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3,5-Dibromobenzyl Alcohol

    • Product Name 3,5-Dibromobenzyl Alcohol
    • Alias Benzyl alcohol, 3,5-dibromo-
    • Einecs EINECS 252-045-5
    • 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

    187765

    Productname 3,5-Dibromobenzyl Alcohol
    Casnumber 38569-10-7
    Molecularformula C7H6Br2O
    Molecularweight 281.93 g/mol
    Appearance White to off-white solid
    Meltingpoint 68-72°C
    Purity Typically ≥98%
    Synonyms 3,5-Dibromo-benzyl alcohol
    Structure Benzyl alcohol substituted with bromine at positions 3 and 5
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=C(C=C(C=C1Br)Br)CO
    Storagetemperature Store at 2-8°C

    As an accredited 3,5-Dibromobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle with a blue screw cap, labeled "3,5-Dibromobenzyl Alcohol, 25g", chemical safety symbols, and batch information.
    Shipping 3,5-Dibromobenzyl Alcohol is shipped in tightly sealed, chemically resistant containers, clearly labeled according to hazardous material regulations. It should be packaged with sufficient padding to prevent breakage and protected from heat, moisture, and direct sunlight. Transport complies with relevant local, national, and international safety and environmental regulations for hazardous chemicals.
    Storage 3,5-Dibromobenzyl alcohol should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as oxidizers. It should be kept in a cool, dry, and well-ventilated area, ideally within a designated chemical storage cabinet. Proper labeling and access control are recommended to ensure safe handling and to prevent accidental exposure or contamination.
    Application of 3,5-Dibromobenzyl Alcohol

    Applications of 3,5-Dibromobenzyl Alcohol in Industrial Manufacturing

    3,5-Dibromobenzyl Alcohol is a specialty aromatic intermediate valued for its unique di-brominated benzyl structure, contributing to the synthesis and performance of advanced materials and fine chemicals. As the actual producer, we supply this raw material in bulk to downstream sectors with controlled quality and detailed guidance for process integration. The following sections present key industrial use cases where our product enhances production cycles, efficiency, and final product properties.

    1. Pharmaceutical Intermediate for Sartan API Synthesis

    Several leading manufacturers in the pharmaceutical sector utilize 3,5-dibromobenzyl alcohol as a crucial building block for synthesizing key intermediates in angiotensin II receptor blockers (ARB), particularly in the preparation pathway for irbesartan and candesartan APIs. Our material participates in a substituted benzylation step, providing selectivity and purity essential for subsequent ring closure and functionalization. Consistent quality and impurity profile control are critical, as regulatory authorities audit each process step and intermediate. Dosage requirements and typical integration depend on process route, batch scale, and targeted regulatory markets.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • European Pharmacopeia (Ph. Eur.) monograph compliance
    • US FDA cGMP (21 CFR Parts 210 & 211)
    • China NMPA Drug Master File registration (where applicable)

    Typical usage ratio

    • 1.10 to 1.15 molar equivalents relative to main reactant, adjusted for route yield and stoichiometry
    • The optimal range is determined by impurity profile and desired conversion rate in the benzylation step

    Downstream process integration

    • Added during the key benzylation step, typically under phase-transfer or polar aprotic solvent conditions
    • Charge timing is controlled by critical process parameters to maintain selectivity

    Final product types

    • Irbesartan API
    • Candesartan cilexetil API
    • Other sartan-class antihypertensive pharmaceutical APIs in developmental pipelines

    2. Agrochemical Synthesis: Precursor for Aryl Bromide Herbicides

    The crop protection industry sources this compound for the synthesis of aryl bromide intermediates crucial in manufacturing post-emergence herbicides. By introducing the dibrominated benzyl substituent early in the synthetic sequence, producers achieve high regioselectivity in subsequent nucleophilic substitution or Grignard coupling reactions. Accurate dosage control and stringent process monitoring minimize undesirable by-products and ensure compliance with agrochemical impurity thresholds set by regulatory agencies across different regions.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products
    • OECD Good Laboratory Practice (GLP) for active ingredient development
    • REACH Registration (Europe)
    • EPA Pesticide Registration Requirements (US, 40 CFR Part 158)

    Typical usage ratio

    • 0.9–1.2 equivalents relative to halogen exchange or coupling partner
    • Precision based on targeted yield and chromatographic purity of downstream aryl bromide intermediate

    Downstream process integration

    • Feedstock for initial coupling or alkylation steps in multi-stage synthesis
    • Process temperature, solvent, and addition rate tailored for scale-dependent impurity control

    Final product types

    • Brominated aryloxyacetic acid herbicides
    • Benzyl-substituted isoxazoline derivatives for weed control
    • Custom halogenated herbicidal intermediates

    3. Performance Polymer Additives in Specialty Coatings

    Producers of advanced coatings and specialty polymers incorporate 3,5-dibromobenzyl alcohol as a reactive monomer for formulating brominated epoxy resins and flame-retardant coatings. The compound integrates through nucleophilic aromatic substitution, furnishing bromine functionality and modifying polymer network characteristics. Carefully managed addition ratios and process temperatures are essential for optimizing mechanical strength, flame resistance, and compliance with fire safety codes in end applications. Each integration protocol reflects both regulatory needs and end-use product specifications.

