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Benzhydryl Bromide

    • Product Name Benzhydryl Bromide
    • Alias Diphenylmethyl bromide
    • Einecs 202-695-2
    • 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

    171416

    chemical_name Benzhydryl Bromide
    other_names Diphenylmethyl bromide
    cas_number 90-99-3
    molecular_formula C13H11Br
    molar_mass 247.13 g/mol
    appearance White to off-white crystalline solid
    melting_point 41-43 °C
    boiling_point 182-185 °C at 15 mmHg
    density 1.39 g/cm³
    solubility_in_water Insoluble
    storage_conditions Store in a cool, dry, and well-ventilated place

    As an accredited Benzhydryl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Benzhydryl Bromide, 25g, is packaged in an amber glass bottle with a tight-sealing cap and labeled for laboratory use.
    Shipping Benzhydryl Bromide should be shipped in tightly sealed, chemically resistant containers, clearly labeled, and compliant with all regulatory requirements for hazardous materials. It must be protected from moisture, heat, and incompatible substances. Transport must follow applicable regulations (e.g., DOT, IATA, IMDG), with appropriate hazard communication and safety documentation included.
    Storage Benzhydryl bromide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect from direct sunlight and keep away from heat. Store under an inert atmosphere if possible, and ensure materials are clearly labeled and secured from unauthorized access.
    Application of Benzhydryl Bromide

    Applications of Benzhydryl Bromide in Industrial Manufacturing

    Benzhydryl bromide is a specialized halogenated intermediate produced by our facility to service key chemical transformation steps in advanced industrial value chains. Its unique reactivity profile, controlled impurity limits, and well-characterized handling parameters support consistent integration into complex downstream processes spanning pharmaceuticals, advanced materials, and fine chemical sectors.

    1. Pharmaceutical Active Ingredient Synthesis

    Benzhydryl bromide directly participates in the quaternization and alkylation syntheses of antihistaminic and anticholinergic pharmaceutical APIs. Its controlled reactivity with nitrogen nucleophiles allows precise N-benzhydrylation, critical for compounds such as diphenhydramine and benztropine. Accurate feed control and impurity management support route reproducibility in regulated pharma manufacturing, where batch traceability and GMP-grade material supply are mandatory for regulatory submission and process validation.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/Ph. Eur./JP compendial monographs for APIs
    • European Medicines Agency (EMA) and US FDA registration guidelines for intermediates
    • ISO 9001 certified quality management in chemical synthesis

    Typical usage ratio

    • Stoichiometric equivalent (1.0–1.2 molar ratio) to amine or nitrogen-containing substrate
    • Adjusted by nucleophile reactivity and downstream yield targets; excess controlled to <5%

    Downstream process integration

    • Direct charged to nitrogen alkylation reactor after base neutralization (typically with NaHCO3, K2CO3, or Et3N)
    • Intermediate isolation and purification prior to final condensation or further derivatization
    • Strict temperature and pH regulation to minimize over-alkylation and side contaminants

    Final product types

    • Antihistamine APIs (e.g., diphenhydramine hydrochloride)
    • Anticholinergic agents (e.g., benztropine mesylate)
    • GMP-grade pharmaceutical intermediates for downstream API synthesis

    2. Fine Chemical and Specialty Intermediate Manufacture

    Within the fine chemical sector, benzhydryl bromide operates as a highly effective benzylation agent for constructing diarylmethane motifs in custom syntheses. It is especially valuable in the design of advanced intermediates for agrochemical and fragrance industries, where selective phenol O-benzhydrylation or amine N-benzhydrylation is required. Careful process control enables end-users to incorporate sterically bulky protecting groups or functional handles for tailored downstream transformations.

