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2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate

    • Product Name 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate
    • Alias Etizolam
    • Einecs 68489-77-2
    • 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

    956296

    Chemical Name 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate
    Molecular Formula C16H13ClFN3·2C4H4O4
    Molecular Weight 601.06 g/mol
    Appearance White to off-white solid
    Solubility Soluble in water and DMSO
    Melting Point Approximately 200-215°C (decomposes)
    Cas Number 119994-67-1
    Storage Conditions Store at 2-8°C, protect from light
    Purity Typically ≥98%
    Synonyms Dalfampridine dimaleate, GABA agonist derivative
    Application Pharmaceutical intermediate; research chemical
    Pka Approximately 7.9 (for primary amine group)
    Logp 2.1 (estimated)
    Stability Stable under recommended storage conditions
    Hazard Classification Non-hazardous for transport

    As an accredited 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed 10-gram amber glass bottle with a tamper-evident cap and detailed hazard labeling.
    Shipping This chemical, **2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate**, is shipped in tightly sealed containers, protected from moisture and light. It is transported as a regulated substance, following all safety, hazardous materials, and temperature control protocols in compliance with local and international regulations. Detailed documentation accompanies each shipment.
    Storage 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep at room temperature (15-25°C) and away from incompatible substances such as oxidizing agents. Ensure the storage area is clearly labeled and accessible only to authorized personnel.
    Application of 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate

    Applications of 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate in Industrial Manufacturing

    As the direct manufacturer of this active pharmaceutical chemical, we supply 2-Aminomethyl-7-chloro-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepine dimaleate to highly regulated pharmaceutical sectors and specialty chemical markets. Our production and quality assurance operate under strict industry standards to suit industrial clients’ requirements for chemical substance traceability, regulatory compliance, and repeatable performance. We focus on key applications with real demand and technical alignment, ensuring every supply batch matches the downstream integration process needs.

    1. Active Pharmaceutical Ingredient (API) for Anxiolytic Drug Formulation

    Major pharmaceutical companies utilize this compound as a key intermediate and precursor in the synthesis of advanced benzodiazepine-based anxiolytics. Process chemists employ rigorous protocols to ensure traceability, lot-to-lot reproducibility, and regulated impurity control. Integration begins at the early stage of multi-step organic synthesis, transitioning the dimaleate form into core scaffold transformation reactions in API plants. Downstream, production lines carry out salt formation, purification, and crystallization. QC labs follow validated stability studies and analytical method controls in all phases up to final API release for formulation teams, who blend the purified intermediate into solid dosage forms.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • US FDA 21 CFR Part 210/211 cGMP requirements
    • European Pharmacopoeia (Ph. Eur.) monographs for related benzodiazepine APIs
    • WHO Guidelines on Quality Assurance of Pharmaceuticals

    Typical usage ratio

    • 0.3–2.2% weight-by-weight of final pharmaceutical batch, adjusted by desired API yield and potency validation

    Downstream process integration

    • Introduced as an early synthetic intermediate in the core molecular assembly step of bulk API production
    • Progresses through controlled hydrogenation, acylation, and crystallization cycles before purification to final dosage grade

    Final product types

    • Oral tablets and capsules for anxiolytic therapy
    • Injectable solutions after further downstream derivatization
    • Bulk API supplied to licensed pharmaceutical finishers
    • Reference standards for analytical and regulatory authorities

    2. Precursor in Central Nervous System (CNS) Active Compound Synthesis

    Specialty intermediates manufacturers employ this raw material in the controlled synthesis of novel CNS-active benzodiazepine analogs used in regulated clinical development and bioactive molecule R&D. Process teams initiate with custom reaction conditions optimized for maleate salt stability and high-purity conversion rates. Detailed solvent and reagent handling minimize side product formation, while validated process analytical technology tracks composition throughout scaling up. Final intermediates undergo downstream modification, such as halogen exchange or amine functionalization, prior to handoff to contract research organizations or pilot production teams.