    Industry compliance standards

    • UL 94 (Flammability Standard for Polymeric Materials)
    • RoHS (Restriction of Hazardous Substances in Electrical/Electronic Equipment)
    • ISO 9001-certified quality control for polymer additives
    • REACH Annex XVII (Brominated Substances Restrictions)

    Typical usage ratio

    • 5–15 wt% in the reactive monomer blend, subject to target flame retardancy and compatibility with other modifiers
    • Formulators adjust within this range based on glass transition temperature (Tg) and polymerization kinetics

    Downstream process integration

    • Charged during pre-polymerization blending or as a post-polymerization functionalization agent
    • Curing step conducted at 120–180°C depending on matrix and cross-linking requirements

    Final product types

    • Brominated epoxy resins for PCB coatings
    • Intumescent fire-protective industrial coatings
    • High-resistance polymer composites for electronic enclosures

    4. Organic Synthesis Intermediate for Industrial Dyes and Pigments

    Manufacturers of performance dyes employ this intermediate in the construction of halogen-substituted aromatic cores, critical for color fastness and chromatic stability in specialty pigments. The alcohol moiety offers a convenient entry point for esterification or etherification, while the dibromo substitution pattern enables site-selective cross-coupling reactions. Dosage and batch incorporation protocol depend on target pigment structure, process throughput, and regulatory pigment impurity limits, particularly in textile and plastics applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dyes
    • ISO 14001 Environmental Management in pigment processing
    • FDA 21 CFR 178.3297 for colorants in food contact polymers
    • REACH SVHC (Substances of Very High Concern) Candidate List

    Typical usage ratio

    • 0.5–2.0 equivalents per pigment-forming aromatic starting material
    • Adjusted for process step (condensation, acylation, or Grignard reaction) and desired molecular weight of the dye

    Downstream process integration

    • Input during aromatic coupling or as a hydroxyl-functionalized linker in pigment backbone construction
    • Batch or semi-batch manufacturing lines, with careful monitoring for side reaction suppression

    Final product types

    • Brominated triphenylmethane dyes for synthetic fibers
    • Color-stable pigment dispersions used in high-performance plastics
    • Functional dyes with improved UV and thermal stability
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    Certification & Compliance
    More Introduction

    3,5-Dibromobenzyl Alcohol: An Everyday Essential for Chemical Synthesis

    Our Hands-On Experience Crafting 3,5-Dibromobenzyl Alcohol

    In the chemical manufacturing world, few aromatic building blocks blend reliability with adaptability like 3,5-Dibromobenzyl Alcohol. We’ve spent years fine-tuning production of this specialty alcohol, ensuring each batch meets the quality standards our partners expect. Creating a consistent supply isn’t only about mastering halogenation and purification processes. It’s about deep familiarity with the molecular structures chemists rely on for complex synthesis, crop protection materials, and pharmaceutical leads.

    You won’t find us trading in generic stock. Our focus lies in direct synthesis, from bromobenzene selection through to the finished crystalline white solid. This means we control every step—halogen ratios, drizzle rates during bromination, reaction temperature, protection from atmospheric moisture, and purity checks by melting point and chromatographic analyses. Even subtle changes in batch size or feedstock character call for vigilant tweaking. One missed detail can throw off the downstream reactivity that customers depend on for making life-changing molecules.

    What Makes 3,5-Dibromobenzyl Alcohol Stand Out?

    Though organic chemistry offers a basket of benzyl alcohols with differing halo substituents, 3,5-dibromo positioning holds unique value. Placing bromine atoms at meta positions activates the aromatic ring for further functionalization, while limiting side reactions less common with ortho- or para-brominated versions. The symmetrical nature of the dibromo substitution grants better predictability in reaction outcomes—especially in Suzuki, Ullmann, or etherification conditions where selectivity and reliability matter most.

