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2,3-Dimethylphenylhydrazine Hydrochloride

    • Product Name 2,3-Dimethylphenylhydrazine Hydrochloride
    • Alias 2,3-Dimethylphenylhydrazine hydrochloride
    • Einecs 239-898-2
    • 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

    579145

    Product Name 2,3-Dimethylphenylhydrazine Hydrochloride
    Synonyms 2,3-dimethylbenzenhydrazine hydrochloride
    Cas Number 825-51-4
    Molecular Formula C8H12ClN2
    Molecular Weight 170.65 g/mol
    Appearance Off-white to light beige powder
    Melting Point 176-179 °C
    Solubility In Water Soluble
    Storage Temperature 2-8°C
    Purity Typically ≥98%
    Chemical Class Phenylhydrazine derivative
    Hazard Statements Harmful if swallowed; irritant

    As an accredited 2,3-Dimethylphenylhydrazine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,3-Dimethylphenylhydrazine Hydrochloride is supplied in a 25g amber glass bottle, securely sealed, with hazard and identification labels.
    Shipping 2,3-Dimethylphenylhydrazine Hydrochloride is shipped in tightly sealed, chemical-resistant containers under dry, cool conditions. Proper labeling and secure packaging in accordance with local and international hazardous materials regulations are essential to prevent leaks and contamination. Handle with care, using appropriate personal protective equipment during transport and upon receipt.
    Storage **2,3-Dimethylphenylhydrazine hydrochloride** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and bases. Avoid moisture and sources of ignition. Clearly label the container and ensure it is kept away from food and drink. Use appropriate personal protective equipment when handling.
    Application of 2,3-Dimethylphenylhydrazine Hydrochloride

    Applications of 2,3-Dimethylphenylhydrazine Hydrochloride in Industrial Manufacturing

    As an original chemical raw material manufacturer, we supply 2,3-Dimethylphenylhydrazine Hydrochloride to downstream partners operating in highly specialized sectors. With an emphasis on targeted industrial value chains, the following sectors exemplify concrete, large-scale applications, with details on regulatory standards, practical dosage design, manufacturing positioning, and finished product relevance.

    1. Pharmaceutical Intermediate for API Synthesis

    This compound is widely used in the pharmaceutical sector as a key hydrazine derivative intermediate during the synthesis of complex Active Pharmaceutical Ingredients (APIs), especially in small-molecule drug development. Both innovator and generic drug producers rely on its high purity to maintain consistent reaction performance in critical diazotization and coupling stages within GMP-compliant settings.

    Industry compliance standards

    • ICH Q7 GMP Guidelines
    • 21 CFR Part 210/211 (USA)
    • Ph. Eur. 10.0 (Europe)
    • USP-NF 2024 (monograph referencing for intermediates)

    Typical usage ratio

    • Applied at stoichiometric equivalence with acylation and diazotization substrates, usually 0.8–1.5 mole per mole depending on API route optimization.

    Downstream process integration

    • Charged directly in the hydrazinolysis or diazo-coupling phase of multi-step organic syntheses for heterocyclic pharmaceutical cores.

    Final product types

    • Anti-tuberculosis drug intermediates
    • Antihypertensive agent precursors
    • Oncology API building blocks
    • Specialty fine chemicals under GMP regime

    2. Agrochemical Synthesis for Crop Protection Agents

    Producers of active agrochemical ingredients employ 2,3-dimethylphenylhydrazine hydrochloride in the construction of functionalized aromatic rings and heterocycles, which form the core of herbicide and insecticide molecules. Scale-up synthesis requires strict batch documentation in accordance with international crop-protection manufacturing standards, due to sensitive downstream applications and regulatory scrutiny.

    Industry compliance standards

    • FAO/WHO - JMPR guidelines
    • ISO 9001:2015 QMS for agrochemical supply
    • China Pesticide Registration (ICAMA)
    • REACH Annex IV/V intermediary usage reporting (Europe)

    Typical usage ratio

    • Used from 0.5 to 2.0 eq. in coupling with chlorinated aromatic feedstocks, with process development determining the precise load to maximize target yield and minimize byproduct formation.

    Downstream process integration

    • Added during the condensation or cyclization stages of nitroso or carbonyl functional group introductions within the active ingredient synthesis route.

