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2-Bromo-5-Nitrothiazole

    • Product Name 2-Bromo-5-Nitrothiazole
    • Alias 2-Bromo-5-nitrothiazol
    • Einecs EINECS 401-060-9
    • 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

    687526

    Chemical Name 2-Bromo-5-Nitrothiazole
    Cas Number 30181-34-3
    Molecular Formula C3HBrN2O2S
    Molecular Weight 209.02 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 112-116°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Storage Conditions Store at room temperature, protected from light and moisture
    Synonyms 2-Bromo-5-nitro-1,3-thiazole
    Smiles Brc1nc([N+](=O)[O-])s1

    As an accredited 2-Bromo-5-Nitrothiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g 2-Bromo-5-Nitrothiazole is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 2-Bromo-5-Nitrothiazole is shipped in tightly sealed containers, compliant with hazardous material regulations. The packaging ensures protection from moisture, heat, and physical damage during transit. Shipping labels include relevant hazard symbols and handling instructions. All transportation follows applicable national and international chemical safety and environmental guidelines.
    Storage 2-Bromo-5-nitrothiazole should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizing or reducing agents. Store at room temperature and ensure proper labeling. Personal protective equipment should be used when handling, and access should be restricted to trained personnel.
    Application of 2-Bromo-5-Nitrothiazole

    Applications of 2-Bromo-5-Nitrothiazole in Industrial Manufacturing

    2-Bromo-5-Nitrothiazole is a high-purity fine chemical intermediate widely used by specialty manufacturers in advanced synthesis processes. This section details practical industrial application scenarios where this compound enters critical downstream production. As a chemical raw material producer, we address the strict technical, regulatory, and processing considerations in each segment.

    1. Pharmaceutical Intermediate for Thiazole-Based API Synthesis

    Several pharmaceutical manufacturers use 2-Bromo-5-Nitrothiazole as a core building block in the synthesis of thiazole-structured Active Pharmaceutical Ingredients (APIs). The nitro and bromo positions facilitate stepwise nucleophilic and selective cross-coupling during key stages of API construction. Customers use our product for process development of anti-infective, anti-inflammatory, and central nervous system drug classes. API synthesis workflows demand strict lot-to-lot reproducibility, documented impurity profiles, and full traceability from raw material sourcing to batch release.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP and EP monographs related to API end-product
    • FDA 21 CFR Part 210/211 manufacturing practices
    • EMA guidelines for starting material documentation

    Typical usage ratio

    • Normally 1.1–1.25 molar equivalents in coupling or cyclization stages; ratio adjusted based on reaction yield and impurity threshold requirements

    Downstream process integration

    • Added during multiple reaction steps, most commonly as halide or nitro precursor for thiazole ring elaboration; follows precise charging order to control regioselectivity and byproduct formation

    Final product types

    • Thiazole-based APIs such as antimicrobial, antineoplastic, and CNS compounds
    • Clinical trial materials for structure–activity relationship (SAR) exploration
    • Reference standards for pharmaceutical quality control

    2. Advanced Agrochemical Synthesis

    Agrochemical producers employ this compound in complex synthesis of thiazole-containing fungicides and insecticides. The nitrothiazole motif appears in advanced crop protection chemicals. Our technical material enters at the intermediate stage, aiding in site-directed modifications for compound libraries. The sector demands traceable supply and documentation for ecological and food safety audits.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO and WHO Specifications for Plant Protection Products
    • ISO 9001-certified production system
    • Local environmental health and safety requirements (e.g., EU REACH, EPA FIFRA in the US)

    Typical usage ratio

    • Generally 0.8–1.3 molar equivalents used per formation step; adjusted for active ingredient yield, minimal waste, and downstream toxicity limits

    Downstream process integration

    • Introduced at the thiazole ring assembly or as a starting halide for further nitrification and cyclization; sequentially built into active compounds by controlled substitution or reduction

    Final product types

    • Thiazole-linked fungicides and insecticide raw active materials
    • Seed treatment agents with regulatory registration
    • Agrochemical technical concentrates for industrial blending

    3. Specialty Dye and Pigment Manufacturing

    Specialty dye manufacturers leverage the unique electron-withdrawing characteristics of nitrothiazole intermediates for syntheses of high-performance pigments. The raw material supports construction of chromophores with targeted spectral properties, required in precision inks and coatings. Applications require consistent purity and trace contaminant control as mandated by customer or government product regulations, especially for export markets.

