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3,5-Bis(Bromomethyl)Toluene

    • Product Name 3,5-Bis(Bromomethyl)Toluene
    • Alias 1,3,5-Tris(bromomethyl)benzene
    • Einecs 229-713-7
    • 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

    876643

    Chemical Name 3,5-Bis(Bromomethyl)Toluene
    Cas Number 1641-61-8
    Molecular Formula C9H10Br2
    Molecular Weight 293.99 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 63-67°C
    Solubility In Water Insoluble
    Density 1.8 g/cm³ (approximate)
    Purity Typically >98%
    Storage Conditions Store in a cool, dry place; keep container tightly closed

    As an accredited 3,5-Bis(Bromomethyl)Toluene 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 100 grams of 3,5-Bis(Bromomethyl)Toluene, sealed with a screw cap, labeled with hazard warnings.
    Shipping 3,5-Bis(Bromomethyl)Toluene should be shipped in tightly sealed chemical containers, protected from light and moisture. It must be handled as hazardous material, following all local, national, and international transport regulations. Use appropriate hazard labeling, and include safety documentation. Avoid exposure to heat, and store upright during transit to prevent leaks.
    Storage 3,5-Bis(Bromomethyl)Toluene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture, heat, direct sunlight, and physical damage. Always ensure proper chemical labeling and keep container tightly closed when not in use to prevent contamination and degradation.
    Application of 3,5-Bis(Bromomethyl)Toluene

    Applications of 3,5-Bis(Bromomethyl)Toluene in Industrial Manufacturing

    As a direct producer committed to precision and quality, we supply 3,5-Bis(Bromomethyl)Toluene to advanced industries that require consistent bromination intermediates for specialty synthesis. This section details the principal downstream sectors utilizing this raw material, with specific notes on compliance, formulation ratios, process step, and end product realizations.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers apply 3,5-Bis(Bromomethyl)Toluene as a core halogenated intermediate for the synthesis of certain active pharmaceutical ingredient (API) building blocks, particularly those targeting anti-cancer, anti-viral, and central nervous system (CNS) therapies. The high-purity compound undergoes controlled substitutions and couplings during multi-step organic syntheses, contributing crucial benzyl bromide moieties required for proprietary and generic small molecule API programs. Integration of this intermediate supports strict traceability under global GMP regulations throughout all stages of processing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • US FDA 21 CFR 210/211
    • EU EudraLex Vol. 4 GMP
    • Chinese Pharmacopoeia quality requirements for pharmaceutical raw materials

    Typical usage ratio

    • Ranges from 0.05 to 0.20 molar equivalents in key alkylation or bromination steps, adjusted by final molecule requirements and the specific synthetic route selected during R&D development

    Downstream process integration

    • Introduced during the benzylation or bromomethylation stage of API construction, commonly fed into batch reactors under anhydrous and inert conditions to ensure selectivity and yield

    Final product types

    • Anti-tumor small molecules (custom APIs)
    • CNS-targeting prototype drugs
    • Antiviral lead compounds
    • Custom halogenated pharmaceutical intermediates

    2. Specialty Polymer Crosslinking Agents

    Polymer producers utilize this dibromo compound as a bifunctional crosslinker, particularly in the formulation of flame retardant thermoset resins and specialty engineering plastics. The chemical structure enables controlled incorporation of bromomethyl functionalities that react during polycondensation or chain extension, imparting enhanced fire-resistance and tailored mechanical attributes to molded parts for electrical, automotive, and construction uses. Strict batch monitoring ensures consistent reactivity and compliance with all downstream safety regulations.

    Industry compliance standards

    • UL 94 Flammability Standard
    • RoHS Directive 2011/65/EU (for restricted substances)
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 for Quality Management in polymer manufacturing

    Typical usage ratio

    • Added at 0.5–3.0 wt% of total resin mass, with precise ratio optimized by end polymer matrix, desired crosslink density, and targeted flame retardancy grade

    Downstream process integration

    • Charged into mixing tanks with resin monomers prior to molding, or co-reacted during in situ polymerization; process typically employs nitrogen blanketing to maintain chemical integrity and batch traceability

    Final product types

    • Halogenated epoxy resins
    • Crosslinked unsaturated polyester resins
    • High-performance thermoset laminates
    • Electrical insulation components

