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Benzofurazan-5-Carbonyl Chloride

    • Product Name Benzofurazan-5-Carbonyl Chloride
    • Alias 5-(Chlorocarbonyl)benzofurazan
    • Einecs 620-367-7
    • 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
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    Specifications

    HS Code

    616196

    Productname Benzofurazan-5-Carbonyl Chloride
    Casnumber 22252-43-3
    Molecularformula C7H3ClN2O2
    Molecularweight 182.57
    Appearance Yellow to orange solid
    Solubility Soluble in organic solvents such as dichloromethane
    Purity Typically >98%
    Storagetemperature Store at 2-8°C
    Synonyms 5-(Chlorocarbonyl)benzofurazan
    Structuralformula O=C(Cl)c1ccc2nonc2c1
    Hazardclass Corrosive
    Application Used in organic synthesis and fluorescent labeling

    As an accredited Benzofurazan-5-Carbonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of Benzofurazan-5-Carbonyl Chloride, sealed, labeled with hazard information and handling instructions.
    Shipping Benzofurazan-5-Carbonyl Chloride should be shipped in tightly sealed containers, under dry and inert conditions. It must be packaged according to hazardous materials regulations, protected from moisture and incompatible substances, and labeled with proper hazard warnings. Transport should comply with relevant international and local chemical shipping guidelines and safety standards.
    Storage Benzofurazan-5-carbonyl chloride should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. It should be kept away from incompatible substances such as strong bases, strong oxidizers, and alcohols. Store under an inert atmosphere, such as nitrogen or argon, to prevent hydrolysis and decomposition. Use appropriate chemical storage protocols.
    Application of Benzofurazan-5-Carbonyl Chloride

    Applications of Benzofurazan-5-Carbonyl Chloride in Industrial Manufacturing

    As a direct manufacturer specializing in benzofurazan-5-carbonyl chloride, we supply this intermediate to a focused range of specialty chemical sectors. This compound's unique reactivity enables selective modifications in complex molecule synthesis, especially where nitroaromatic functionalities and carbonyl chloride groups are essential. Below we detail precise downstream applications, industry compliance criteria, formulation ratios, process integration, and types of finished goods.

    1. Advanced Fluorescent Dye Synthesis for Analytical Reagents

    Benzofurazan-5-carbonyl chloride provides a reactive carbonyl chloride group used in the derivatization of amines and thiols during the production of fluorescent labels for HPLC and capillary electrophoresis kits. Producers introduce it at the post-coupling stage to form N-substituted benzofurazan derivatives with strong fluorescence, widely used in bioanalytical detection reagents. The material's purity and consistency are critical, meeting analytical sector requirements—every batch undergoes trace impurity screening to ensure reproducibility for diagnostic formulation partners.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • REACH (EC) No 1907/2006 for registered substances (when applicable in the EU)
    • IUPAC Nomenclature and Pharmaceutical Quality System guidelines (for reagents used in regulated environments)
    • Supplier auditing protocols set by life science analytical kit producers

    Typical usage ratio

    • 0.05–0.2 molar equivalents in dye synthesis formulations, calculated relative to the analyte’s amine or thiol component; precise addition adjusted based on targeted fluorescence intensity and labeling efficiency

    Downstream process integration

    • Added post-core dye synthesis, during acyl chloride coupling with analyte (amine/thiol) substrates
    • Requires strict anhydrous and inert atmosphere conditions
    • Followed by purification via recrystallization or column chromatography
    • QC includes fluorescent spectrum assessment and trace-level purity analysis

    Final product types

    • Pre-packed HPLC fluorescent derivatization kits
    • Labeling reagents for amino acid quantitative analysis
    • Custom fluorescent probes for laboratory research
    • Capillary electrophoresis fluorescent derivatization agent sets

    2. Precursor in Nitroaromatic Pharmaceuticals Development

    Pharmaceutical manufacturers use this compound as a key intermediate to introduce and functionalize the benzofurazan scaffold in new chemical entity (NCE) drug R&D, especially for nitroaromatic frameworks targeting anti-infective, antiviral, and CNS-active molecules. Integration occurs at the late-stage intermediate coupling step, where the carbonyl chloride group reacts with protected amines or aromatic nucleophiles. Strict controls over stoichiometry and impurity profiles ensure regulatory compliance for pharmaceutical intermediates.

