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4-Bromo-3-Nitro-Benzaldehyde

    • Product Name 4-Bromo-3-Nitro-Benzaldehyde
    • Alias 4-Bromo-3-nitrobenzenecarbaldehyde
    • Einecs 629-023-7
    • 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
    VTB
    Specifications

    HS Code

    181625

    Chemicalname 4-Bromo-3-Nitro-Benzaldehyde
    Molecularformula C7H4BrNO3
    Molecularweight 230.02 g/mol
    Casnumber 619-08-9
    Appearance Yellow to yellow-brown solid
    Meltingpoint 146-150 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and DMSO
    Storagetemperature Store at room temperature, in a dry, cool, well-ventilated place
    Smiles O=Cc1ccc(Br)c([N+](=O)[O-])c1
    Inchi InChI=1S/C7H4BrNO3/c8-6-1-2-7(5(3-6)9)10(11)12/h1-3H

    As an accredited 4-Bromo-3-Nitro-Benzaldehyde 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 25 grams of 4-Bromo-3-nitro-benzaldehyde, sealed, labeled with hazard warnings, and product information.
    Shipping 4-Bromo-3-Nitro-Benzaldehyde is shipped in tightly sealed containers, compliant with chemical safety regulations. It is packaged to prevent moisture, light, and contamination, and typically transported as a hazardous material. Shipping documentation includes hazard classifications, and handling instructions must be strictly followed to ensure safe transit and delivery to the destination.
    Storage 4-Bromo-3-nitro-benzaldehyde should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it separated from incompatible substances such as strong oxidizers and reducing agents. Ensure proper labeling, and limit exposure to heat or open flames. Store at room temperature and follow all relevant safety and regulatory guidelines.
    Application of 4-Bromo-3-Nitro-Benzaldehyde

    Applications of 4-Bromo-3-Nitro-Benzaldehyde in Industrial Manufacturing

    4-Bromo-3-nitro-benzaldehyde serves as a critical aromatic intermediate in several downstream manufacturing segments requiring consistent purity and reliable performance. Our production supports diverse industries ranging from advanced pharmaceuticals to specialized agrochemical synthesis, each with distinct technical protocols, compliance benchmarks, and integration needs. Below we detail the major real-world industrial applications based on direct customer feedback and process validation.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Heterocyclic Compound Intermediate

    This compound is widely used for constructing key intermediates in the synthesis of heterocyclic APIs, notably in the development of certain antibacterial, antiviral, and antihypertensive drug candidates. Multinational pharmaceutical plants value its high selectivity in nucleophilic aromatic substitution, enabling efficient route design for late-stage precursors. Its utility in these syntheses is determined by product-specific process safety and impurity control regimes under cGMP conditions.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4: GMP Guidelines for Human and Veterinary Drugs
    • USP, EP, JP Pharmacopoeia intermediate specifications for intended APIs
    • FDA 21 CFR Part 211 for finished pharmaceuticals (upstream relevance)

    Typical usage ratio

    • Ranges from 0.3 to 1.2 molar equivalents as a key step intermediate
    • Exact proportion depends on the stoichiometry of target API and route optimization

    Downstream process integration

    • Introduced during core ring closure or substitution step following nitration and bromination
    • In-process monitoring for residual starting material via HPLC
    • Can be handled in batch or continuous flow reactors depending on volume
    • Product purification designed to meet isolated intermediate purity ≥99.0%

    Final product types

    • Heterocyclic drug intermediates (e.g., pyridine- and quinoline-based APIs)
    • Finished antibacterial and antihypertensive drugs after further downstream synthesis
    • Advanced pharmaceutical research intermediates

    2. Agrochemical Intermediate for Selective Herbicide Synthesis

    Formulators in the agrochemical industry utilize this compound as a building block for several modern herbicide molecular scaffolds. Its electron-deficient aromatic framework makes it suitable for coupling and functionalization, which is essential in constructing substituted aromatic systems found in selective weed control agents. Most plants using this material operate under strict environmental monitoring and often require multi-step purification protocols.