    Industry compliance standards

    • REACH (EC) No 1907/2006 for safe chemical handling and reporting
    • ISO 9001:2015 for documented process traceability
    • OECD Guidelines for Testing of Chemicals (preclinical, safety phases)

    Typical usage ratio

    • 10–25% molar ratio as precursor, modulated by required analog variation and reaction yield optimization studies

    Downstream process integration

    • Enter synthesis in batch reactor as main amine feedstock
    • Engage in further cyclization, halogenation, or N-alkylation via site-specific chemistries validated by customer R&D teams

    Final product types

    • CNS-active molecular scaffolds for clinical candidate selection
    • Advanced benzodiazepine libraries for drug discovery screening
    • Synthesis-grade reference samples sent to pharma innovators
    • Lead compounds for in vivo neuroscientific research

    3. Custom Synthesis in Contract Manufacturing for Clinical Development

    CRO and CDMO customers order this raw material for clinical phase custom molecule synthesis under controlled conditions. The initial maleate salt is precisely weighed, dissolved, and dosed per project-specific synthesis batch sheets, complying with non-GMP and GMP contract standards as needed. Integration occurs in modular reactor systems with tight temperature and pH control. The chemical undergoes multi-step conversion to generate highly pure clinical development candidates. Each stage involves full batch record documentation, impurity tracking, and isolated intermediate transfer, supporting transparent regulatory auditing and sponsor review.

    Industry compliance standards

    • GMP or non-GMP synthesis protocols (as per clinical phase specification)
    • ICH M7 for mutagenic impurity control
    • EU Clinical Trial Regulation No 536/2014 for investigational medicinal products
    • ISO 13485 for quality in medical device-active compounds (where required)

    Typical usage ratio

    • Variable from 1–12% by total mass of target molecule, determined by clinical batch size and contracted synthesis route

    Downstream process integration

    • Batched into primary reactor vessel with controlled feed-in for time-dependent reaction
    • Chemical transformation and purification staged for handover to secondary synthetic block or scale-up

    Final product types

    • Clinical trial-grade benzodiazepine derivatives
    • Regulatory submission samples for IND or CTA filings
    • Reference standards for safety and bioequivalence testing
    • Pre-commercial scale molecules for confirmatory batch production

    4. Reference Substance Supply for Analytical Laboratories

    Chemical analysis laboratories, contract testing centers, and regulated manufacturers routinely source this material as a certified reference substance for validating benzodiazepine identity, purity, and pharmacopoeial conformity by HPLC, LC-MS/MS, and NMR. The material serves as a calibration benchmark and impurity profile comparator for drug quality assurance. Our supply conforms to analytically certified batch consistency, packaged under inert conditions for maximum chemical stability and traceability, supporting routine compliance audits and laboratory accreditation survey audits.

    Industry compliance standards

    • USP General Chapter <467> Residual Solvents testing
    • ISO/IEC 17025 accreditation for analytical competence
    • European Pharmacopoeia 2.2.46 Chromatographic Separation Techniques
    • FDA cGMP analytical method validation guidelines

    Typical usage ratio

    • 1–10 mg per test run, precise weight adjusted based on assay method and calibration requirements

    Downstream process integration

    • Weighing and solution preparation for primary calibration curve setup
    • Blind spiking for assay validation and system suitability checks in routine and audit-focused analytical runs

    Final product types

    • Pharmacopoeial reference standards
    • Secondary working standards for QC labs
    • Batch release quality control samples
    • Certified calibration solutions for regulatory inspection
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    Certification & Compliance
    More Introduction

    2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate: A Closer Look from the Manufacturing Floor

    Understanding the Chemistry at Its Core

    On the production line, chemistry isn’t just theory—it’s a series of precise steps, every batch a reflection of attention and experience. Among the compounds we’ve committed to producing, 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate stands out for the challenge that each synthesis cycle brings. We didn’t land on this route because it was the simplest. The molecular structure, with its 7-chloro and 2-fluorophenyl groups, responds differently to each adjustment in pH or solvent volume. Here, each technician keeps a close eye on the color change, crystallization onset, and exotherms—factors that textbooks rarely capture in full.

    This compound belongs to a subset of benzodiazepine derivatives favored by researchers due to a particular profile shaped by the chloro and fluorophenyl substitutions. These small changes in the backbone dramatically influence pharmacological utilities, which is why investigators continually seek purer, more consistent output. Over the years, we’ve adjusted our reactors, refined the order of addition, even swapped out specific filtration media to ensure yields never come at the expense of degradation or excess solvent carryover. Every lot ships with data sheets written from the workbench, not just processed by analysts behind glass.

    Specifications Rooted in Practical Realities

    Specs for this product reflect the fine balancing we strike every shift. Working with a molecular weight just short of 500, the salt form—dimaleate—helps address solubility and handling concerns. Crystalline conversion under controlled humidity avoids sticky clumping, which matters much more during pilot production than in small beaker tests. Typical production cycles offer purities exceeding 99%, both by HPLC and NMR. We monitor not just the primary peak but sidelined impurities and byproducts that creep in when temperature or pressure slips out of range.