    Industry compliance standards

    • ICH Q7 GMP Guidance for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 (for drug substance suppliers)
    • EU GMP Guidelines Part II for raw materials
    • Documentation of traceability and impurity mapping for APIs

    Typical usage ratio

    • Ranges from 1.0–1.2 molar equivalents for direct amide or ester couplings in custom synthesis; the ratio is adjusted to drive reactions to completion while minimizing byproduct generation

    Downstream process integration

    • Introduced after core scaffold assembly, typically in solvent-based coupling reactors under chilled or controlled-temperature conditions
    • Followed by isolation and purification through preparative chromatography or crystallization
    • Used in the preparation of clinical trial API batches and medicinal chemistry libraries
    • Stability and residual solvent analysis completed prior to QP release

    Final product types

    • Semi-synthetic APIs featuring nitrobenzofurazan heterocycles
    • Novel small molecule candidates in antiviral and anti-bacterial pipelines
    • Specialty CNS drug intermediates requiring benzofurazan modifications

    3. High-Energy Material Additive for Specialty Explosives

    Specialty energetic material formulators implement benzofurazan-5-carbonyl chloride to manufacture tailored benzofurazan derivatives sought for their electron-withdrawing structure, modulating burn rates and sensitivity in precision detonators and booster compositions. Material addition is timed to the energetic precursor’s post-nitration or amidation phase, achieving exacting performance requirements. The application demands rigorous tracking of nitrogen content, thermal stability, and safety characteristic certifications.

    Industry compliance standards

    • UN Manual of Tests and Criteria for explosives (Section 2: classification, sensitivity)
    • US ATF Regulation 27 CFR Part 555, Subpart K—Storage, handling and manufacture
    • Defense Federal Acquisition Regulation Supplement (DFARS)—Energetic materials control
    • Internal QC and traceability in compliance with military procurement protocols

    Typical usage ratio

    • 1–3 wt% as additive or reactant, incorporated based on energetic formulation designs targeting specific detonation velocity or stability profiles; ratio is determined through small scale composition validation tests

    Downstream process integration

    • Added during post-nitration functionalization, typically via closed reactor systems to manage exothermicity
    • Processed under controlled temperature with in-line monitoring of exotherms and evolved gases
    • Followed by granulation, blending, and pressing into composite explosive elements
    • Final assembly in compliance with approved plant safety protocols

    Final product types

    • Detonator boosters for high-reliability initiation systems
    • Precision pyrotechnic charges for aerospace separation mechanisms
    • Custom explosive inserts for oil well perforation charges

    4. Functional Material Synthesis for Polymer Modification

    In advanced polymer chemistry, researchers and specialty manufacturers employ benzofurazan-5-carbonyl chloride to graft benzofurazan groups onto selective polymer backbones, enhancing charge transport, UV response, or fluorescence in specialty coatings and electronic materials. The compound enters at the post-polymerization functionalization phase, requiring stringent control over the degree of functionalization to balance material properties. Product traceability and consistency are ensured through batch-level FTIR and NMR analysis.

    Industry compliance standards

    • ISO 9001:2015 for specialty polymer production
    • RoHS Directive (EU) 2011/65/EU (as applicable for electronics-grade coatings)
    • REACH Registration (EC) No 1907/2006 for substances imported into Europe
    • Internal hazardous substance monitoring protocols for downstream electronics partners

    Typical usage ratio

    • Typically 0.2–1.0 wt% relative to base polymer in batch modification, adjusted according to target level of functional substitution and desired optical or electrical characteristics

    Downstream process integration

    • Reactive addition to functionalize pre-formed polymer chains via acylation or amidation reactions
    • Utilized in solvent-cast, melt-extrusion, or in-situ solution modification systems
    • Post-functionalization purification through solvent extraction, precipitation, or membrane filtration
    • Microstructural analysis by GPC, FTIR, and NMR conducted for every lot

    Final product types

    • Photoresponsive polymer coatings for printed circuit boards
    • Emission-tuned polymer films for display device layers
    • Conductive or fluorescentant polymer composites for optoelectronics
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    Certification & Compliance
    More Introduction

    Benzofurazan-5-Carbonyl Chloride: Precision Chemistry from the Manufacturer’s Bench

    What We Know about Benzofurazan-5-Carbonyl Chloride

    With decades in the fine chemicals business, our team has watched demand shift and grow in many specialty arenas, but requests for high-purity heterocyclic chlorides always stand out. Benzofurazan-5-Carbonyl Chloride, model BFC-5CCl, gains frequent attention from both pharmaceutical and agrochemical developers. It’s not the easiest compound to handle, but those who rely on it value the clarity and control it brings to their target reactions.

