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Benzylhydrazine Dihydrochloride

    • Product Name Benzylhydrazine Dihydrochloride
    • Alias Benzylhydrazine, 2HCl
    • Einecs 229-687-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    354289

    Chemical Name Benzylhydrazine Dihydrochloride
    Cas Number 52417-22-4
    Molecular Formula C7H12Cl2N2
    Molecular Weight 195.09 g/mol
    Appearance White to off-white solid
    Melting Point 184-188°C (lit.)
    Solubility Soluble in water
    Purity Typically ≥97%
    Storage Temperature 2-8°C
    Synonyms α-Phenylhydrazine dihydrochloride
    Smiles NNCc1ccccc1.Cl.Cl
    Hazard Statements Harmful if swallowed, causes skin and eye irritation

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

    Packing & Storage
    Packing Benzylhydrazine Dihydrochloride, 5g, supplied in a tightly sealed amber glass vial with a tamper-evident cap and hazard labeling.
    Shipping Benzylhydrazine Dihydrochloride should be shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material, so transport must comply with applicable regulations for chemicals, including proper labeling and documentation. Shipping should be via ground or air methods that meet safety standards for corrosive and toxic substances.
    Storage Benzylhydrazine Dihydrochloride should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator temperature). Ensure compatibility with surrounding chemicals and store away from oxidizing agents and sources of ignition. Use appropriate labeling and secondary containment to prevent accidental spills or exposure.
    Application of Benzylhydrazine Dihydrochloride

    Applications of Benzylhydrazine Dihydrochloride in Industrial Manufacturing

    Benzylhydrazine dihydrochloride serves as a specialized intermediate in selected chemical manufacturing sectors where precise control over hydrazine derivatives supports innovation in pharmaceutical synthesis, advanced materials, and diagnostics. As an original manufacturer, we enable consistent quality and process reliability for demanding downstream users through rigorous quality control and full regulatory traceability.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers utilize benzylhydrazine dihydrochloride primarily in the preparation of hydrazine-based intermediates required for active pharmaceutical ingredient (API) synthesis. Careful control of moisture, purity, and residual solvent content is essential, as the intermediate participates in key condensation and cyclization reactions for the production of antihypertensive and anticancer agents. Our high-purity material supports process repeatability in both pilot and commercial API lines.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <795> for intermediate synthesis hygiene
    • EU GMP Part II: Basic Requirements for Active Substances Used as Starting Materials
    • CFR Title 21 for trace residue and impurity controls

    Typical usage ratio

    • Employed at 0.5–1.2 molar equivalents relative to the ketonic or aldehydic coupling partner in specific step reactions; final ratio determined by API synthesis route and desired conversion yield

    Downstream process integration

    • Charged directly into batch reactors during hydrazone condensation or heterocycle formation steps, typically following solvent charging and pH adjustment; reaction proceeds with downstream isolation and purification of pharmaceutical intermediates

    Final product types

    • Intermediate for antihypertensive drug substances
    • Building block in antitumor agent production
    • Precursor in CNS-active compound development
    • Hydrazone-based intermediates for further derivatization

    2. Agrochemical Research Compound Synthesis

    Our compound plays a critical role in research-stage and pilot-scale agrochemical laboratories, where its hydrazine functionality enables the synthesis of novel pesticide or herbicide candidate molecules. The high reactivity profile supports acylation and heterocyclic construction in days-long campaigns aimed at developing selective crop protection agents, with stringent monitoring for trace contaminants under regulatory review.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 quality management system for research chemical production
    • REACH Regulation (EC) No 1907/2006 (for R&D use and registration)

    Typical usage ratio

    • Added at 0.8–1.5 mol equivalents with respect to the acylating or aldehyde counterpart; exact amount tailored to target molecule architecture and research protocol scale

    Downstream process integration

    • Introduced in early-stage syntheses during hydrazone or imine coupling steps; product subsequently purified via crystallization or chromatography for analytical screening or biological assay submission