    Moisture content hovers below 0.5% thanks to vacuum dryers timed against internal dew point monitors. Particle sizing ensures anything meant for further formulation remains free-flowing and predictable, a detail noticed most during downstream blending. Unlike some manufacturers who batch through batch without recalibrating instrument drift, our operations crew brings regular reference samples and recalibrates after every shift change.

    How This Compound Is Used Across Sectors

    Chemists choose this benzodiazepine derivative for a mix of utility and dependability. It serves as an intermediate in active pharmaceutical ingredient (API) research, sometimes as a core element of CNS drug design. Research partners have explored its potential as a scaffold—other ring structures can be built off its backbone or modified through alkylation or acylation reactions. Medicinal chemistry labs look for stable, easy-to-handle compounds, and our dimaleate salt checks those boxes due to its strong shelf stability and predictable reactivity.

    Outside the direct realm of drug design, this compound finds roles in target identification studies, often as a positive control due to its well-characterized interaction profiles. Experienced formulators, especially those designing reference standards, reach for our batches because the impurity profile is both low and consistent, cutting down on downstream purification time. Even life science supply companies, building compound libraries or screening kits, rely on source quality and continuity batch-to-batch, a guarantee that only comes from those making their processes transparent.

    Tangible Differences from Other Benzodiazepines

    Industrial chemists rarely see product choice as a matter of preference. Each derivative brings certain risks and advantages. Compared with standard benzodiazepines, this fluorophenyl-chloro compound offers sharper selectivity in receptor-binding profiles—a feature that has attracted attention in both academic and commercial circles. In practical terms, this means broader applications in structure-activity relationship (SAR) studies, beyond what more generic diazepine salts provide.

    Handling characteristics matter too. This product doesn’t cake in its container nor does it emit off-odors, thanks to benchmark solvents and double-filtration before crystallization. Other suppliers may market similar molecules in less stable forms—hydrochloride or free base—yet these often struggle with moisture-induced degradation or fluctuating assay values. We stick to the dimaleate salt because years of bench and pilot-scale runs have demonstrated stable shelf life under varying storage conditions, tolerating wide humidity swings without visible color shift or structural breakdown.

    Technicians noted early on that this compound resists breakdown during exposure to mild light and oxygen, reducing the number of ‘out-of-spec’ lots. Other benzodiazepine derivatives can show telltale signs of breakdown, like yellowing or extraneous IR peaks—outcomes that lead to wasted time and rework. Real-world evidence, from our own lot tracking system, shows the rate of rejected material for this product remains lower than for comparable compounds.

    Traceability and Transparency Built Into Every Batch

    Years ago, quality audits uncovered the downstream headaches caused when sources are murky or data sheets feel abstract. Our plant responded by building direct traceability into each production run. Lot numbers tie to specific reaction logs, equipment calibration records, and even names of crew handling the batch—no black boxes. This brings confidence downstream, especially for clients facing regulatory scrutiny or needing to track impurities back to the source.

    Every specification published online or sent with a shipment comes off the actual control records, not boilerplate. When an unexpected variance is flagged, our team steps in on the same day for root-cause review. Improvements have real impact: one tweak to the filtration stage eliminated a stubborn chromatographic impurity that had tripped several external partners’ QC checks. Being the manufacturer, not just a supply intermediary, means we confront and address each feedback loop directly.

    Process Evolution Backed by On-the-Ground Experience

    Process tweaks happen here with full buy-in from floor staff who actually run the reactors or dryers, not just from the R&D office. One year, during a particularly humid stretch, final product started trending high on moisture assays. Instead of writing off product or making customers wait, our shift supervisor tested a new desiccant schedule—swapping out precharges at mid-cycle. Within a week, assay values came back within expected range, and no customer noticed any delay. These kinds of practical interventions stack up over decades, shaping a process that is both robust and adaptable.

    Our data packs with each shipment reflect hands-on knowledge: melting points, IR and NMR fingerprinting, even photostability data from in-plant storage studies. We leave in comments from both quality and production, whether it’s a slightly longer drying time or a forewarning about a minor batch-specific deviation. Years ago, larger competitors circulated product that looked good on paper but fell short in real-world screening. Our feedback loop with partners remains our strongest differentiator—direct communication without marketing buffers or legalese.

    Safety and Environmental Responsibility

    Operating a plant that handles active intermediates like this benzodiazepine derivative brings responsibility. Vent scrubbers, solvent recovery, and stringent PPE protocols are routine. Tank changeouts, line flushes, and filtered exhausts safeguard not only our staff but also the town downstream from our pipes. Years of meticulous monitoring and close calls with process upsets have taught us to stay vigilant, never leaning on automation to replace oversight.

