Products

Dichlorobenzyl Alcohol

    • Product Name: Dichlorobenzyl Alcohol
    • Alias: DCBA
    • Einecs: 202-918-9
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    465018

    Chemical Name Dichlorobenzyl Alcohol
    Molecular Formula C7H6Cl2O
    Molecular Weight 177.03 g/mol
    Appearance White crystalline solid
    Melting Point 52-54°C
    Boiling Point 283°C
    Solubility In Water Slightly soluble
    Odor Faint aromatic odor
    Cas Number 1777-82-8
    Density 1.38 g/cm³
    Pka 11.6
    Storage Conditions Store in a cool, dry, well-ventilated area
    Uses Antiseptic, ingredient in throat lozenges
    Synonyms 1,3-Dichloro-2-(hydroxymethyl)benzene
    Stability Stable under recommended storage conditions

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

    Packing & Storage
    Packing The packaging is a 500g amber glass bottle, tightly sealed, featuring a clear hazard label for Dichlorobenzyl Alcohol and handling instructions.
    Shipping Dichlorobenzyl Alcohol should be shipped in tightly sealed containers, protected from moisture and light. It is generally classified as a non-hazardous substance, but care must be taken to avoid spills and leaks. Store and transport at room temperature, following standard chemical safety protocols and local regulations for non-hazardous organic compounds.
    Storage Dichlorobenzyl Alcohol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from heat sources, direct sunlight, and incompatible materials such as strong oxidizers. Ensure the storage area is equipped with proper spill containment and fire suppression systems. Clearly label the container, and keep it out of reach of unauthorized personnel.
    Application of Dichlorobenzyl Alcohol

    Applications of Dichlorobenzyl Alcohol in Industrial Manufacturing

    As a dedicated manufacturer of Dichlorobenzyl Alcohol, we support industrial partners in high-value downstream sectors. Our material integrates into clearly defined applications where its antimicrobial and preservative functions deliver concrete performance advantages. Below we outline the major industrial uses, each with detailed technical parameters and compliance information.

    1. Pharmaceutical Lozenges and Throat Sprays

    Pharmaceutical manufacturers routinely employ our material as a topical antibacterial component in lozenges and throat sprays for symptom relief products. It enters formulations in precision-controlled amounts, preventing microbial growth and contributing to the therapeutic profile under stringent medicinal standards. Quality control teams rely on validated dosing and documentation systems to comply with global regulatory demands, especially for products exported across markets with differing pharmacopoeial requirements.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.)
    • United States Pharmacopeia (USP)
    • Good Manufacturing Practice (EU GMP, FDA cGMP)
    • Medicines and Healthcare products Regulatory Agency (MHRA) product licenses

    Typical usage ratio

    • 0.1% to 0.4% w/w in finished lozenges or spray solutions; exact dosing determined by required antimicrobial efficacy, flavor load, and local regulations

    Downstream process integration

    • Added during the wet blending phase for syrup or tablet mass, before active ingredient introduction and final granulation or liquid filling steps

    Final product types

    • Medicated throat lozenges
    • Antibacterial oral sprays
    • Symptomatic relief pastilles

    2. Oral Care Solutions and Mouthwash Preparations

    Producers of mouthwash and other oral hygiene products use our material as a broad-spectrum preservative, targeting bacterial contamination risks in water-based formulas. Technical teams carefully validate its inclusion to ensure formula clarity, palatability, and prolonged shelf stability, while adhering to regulatory documentation and toxicology assessments common to the oral care sector. Processing engineers monitor pH and excipient interactions to maintain efficacy throughout the shelf life.

    Industry compliance standards

    • Cosmetic Regulation (EC) No 1223/2009
    • ISO 22716 for Good Manufacturing Practices
    • U.S. FDA OTC Monograph for Oral Health Care Drug Products
    • Japan Standards of Cosmetics Ingredients (JSQI)

    Typical usage ratio

    • 0.05% to 0.2% w/v according to microbial challenge study data and country-specific maximum preservative concentrations

    Downstream process integration

    • Dosage occurs during the formulation liquid-mixing stage, prior to flavor and coloring additions, with continuous stirring to ensure consistent dispersal

    Final product types

    • Mouthwashes and rinses
    • Antibacterial dental gels
    • Oral disinfectant solutions

    3. Veterinary Topical Solutions and Hygiene Sprays

    Veterinary pharmaceutical formulators implement dichlorobenzyl alcohol as a preservative and antimicrobial in topical wound sprays, ear cleansers, and disinfectant washes intended for animals. Quality assurance teams must demonstrate ingredient traceability and absence of residues in compliance with veterinary drug authorities. Processing requires close control over ingredient compatibility to maintain stability in aqueous and semi-solid delivery formats.