    Final product types

    • Novel fungicide screening candidates
    • Herbicide and insecticide investigational leads
    • Synthetic route intermediates for regulatory submissions
    • Reference standards for analytical method development

    3. Specialty Polymer Crosslinker Synthesis

    Benzylhydrazine dihydrochloride enables the creation of high-performance polymer crosslinkers, particularly in the synthesis of hydrazide crosslinked polyacrylates and hydrogels for advanced materials. Strict residual monomer analysis and impurity profiles are managed as part of the polymer plant’s QA, ensuring the hydrazine moiety is available for post-polymerization modification.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • EN 14028: Chemical crosslinkers for plastics
    • REACH regulations for industrial polymer intermediates
    • U.S. EPA TSCA reporting for new chemical substances

    Typical usage ratio

    • Incorporated at 0.3–0.7% wt/wt of total monomer feed depending on target crosslink density and polymer application (e.g. sensor vs. biofilm-resistant coatings)

    Downstream process integration

    • Dosed during or immediately prior to post-polymerization crosslinking step; reaction conducted under controlled temperature and inert atmosphere, with subsequent stripping and curing

    Final product types

    • Hydrazide-crosslinked polymer resins
    • Water-absorbent hydrogel components
    • High-strength, solvent-resistant adhesives
    • Specialty films for biosensor substrates

    4. Radiopharmaceutical Labeling Agent Synthesis

    In nuclear medicine and tracer diagnostics, researchers leverage benzylhydrazine dihydrochloride for the synthesis of radio-labeling precursors, particularly for the conjugation of hydrazine groups to biologically active peptides or ligands. Precise batch qualification, trace metal analysis, and adherence to radiochemical purity standards are critical at this stage, as the resulting derivatives must withstand subsequent radiolabeling processes used in PET and SPECT tracer manufacturing.

    Industry compliance standards

    • U.S. Pharmacopeia (USP) Chapter <823> Radiopharmaceuticals for Positron Emission Tomography
    • Good Radiopharmacy Practice (GRPP, EANM Guidelines)
    • ISO 13485: Quality management for medical device intermediates
    • CFR Title 21 Part 212: cGMP for PET drugs

    Typical usage ratio

    • Utilized at stoichiometric or slightly excess quantities—1.0–1.2 equivalents relative to the activated ester or peptide substrate, refined depending on molecular weight and labeling yield requirements

    Downstream process integration

    • Hydrazine intermediate added after primary peptide synthesis and initial purification; the conjugation reaction is performed immediately before radioisotope attachment, followed by HPLC purification

    Final product types

    • Radiolabeling precursors for PET/SPECT tracers
    • Hydrazine-functionalized peptide reagents
    • Targeted imaging agent intermediates
    • Diagnostic test batch components

    5. Analytical Derivatization Reagent Production

    Chemical analysis laboratories deploy benzylhydrazine dihydrochloride to create derivatization agents that react selectively with carbonyl compounds. These reagents enable enhanced detection sensitivity in HPLC or GC workflows, supporting trace-level quantification of aldehydes and ketones in pharmaceutical, food, and environmental analysis. Strict batch release protocols verify absence of interfering side-products.

    Industry compliance standards

    • ISO/IEC 17025:2017, General Requirements for the competence of testing and calibration laboratories
    • AOAC International: Official Method guidelines for derivatization chemistry
    • USP General Chapters <1225> and <621> for analytical method validation
    • EPA SW-846 Method 8315A (Carbonyl Derivatives by HPLC)

    Typical usage ratio

    • Formulated at 0.2–0.4% by volume in derivatization reagent mixtures; final dosages adjusted according to analyte concentration and detection limits sought by the laboratory

    Downstream process integration

    • Employed during sample preparation as part of pre-injection reagent mixes; after mixing with carbonyl-containing samples, the derivatized analyte is further processed for chromatography analysis