    Waste minimization runs parallel to efficiency. Spent solvents from synthesis stages recycle through our recovery units, reducing both input costs and landfill load. Where cross-contamination could threaten neighboring lines, full system validations guarantee only what’s meant to run, runs. Regenerable resins serve for purification, and routine audits ensure nothing slips through the cracks. We track our environmental indicators openly because anyone who’s worked with these chemical classes knows public trust is only as strong as yesterday’s water sample.

    What Our Team Has Learned Over the Years

    Continuous production sharpens focus on details that brochures never mention. Certain employees only trust a batch once they sniff the final flask—having found years ago that off-odor predicts off-spec. Process engineers lean on upstream analytics to flag incipient issues ahead of time, but nothing replaces the experience of a technician catching a chromatogram that looks ‘off’ by a subtle shoulder on the main peak.

    Clients looking for a supplier with their own skin in the game ask questions that go beyond certificates. They want to know what really goes into the process, how solvent changes affect batch quality, why shelf life sometimes varies by shipment. Only a manufacturer, managing synthesis day-to-day, provides these answers with authority. We talk honestly about failure: a line swap that carried trace chlorinated residue into an otherwise clean run, or a miscalculation in scale that forced a rework. Learning here stays with the team, driving small changes that improve every subsequent batch.

    Challenges and the Way Ahead

    Production always brings up fresh problems. Solvent pricing, supply chain hiccups, and regulatory changes don’t warn you before they hit the order book. Years back, we faced a sudden shortfall in a precursor—caught late on a Friday when deliveries stopped. Instead of pausing, the team brainstormed late and sourced a backup, rerouting synthesis to accommodate the change. The structure and integrity of the product stayed consistent, but we saw firsthand how flexibility matters.

    Facing increasing scrutiny from regulatory bodies and rising client expectations, documentation gets more detailed each year. Our response has been to invest in both people and systems. Batch records cross-reference all analytical results, and we spend weeks onboarding each staffer to the specific quirks of each compound line. Problem-solving isn’t limited to the lab notebook but involves real-time interventions and direct communication with clients should an issue arise.

    Serving a Diverse Client Base?

    Chemical companies, academia, and government labs source this compound for unique projects. Each has its own expectations and pain points. Some prioritize long-term storage under variable conditions—our dimaleate formulation addresses those needs by holding up to heat and humidity. Others push for near-zero impurity profiles, which we meet through redundant purification cycles and ongoing method validation.

    We stay alert for feedback, treating each complaint or test failure not as a nuisance but as a lesson to fold back into the process. Direct lines between production, QC, and clients foster trust—a resource as tangible as any flask of finished product. Our annual audits with external partners often set new bars for both traceability and openness, rather than just box-checking for compliance.

    Why Direct Manufacturer Knowledge Matters

    Resellers and traders might offer convenience, but they don’t feel the consequences when a lot fails downstream testing. Only those who handle the raw materials, run the reactors, and see batches from start to finish can answer detailed questions and explain why a shipment may have tiny batch-to-batch differences. Issues with 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate—be it unexpected moisture upticks or microimpurity spikes—are the manufacturer’s to own, fix, and communicate about honestly. Repeat clients stay with producers willing to stand by these challenges, not deflect them.

    Experience shapes every product leaving our facility. Site visits from partners are welcomed, not skipped. Troubleshooting is collaborative, not transactional. We invite questions as much about our site operations as about the compound’s analytical results. The trust this builds extends far beyond a single purchase order.

    Refining for the Needs of Today and Tomorrow

    Shifting research needs and tighter quality requirements keep us adapting. Advances in chromatographic separation, impurity tracking, and in-situ monitoring have driven better output over the past decade. Real-world input from researchers working with our compound becomes guidance for upgrades—whether to isolation hardware, drying cycles, or in-line analytics.

    Projects these days often require customization—alternative particle sizes, custom solvent footprints, tailored impurity tolerances. As the manufacturer, we welcome these requests, seeing them as opportunities to stretch operational range and learn. Bulk runs, kilo labs, and even gram-scale pilot batches each receive full documentation and batch-specific handling that mirrors client expectations for their final application.

    Conclusion from Decades of Manufacturing

    Making 2-Aminomethyl-7-Chloro-2,3-Dihydro-5-(2-Fluorophenyl)-1H-1,4-Benzodiazepine Dimaleate isn’t just about pushing out another chemical. It’s a collaboration built on years of practical know-how, a continual tweaking and troubleshooting that never really ends. Choice of salt form, direct handling, and process control show up in every assay and lot report—and drive the reliability our partners depend on. For buyers who care about quality that’s real, we offer more than material; we share the commitment behind each batch, every single time.