    Industry compliance standards

    • World Organisation for Animal Health (WOAH/OIE) standards
    • European Medicines Agency (EMA) veterinary medicines guidelines
    • Veterinary pharmacopoeias (Ph. Eur. Veterinary)
    • GMP standards for veterinary drugs

    Typical usage ratio

    • 0.05% to 0.3% w/w, determined by finished product type and required antimicrobial spectrum

    Downstream process integration

    • Introduced during pre-emulsification or solubilization steps, before package sterile filtration or aseptic filling for spray and cream formulations

    Final product types

    • Veterinary wound care sprays
    • Animal ear cleansing solutions
    • Topical disinfectant liquids

    4. Personal Hygiene and Intimate Care Products

    Manufacturers leverage the strong antimicrobial action in intimate hygiene wipes, feminine care wash liquids, and foaming cleansers. Strict formulation controls and challenge testing verify the preservative’s performance within consumer safety margins. Regulatory documentation includes preservative approvals and product efficacy studies, aligned to the specifics of personal care and hygiene segment compliance.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • FDA 21 CFR for cosmetic ingredients
    • ISO 29621 (Guidelines for the microbiological quality of cosmetic products)
    • SCCS Opinions for preservatives

    Typical usage ratio

    • 0.05% to 0.2% w/w in aqueous or emulsion-based formulas, adjusted for compatibility with detergents, surfactants, and fragrance loads

    Downstream process integration

    • Blended with other preservatives during the water phase of batch production, prior to surfactant addition and emulsification; monitored with in-process testing

    Final product types

    • Intimate area liquid cleansers
    • Feminine hygiene wipes
    • Personal foam and gel washes

    5. Ophthalmic Solution Preservation

    Ophthalmic product formulators employ dichlorobenzyl alcohol in non-prescription eyewash and cleaning drops to control microbial risks, subject to rigorous risk assessments and preservative challenge testing. Production involves ultra-purified water and cleanroom compounding, requiring batch records that document all preservative usages as part of quality release. Variations in dosage reflect strict limits set for ocular safety and comfort.

    Industry compliance standards

    • International Council for Harmonisation ICH Q7
    • United States Pharmacopeia Chapter <797> and <1151>
    • European Pharmacopoeia monographs for ophthalmic preparations
    • ISO 13485 (Medical devices QMS for sterile products)

    Typical usage ratio

    • 0.01% to 0.08% w/v, strictly controlled per finished batch based on preservative effectiveness studies and comfort/toxicology reviews

    Downstream process integration

    • Added to the water phase under cleanroom conditions, prior to final sterile filtration and aseptic packaging operations

    Final product types

    • Non-prescription sterile eye rinses
    • Contact lens cleaning and storage solutions
    • Pre-moistened ophthalmic wipes

    6. Surface Sanitizer Formulations for Healthcare Facilities

    Our material functions as an antimicrobial additive in surface disinfectant liquids produced for hospitals, clinics, and laboratory environments, where microbial resistance and efficacy validation are mission-critical. Regulatory-compliant batching and continuous process verification allow chemists to produce surface cleaners with sustained biocidal activity, supporting infection prevention teams in highly regulated sectors.

    Industry compliance standards

    • EN 1276 (Quantitative suspension test for bactericidal activity)
    • EPA List N (Disinfectants for use against viral and bacterial pathogens)
    • FDA QSR (21 CFR 820) for medical device surface cleaners
    • ISO 9001 for manufacturing process control

    Typical usage ratio

    • 0.08% to 0.15% w/v, established by surface contact time requirements and target pathogen profiles

    Downstream process integration

    • Introduced after base solvent/blend in aqueous or alcohol-based disinfectant mixers, with batch kill-test verification post-dispersion

    Final product types

    • Hospital-grade disinfectant sprays
    • Clinical wipe solutions
    • Lab bench sanitizer liquids

    Free Quote

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    Certification & Compliance
    More Introduction

    Dichlorobenzyl Alcohol: A Practical Look from the Workshop Floor

    Our Experience Manufacturing Dichlorobenzyl Alcohol

    Dichlorobenzyl Alcohol has been a regular part of our production line for many years, mainly because of its valued role as an antimicrobial and preservative in pharmaceuticals and personal care products. From raw input through the final packaging, we work with this compound daily, watching its journey as it moves from a raw chemical to a finished product ready for shipment. Over time, long runs in our own reactors have shown us how consistency matters. Any small deviation in reaction timing or purification steps changes the product’s clarity, odor, and purity—factors that our customers notice right away.

    The batch regularly leaves our facility in crystal-clear, white, needle-like solid form, which our team requires to meet tight specifications. Each lot is sampled, dissolved in the lab, and checked for residual starting materials using HPLC. Moisture control is critical, because even a trace can accelerate breakdown, leading to a yellow tint or loss of performance for end use. We source our starting dichlorobenzene from vetted suppliers, but the real craft happens under our own roof: careful pH adjustment during the conversion to keep corrosive byproducts out, and slow cooling to ensure the right crystal habit. By the time product reaches the drum, it has been shaped as much by our process as by the chemical formula itself.

    Product Specifications—The Real-World Details

    Most buyers look to us for CAS No. 1777-82-8, which matches the 2,4-dichlorobenzyl alcohol isomer commonly used as an antiseptic. This specific form stands out thanks to a favorable melting point range between 54°C and 57°C, a manageable density, and sufficient stability for multi-year shelf life if stored in a dry, cool warehouse. Our finished product usually tests at 99% minimum purity by HPLC, with less than 0.3% water and minimal organic impurities.