    Final product types

    • Precursor intermediates for triazole and pyrazole herbicides
    • Insect growth regulator scaffolds
    • Pesticide candidate molecules for research trials
    • Registered pesticide manufacturing streams

    3. Dye and Pigment Intermediate Manufacturing

    Industrial dye and pigment makers use this hydrazine derivative for azo coupling reactions that create vivid and persistent colorants. Its unique methyl group substitutions influence chromophore formation and result in products with improved fastness and hue stability. Compliance with sustainability and textile accessory regulations is crucial, given end-consumer safety and environmental health considerations.

    Industry compliance standards

    • OEKO-TEX Standard 100
    • ZDHC MRSL v3.1
    • EU Regulation (EC) No 1907/2006 (REACH)
    • EN ISO 9001:2015 for dye manufacturing

    Typical usage ratio

    • Typically dosed at 0.7–1.3 eq. against primary aromatic amines or diazonium salts in coupling reactions; optimized by desired pigment intensity and batch reactivity testing.

    Downstream process integration

    • Enters the batch after diazotization of the aromatic amine, with immediate reaction leading to mono- or bis-azo pigment core.

    Final product types

    • Textile azo dyes for synthetic and cellulosic fibers
    • Resistant pigments for automotive coating
    • Specialty inks for industrial and digital printing
    • High-stability pigments for plastics compounding

    4. Specialty Analytical Reagents Production

    Chemical analysis and research laboratories utilize 2,3-dimethylphenylhydrazine hydrochloride as a derivatization agent for carbonyl compound identification and quantitation, crucial in pharmaceutical, environmental, and forensic testing. The production of such reagents demands precision control in purity and trace-metal content, supporting strict analytical method validation in regulated laboratory environments.

    Industry compliance standards

    • ISO/IEC 17025:2017 laboratory accreditation
    • USP Analytical Reagents chapter reagent requirements
    • GLP (Good Laboratory Practice) principles
    • EPA SW-846 for method compliance (environmental methods)

    Typical usage ratio

    • Solution preparations from 0.02–0.2% w/v in analytical solvents; precise volumetric addition depending on derivatization reaction stoichiometry.

    Downstream process integration

    • Introduced during reagent kit assembly or before analytical separation techniques (e.g., HPLC sample prep, GC derivatization) for high specificity detection workflows.

    Final product types

    • Commercial carbonyl-detecting reagent kits
    • Reference standards for HPLC/GC-MS calibration
    • Material testing controls for environmental sampling
    • Custom analytical solutions for OEM laboratory brands

    5. Chemical Research in Academic and Industrial Innovation

    Universities and R&D departments of chemical companies apply this compound as a specialized building block in novel heterocyclic chemistry, structure-activity relationship (SAR) studies, and synthesis of molecular probes. The demand for high lot-to-lot reproducibility and traceable documentation ensures suitability for research findings and experimental process records that stand public scrutiny or patent reviews.

    Industry compliance standards

    • Sigma-Aldrich and ACS chemical reactivity grading
    • ISO 9001:2015 research supply standards
    • GLP-compliant laboratory recordkeeping practices
    • Institutional chemical safety protocols

    Typical usage ratio

    • Applied in equimolar to moderate excess (1–3 eq.) to address variable reactivity in exploratory syntheses, documented by experimental rationale.

    Downstream process integration

    • Integrated at the reagent addition stage in project-specific synthetic routes, primarily for constructing substituted hydrazones or diazo derivatives.

    Final product types

    • Novel polycyclic heterocycle libraries
    • Structure-labeled chemical probes for bioassay
    • SAR compound sets for drug discovery
    • Patent-submission small molecules
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    Certification & Compliance
    More Introduction

    2,3-Dimethylphenylhydrazine Hydrochloride: An Industry-Ready Reagent from Direct Production

    Molecule Background and Model

    Coming straight from our own reactors, 2,3-Dimethylphenylhydrazine hydrochloride stands out among arylhydrazine salts. Our experience producing this compound has made one thing clear: consistence in structure and impurity control matter for research, pharmaceuticals, and specialty synthesis. This molecule, with two methyl groups ortho and meta to the hydrazine function, brings a blend of stability and reactivity. Standard hydrohalide crystallization yields a white to slightly off-white solid, with reliable purity not only by HPLC but also by GC testing. From lot to lot, you can expect consistent melting points and a product that handles storage over typical temperature ranges, thanks to rigorous control over neutralization and isolation steps.