    We’ve compared runs using standard benzyl alcohol, mono-bromobenzyl variants, and even other dihalo analogs. The feedback is clear: 3,5-dibromobenzyl alcohol gives noticeably better yields in certain pharmaceutical intermediate steps, cuts down the isolation of byproducts, and improves crystal purity in final recrystallizations. More bromine atoms at the right positions open up niche reactivity channels unavailable to mono- or para-halogenated alcohols.

    Specifications Shaped by Real-World Demands

    While the literature lists this product under CAS 6263-34-1, it’s the smaller details that often make the difference. Purity targets stretch beyond 98%. We screen for residual brominated side-products and offer material in crystalline form to ease accurate weighing and dissolution. Every lot moves through vacuum-drying, hands-on melting point measurements, and spectral validation with NMR and GC analysis. End-users in pharmaceuticals, agrochemicals, and advanced materials benefit because tighter specs trim away unpredictable variables in multistep synthesis.

    We manufacture by weighing actual feedback from research teams and formulators. Most opt for the solid white crystals with a melting point generally around 66-68°C. This helps confirm identity and guides storage strategies—critical for labs that must avoid product degradation. Solubility profiles in organic solvents like dichloromethane, ethyl acetate, or THF stem from user reports. Chemists appreciate the ease of stock solution prep compared to oils or tars from other functionalized alcohols.

    Usage: Building Complexity with Confidence

    You’ll see 3,5-dibromobenzyl alcohol mentioned in synthetic methods papers, especially in pharmaceutical research. The compound steps up as a pivotal intermediate in elaborating complex molecules, making use of its di-brominated core to install aryl groups, ethers, or esters on the benzyl position. For example, in halogen-metal exchange or cross-coupling protocols, the stability and accessibility of the 3,5-positions allow for reliable transformation to more demanding frameworks.

    Research teams tackling heterocycle synthesis or generating aryl ethers lean on this product because it helps bypass multi-step protection/deprotection routines. The bromines act as anchor points for metalation or catalytic cycles, so the synthetic path clears up. This efficiency translates to more grant dollars saved, better reproducibility, and fewer headaches troubleshooting unwanted byproducts. Every time a pilot scale-up gets stuck on low purity caused by problematic bromide content, our customers recount how sticking with our material brought yields back in line.

    Crop protection chemistry also draws heavily from dibrominated benzyl alcohols. Analog design for new active ingredients often hinges on halogen placement, and meta-bromines are documented for improving lipophilicity or modifying metabolic routes in target species. 3,5-Dibromobenzyl alcohol slips smoothly into these synthetic routes, supporting biologists and formulation chemists who count on exacting halogenation patterns for structure-activity relationships.

    Other fields like polymer science and specialty colorant design increasingly survey the space of brominated aromatic alcohols because of the robust reactivity they offer. In every application, preparation and isolation of pure product without discoloration or residual solvents guides us in process choices and packaging.

    Comparing 3,5-Dibromobenzyl Alcohol to Other Benzyl Alcohols

    Choosing among benzyl alcohols with various halogen placements marks a key step for chemists. In our shop, we’ve experienced the headaches that come with competing isomers—product isolation grinds to a halt when ortho- or para-brominated contaminants sneak in. 3,5-Dibromobenzyl alcohol cuts these headaches by giving you a single, well-characterized dihalide, so downstream transformations run smoothly.

    Mono-brominated benzyl alcohols sometimes tempt as cheaper options, but over time, we’ve seen clients circle back to our di-bromo grade. They report fewer impurities, more predictable coupling efficiency, and less effort purifying their target molecules. The difference comes down to repeatable reactivity patterns springing from the meta-bromo orientation, along with the lower risk of unwanted side products during catalytic processes.

    Double-checking every shipment for melting point and spectral matches also distinguishes a true manufacturing operation from a repackaging or trading house. We’ve encountered cases where labs bought from traders, found inconsistency in physical form or purity, and needed an overnight resupply to keep projects on track. Our reputation rides on this distinction—it means less requalification, faster route scouting, and smoother scale-up in industrial processes.

    Quality Means More Than Purity Numbers

    For most users, technical product pages rarely surface the hidden variables that impact results. Our team's focus on crystallinity and thermal behavior comes from watching how small changes in drying or filtration mess with handling in gloveboxes or automated dispensers. A bit too much solvent retained in the crystals and you’ll find material that cakes, clumps, or melts prematurely. We’ve invested in incremental upgrades—growing crystals under controlled cooling, running extended vacuum cycles, and triple-sealing packaging. All those incremental improvements add up to less waste, greater shelf stability, and easier scaling for custom runs.