    Industry compliance standards

    • EN 71-3 requirements for pigments in toys and plastics
    • OEKO-TEX and ZDHC guidelines for textile auxiliary agents
    • RoHS/REACH compliance for pigments in electronics and packaging
    • ASTM D476 pigment testing standards

    Typical usage ratio

    • Between 0.5–1.5 molar equivalents based on chromophoric development and color intensity requirements; ratio determined by final hue consistency and stability under light/heat stress

    Downstream process integration

    • Charged during azo coupling or subsequent condensation steps to achieve required absorption spectrum; typically processed in micro-batch reactors for color consistency

    Final product types

    • Specialty dyes for security inks and non-impact printing
    • High-end pigments for automotive and industrial coatings
    • Textile colorants for technical fabrics

    4. Electronic Material Precursors for Organic Semiconductors

    Electronics and material science companies utilize this intermediate as a precursor for synthesizing thiazole-functionalized organic semiconductors and light-emitting materials. The compound’s dual electron-withdrawing substituents promote charge transport in final devices. The application requires rigorous control of metallic and organic impurities, batch reproducibility, and detailed supply chain documentation for semiconductor QC systems.

    Industry compliance standards

    • IEC 60747 standards for semiconductor quality assessment
    • JIS C5016 evaluation for organic light-emitting materials
    • ISO 14001 for environmental management in electronic material production
    • Customer-driven material qualification protocols for microelectronic fabrication

    Typical usage ratio

    • Commonly charged at 0.9–1.1 molar equivalents per polymeric or small molecule backbone; precise ratio varies by target mobility and dielectric breakdown profile

    Downstream process integration

    • Added to pre-polymerization step for organic electronic precursor synthesis; followed by vacuum sublimation or chromatographic purification before device integration

    Final product types

    • Organic semiconductors for flexible OLED displays
    • Photoactive layers for organic photovoltaic devices
    • Sensors and thin-film transistors with advanced functionalization
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    Certification & Compliance
    More Introduction

    2-Bromo-5-Nitrothiazole: A Closer Look at a Key Intermediate

    Our Direct Experience in Making 2-Bromo-5-Nitrothiazole

    Bringing 2-Bromo-5-Nitrothiazole from the bench to industrial scale has shaped how we approach complex heterocycle manufacture. Early pilot batches of this compound taught us that getting the thiazole backbone right is only a part of the challenge—the positioning of both the nitro and bromo groups demands constant care. Most of the difficulties arise in balancing yield and purity during halogenation. Years spent finetuning the reaction parameters reflect the realities of working with aromatic bromination, especially when nitro functionalities are present. Every improvement in our plant comes after direct testing—no shortcut to scaling up a sensitive synthesis.

    Model and Specifications as We Deliver Them

    2-Bromo-5-Nitrothiazole typically leaves our site as a bright yellowish solid, crystalline in form. Batch-to-batch consistency shapes every quality audit and internal review we carry out. We monitor for a melting point in the expected range around 170 to 173°C, with nearly all lots meeting a purity specification above 98% by HPLC, reflecting the reliability required by our pharmaceutical and agrochemical partners. Our process routes allow us to offer the compound in kilogram to multi-ton lots, packed in tightly sealed, light-resistant containers.

    Every bottle or drum contains more than just raw material. The real story is in the tight controls: residual solvent limits, controlled particle size (for flow in downstream steps), and thorough impurity profiling. We've found that slight deviations in raw materials shift the impurity profile considerably. This is why raw input selection—right down to the grade of sulfur and bromine—is never left to chance.

    What Differentiates Our 2-Bromo-5-Nitrothiazole from Others on the Market

    After decades serving custom synthesis contracts, we've seen that impurity loading comes as much from upstream sources as from the main reaction vessel. Not all suppliers catch this. We seldom find outside material with the same purity profile that matches ours, especially with respect to isomeric thiazole byproducts. Many commercial sources offer thiazole halonitro compounds in variable blends, reflected in inconsistent chromatographic signatures.

    Large-scale chemical plants sometimes handle thiazole intermediates on multipurpose lines, but cross-contamination leaves traces in the final product. Our site dedicates production vessels to sulfur-nitrogen-heterocycle chemistry during every run. This allows a level of root-cause tracking unmatched by contract packers or traders. Feedback from our long-term partners in life sciences shows tighter control over impurities often translates into improved batch-to-batch performance later in the pipeline.