    Industry compliance standards

    • REACH (EC 1907/2006) compliance for chemical intermediates
    • ISO 9001:2015 Quality Management Systems
    • Responsible Care Process Safety Protocols (CEFIC/ACC)

    Typical usage ratio

    • Typically 0.9–1.1 molar equivalents per target nucleophile functional group
    • Adjusted upward for multi-site protection or batch-scale losses

    Downstream process integration

    • Introduced to stirred reactor with pre-weighed nucleophile and solvent (DMF, DCM, or THF)
    • Stepwise addition in the presence of base (K2CO3 or NaOH) for controlled mono-benzhydrylation
    • Visitor sampling for QC confirmation prior to workup and extraction

    Final product types

    • Diarylmethane-based fine chemical intermediates
    • Phenol and amine-protected specialty compounds
    • Custom-designed fragrance precursors
    • Agrochemical advanced building blocks

    3. Polymer and Resin Modification

    In specialty polymers, benzhydryl bromide delivers highly controlled arylation functionality, most notably in cationic resin modification and engineering of crosslinkable thermosets. Its ability to generate benzhydryl-substituted moieties via electrophilic aromatic substitution or nucleophilic catalysis supports precise alteration of thermal and mechanical properties, providing manufacturers with a means to introduce unique steric and hydrophobic attributes into high-value materials designed for electronics, coatings, or specialty adhesives.

    Industry compliance standards

    • ISO 9001 management of polymer modification operations
    • RoHS Directive (2011/65/EU) and REACH registration for materials entering EEE supply chains
    • ISO 14001 Environmental Management for resin additive processing

    Typical usage ratio

    • Applied at 0.2–2.0 weight percent depending on targeted degree of functionalization
    • Exact proportion determined by resin functionality and end-use property targets

    Downstream process integration

    • Dosed directly into monomer or polymer melt stage, with in situ monitoring of reaction endpoints (temperature, viscosity)
    • Integration with radical or ionic polymerization systems
    • Real-time IR or NMR verification of benzhydryl group incorporation prior to curing, extrusion, or compounding

    Final product types

    • Modified cationic exchange resins for water treatment systems
    • Electronic-grade thermoset materials with enhanced dielectric properties
    • Surface-functionalized coatings and adhesives
    • Engineered specialty polymers for high-performance applications

    4. Laboratory Reagent and Chemical Synthesis Services

    Analytical and custom synthesis laboratories depend on benzhydryl bromide as a reference-grade alkylating agent in screening and structure-activity research. Laboratories engage its high purity for the creation of protected amines, carboxamides, and selective functional group transformations on pilot and kilo-scale. The well-defined physicochemical data, stability, and homogeneous particle distribution from our manufacturing facilitate direct application in demanding method development and analytical standards services.

    Industry compliance standards

    • ISO/IEC 17025 requirements for analytical laboratories
    • GLP (Good Laboratory Practice, OECD)
    • Accredited chemical reference material traceability standards
    • Material Safety Data Sheet (MSDS) and GHS-compliant labelling

    Typical usage ratio

    • 0.5–1.5 equivalents per synthesis target on millimole to mole scale in research protocols
    • Experimental ratios modified per substrate structure and desired yield optimization

    Downstream process integration

    • Dissolved in dry organic solvents followed by dropwise addition to nucleophile at 0–40°C
    • Reaction monitored by TLC, HPLC, or GC for endpoint determination
    • Post-reaction neutralization, organic extraction, and product isolation by preparative chromatography

    Final product types

    • Standardized analytical reference materials
    • Small-scale drug analogs and model synthetic intermediates
    • Protected heterocycles, peptides, and amines for custom services
    • Academic and contract synthesis outputs supporting process R&D
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    Certification & Compliance
    More Introduction

    Benzhydryl Bromide: Experience from the Lab Floor

    Benzhydryl bromide has carried a quiet reputation in our industry for many years. As chemists who regularly handle aromatic bromides, we care about reliability and confidence in our tools—listed proudly on our drums is benzhydryl bromide, manufactured and purified according to rigorous batch details that we’ve refined year on year. Our brand DNA is all about knowing the ground truth behind the molecules and what they bring to processes large and small. For benzhydryl bromide, we keep quality in the forefront because mistakes here ripple into everything that follows down the line.