    3. Agrochemical Intermediate Manufacturing

    Leading crop protection companies employ this raw material as a precursor within the synthesis of novel active ingredients for herbicides and insecticides. The dual bromomethyl functionality enables selective introduction of reactive sites onto aromatic ring systems, establishing custom scaffolds for further functionalization. Efficient integration in pilot and commercial production supports batch-to-batch uniformity, tracking from material receipt through advanced downstream transformations and formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Technologies
    • ISO 9001:2015 (for agrochemical operations)
    • Globally Harmonized System (GHS) for safe handling and labelling
    • China Ministry of Agriculture GB chemical registration rules

    Typical usage ratio

    • Applied at 0.1–0.8 equivalents relative to main aromatic synthesis intermediates, tailored to target yields and impurity minimization in multi-step processes

    Downstream process integration

    • Charged to reactor following initial aromatic precursor functionalization; reacts under base, phase transfer, or catalytic conditions to form key bromo-aromatic units before further derivatization

    Final product types

    • Precursor compounds for selective herbicides
    • Building blocks for insecticidal synthesis
    • Custom pesticide intermediates
    • High-value crop protection agents

    4. Fine Chemical Building Block for Liquid Crystal Synthesis

    Manufacturers of advanced display materials integrate 3,5-Bis(Bromomethyl)Toluene into the synthesis of tailored liquid crystal monomers for LCD and OLED panels. The symmetrical dibromomethyl framework enables precise control over molecular alignment, promoting enhanced display clarity and temperature stability. Customized process conditions and inline QC ensure batch reproducibility for downstream panel assembly and device integration, with full traceability across materials used in electronic-grade applications.

    Industry compliance standards

    • IEC 61249-2-21 (Halogen-free requirements for display substrates)
    • JPCA-ES-01 (Japan Printed Circuit Association Environmental Standards)
    • ISO 9001:2015 for electronics materials production
    • RoHS Directive (lead, mercury, PBB, PBDE restrictions)

    Typical usage ratio

    • Utilized at 0.02–0.12 molar equivalents, adjusted based on targeted molecular lengths and mixture formulations for specific liquid crystal properties

    Downstream process integration

    • Fed into high-purity reactors for controlled bromination and Friedel-Crafts-type reactions; subsequent purification yields liquid crystal monomers for blending or further functionalization

    Final product types

    • Twisted nematic liquid crystal monomers
    • Advanced liquid crystal mixtures for TFT-LCD screens
    • OLED panel compounds
    • Specialty display materials for aerospace and medical imaging

    5. Reactive Intermediate for Custom Dye Synthesis

    Dyestuff manufacturers select this compound as a key brominated building block for synthesizing specialty dyes, pigments, and optical brighteners. Its bromomethyl arms allow controlled coupling and extension of conjugated systems, which are then further modified by azo or anthraquinone chemistry. The ability to introduce complex aromatic frameworks through high-yield, low-residue pathways contributes to improved color intensity and fastness for technical textiles and specialty coatings.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Safety and Chemical Residue Limits)
    • ISO 14001:2015 (Environmental Management Systems)
    • REACH Annex XVII (Restrictions on Substances in Dyes)
    • EPA 40 CFR Part 721 (Significant New Use Rules for chemical substances)

    Typical usage ratio

    • Formulation concentrations range from 0.3 to 2.0 weight percent in dye precursor synthesis, optimized by chromophore target strength and performance profile

    Downstream process integration

    • Added to aromatic starting material during nucleophilic substitution, cross-coupling, or condensation stages; isolation and purification follow, ensuring high purity for subsequent dye formation

    Final product types

    • High-fastness disperse dyes
    • Optical brighteners for synthetic fibers
    • Special effect pigments for plastics and inks
    • Functional textile dye intermediates
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    Certification & Compliance
    More Introduction

    3,5-Bis(Bromomethyl)Toluene: A Manufacturer’s Perspective

    Understanding 3,5-Bis(Bromomethyl)Toluene

    Producing 3,5-Bis(Bromomethyl)Toluene has taught us that consistency in quality transforms downstream synthesis. The compound, often referenced by its CAS number 623-15-4, doesn’t just serve as a chemical input; it shapes the very foundation of advanced organic synthesis in specialty and performance chemicals. Laboratories and industrial clients rely on us because the reliability of this intermediate defines the yield, purity, and economic viability of their own final products.

    Our plant focuses on this compound because of its unique substitution pattern on the toluene ring. Technicians witness clear evidence at every stage—the positions of the bromomethyl groups at the 3 and 5 carbons allow for selective reactions that can’t be achieved with monosubstituted or differently arranged derivatives. This arrangement opens routes in synthesis that save time, reduce waste, and offer higher value.