    Specification and Quality Control

    Making thousands of kilograms each year, we have gained real hands-on know-how for what chemists require. Our 2,3-dimethylphenylhydrazine hydrochloride consistently exceeds the 98% purity threshold. Residual solvents rarely exceed 0.5% by weight following our multi-stage drying. Test data comes straight from our on-site analytical suite, with outcomes measured by HPLC, melting point, and NMR—directly from production batches, not just pilot samples. We don’t see a lot of ambiguity when it comes to color, crystallinity, or residual moisture, so labs and plants can rely on batch-to-batch consistency.

    Those working with sensitive transformations—such as azo couplings, pyrazole syntheses, or pharmaceutical API intermediates—appreciate that low-level metal catalysts, halide residues, and conformational purity affect downstream performance. Our direct process design controls for trace Fe and Cu below 10ppm, with sodium, potassium, or magnesium rarely detectable in finished product. At the user’s bench, this translates into reproducible conversion and less troubleshooting during process scale-ups or kilo lab campaigns. That’s a direct result of in-house reactions, close process monitoring, and the lack of intermediate repackaging or blending, so you never have to wonder how long the product sat in a third-party warehouse.

    Applications and Practical Use Cases

    2,3-Dimethylphenylhydrazine hydrochloride exerts its value in formation of arylazo compounds, heterocyclic intermediates, and as a versatile foundation for pharmaceutical research. We receive direct feedback from scientists looking for specific N-N coupling selectivities or seeking to minimize tar formation. Pyrazole and related five-membered rings start with compounds like ours, especially for exploratory process chemistry in small molecule drug development. Bulk pharmaceutical customers use it in controlled, multistep syntheses that hinge on a reliable hydrazine component. Analytical reference labs request our material for assay development, knowing the importance of lot-to-lot uniformity and documented impurity profiling.

    Taking one example from the pigments sector, 2,3-dimethylphenylhydrazine hydrochloride reacts cleanly with a range of benzaldehyde derivatives, forming scavenging intermediates for azo dye coupling. This means less rework, fewer isolation problems, and purer colorants on the finishing line. We’ve seen similar performance when supporting fermentation-derived intermediate syntheses, where reactivity and controlled by-product formation can impact yields upstream of API isolation. Researchers in university and biotech labs have relied on our direct production for scaling up gram-to-kilogram quantities, emphasizing solid form homogeneity and ease of dissolution into various organic or acidified solvents.

    Differences from Other Hydrazines and Derivatives

    Few hydrazine compounds offer both the methyl shielding on the phenyl ring and the salt stability provided by the hydrochloride form. Compared to unsubstituted phenylhydrazine hydrochloride, the 2,3-dimethyl variant resists oxidation and copes better in exposed storage due to reduced electron density around the core nitrogen. This alteration changes not just physical stability but also alters the electronic profile, impacting reaction selectivity in metal-catalyzed transformations and in azocoupling. The hydrochloride salt’s manageable deliquescence makes it simpler to work with than phenylhydrazine base or hydrazone tars, especially in plant environments lacking sophisticated air-drying systems.

    Other isomeric dimethylphenylhydrazine salts—such as 2,4- or 3,4-dimethyl analogues—suffer from greater by-product formation in common coupling steps. Feedback from a handful of scale-up campaigns points to smoother isolation from mixed solvents and less matrix interference in downstream analytical work. Some manufacturers favor cheap, bulk phenylhydrazine base, but our customers tell us that impurity-prone grades lead to batch failures or complex purification setups. With 2,3-dimethylphenylhydrazine hydrochloride, our continuous improvements in filtration and agitated drying mean users spend more time on chemistry and less resolving process bottlenecks.

    From our experience, the hydrochloride salt packs more densely than acetate or sulfate versions, reducing dust formation and lowering potential exposure risk during open transfers or weighing. On top of this, our direct process control eliminates unknown residuals often introduced during third-party repackaging. Real traceback to batch records, certificates signed off by in-house chemists, and open-door communication set us apart from outside traders. Requests for special particle sizing, liquid suspensions, or blended hydrazines come with freighter, not container, timelines.

    Handling and Storage Insights

    This compound, like many hydrazine-derived solids, demands thoughtful storage and safe transfer practices. Our packaged product lands in double-lined, moisture-resistant bags tested for robust transit, then packed in steel drums or thick HDPE pails based on order size. Handling teams with years of experience will notice the faint, distinct odor of a well-synthesized arylhydrazine salt but will not experience the excessive fume issues that plague less refined grades. Direct-from-factory shipments reduce lag in the distribution chain, cutting back on internal moisture pickup and unintended side-product growth.