    Final product types

    • Aldehyde and ketone derivatization agents for HPLC/GC
    • Packaged analytical reagent kits
    • Certified reference materials for quality assurance
    • GC-HPLC method development standards
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    Certification & Compliance
    More Introduction

    Benzylhydrazine Dihydrochloride: Chemistry that Drives Progress

    Bringing Benzylhydrazine Dihydrochloride into the manufacturing line marks a genuine step forward in synthetic versatility. As a manufacturer who has worked through countless batches and reactor runs, I’ve come to appreciate the unique role this compound plays in advanced organic synthesis. The evolution of fine chemicals often depends on reliable access to specialized reagents. Benzylhydrazine Dihydrochloride isn’t as common as hydrazine monohydrate, and the difference isn’t trivial—subtle changes in the molecular structure translate into noticeable advantages in targeted reactions.

    How Benzylhydrazine Dihydrochloride Sets Itself Apart

    The core of this reagent lies in its hydrazine functionality, protected and modulated by the benzyl group. This extra level of design opens up reactions that are impractical or inefficient if you start with less tailored hydrazine salts. I have seen more consistent results with aryl diazotization, selective reductive amination, and heterocycle construction when using this compound, particularly under scale-up conditions where reproducibility remains a constant pressure point.

    The two hydrochloride counterions also make a clear difference in solubility and handling. Compared to free base benzylhydrazine, the dihydrochloride form reduces volatility and limits atmospheric degradation. That means fewer headaches related to stabilizing raw materials on the shelf, safer transfer protocols, and less unplanned downtime to sort out degraded reagents. We all know that even small losses in reactivity can mean schedule setbacks, off-spec products, and wasted materials. Over time, there’s no substitute for stability in stock.

    Quality Matters: What We’ve Learned by Making It Ourselves

    Over the years, I’ve seen subtle shifts in outcome linked directly to raw material purity. Even with low active content, trace impurities in the precursor hydrazine or solvent residues can escalate into downstream reactivity or crystallization problems. Purity in Benzylhydrazine Dihydrochloride isn’t simply an academic number—we track it daily using HPLC, verify chloride content with titration, and scrutinize batch consistency by melting point. Our on-site analytical work points directly to less batch-to-batch variation when compared with materials from third parties who may introduce middleman storage or transport exposures. This discipline gives our customers less variability on the line, and we’ve built several multistep pharmaceutical and agrochemical intermediates in-house using Benzylhydrazine Dihydrochloride as a necessary step; quality shows up not just on spec sheets, but on yield, filtration time, and the ease of washing residues from reactors.

    Our processes avoid recycled solvents, which tend to introduce trace aldehydes or amines that crop up in later analyses. During drying and packaging, maintaining a low humidity, controlled environment helps reduce caking, and we prefer smaller-volume packaging for labs and small pilot plants to prevent unnecessary air exposure. When we ship kilo-scale lots for production teams, we ensure direct tracking from our reactor through to finished product, so every kilogram reflects the same care applied to smaller batches. These steps simplify regulatory audits and technical onboarding, especially for regulated markets like pharmaceuticals or crop protection.

    Spec Sheets Don’t Tell the Whole Story

    A fraction of a percent makes little sensation in the datasheet, but too many times such differences have led to customer complaints or costly troubleshooting. Early on, we noticed downstream anisotropy in certain crystallizations if the sodium content exceeded a certain threshold, often due to incomplete removal during washing. That’s not a figure you’ll see on a typical specification, but after the first call from a scale-up chemist fighting with filters, that detail is impossible to ignore. The fine dust that accumulates inside valves, the color changes noticed at the bottom of a storage drum, or the extra rinse cycles necessary after a viscous charge—all these little technical wrinkles point back to process controls we keep tight on our end.