    Product Model and Specifications

    Consistent color and purity often act as silent signals for batch quality. We manufacture 3,5-Bis(Bromomethyl)Toluene in technical and high-purity grades, always with strict compositional targets. Typical batches contain a minimum assay of over 98% GC purity, verified through in-house instrumentation before any shipment leaves our facility. Trace moisture and residual solvents can derail reactions, so our production lines use vacuum drying and sealed packaging to retain performance for clients.

    Granularity and melting point are more than numbers in a data sheet—they inform users about stability, handling suitability, and storage life. The off-white crystalline appearance remains uniform from batch to batch. Each drum or bag reflects deliberate care around drying, screening, and transfer processes to avoid clumping and ensure batch homogeneity.

    Why Users Turn to 3,5-Bis(Bromomethyl)Toluene

    Years of feedback from partners in polymers, pharmaceuticals, and flame retardant production shape our view of this intermediate. In polycondensation chemistry, the symmetry of the two bromomethyl groups delivers an advantage. Users find substitution reactions on either end proceed with similar yields and predictable outcomes. We’ve seen this streamline production runs for dialkyl-substituted resins and ligands.

    In pharmaceutical synthesis, precision matters. Regioselectivity of functionalization can’t always be left to chance. Our product’s structure offers synthetic organic chemists a route to build intricate molecules with greater certainty. One pharmaceutical client improved their core yield by 9% after switching from a disubstituted toluene with both bromomethyls on adjacent positions to our 3,5-variation, cutting byproducts and saving valuable column time.

    Flame retardants depend on bromine content and distribution. Bifunctional toluenes, especially with robust purity and stable crystalline form, enable more effective grafting during copolymerization or additive production. We hear from plastics producers about improved flame test scores and easier blending, with less need for repeated purification cycles.

    Comparison With Other Benzyl Bromides

    While there are many benzyl bromide derivatives on the market, not all bring the same reactivity profile. The classic benzyl bromide carries a single bromomethyl group on the toluene ring. Labs often start with this simpler compound for substitutions, but once dual reactivity or symmetry become vital, the search moves to more specialized analogs.

    Our 3,5-disubstituted compound offers a distinct advantage over its 2,4- and 2,6-counterparts. Placement of the bromomethyls in non-adjacent positions reduces the risk of side reactions due to steric hindrance. Chemists can approach both sites with less risk of over-alkylation or undesired crosslinking, which ultimately means less cleaning up in the final stages of synthesis.

    Monosubstituted toluene derivatives may work for single-arm functionalization, but for users who need bifunctional centers, our 3,5 arrangement reduces byproducts and increases yield. In industrial alkylation, this translates into higher efficiency and cleaner waste streams.

    Safety, Handling, and Environmental Considerations

    Our role as manufacturers comes with responsibility. 3,5-Bis(Bromomethyl)Toluene requires strict controls in storage and transfer. Staff who handle product storage, weighing, and packaging wear chemical gloves and respirators—not just to comply with regulations, but because maintaining personal health ensures continuity on the line. Brominated organics can irritate the skin and mucous membranes, and our team undergoes regular safety training and monitoring.

    We’ve built secure loading and unloading routines for both small containers and bulk drums. All liquid spills pass through closed circuit containment and treated waste routes, using in-house analytical tools to monitor effluent for bromide content. We share these protocols openly with major clients, because process transparency builds long-term trust and keeps both sides aligned on safety improvements.

    During packaging, our operators fill and seal containers within inert-atmosphere gloveboxes. By limiting exposure to air, we cut down on moisture uptake—critical, since hydrolysis eats into effective bromide content and harms reactivity downstream. Every outgoing shipment includes batch traceability and storage tips grounded in years of real-world experience.

    Addressing Industry Needs

    Our daily operations run on questions from clients. Polymer manufacturers ask how to push grafting efficiency without spiking costs. Specialty chemical companies want to move toward greener processes, looking for reduced halogen waste or safer handling. We channel these demands into the heart of our process improvement.

    Raw material quality starts with supplier vetting. Our bromine sources undergo full-spectrum impurity checks, and supply contracts demand traceability up the supply chain. We’ve learned that any fluctuations here show up quickly in our reactors as color shifts or off-odors. Rejects don’t see daylight, and our waste is neutralized on-site before disposal.

    Several clients in Japan and Europe request heavy-metal screening, well beyond mandated limits, in line with their own environmental commitments. Incorporating dual-stage purification before final packing reflects their expectations and helps us develop better processes over time.

