific chromophoric and stability properties. Firms use it in reactions with selected aromatic aldehydes or ketones, forming conjugated systems that define the target spectrum profile. The process emphasizes highly controlled temperature and pH to maintain compound color integrity and avoid formation of side isomers or insoluble by-products. Strict impurity checks assure that pigments meet sector criteria for colorfastness and non-toxicity.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys – Migration of Certain Elements (for toy and children’s item pigments)
    • ISO 9073-10 Nonwovens–Pigment Quality Determination
    • EU REACH Annex XVII (Chemical safety for dyes and pigments in finished goods)

    Typical usage ratio

    • 0.5–1.5 molar ratio relative to aromatic carbonyl compound; ratio optimized for maximum color yield and pigment fastness requirements

    Downstream process integration

    • Added during dye-coupling or pigment precursor condensation stage, typically under continuous monitoring by UV/VIS spectroscopy

    Final product types

    • Specialty hydrazone-derived dyes for textiles, inks, or plastics
    • Industrial pigments with custom chromophore performance
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    Certification & Compliance
    More Introduction

    3-Hydroxybenzylhydrazine Dihydrochloride: Built for Real Work in Real Labs

    Working with the Substance, Not a Catalog Listing

    In the world of advanced chemical synthesis, suppliers and resellers often throw quite a lot of jargon at you. For us on the manufacturing line, talk comes after results. 3-Hydroxybenzylhydrazine dihydrochloride is not just another name in a booklet. Every batch coming out of our reactors gets strict, hands-on scrutiny before it hits your shelf. This isn’t the kind of material you buy to keep in storage; it’s for people who know exactly what they need from a coupling agent or intermediate that pulls its weight through early research, pilot trials, and production scale-ups.

    A Practical Introduction to 3-Hydroxybenzylhydrazine Dihydrochloride

    This compound, in its pure dihydrochloride salt form, holds a special place for researchers and process chemists developing pharmaceuticals and fine chemicals. We have seen it called on in multiple synthetic routes, especially where the benzylhydrazine core proves handy in constructing challenged analogs or enabling controlled functional group transformations.

    Our primary offering uses a model based on strong, proven routines: the starting material matches tight purity demands and specifications keep batch variance down. In practical terms, our standard is >98% purity as tested by HPLC, colorless-to-off-white crystalline solids, and well-documented solubility profiles (read: good water compatibility, easy mixing in common polar solvents). Each batch cycle carries documentation showing actual, not theoretical, analysis. No mystery peaks or unexplained degradants in the spectra—what you read is what you get.

    Where Our Product Comes Into Its Own

    In pharmaceutical R&D, time counts as much as raw yield. This salt’s robust character makes it perfect for medicinal chemists looking to build hydrazone libraries or couple aromatic fragments. We’ve provided this compound for both one-pot screening processes and stepwise syntheses, where control over reactivity is essential. Several teams reported back: side reactions stay minimized with our dihydrochloride version, as opposed to the free base or mono-HCl alternatives, which can behave unpredictably under standard conditions. The double salting not only stabilizes the molecule but gives you fewer surprises during workup or scale translation.

    Hydrazines aren’t universally loved—they get suspicion for their potential redox activity and volatility in the wrong forms. This is where in-house technical feedback makes the difference. Our dihydrochloride salt cuts down on dusting, lessens volatility, and moves cleanly from scales of grams to kilograms without drama. Several years back, a pharma customer attempted a direct swap with a mono-HCl sourced elsewhere, leading to stubborn decomposition and batch failures. Returning to our preparation, they saw not only higher yield but also less off-odor and longer material shelf life. These lessons don’t show up in catalogs, but in real returns from monitoring actual use cases.