    I recall supporting a team working on a nitrogen-containing pharmaceutical scaffold. Hydrazine, in its usual forms, failed to give satisfactory selectivity. Use of Benzylhydrazine Dihydrochloride gave both improved regioselectivity and eliminated the stubborn side product seen previously. The project saved weeks of development time and cut purification steps. We share these observations with R&D teams looking to transition reactions from bench to pilot scale. Sometimes the fastest path forward means working backward from trouble—and often the right choice in hydrazine derivative decides the margin between 90% and 95% isolated yields.

    Why Direct Manufacturing Makes a Difference

    Dealing first-hand with our own plant means we have control at every stage, and that includes the ability to customize particle size, lot size, and purity. We can offer options such as increased batch size or finer micronization when requested. From a workflow standpoint, smaller crystals are favored in some continuous flow equipment; larger, less cohesive crystals aid larger batch processing by simplifying handling. We’ve implemented feedback from users who prefer certain formats, knowing it can reduce dust in the air, improve flow rates, and save manual labor downstream.

    Manufacturing at scale means constantly assessing the lifecycle of all intermediates and byproducts. We recover and reuse process solutions where contamination won’t compromise final content, but never at the expense of quality for final product. Unlike resellers or brokers, we keep thorough logs of every process adjustment, allowing us to troubleshoot almost anything reported by users. Face-to-face troubleshooting means avoiding weak links in the supply chain and creating a culture of accountability in production. Knowing the traceable path from raw hydrazine to finished Benzylhydrazine Dihydrochloride strengthens confidence across the value chain, especially for regulatory and analytical teams downstream.

    Applications in Modern Synthesis

    Benzylhydrazine Dihydrochloride turned out to be a useful niche material in several reaction classes. It acts well as a building block for azines, especially when more basic or less nucleophilic conditions would compromise selectivity. Beyond that, its use in selective monoalkylation and as a precursor for specialty heterocycles has grown steadily in the fine chemical sector. We have supplied this compound to researchers aiming to streamline indole and pyrazole ring construction—a testament to its flexibility and the incremental improvements that matter in the lab and plant.

    We are often approached with questions about workarounds using regular hydrazine salts or other simple hydrazine derivatives. Our long-term view, from both efficiency and safety perspectives, shows that Benzylhydrazine Dihydrochloride can offer distinct operational advantages, from handling and storage through to the yields in downstream reactions. The presence of the benzyl group not only helps manage the electron density in the intermediate, but it also acts as a recognizable handle for later synthetic manipulations, including deprotection, without risking formation of intractable byproducts. This has helped several projects bypass costly purification steps or avoid impurity-related setbacks.

    Comparisons to Other Hydrazine Reagents

    Many customers ask whether Benzylhydrazine Dihydrochloride can substitute for phenylhydrazine, hydrazine hydrate, or even methylhydrazine. The answer comes down to targeted results. Each functional group modulates reactivity and downstream chemical behavior in different ways. Unlike the more toxic, volatile methylhydrazine, Benzylhydrazine Dihydrochloride provides a favorable balance between functional group compatibility and manageable storage. It won’t evaporate as fast or create unstable intermediates prone to decomposition on standing.

    Pharmaceutical and crop protection chemists see the clear advantage in reactions demanding selectivity, particularly with sensitive aryl or alkyl halides, where the benzyl protection prevents unwanted side reactions. Standard hydrazine hydrate often oversaturates many systems with basicity, while the dihydrochloride version here keeps things manageable, reducing risks of exotherms or uncontrolled reactivities. This same property enables it to function efficiently as an intermediate, taking pressure off downstream purification and minimizing unwanted impurity profiles.

    From my own experience, substitutions involving Benzylhydrazine Dihydrochloride tend to outperform those with cheaper hydrazine derivatives in stepwise syntheses. Losses to side reactions, clean-up time, and even final product odor can add up quickly when upstream quality is inconsistent. The benzyl-protected hydrazine makes backward integration into more complex scaffold builds much cleaner, and those savings show on every scale, whether running 100-gram lab jobs or multi-kilo commercial production lots.