    The topic of trace metal or oxidizable impurity content sometimes falls flat with suppliers. Through years of conversations with medicinal chemists and formulators, we’ve understood the unseen risks poorly controlled material brings. Our team runs periodic impurity sweeps using GC-MS and ICP-OES, especially for catalyst-sensitive syntheses where hidden contaminants stall expensive reactions. That means end users spend weekends in the lab running reactions instead of chasing down contamination sources—less overtime, more productive science, better project morale.

    Supporting Customization Without Cutting Corners

    Some customers need larger custom lots or unique packaging sizes to match their batch scheduling. We’ve seen requests evolve from half-kilo pilot runs for route scouting to regular multi-kilo shipments supporting scale-up in pilot plants. Adapting to these requests, we’ve expanded our filtration and drying gear and built out batch tracking so clients know exactly which process history accompanies each lot.

    A handful of applications ask for extra specifications. One example: an advanced materials group looking for ultra-low residual solvents due to downstream polymerization. Working alongside them, we iterated on our drying steps, monitored headspace volatiles, and delivered batches that met demanding criteria without compromising throughput. We see support as more than responding to requests. It’s a collaboration, sharing firsthand what we’ve learned from hundreds of multi-kilo syntheses as well as pitfalls that have cost us time and material.

    Honest Practices and Safe Handling

    Safety in manufacturing starts long before bottling. 3,5-Dibromobenzyl alcohol’s composition makes it less volatile than simple benzyl alcohol, but that doesn’t remove all hazard. Our facility avoids dust generation, uses closed-transfer equipment, and trains crew to anticipate the heavy, distinctive odor brominated aromatics sometimes release. Environmental protection comes first, so spent solvents and filtrates get managed through local recovery and incineration partners, never down the drain.

    Our colleagues on the research and lab side appreciate detailed documentation. We share experience-driven tips for storage—cool, dry, away from light and oxidizers. In our own storage drums, product stability runs well over a year, provided temperature and moisture swings are kept in check. We see every outgoing shipment as a reflection of our own commitment to responsible supply, right down to labeling expiration dates based on real shelf life, not just paperwork conventions.

    The Real-World Impact of Reliable Manufacturing

    Pharmaceutical companies, fine chemical makers, and university labs rely on tightly specified starting materials like 3,5-dibromobenzyl alcohol to innovate quickly and on budget. We’ve watched as a single out-of-spec batch delayed months of discovery work or, worse, forced price renegotiations for failed pilot campaigns. We take pride in offering batches that arrive with clear origins, transparent process histories, and consistent analytics, all built from decades of chemical know-how—not abstract corporate claims.

    We regularly host customer audits, walk through our production floors, and discuss how traceability down to the source helps meet both regulatory and practical requirements. A lot of our expertise comes from old-fashioned troubleshooting—noticing a subtle change in the color of a distillation cut or a shift in NMR baseline, then tracing it back to a new lot of bromine or benzaldehyde. We build long-term trust on being able to share stories of what worked, what didn’t, and how the learning shaped our processes.

    Future Directions: Meeting Evolving Synthesis Trends

    Every year brings questions from the research frontier. Could meta-dibrominated alcohols improve environmental degradation profiles for new crop protection candidates? Do emerging green chemistry techniques change the required purity or contamination profiles? With new catalysis methods, is meta placement offering even greater selectivity? Having a direct hand in manufacturing helps us spot shifts in demand—sometimes chemists call us after reading a new journal article, looking for kilo quantities to try out a reaction never before scaled.

    We take these conversations seriously. Their urgency shapes which process tweaks and expansions come next on our production floor. One forward-thinking project involved shifting a purification step to a greener solvent, requested by a customer focused on sustainability audits. Anticipating synthetic trends and building flexibility into our manufacturing allows quick pivoting between custom lots and standard runs, so innovative groups don’t have to stall discovery cycles waiting for supply chain catch-up.

    Partnership Built on Shared Experience

    Every drum, bottle, and flask of 3,5-dibromobenzyl alcohol that leaves our facility represents years of lessons learned—batch records improved, purification traps replaced, testing protocols revised, and customer advice heeded. Unlike a trader, we can draw on direct hands-on troubleshooting, show real batch data in customer visits, and adapt in real time to evolving regulatory and scientific challenges. Our deep experience not only helps bring products online faster but also prevents costly detours on the customer’s bench or plant floor.

    If your team faces hurdles with aromatic coupling, struggles with yield drags, or chases after problematic isomer mixing, our experience stands ready for consultation. We know that every gram counts—not just for cost, but for timelines and the livelihoods tied to reliable research and production. With a steadfast eye on practical chemistry and an open channel for customer feedback, our real-world commitment to quality, transparency, and ongoing learning means each batch of 3,5-dibromobenzyl alcohol delivers more than molecular weight and purity numbers—it brings trust and collaboration to every stage of your project.