    Industry compliance standards

    • ISO 9001:2015 for process and quality management systems
    • FAO/WHO Specifications for Plant Protection Products
    • REACH registration and use compliance for hazardous substances
    • OECD Guidelines for the Testing of Chemicals (relevant to intermediates)

    Typical usage ratio

    • Applied at 0.5–1.5 molar equivalents in multi-step synthesis
    • Adjustment based on the complexity of the target herbicide and yield considerations

    Downstream process integration

    • Charged as core coupling reactant following aromatic substitution or reduction reactions
    • Integrated into multi-vessel synthesis with in-process GC-MS for contaminant tracking
    • Mainly used in semi-batch production lines with phase separation steps
    • Adheres to hazardous material handling and waste disposal protocols on-site

    Final product types

    • Triazine and pyridine-based herbicide technical concentrates
    • Bulk pre-mix herbicide formulations
    • Custom synthesis intermediates for patented agrochemicals

    3. Dye Intermediate: Advanced Organic Pigment Manufacturing

    Dye manufacturers employ this aromatic aldehyde primarily as a precursor for synthesizing nitro and bromo substituted azo dyes and acid dyes. Its highly directed reactivity towards diazotization makes it an ideal candidate for introducing chromophoric groups onto large-molecule pigment bases. Producers in the textile and specialty pigment sectors monitor purity and isomer content closely via finished product colorfastness and migration testing, particularly for regulated markets.

    Industry compliance standards

    • Oeko-Tex® Standard 100 (for textile dye endpoints)
    • EN 71-3:2019 (for pigment use in toys and children’s articles)
    • REACH Annex XVII for restricted dye components
    • ISO 105-E04 for colorfastness to perspiration

    Typical usage ratio

    • 1.0–2.0% w/w of the total dye formulation batch
    • Can be increased to 2.5% when deeper shade intensity or specific hues are desired

    Downstream process integration

    • Introduced at the pigment coupling reaction after sulfonation
    • Followed by reduction, filtration, and spray-drying
    • Final blending with dispersants and stabilizers according to customer specification
    • Batch QC includes shade, solubility, and residual aromatic impurity analysis

    Final product types

    • Nitrobenzaldehyde-based azo dyes for fabric dyeing
    • Specialty pigments for printing inks and plastics
    • Mixed-colorants for automotive and industrial coatings

    4. Fine Chemical Synthesis: Building Block for Aroma & Flavor Intermediates

    Chemical processors specializing in the synthesis of high-value aroma intermediates deploy this material as a critical aromatic precursor. Through selective condensation and further functional group modifications, it enables the production of flavoring compounds used in perfumery and specialty fragrances. Downstream processors demand robust analytical proof for all trace cross-contaminants in accordance with food and fragrance safety regulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) safety standards
    • ISO 9235:2013 for definition of fragrance raw materials
    • FEMA GRAS (Generally Recognized as Safe) program for flavor intermediates
    • Hazard Analysis Critical Control Point (HACCP) requirements in food additive production

    Typical usage ratio

    • 0.2–0.7% by weight in synthesis batches for aroma compounds
    • Ratio adjusted based on the target aldehyde or substituted aromatic endpoint

    Downstream process integration

    • Added as a condensation reactant in forming Schiff bases or oxime derivatives
    • Products undergo reflux, fractional distillation, and vacuum drying
    • QC sampling for residual halogen and nitro impurities at each stage
    • Storage under inert conditions to prevent oxidation prior to blending

    Final product types

    • Aldehyde-based aroma intermediates for perfumery
    • Flavor chemicals for food-grade applications (subject to GRAS approval)
    • Specialty fragrance bases for cosmetics and personal care

    5. Material Science: Precursor for Functional Polymer Modification

    Specialty polymer manufacturers integrate this compound as a functional monomer or chain-end modification agent to impart specific electronic or UV-absorbing properties to advanced plastics and resins. This role is especially important in engineering polymers for electronics, coatings, and housing materials, where halogenated-nitro aromatic compounds increase resistance to degradation and enable processability under controlled conditions.