    Our production line for Benzofurazan-5-Carbonyl Chloride runs on site using a batch synthesis route developed through years of process hazard analysis, scale-up trials, and feedback from formulation chemists. Not all carbonyl chlorides tolerate upstream impurity load; BFC-5CCl’s method forces a slow chlorination under controlled low temperature. Small changes in reagent quality or temperature disrupt the selectivity, so consistent manufacturing starts with disciplined feedstock screening. For our current lots, we maintain greater than 98.5% assay by HPLC, residual moisture below 0.05%, and manage residual organic solvents through distillation under reduced pressure.

    The Role of Benzofurazan-5-Carbonyl Chloride in Synthesis

    People who use Benzofurazan-5-Carbonyl Chloride are often looking to turn a simple amine, alcohol, or thiol into an advanced intermediate with selective activation points. Its reactive carbonyl chloride moiety does not forgive mistakes in stoichiometry or temperature, but with rigorous technique, it lets chemists build off the benzofurazan ring to add properties like fluorescence, pharmacophoric functionality, or unique redox behavior. Our lab work typically pairs it with nucleophilic amines in controlled microreactors, and we keep eye protection and strong ventilation protocols at the fore. The light-yellow, sometimes coriander-shaded solid tends to hydrolyze against ambient humidity, so users move fast and glove up before opening bottles.

    We see BFC-5CCl as a backbone for both large-scale API development and research-scale fluorescent tagging workflows. Unlike simple acyl chlorides, the benzofurazan chromophore confers additional detection and tracking power, particularly in imaging-based pharmacology or environmental tracing studies. For us, the challenge has always been supplying lots that remain bright, easily dissolvable, and predictable across batches.

    Making a Difference from Other Carbonyl Chlorides

    Not all carbonyl chlorides behave the same in the lab, and that is evident for anyone who’s juggled the likes of benzoyl chloride or other substituted aromatic acid chlorides. Benzofurazan-5-Carbonyl Chloride, with its heteroatom scaffold, interacts uniquely with electron donors, often forming tighter or more rigid intermediates. Those looking to prepare advanced heterocyclic ureas or carbamates find the electronic structure lets them skip auxiliary steps, ultimately saving days of purification. Engineers in our pilot plant report that the less-volatile benzofurazan ring reduces unwanted side products compared to monocyclic chlorides or simple aliphatic analogues.

    The photophysical traits of this molecule matter heavily in analytical and life sciences work. Standard carbonyl chlorides, though useful, do not allow direct tracking under UV or visible light. With BFC-5CCl, the intrinsic fluorescence of the benzofurazan core adds new layers of information. Teams in environmental forensics take advantage by tagging unknown nucleophiles and scanning for contamination plumes at very low concentrations. In our own labs, we quantify product yield by direct fluorometry rather than chasing faint NMR peaks.

    Quality Commitment as Source Manufacturer

    Those who work in scale-up chemistry know the frustration when the upstream batch varies from the last. We’ve learned that reproducible outcomes from Benzofurazan-5-Carbonyl Chloride hinge on two priorities: raw material selection and process discipline. Our suppliers remain vetted, often following years of collaboration around aromatic nitro intermediates. People often ask why we run such tight controls on moisture and trace metals, and the answer is always downstream reactivity. Even trace levels of iron or copper degrade product quality, so we analyze every lot by ICP-OES before moving to reactor charging.

    From brominated side products to over-chlorinated residues, these unwanted signals show up more easily in a chromophoric system like benzofurazan. By holding our production under nitrogen and packaging material in desiccated containers in line with transport requirements, we aim to reduce the risk for project chemists. The results speak for themselves: fewer failed coupling steps, crisper analytical traces, and a lower burden on post-reaction workups.

    User Experience from Lab to Plant

    Over the years, custom synthesis teams have described the difference between working with this compound and other acyl chlorides as a matter of ‘confidence in the bottle.’ Some new users expect it to flow or reconstitute as easily as benzoyl chloride, but a compact, crystalline morphology dominates. It stores best at refrigerated temperatures, and direct transfer under dry nitrogen lets users skip annoying clumping or ‘caking up’ that tends to steal time in an air-sensitive glove box.

    Scale-up efforts reveal why purity and shelf life make such a financial difference. Low-grade lots tend to decompose upon storage, forming acids that neutralize costly bases or cause sticky tar in glassware. Our large-scale partners report that handling quality material gives more predictable stoichiometry, less wasted time in cleanup, and fewer fiber filterings at kilolab scale. In pooled data from customers across three continents, yields in peptide coupling improved by up to 8% using our product versus commercial preparations, reducing waste acid and chlorinated byproducts.