    Safety and Handling Insights

    We don’t take shortcuts on storage or shipping protocols. Dihydrochloride form brings key handling advantages. It’s less volatile, posing fewer risks of workplace exposure during weighing or transfer. Over the years, switched drums containing loose base or hydrate forms back to dihydrochloride format after repeated user feedback, citing both ease of handling and a dramatic reduction in airborne hydrazine. Almost every technician values packaging designed for clean, single-use openings. Accidental spills of the solid version are easier to contain and clean, unlike liquid hydrazine that can evaporate and create hazardous conditions quickly.

    Continuous monitoring of chloride content reduces risks of decomposition that can occur under high humidity or overexposure to air. Several studies have shown that hydrazine salts display better shelf stability compared to their free base counterparts, and in practice, that means longer usable product life with minimal loss of performance. Our recommendations sometimes include shorter shelf lives than theoretical maximums, because we prioritize real on-site storage conditions over theoretical models. Frequent customer feedback has pointed out that tight packaging and controlled stocks do more to preserve material quality than simply relying on specification numbers.

    Supporting Progress in Research and Industry

    In my years working with both startup tech companies and established multinationals, trends in research priorities often shift rapidly. More sustainable syntheses, better selectivity, cleaner emissions—all guide the choices in reagents. Benzylhydrazine Dihydrochloride plays an underappreciated role here, granting access to functionalized hydrazines without the same regulatory burdens as more hazardous free hydrazine handling. Its efficient incorporation into complex molecules saves time and waste, and technical support from a manufacturer familiar with both bulk and small-scale needs gives real-world value when results are on the line.

    I’ve attended dozens of technical review meetings and project launches. The common thread linking successful scale-up projects isn’t just brilliant chemistry—it’s reagents that work as expected, time after time, across shifting process parameters. The benefits of Benzylhydrazine Dihydrochloride become most obvious in these critical transition points, when the cost of troubleshooting spikes and the tolerance for surprises drops. Its contribution isn’t just in raw reactivity, but in the dependable control it provides to both process and product teams.

    Meeting Modern Production Demands

    Every batch carries the stamp of engineering decisions made for manufacturability and scale-up. By maintaining close technical dialogue between users and process teams, we’ve optimized our formulation and packaging to support today’s requirements for on-time, safe, and reproducible chemistry. Our ability to adapt to tailored processes is driven by first-hand insight into customer workflows and the challenges of integrating new materials into existing product lines.

    Pretending every application of Benzylhydrazine Dihydrochloride carries the same weight would be misleading. Each industry, project, and even team within a customer site will notice different process advantages: whether it’s fewer solids to manage during downstream filtration, improved tolerance for oxygen or water in the system, or simply the convenience of a non-volatile, crystalline solid over tricky liquids. Our attention to detail means even fringe cases in application are documented and, where necessary, new experiments are run to gather data. That’s the value of direct production over simple resale of commodity chemicals: process knowledge becomes part of the product.

    The Importance of a Reliable Partner

    In a world punctuated by supply-chain volatility and new chemical regulations, relying on robust, locally produced intermediates supports not just compliance, but also the creative edge of R&D. Benzylhydrazine Dihydrochloride, with its carefully controlled profile, offers an avenue for problem-solving that resonates with every chemist who’s weighed, stirred, or filtered their way through a difficult process. It’s not just about selling a chemical—it’s about offering assurance that each unit meets the standards demanded by research, manufacturing, and regulatory teams.

    Experience teaches that every improvement—no matter the step in production—echoes further down the line. Performance in synthesis produces cleaner products, reduces emissions, and brings more value than any abstract claim to consistency. Benzylhydrazine Dihydrochloride, integrated thoughtfully with the knowledge gained from the shop floor to analytical bench, is far more than a line on a specification form; it’s a foundation for progress, built through real-world chemistry and shared trust in enduring quality.