    Industry compliance standards

    • ISO 14001:2015 for environmental management
    • UL 94 flammability standards for treated polymers
    • RoHS Directive 2011/65/EU compliant for restricted substance levels
    • ASTM D638/D882 for polymer tensile and physical properties

    Typical usage ratio

    • Functionalization dosed at 0.1–0.6% of total polymer mass
    • Optimization based on targeted end-use physical and UV properties

    Downstream process integration

    • Charged during pre-polymer functionalization or melt blending phase
    • Covalent incorporation under elevated temperature (80–200°C)
    • Final resin stabilization via post-processing with antioxidants
    • Continuous monitoring for unreacted monomer via FTIR or GC analysis

    Final product types

    • UV-resistant polyesters and polyamides
    • Flame-retardant plastic housings and enclosure materials
    • Functionalized resins for electronic encapsulation and conformal coatings
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    Certification & Compliance
    More Introduction

    4-Bromo-3-Nitro-Benzaldehyde: Our Experience Manufacturing High-Purity Aromatic Intermediates

    Introduction

    Over the last decade, our team has grown alongside technology and customer demand in the fine chemicals industry. 4-Bromo-3-nitro-benzaldehyde represents one of the most requested aromatic building blocks for us. Our factory started producing this compound when the shift toward specialized drug development and colorant synthesis picked up speed. At that point, reliable sourcing of halogenated nitrobenzaldehydes often held up entire research projects. Our chemists took it as both a challenge and an opportunity. Direct feedback from researchers and process development engineers has shaped how we produce and test this product.

    Unique Challenges of 4-Bromo-3-Nitro-Benzaldehyde Manufacturing

    In the lab, it seems simple to brominate and nitro-formylate a benzene ring. Scaling up always reveals the real complexities. Over years of scale-up batches, we identified several critical points for ensuring the quality of 4-bromo-3-nitro-benzaldehyde. Some challenges come from bromine handling itself. Strong odors, volatilization, material loss, and corrosion issues force ongoing investment in containment and ventilation.

    Nitration brings a second level of scrutiny. Reactions drift to unwanted product if the conditions go outside the narrow window. Early efforts with small batch chemostats helped us dial in temperature, reagent speed, and mixing patterns. Even today, we don’t rely on just in-line temperature sensors; hands-on checks and regular lab analytics keep our batch data in check.

    After reaction, separating trace poly-brominated impurities makes a significant difference for users working on advanced pharmaceuticals. High-performance column purification and careful temperature control during drying both help keep impurity profiles sharply within customer specifications. This is where our own experience makes the most difference; more than one project has been saved by a production team spotting subtle changes in crystal habit or color shade before they impacted a final batch.

    Specifications and Reliable Quality

    We manufacture 4-bromo-3-nitro-benzaldehyde with an assay target above 98 percent. Our isolation method minimizes chlorinated byproducts and keeps the moisture below one percent. Over many years, the dark yellow crystalline powder remains the form customers prefer, and constant feedback reinforces that color and particle size have a clear impact on downstream filtering and reactivity.

    We routinely test each lot by GC, HPLC, and NMR to confirm structure and purity. On top of standard batch logs, our shift teams annotate every deviation in a physical notebook—old-school, but nothing beats the immediacy when investigating batch-to-batch variation. Inquiries often come with a request for custom particle size or particular drying conditions. This isn’t a sideline; it's often dictated by each syntheses’ filtration and solubility constraints. We accommodate these because they are practical needs, not abstract preferences.

    Some customers connect with us specifically because they’ve had issues with oxidative decomposition from less controlled suppliers. Stable storage starts at drying and extends to packaging. We use double-sealed, lined containers and always encourage prompt use to avoid exposure to humidity or light, which can degrade aldehydes over time.

    End Uses and Customer Needs

    Most of our global shipments of 4-bromo-3-nitro-benzaldehyde support medicinal chemistry work, especially intermediate-scale syntheses for research APIs and advanced intermediates. Our early partnerships came from universities and contract research organizations struggling to find reproducibly pure material. Later, dye and pigment producers came on board, especially those building specialty azo and anthraquinone derivatives. The exacting color requirements of these users taught us the value of strict lot tracking and physical property recording.

    Pharmaceutical customers often ask about possible metal contamination and nitro carryover. Part of our QC includes regular trace heavy metal analysis by ICP, and we supply typical results to customers without delay. Whenever a new project kicks off, scale-up usually starts at the low kilo range in glass. Our commercial customers in pigments or polymers usually go larger, sometimes requiring drum-scale batches or continuous supply. We work tightly with both groups to match delivery arrangements and order size to their needs.