    Our Benchmarks for Quality

    The difference shows up during synthesis. We work from pharmaceutical-grade benzophenone batches, so the product’s clarity, purity, and physical handling all meet the same standards we would expect if we wore our customer’s lab coat. Under controlled temperatures, with close attention to stirring rates and real-time analysis, our process yields benzhydryl bromide (C13H11Br) that crystallizes bright and without the yellow cast that sometimes signals incomplete reaction. Purity standards (by GC and NMR) consistently verify levels above 99%. We know well that even trace byproducts can block downstream transformations or lower overall yield. Some products from other sources arrive with the faint smell of degradation—those that don’t carry strict in-process controls often give surprises after only a short time on the shelf. Our regular in-house stability monitoring flags those risks before they ever reach the customer.

    Technical Profile and Specifications

    We supply benzhydryl bromide as free-flowing, white crystalline powder. The substance reports a melting point in the mid-40s Celsius, though impurities can bring this number down rapidly. Moisture sensitivity proves minor but non-negligible for long-term storage; even fully capped, high humidity environments will eventually produce clumping and surface discoloration, which we observe during accelerated aging studies. The theoretical molecular weight sits at 233.13 g/mol, and our certificate of analysis covers scan data for bromine content, residual solvents, and overall organic purity. By intentionally keeping solvents like toluene below strict cutoffs, we avoid many problems in catalyzed systems, especially in Grignard and Friedel-Crafts reactions.

    How Benzhydryl Bromide Earns Its Place

    This compound finds a place in multiple transformation routes. As a manufacturer, we see the most demand from two segments: pharmaceutical API synthesis and specialty chemical intermediates. For drug synthesis, benzhydryl bromide’s popularity comes from its use in protecting group strategies—its benzhydryl group is easy to install on alcohols and amines, and just as easy to remove under mild acidolysis or hydrogenolysis conditions. We’ve worked with clients needing kilogram-level campaigns for antihistamines, antidepressants, and even certain antitumor agents. The upfront purity of benzhydryl bromide often determines the number of purification steps needed later. We spot the difference in customer feedback: fewer reports of “strange byproducts” or “unusual spot on TLC” when our product forms the starting point.

    In non-pharma settings, benzhydryl bromide’s alkylating strength stands out. The molecule carries a positive charge denisty at the benzylic carbon, making it a favored substrate for nucleophilic substitution. We have customers who make triphenylethylene derivatives on pilot scale—some of these build starting polymers for specialty coatings, others end up as advanced ligands for catalysis. The convenience comes from the bromide leaving group, and we know from our experience that bromide is less prone to hydrolysis or decomposition than its chloride cousin under lab ambient conditions, yet still reactive enough to enable a good SN1 and SN2 balance. Operators in custom synthesis often ask us to share spectroscopic profiles and aging data, and our technical team has handled enough batch-to-batch comparability work to advise on real-world differences.

    Comparisons with Similar Reagents

    Benzhydryl chloride sometimes comes up in the request roster, but years of direct application show that benzyl bromide delivers higher yields and cleaner conversions in key alkylation assays. Bromide as a leaving group initiates substitution reactions faster than chloride, especially with less reactive nucleophiles. The environmental tension comes into play as well—a bromide can be easier to manage in downstream separation protocols, especially when scaling up to kilogram and ton scale. For those working with biaryl linkages or seeking easier workups, benzhydryl bromide simply generates fewer purification headaches due to milder side-product profiles.

    Compared to benzyl bromide, benzhydryl bromide carries the extra phenyl ring. That ring stabilizes the intermediate carbocation in many reactions. Practically, this enables better selectivity and higher control during more complex alkylation steps. We’ve had feedback sessions with researchers scaling up custom antipsychotic precursors—where benzyl bromide brought a wider variety of byproducts, benzhydryl bromide finished the run with higher mass balance.