    Resolving Longstanding Challenges

    Early on, difficulty in controlling particle size and dryness led to packing issues and unnecessary losses for end-users. Our team invested in new multi-step drying systems that use programmable heating and vacuum staging, so each batch reaches optimal dryness without runaway decomposition.

    Initial struggles with container fouling and product compaction taught us the value of inert packaging and prompt turnover. By designing logistics schedules around client run rates, we cut warehouse time and ensure material arrives fresh, with no need for extra breaks or grinding.

    Not all applications demand the strictest purity, but we maintain two distinct production lines. One delivers standard technical grade for bulk use in resins and intermediates. The other line stays set aside for high-purity applications, with tighter filtration and more rigorous analytical oversight. End-users choose what fits best, and our operation stays flexible enough for both.

    Applications That Drive Innovation

    We see our product’s real impact in end-use stories. Polymer manufacturers call us to share new resin formulations that take advantage of the product’s bifunctional activity. The predictable reaction at both bromomethyl sites means they isolate higher yields on first pass, and the absence of closely-positioned groups reduces unwanted cross-linking. Better control over structure leads to stronger, more consistent performance characteristics in the finished polymers.

    In pharmaceutical research, synthetic teams favor our product for its unique substitution pattern. Freely reacting both bromomethyl arms, they can build up complex aromatic frameworks, necessary for novel active molecules. Some researchers comment on skipping intermediate protection steps, saving weeks and resources.

    Manufacturers of flame retardant chemicals value the high bromine content—needed to meet strict regulatory standards worldwide. Less waste during formulation, thanks to high purity and stability, results in uniform flame retardancy without costly reprocessing. Feedback from downstream users regularly points to higher compliance rates and smoother integration into masterbatches.

    We learn from every customer-provided case report or test result, using fresh data to tweak upcoming batches. Our technical staff share field data internally, from viscosity shifts in heat-sensitive reactions to flowability in automated feeders. This creates a feedback loop that sharpens production standards and keeps quality high across the board.

    Improvements Through Continuous Investment

    Investing in better manufacturing assets pays off quickly. Our latest reactor series uses load cells and real-time analytics for tighter process control, which delivers cleaner product and better repeatability. We continue to replace legacy plant assets with modular containment systems, so product contamination or cross-reaction doesn’t keep scaling up with larger batch sizes.

    On the analytical side, chromatography and mass spectrometry give operators instant in-line checks. If a deviation appears, techs spot and fix it before full-scale batches go out. Keeping active maintenance routines and up-to-date instrumentation guards against drift and maintains the reliability our clients expect.

    We don’t work in a vacuum. Regular audits and process reviews by independent assessors ensure every improvement meets industrial standards and client expectations. Turnarounds and process upgrades are communicated openly to those who trust us most—our steady repeat customers across industries.

    Adaptation to Regulatory Changes

    The chemical industry meets constant regulatory evolution. Over the last decade, we’ve observed increased scrutiny toward halogenated intermediates on multiple continents. This drives improvements, not just in documentation but in cleaner synthesis and safer routes. Our early adaptation to stricter reporting and shipment measures for 3,5-Bis(Bromomethyl)Toluene enables us to deliver material smoothly into regulated markets.

    Auditors demand more than simple purity checks. They seek full traceability batches, confirmed compliance to REACH, TSCA, and similar programs. We train our people in the shifting language of compliance so no shipment gets held due to a missing certificate or incomplete disclosure. These systems don’t just help the buyer; they keep our operation watertight, reduce recall risk, and raise professional pride on our end.

    Lessons Learned and Looking Forward

    Every challenge in manufacturing 3,5-Bis(Bromomethyl)Toluene creates a ripple effect across industries using it. We keep learning alongside our customers. New applications, whether in energy storage or specialty polymers, push us to understand how slight shifts in purity, moisture, or substitution pattern can spark new ideas—or sudden headaches.

    Looking back over years in this field, we see the value in long-term relationships built on transparency, reliability, and technical collaboration. Anticipating new trends in green chemistry or process automation means adapting our plant, retraining staff, and regularly consulting with external experts. As new regulatory changes emerge, we move beyond compliance and target greener, more cost-efficient routes to the same trusted products.

    We approach each batch as more than a simple unit for sale; it stands as a reflection of everything learned from past feedback, near misses, and customer insights. The next generation of applications, from smart materials to breakthrough therapeutics, depends on every link in the supply chain upholding these shared standards. As the actual manufacturer, not just a signpost in the distribution chain, we stand ready to meet each new challenge with open ears and a sharp focus on quality, safety, and mutual success.