    Comparison with Related Aromatic Aldehydes and Intermediates

    It rarely makes sense to consider 4-bromo-3-nitro-benzaldehyde in isolation. Our catalog includes several aromatic aldehydes, each differing by substitution and position on the ring. In comparison, the 4-bromo and 3-nitro pattern creates both unique electron density and reactivity. This is especially useful in Suzuki coupling and other Pd-catalyzed transformations, allowing customers to further elaborate the molecule with high selectivity.

    Some users try switching from 3-bromo-4-nitro-benzaldehyde or related analogs, only to discover that regioisomeric purity changes both reaction rates and byproduct profiles. Other aldehydes lacking the nitro or bromo group react differently in condensation or nucleophilic aromatic substitution. Customers often describe a sharp difference in intermediate stability and color tone in pigment work or in downstream amine/imine conversions.

    We occasionally supply both 4-bromo-3-nitro-benzaldehyde and its isomers to comparative labs, but our advice remains that switching between them for cost rarely pays off, due to the direct impact on yield and product profile. The majority of customers who adopt this compound do so for specific, target-driven chemistry, not as a general aromatic aldehyde.

    Why Consistency Matters—Real Impact on Research and Production

    Consistency makes or breaks a project. Our position as a direct producer allows us to control every variable, from raw material quality to in-process testing and finished product isolation. Customers have reported problems with resellers who can only guarantee nominal purity but lack control over stereochemistry or contaminant profile.

    Some projects march to FDA or EMA oversight, and small fluctuations lead to analytical headaches. If a lot fails to match analytical references by more than a fraction of a percent, results from bio-assay or physical processing start to shift. Chemistry teams don’t want to tweak conditions every time new material arrives. Our ongoing direct communication with technical managers and process chemists supports long-term partnerships, ensuring each batch delivers no surprises.

    Supporting Solutions for Customer Challenges

    Many users encounter time and again the issue of inconsistent supply and unpredictability. This may result in delayed project timelines, bottlenecks, and wasted batches. We built our processes with backup raw material sources and carefully planned production scheduling to make sure lead times stay short. Order spikes, regulatory changes, and shipping disruptions can still happen, but our team is continuously trained and ready to adjust supply to meet demand.

    Waste management and environmental compliance mean more than just box-ticking. We handle all halogenated and nitro wastes at the site, ensuring full regulatory traceability. Our teams monitor VOC emissions and handle residues for off-site destruction with certified partners.

    Many first-time buyers want advice on handling and reactivity. While safety data is required, tactile advice—such as minimizing open transfers or protecting the powder from excess airflow—prevents avoidable losses and exposure.

    Continuous Improvement: Listening and Upgrading Skills

    The fine chemicals market and synthetic methodology evolve year by year. As a manufacturer, we cannot stand still. Our R&D bench tests alternative bromination methodologies to reduce hazardous byproducts and energy use. We invest in both new equipment and operator skill—embracing process automation, but also encouraging supervisors to record and share troubleshooting successes and failures.

    Processor upgrades have led to significant reduction in batch rework rates, and tighter humidity controls at the drying stage resulted in noticeably improved shelf-life, which in turn wins appreciation from end users facing longer inventory cycles.

    Traceability and Documentation

    Every drum and jar leaves our facility with a full production log, not just a certificate of analysis. This degree of documentation helps end users comply with regulatory requirements and simplifies tracking results through their own supply chain or quality system audits. For customers designing in silico processes or analyzing batch-to-batch product performance, our technical support team pulls historical process and analytical data to provide greater insight.

    Looking to the Future

    The need for reliable, well-characterized intermediates continues to rise, especially as molecular design and advanced formulation trends continue. Our ongoing mission is to match product quality to application needs and keep communications direct and open.

    Research chemists and large manufacturers have taught us flexibility, transparency, and speed are non-negotiable. Our journey manufacturing 4-bromo-3-nitro-benzaldehyde reflects our broader approach: practical, informed by real-world feedback, and always ready for new challenges as science moves forward.