    Attempting this molecule’s substitution with benzhydryl iodide brings tradeoffs. Iodides are more reactive but challenging to store due to higher instability and increased risk of side reactions, especially with common nucleophiles that might otherwise tolerate bromides. We experimented directly with this at pilot scale, only to discover shorter shelf life and greater handling complications for iodide analogs, leading to wasted raw materials in a setting that already runs lean margins.

    Practitioner Eyes: Handling and Storage

    Inside the plant, our teams rely on good storage protocol—airtight packaging, cool and dry warehouses, and simple but robust labeling practices. Unlike some highly reactive alkyl halides, benzhydryl bromide does not require elaborate inert-atmosphere handling, though we always recommend minimizing prolonged light or heat exposure. We use glass or high-density polyethylene bottles during preps and recommend them for laboratory use, based on real-world resistance to both bromine corrosion and volatility loss.

    Bench chemists in scale-up groups often comment on ease of weighing, dissolving and filtering, as the crystals dissolve well in common organic solvents like dichloromethane, chloroform, and ether. Some competitors supply material with needle-like crystals that bind moisture and clog transfer lines; through continuous process improvements, we target plate-like morphology where possible to minimize dust and maximize pourability.

    From direct feedback, our manufacturing runs avoid excessive fines in the final blend, which means fewer dust clouds during bulk transfer—a practical workplace safety and ergonomic issue. While smaller batches carry more control, large-scale blends sometimes produce variable particle sizes. Regular sieving and blending after crystallization keep our powder consistent batch to batch, an effort emphasized by our operations managers after receiving repeated customer praise on ease-of-use.

    Environmental and Regulatory Transparency

    Compliance starts at our raw material source. Benzhydryl bromide is categorized as a specialty chemical and monitored under various national customs and transportation rules due to its potential dual-use in both legal and non-peaceful applications. Our compliance record comes from careful attention to sourcing, inventory tracking, and documentation. We conduct regular third-party audits to make sure all production matches regulatory benchmarks. As with other brominated intermediates, wastewater and venting controls sit at the front line. Our scrubbers, activated carbon beds, and multi-stage condensers keep emissions well below regulatory thresholds, a lesson hard earned in our plant commissioning years back.

    Waste handling draws equal vigilance. Unreacted raw streams and off-spec materials are collected under Class II hazardous waste protocols, labeled clearly, and shipped quarterly using fully licensed contractors. Our technical team reviews waste streams with both environmental health staff and customers launching greener processes. Using experience from plant upgrades, we assist those aiming for full bromide ion recovery or in-plant recycling—sometimes prepping custom grades with tighter impurity cutoffs or specific solvent restrictions to support greener synthesis and easier product compliance.

    Product stewardship in brominated aromatic chemicals means tracking emerging regulations worldwide. Recent updates in EU REACH, US TSCA, and Asia-Pacific frameworks prompt regular reviews of our safety data sheets and risk assessments. We report hazard and exposure information openly, attached to each lot code, and conduct regular training for downstream users. On the rare occasion of batch non-compliance, recall and notification procedures operate within hours—well-tested in live drills—ensuring products in the supply chain remain safe, legal, and high-confidence.

    Supporting Customers Upstream and Downstream

    Direct relationships with scale-up chemists, pilot plant engineers, and R&D project leaders offer insight into daily challenges involving benzhydryl bromide. Some customers need pure, large-scale runs for API intermediates, while others run explorations for new ligands in asymmetric catalysis. We keep in touch through technical troubleshooting, guided use protocols, or advice on synthesis scaling. Chemists seeking protection strategies for alcohols and amines share their individual set-ups; every year, our team helps optimize protocol details, saving them time, raw materials, and late-stage batch failures.

    Certain applications require total traceability for every raw component that touches the reactors. Here, our rigorous batch level documentation plays a major role. Customers in regulated fields routinely request full chain-of-custody logs, down to the hour-by-hour cooling and crystallization stages. Our team provides original production and purification logs, complete with full spectral scans, which software audits against specification targets—an investment that paid off for a customer needing FDA submission-quality data for a rare orphan drug precursor.