    Not All “3-Hydroxybenzylhydrazines” Behave Equally

    You’ll find various hydrazine sources promising high purity, high conversions, or “custom” grades. But walk through their process specs and you’ll spot missing details—water content, trace ion analysis, or unexplained batch inconsistencies. Our team has had enough close calls; we take nothing for granted. Trace chloride and iron specs get documented with ICP-OES and ion chromatography. That reduces the risk of introducing rogue metals or ionic noise into your syntheses. Long-term stability studies (our own, not lifted from a reseller’s sheet) confirm that sealed, properly stored product will perform as promised for at least one year.

    Free base hydrazines or mono-HCl salts might look cheaper on paper. If you have ever tried to run a late-stage peptide coupling or reductive amination, you know that off-the-shelf mono-HCl lots can drift in color, purity, and workup convenience. We’ve observed inconsistent pH behavior and non-repeatable crystallization profiles in samples from competing suppliers. That’s why we focused our method on salt form consistency—far less chance of clogging lines or introducing unwanted byproducts, especially at scale.

    Supporting Efficiency and Safety—From Synthesis to Application

    A large part of our work at the plant is hands-on—packing, blending, granulating, or breaking up lumps by hand when required. This lets us spot issues before you do. Hydrazines deserve respect for their hazards. Handling the dihydrochloride form instead of the volatile free base means less exposure risk and smoother compliance with in-house waste protocols. End-users report far fewer handling headaches with our material versus less stable alternatives. Powdered or granular, consistent flow properties have kept automated dosing systems running without interruption.

    Every container leaving our facility has a tracked batch passport. This isn’t just for paperwork; it’s the only way to trace subtle differences batch-to-batch and help end-users pinpoint the source of a sudden blip in their process. We field regular technical calls and know that practical support is more useful than a generic SDS. If your team ever struggles with solution preparation, solid dispersion, or troubleshooting an impurity, our in-house chemists can draw on thousands of hours making, shipping, and handling these products—no need to call into an anonymous service center.

    How We Compare: Differences from Off-the-Shelf or Repackaged Products

    It’s easy for traders and third parties to focus only on data sheets. We’ve tested dozens of “standard” or “research” grade competitors, sometimes sourced globally, and the results are rarely consistent. Slightly lower-grade material can be handled for routing screening, but as soon as you step up to kilo-quantities or into regulated workflows, the cracks show: variable lots, batch odors, unexplained sediment after storage, trouble in dissolution tests. Our process keeps an eye on key details: moisture content, salt content, and heavy metals meet or exceed common regulations—not because labels demand it, but because cleaning up a failed batch always costs more than doing it right in the first place.

    Some suppliers advertise tailored pack sizes or “custom packaging.” For us, it goes deeper. After feedback from peptide teams and medicinal chemistry groups frustrated by clumping, we adjusted our packing method to reduce static and maintain shipper security—no “mystery dust” or over-pressurized liners, and always sealed in inert conditions. We know from experience a stable material on paper means little if it fails during scale-up. Reports from peptide and API teams made it clear: our salt’s reproducible melting profile and clean dissolution in buffered and unbuffered aqueous solutions means less time spent on chipping or column clogs.

    Supporting Structured Research and Unstructured Problem Solving

    We’ve watched trends in pharma and life sciences and witnessed the shift from bulk commodity reagents to targeted intermediates. The need for reliability becomes clear after a couple of failed scale-ups. Medicinal chemists, especially those working with sensitive backbones or late-stage analogs, rely on hydrazines with well-documented impurity profiles; there’s enough unpredictability in synthesis without questioning your core input. Our Q.C. discipline comes from decades in the trade: we control not just the headline assay reading, but also the side impurity profiles, to keep your troubleshooting simple.

    There’s a practical side to this field that gets overlooked. Repeatedly, research labs discovered their third-party compound stock had drifted outside specifications, leading to issues like batchwise impurity spikes or failed purifications. We maintain a comprehensive sample archive stretching back years. This lets us compare any “problem” batch to historical reference lots—a valuable resource for pharma partners who form long-term projects. Our experience shows that solving problems on the factory floor helps the end-user just as much as lab-based research.