    Supporting Discovery from Development to Manufacturing

    Manufacturing teams need compounds that do more than just meet spec sheets. They need reliability batch after batch. With benzofurazan-5-carbonyl chloride, the stakes are high: inconsistent profiles drive up rework costs and delay downstream development. We commit to publication-level transparency, sharing not only assay values but also trace impurity profiles, certificate of analysis details, and near real-time feedback for process deviations.

    Early-stage labs using BFC-5CCl often pivot quickly between structure-activity series, requiring sub-gram to multi-kilogram quantities without question on identity. We offer both standard 25g packs for initial screens and multi-kilogram drums for scale-up, each subjected to the same release criteria. Feedback from these teams confirms that lot-to-lot consistency builds trust, allowing them to avoid adjusting protocols or running excess controls.

    Long-Term Value to Science and Industry

    The benzofurazan platform opens technical routes not easily accessible with simple benzene-based carbonyls. Fluorescent detection supports real-time tracing in biosystems and environment. Phosphorylation and glycosylation studies benefit from the electron richness of the ring, offering new pathways in carbohydrate and nucleotide chemistry. One customer in the diagnostics field described a leap in detection sensitivity after switching to BFC-5CCl for protein derivatization compared to standard phosgene surrogates.

    Pharmaceutical manufacturers recognize another benefit: benzofurazan-5-carbonyl chloride supports high selectivity peptide coupling, especially where side-reactions with simpler reagents proved intractable. Better reactivity towards hindered amines, fewer hydrolytic breakdowns, and easier isolation—those are claims we can back up with internal figures and end-user validation. Our data show that in over 90% of trials involving sterically challenging amines, customers see cleaner chromatographic results and higher yields.

    Troubleshooting and Process Solutions

    With a sensitive acid chloride like BFC-5CCl, the main headaches show up around moisture management, shelf life, and reaction exotherms. Technicians in our plant learned early on that closed-system charging and rapid transfer shave hours off cleanouts and reduce the load on operator training. We train partners on low-temperature handling and pressure relief to keep runaway exotherms in check. Not everyone realizes the tendency of this compound to release HCl gas on contact with even minute traces of water; proper ventilation and neutralization stations prevent corrosion issues.

    Reuse of spent packaging can be an issue for facilities that don’t dedicate specific hardware to acid chlorides. We only use UN-approved fluoropolymer-lined containers and advise against glass storage for long durations. One client in peptide manufacturing explained that adopting our polyethylene jugs eliminated plugged dispensing lines, which had plagued them when using competitors’ glass-packed material.

    Environmental & Regulatory Considerations

    Manufacturers have felt growing scrutiny about the downstream fate of specialty acid chlorides. We’ve invested in greener synthesis steps, minimizing volatile byproduct release and scaling solvent recycling internal to our plant. Because chlorinated aromatics may pose a hazard to aquatic systems, we support our customers with waste handling consultation and on-site neutralization protocols.

    International standards for specialty intermediates push the regulatory bar higher each year. Our documented impurity tracking, hazard labeling, and QA archiving have passed regional audits without incident. We never sidestep legal requirements for hazard communication, and train our team to keep detailed batch records for at least 10 years—a practice we recommend up and down the value chain.

    Future Prospects and Evolving Applications

    Niche compounds like Benzofurazan-5-Carbonyl Chloride may never hit the tonnage reports of commodity chemicals, but their impact can ripple through scientific progress. In-house research explores new derivatives aimed at increasing aqueous solubility and reducing dark reaction rates, hoping to meet the next wave of analytical and diagnostic challenges. Collaborations with academic groups help us pilot microreactor-based fluorogenic probes, seeking both greener footprints and higher modularity.

    While some carbonyl chlorides fade in relevance as alternatives pop up, Benzofurazan-5-Carbonyl Chloride persists in crucial roles far beyond what its molecular weight might suggest. Whether in tracking nerve agent degradation in soil or supporting chiral separations for advanced therapies, it earns its reputation as a tool for innovators—and those committed to precise, responsible chemistry. Customers who have spent decades wrestling with less cooperative acyl chlorides report relief and a renewed drive for efficiency when they add our BFC-5CCl to their toolkit. The stories we hear push us to refine, invest in better analytics, and maintain an unwavering focus on performance and trust.