    Not all support is technical. Occasionally, product misuse or misconceptions show up—like attempted direct substitutions from benzyl bromide without tuning reaction times, or storing open drums in humid environments. Drawing on years on the plant floor, we update our FAQs with new troubleshooting notes each season. The technical service team runs regular webinars and white paper releases, openly discussing both pitfalls and workarounds for common benzhydryl bromide handling questions.

    Ongoing Research and Innovation Paths

    Process efficiency drives margin and safety gains. Recent investments in continuous flow synthesis cut reaction time for our benzhydryl bromide plant by 40%, while at the same time dropping batch variability scores significantly below previous benchmarks. Through side-by-side comparative NMR and GC analytics, our R&D staff validated tighter control over byproduct formation and improved crystallization morphology—critical in customer applications demanding high filtration rates for later stages.

    We share our findings with select partner companies pursuing new chiral resolving agents and high-stability polymers. Benzhydryl bromide appears in custom derivatization workflows for specialty chemical building blocks, where its unique two-ring structure creates a wider range of coupling chemistries. Here’s where differences matter: we note that benzhydryl bromide outperforms single-ring analogues as a scaffold for developing UV-stable or photoreactive molecules. Real-world testing in our own labs produced incremental yield improvements and sharper selectivity when switching to benzhydryl bromide over older alkyl halides.

    Every year, customer applications guide us into previously untested ground—catalysis researchers requesting insights on reactivity with new ligand pools, medicinal chemistry teams probing for better dropping and filtering regimes, and process chemists running modeling simulations on alternative solvent systems. Our technical staff approaches each new application as a laboratory-scale pilot, echoing the same hands-on experimental method that built our manufacturing backbone.

    Lessons from Daily Operations

    Producing benzhydryl bromide brings home the lesson that small mistakes echo through entire value chains. A short washing step here, a slight solvent leftover there—quality slips crop up without constant attention and an experienced team watching every variable. Our operators rotate through each stage of the plant to spot minor issues that could snowball at scale. Weekly debriefs between production and QC teams close the gap between what’s written on the batch sheet and what happens on the ground.

    Thin profit margins don’t allow for complacency. As a primary manufacturer, we constantly balance input costs—phenyl-based starting materials, bromine reagents, energy for cooling and crystallization—against a global benchmark for purity and reliability. We share strategies with partners: shifting sourcing to lower-impurity benzophenone suppliers, implementing stricter ratios in bromination runs, and piloting new waste treatment chemistries to cut disposal costs while reducing environmental impact.

    Demand sometimes swings unpredictably. Laboratory orders one month may presage a run on ton-scale pharmaceutical syntheses six months later. We’ve learned not to chase short-term price drops at the expense of long-run customer trust. Instead, we double down on safe logistical practices and transparent communication. Plant expansion plans are always stress-tested against actual market feedback and long-term customer partnerships.

    Safety, Trust, and Looking Ahead

    On the plant floor, safety matters most when handling benzhydryl bromide. Each transfer, each blend, and every analytical sample reflects a hard-won culture of vigilance. The staff pays attention to things like PPE compliance, controlled ventilation, and documented batch changes. Site safety drills for both product spills and health incidents occur monthly—lessons learned from close calls ensure readiness claims ring true.

    Our ethics policy guides both sourcing and sales. Benzhydryl bromide production carries a responsibility to verify the end use, especially with tighter regulations on dual-use chemicals and concerns over diversion. Staff training and regular compliance checks follow both legal requirements and our internal code of conduct, aiming to serve responsible science and safe industry operations.

    After two decades in chemical manufacturing, we see real value in close relationships—being open with specification advances, supporting worker-centric process improvements, and developing new supply models that keep both cost and quality in view. Benzhydryl bromide’s journey, from feedstock drum to finished flask or reactor, stands as a test of our reputation. By sharing what we’ve observed and learned—failures included—we help everyone in the value chain solve problems better, faster, and safer.