    Uses and End Markets Informed by Real Demand

    2-Bromo-5-Nitrothiazole doesn’t find itself on commodity rosters. It fills a unique role as a starting block for API and agrochemical discovery, supporting efforts in kinase inhibition, antimicrobial research, and industrial seed chemistry. Customers designing thiazole-based compounds demand consistent reactivity so that synthetic routes do not drift between campaigns. Our own technical teams collaborate with users at the method development stage; we’ve learned the headaches that arise from inconsistent input. Our ongoing process dialogue (not just shipping product) makes sure our partners get uninterrupted supply for the lead optimization phase and beyond.

    We often find our customers using this compound as a coupling partner for Suzuki-Miyaura and Stille-type cross-couplings, where the bromine on the heterocycle undergoes selective activation. Nitro functionality guides regioselective modifications, making our product a popular choice for researchers designing highly functionalized heterocycles. Knowing where and how reaction kinetics slow or accelerate in these systems, we adjust our crystallization and purification steps to avoid latent inhibitors or reactive debris passing through. Technical troubleshooting, not simple specification-matching, keeps synthesis moving forward in these fields.

    Safeguarding Supply and Quality—How Experience Matters

    Market disruptions lay bare the risks of overreliance on generic supply chains for critical intermediates. We’ve watched market swings move the availability of thiazole precursors overnight, especially as regulatory changes have tightened global shipments of bromine-based chemicals. We invest in backward integration—a direct stake in the chains that supply our most sensitive starting materials. Owning these relationships means our delivery does not stall behind “unforeseen” raw material disruptions.

    Having sat across from underwriters, auditors, and procurement leads, one thing stands out: they trust sourced materials with documented control. In-house testing, batch-specific certificates, and transparent traceability are non-negotiable for their upstream risk management. We’ve built our reputation on not cutting corners under pricing pressure. While distributors can repackage or broker intermediates, only manufacturers with site control and regulatory compliance can fully vouch for their output. We run our quality checks in-house, avoid passing off basic analysis certificates from partners, and track all critical process changes directly.

    The global market now looks harder at where fine chemicals come from. Issues once considered minor—unexpected trace contaminants, batch variability, noncompliant waste management—regularly push projects off timeline. Our firsthand familiarity with export controls and regulatory requirements, honed serving GxP and ISO-audited downstream clients, puts us in position to cater to the higher end of process-driven industries. Instead of relying on density of distribution networks, our advantage comes from standing behind every kilo we ship.

    Product Handling and Technical Support: Lessons from the Field

    Extensive feedback from labs and pilot-scale facilities taught us the practical realities of handling 2-Bromo-5-Nitrothiazole. Its sensitivity to prolonged exposure to moisture and light, along with a known tendency to cake over time, means we take storage and shipment seriously. Our dispatch protocols call for inert packing, moisture barrier linings, and tamper-evident sealing—not because it markets well, but because customer complaints have shown that such measures make the difference between a reproducible process and a costly rerun. Temperature logs for sensitive shipments are standard procedure.

    Operators who’ve worked with this nitrothiazole in plant settings know to expect occasional dusting and a strong odor signature. Our technical briefing includes safe handling guidelines evolved from direct plant experience. Safety is not just an SOP formality; we maintain real-time connections between our process technologists and customer R&D groups, facilitating trust, especially for those working in regulatory environments where batch traceability matters.

    Why Quality and Process Understanding Go Hand in Hand

    Downstream chemists often ask for more information than what specification sheets provide. They want to understand the fate of minor impurities, not simply the headline purity number. Based on this feedback, we test for potential side-products such as dibromo or dinitro homologues and ensure systematic rejection of any batch that exceeds agreed thresholds. Controlling the exact site of bromination—limiting overbromination and polysubstitution—was a major milestone we reached only after exhaustive reengineering of our chlorination and bromination protocols.

    A key differentiator is our attention to reaction workup and isolation. Early attempts at solvent-switch crystallizations failed to deliver consistent bulk product. By working hand-in-hand with engineers and process chemists, we moved to stepwise cooling profiles and solvent mixtures that both foster high recovery and minimize formation of off-color or poorly soluble fractions.