    Customers working on multi-shift schedules want product to flow on demand and not harden or clump under local seasonal conditions. Our bulk lots move through rotation within a matter of weeks, not months, eliminating concerns about long-term shelf carryover frequently seen with ship-around inventories. Closed transfer systems and regular condition checks help minimize handling risks, with our technical support always available about containment, cleanup, or material evaluation.

    Sustainability and Regulatory Commitment

    Producing hydrazine intermediates comes with significant environmental and regulatory oversight. Over the years, our facility has adopted solvent recovery and recycling systems directly into the reactor suites making this product. Emission controls, closed reactors, and in-house neutralization reduce volatilized organic load. Strict adherence to registration and export law comes standard, with all current output documented for compliant pharmaceutical and industrial use destinations. Waste minimization isn’t lip service; solvent and by-product streams cycle into compatible waste-to-energy or high-temperature destruction options, avoiding local environmental discharge.

    Feedback from customers in regions applying stringent REACH or TSCA guidelines informed improvements in our isolation and tracking processes. This means not only do our finished goods ship with full material identity, impurity, and trace element sets, but upstream production also leaves a smaller environmental footprint than legacy syntheses. In our daily operations, continuous improvement loops fix process leaks, recover evaporated solvents for re-use, and drive down total chemical inventory through on-demand, short-lead batch production. Direct production relationships allow rapid feedback and ongoing adaptations to new regulatory or paperwork demands, which bulk traders and distributors seldom offer.

    Technical Support and Troubleshooting Experience

    Years spent talking directly with chemists give us a strong sense of the real-world issues they face—unplanned color impurities, unexpected reactivity loss, variable batch-to-batch outcomes. One pharmaceutical partner recently flagged a subtle drop in product yield during a ring-forming step. Working from our own data, we pinpointed a minor uptick in moisture content and successfully adapted a drying protocol, resulting in restored yields on the next run. Real product support doesn’t come from reading spec sheets but from seeing analytical data match performance in live process equipment.

    We prioritize both consistency and transparency. Each finished lot comes with a full analytical profile confirmed by an on-site chemist who can explain not just the numbers but also the synthetic pathway and conditions that led to those results. Process questions from customers, whether about adaptation for a new solvent or troubleshooting trace impurity effects, always receive a real explanation—not simply templated advice. For those scaling up or developing new processes, access to technicians who have run full-scale synthesis themselves closes the gap between small-batch experimentation and true production.

    Supply, Lead Times and Industry Relations

    Proximity to several api and pigment plants means our production scheduling reflects not just our own forecasts but also the real needs of ongoing campaigns. Weekly coordination with key users gives us a head start planning production and testing so that lots ship tight to demand. Because finished material moves rapidly out of the building, customers don’t experience the shelf-aging or repackaging common with distributed inventory. In stable markets, this translates into short, predictable lead times—for kilo-scale pilot work or ton-sized bulk orders.

    Maintaining direct relationships matters for everyone’s peace of mind. Researchers needing rapid turnaround of small, research-scale samples call on our plant chemists directly. Larger end-users often request site audits, process summaries, or regulatory documentation, all of which we can accommodate based on hands-on knowledge, not secondhand information. We frequently receive requests for alternative specs or performance tweaks and treat these as opportunities to improve. Open dialogue with buyers and development teams shapes our quality standards and packaging protocols; experience working side-by-side with on-site users has driven our overhaul of drying, filtration, and packaging systems for maximum reliability.

    Looking Forward: Real-World Problem Solving in Hydrazine Chemistry

    2,3-Dimethylphenylhydrazine hydrochloride typifies what’s possible when a manufacturing chemist keeps both process control and collaborative feedback front and center. We have watched fields of use expand over the years, from classic dye manufacturing to cutting-edge medicinal chemistry and green process development. Much of the product’s current quality stems from open engagement with users who test our limits and challenge standards, forcing us to keep evolving.

    As novel synthetic routes and greener practices grow in importance, continuous review and adaptation in production and waste minimization remain part of our day-to-day practice. Bringing together raw material selection, reactor design, and product handling into a real-world production loop has made a difference in outcome and reliability for hundreds of customers worldwide. Solid feedback drives active improvement; each resolved issue gets fed back into new batch strategies.

    Our journey with 2,3-dimethylphenylhydrazine hydrochloride demonstrates what’s achievable by eliminating the barriers between manufacturer and end user, bridging the gap between hard data and hands-on chemistry. We believe this direct connection brings out the best in our products and in the results our customers generate.