    A Commitment to Real Quality, Not Just Paperwork

    Processors in regulated industries know the agony of reworking a batch or scrapping a week’s worth of pilot plant material. By providing a product that stays consistent from one shipment to the next, we keep more lines running—and more researchers focused on their science, not their supply headaches. Off-color, off-odor, or subtly degraded lots can kill morale and sap budgets. Our process spans from raw material inspection to multi-point Q.C. release. We do this not to meet regulatory protocols, but because every scrap of poorly characterized input means a risk to someone’s valued time and output.

    Multiple customers have thanked us not just for timely deliveries or adherence to paperwork requirements, but for spotting and alerting them to subtle differences before anything gets to their dock. These stories often go unreported but speak to the practical advantage of a manufacturer owning the process, catching issues that a “buy-and-ship” dealer simply can’t see from behind a desk.

    Responsible Handling and Field-Tested Reality

    Those who spend their careers around hydrazines know well the importance of safety and predictability. Our bulk packs and smaller research units get the same supply chain attention—shipped under validated conditions, monitored for temperature excursions, and tracked every step. None of the “gray-market” worries about counterfeit or relabeled bulk stock. What reaches your project passes through our hands, not an unknown middleman.

    A prime example from recent years: feedback from synthetic biochemists highlighted the improved resistance of our product to hydrolysis under ambient lab humidity, compared with alternatives that rapidly lost mass and purity over only a few days. We traced this issue to poorly controlled drying and storing protocols at competitors’ plants, resulting in residual moisture, lower shelf stability, and customer frustration. Regimented control of our own process—insisting on monitored humidity, tight validation of drying cycles, and accurate moisture readings—produces a product that delivers on paper and in practice.

    Supporting Future-Oriented Innovation

    As manufacturing specialists, we make it routine to adapt in response to researcher input. Researchers pushing beyond traditional synthesis typically need tighter control: better selectivity in fragment coupling, lowered side reactions during downstream derivatizations, and analytic traceability for regulatory submissions. By working alongside our clients, rather than just shipping out catalog items, we can document, adapt, and refine both the chemistry and the delivery—meaning less guesswork on scale-up and less troubleshooting in regulated or late-stage projects.

    For those in universities and industry alike, we haven’t built our reputation on claims—we rely on real experience and an unwillingness to accept mediocrity. If you have a specialized inquiry, want historical comparison data, or need a specific impurity tracked, our process engineers work with you, not around you. This isn’t “one size fits all.” The difference between reliable R&D output and a week spent cleaning up failed reactions lies not in marketing terms, but in a consistent, technically sound product.

    Putting Quality on the Bench, Not Just the Label

    Consistency is what keeps the process moving, week after week, from screening bench chemists to pilot plant technicians. We have seen firsthand the value of anticipating problems before they reach the customer: powder flow, dissolution trouble, unwanted solvent adducts, or sudden out-of-spec degradation. By addressing these from the manufacturing side, not waiting for an end-user complaint, we reduce downtime, increase productivity, and help keep projects on track. The result is a material that meets expectations every time, not just in documentation but in everyday work—the kind of outcome we wish every supplier cared enough to offer.

    Real Partnerships Make All the Difference

    We make decisions daily—about raw stocks, process order, quality analysis, and packaging—that affect not just our output, but your lab’s throughput and reliability. We know what it takes to offer a product that supports fast bench chemistry, meets regulatory scrutiny, and endures the messiness of scale-up without adding risk. That understanding does not come from spec sheets or sales pitches. It comes from years on the plant floor, feedback loops across the supply chain, and a belief that being a manufacturer means more than filling a barrel and shipping a label.

    This is why researchers and companies who care about both their daily process and their bottom line continue to choose our version of 3-hydroxybenzylhydrazine dihydrochloride. Reliable, repeatable, process-friendly—built from the ground up, not just filled and forwarded. It’s work we take pride in, results we stand behind, and trust we earn, one batch at a time.