    Long-term relationships with pharmaceutical customers have shown that lot-to-lot variability hits performance in later-stage synthesis. The “invisible” differences—trace metals, residual halides, non-thiazole organics—surface only during scale-up. That insight feeds into our own plant audits, batch recordkeeping, and corrective measures. We devote resources yearly to reviewing analytical standards so our tests remain ahead of evolving regulatory and internal benchmarks.

    Comparing 2-Bromo-5-Nitrothiazole with Other Halonitrothiazole Derivatives

    2-Bromo-5-Nitrothiazole fills a specific niche among halonitrothiazoles. Its bromine at position 2, combined with the nitro at position 5, confers a unique reactivity profile compared to, say, its 4-nitro or 2-chloro cousins. Cross-coupling efficiency, regioselectivity in nucleophilic substitutions, and the stability under common cross-coupling conditions all vary with such variations. Clients with discovery programs focused on kinase inhibitors or plant growth modifiers routinely confirm that switching the halogen alters downstream yield and even patent strategy.

    Our line covers several bromo and nitrothiazole isomers, but the 2-bromo-5-nitro variant remains the first choice for most users developing electron-deficient heteroaromatic compounds. Where other isomers have their place—for example, ortho-brominated or para-nitro variants for specialized cross-couplings—customer feedback consistently highlights the easier handling, storage, and reactivity of our 2-bromo-5-nitrothiazole.

    Those who sample materials from general supply channels often run into problems with off-color or lower-melting materials, a hallmark of inadequate separation at the purification stage. We invested in column and slurry-tray systems specifically sized for this product, not generically retrofitted for alternating projects.

    Whether handled as a dry solid, or dissolved for continuous processing, tight reactivity ranges matter. Some users purchasing from general traders report sluggish couplings or crystallization problems. Our product testing program peaks for precisely these end-use metrics, going beyond raw HPLC purity and focusing on application-driven requirements. This selects for the specs our long-term users demand, and avoids false economies from loosely specified bulk product.

    The Path Forward: Innovations and Industry Demands

    The regulatory climate and user expectations keep shifting. Our plant teams see greater scrutiny placed on solvent use, waste minimization, and the carbon footprint of halogen and nitration steps. We have responded by implementing closed-loop solvent recovery, on-site waste processing, and strict emissions controls. Investors and value chain partners care about compliance and sustainability, and so do our engineers—if only because their own job satisfaction ties into running a clean, safe site.

    Solvent consumption, once an afterthought, now figures in every plant-level audit. We build our main solvent recovery towers with the dual mandate: maximize throughput, minimize ecological and financial waste. Efforts to avoid excessive mother-liquor disposal led to new filtration protocols and tankage layout. These changes didn’t arise from a regulatory memo—but out of daily conversations with our engineers and foremen flagging pain points.

    Energy intensity remains an issue—for bromination and nitration we still require chilling and controlled reagent dosing. We’re constantly trialing reactor improvements and route modifications aimed at lowering the aggregate energy requirement by reducing the number of process steps or identifying milder oxidants and halogen sources.

    Years of direct experience making and troubleshooting thiazoles have shaped our approach to process optimization. Analytical teams routinely gather input from end users about downstream reactivity and isolation challenges. The incentive is not abstract: slower, dirtier reactions downstream slow progress for everyone.

    Why Real Manufacturing Commitment Matters

    The market for thiazole intermediates is not forgiving of shortcuts. End users in pharma, agrochemicals, and research are demanding sharper batch records, compliance documentation, and insight into every step—well before they engage a supplier. We opened our facility tours to technical visitors and respond to audits without outsourcing process explanations to outside consultants. Our ability to answer technical questions comes from daily, year-round engagement with the product—not from cobbling together information from disparate batch records or outside labs.

    Anyone working with sensitive nitrogen- and sulfur-containing heterocycles knows the real-world pitfalls: inconsistent raw inputs, contamination from recycled solvents, or improper scale-up can derail a synthesis program. Most intermediates are not forgiving about where and how they’re made. Our investment in upstream chemical control, dedicated plant infrastructure, and tight batch analytics pays direct dividends for the customer, who gains reliability and faster project timelines.

    Moving forward, we draw on both customer input and plant team insights to keep our process reliable, flexible, and up to new regulatory standards. As experienced chemical manufacturers, we know that trust in the supply chain depends on shared standards, transparency, and active problem-solving at every turn. We take pride in standing behind our product, not just shipping it.