    Physical properties get just as much attention as chemical purity. Good dichlorobenzyl alcohol forms resilient, non-caking crystals. From our own hands-on experience, poorly crystallized product signals trouble: dustiness, off-odors, or reluctance to blend in formulation tanks, all hassles for downstream users in pharma, oral care, and hygienic wipes. In our own plant, we judge a successful batch by its free-flowing feel and faintly sweet, slightly medicinal aroma. This isn’t just about aesthetics—these cues tell us everything has gone right in process control.

    Our product’s molecular weight comes in at 191.04 g/mol, and we log every batch number with dates and operator signatures, so every shipment can be traced back to its roots. The process relies on closed systems to avoid airborne dust during blending, since inhaled dichlorobenzyl alcohol can cause irritation. Workers who handle it daily use gloves and fitted masks. We share the same MSDS sheets with our downstream customers that guide our own plant protocols, so everyone up and down the supply chain works from real-world knowledge, not theory.

    Key Uses and Real Applications

    Dichlorobenzyl alcohol doesn’t stay in our warehouse long. Most drums leave the plant on their way to cough lozenge production lines, hospital-grade mouthwashes, and topical antiseptic solutions. We hear back often from oral care formulators and contract manufacturers about why they return to this compound: reliable pathogen control, a mild flavor profile, and a record of safety stretching back decades. In the laboratory, it breaks bacteria’s cell membranes efficiently at low concentrations, slowing the spread of infection in the mouth and throat with fewer side effects than more aggressive actives.

    Some of our biggest customers use it as a synergist with amylmetacresol or other mild local anesthetics, boosting the total antimicrobial effect while softening the burning sensation some other actives produce. Pharmacies and oral care brands lean on dichlorobenzyl alcohol because it performs in both sugar-based pastilles and modern sugar-free lozenges. Blending goes smoothly, and the compound dissolves evenly—less clumping, less downtime cleaning tanks. We’ve worked with facilities who’ve clocked the difference, appreciating fewer reject batches thanks to reproducible performance.

    Beyond cough drops, manufacturers of throat sprays, hard-candy style disinfectants, and even some veterinary washes purchase from us thanks to the predictable action of this compound. Rarely, we’ve seen requests from personal care producers, who value its microbial control properties for niche handwashes, ear cleaners, or certain deodorants. These are small but steady outlets that prove the versatility of well-made dichlorobenzyl alcohol.

    What Sets Our Product Apart

    The chemical market is crowded, with a lot of dichlorobenzyl alcohol that looks similar on a specification sheet. Our edge has always come from running our own, vertically integrated lines. We control the process right from the initial dichlorobenzene charge, so any deviation—be it a blip in conversion yield or a hiccup in filtration—gets addressed by someone two doors down. Having hands and eyes on each batch means impurities or off-spec output seldom make it past day-shift inspection, let alone into finished goods.

    We sample every drum, not just a token few. It’s labor-intensive, but our customers see almost zero rejected shipments. We load from the same tanks for export as for our domestic customers, with no split grades or “special exports.” This matters, because inconsistent quality is a headache all chemists recognize. Nothing disrupts a pharmaceutical production line faster than variable ingredient performance. Over the years, only a handful of customers have come back with quality complaints, and almost always, these have traced to storage damage or rare transit mishaps, never our own plant output.

    Our main distinction is the clarity and odor of our crystals. End users tell us repeatedly how much easier our product is to process; free from caking, and compatible with high-speed blending. The compound’s melting point range remains narrow, a sign it is well crystallized and free from significant side-products. In our experience, batches that harden into blocks over time indicate problems with trace moisture or off-isomer formation, so every fill is checked for density and texture.

    Many producers offer dichlorobenzyl alcohol in both technical and pharma grades. After some tough lessons with cross-contamination on contract lines outside our facility, we keep strictly separated lines for pharma-grade output. Raw material inlets and transfer lines stay color-coded. We’ve invested years in making cleanup and operator training second nature, so the pharma-grade never picks up any traces from non-pharmaceutical runs. Our technical grade, still high-purity, serves well in nonmedicinal applications where the highest certification isn’t needed, but we never pass off one for the other, sparing everyone in the chain from regulatory issues later.

    Managing Consistency—A Manufacturer’s Perspective

    Constantly checking the small details keeps our batches reliable. Staff rotate through both lab and plant to reinforce know-how, since production reality rarely matches textbook theory. We’ve worked through times when antisolvent quality shifted, or utility power dipped; when equipment age showed up as slow cooling rates; when even a new tank lining altered the end-product aroma. Every step matters. We have rigid logs that track who mixed, who tested, and who packed each shipment, so questions months later can be answered with facts, not guesses.

    We learned early that controls need to extend to packaging. Some drums become brittle in cold weather and leech trace chemicals back into the product. Our team sought out suppliers with BPA-free liners, tested for leachables, and now spec every drum for high-barrier, contamination-resistant surfaces. When we switched supplier a few years ago, the impact on odor was immediate, with downstream customers noticing cleaner product as a result.

    Handling temperature excursions during shipping raised another lesson. Even on reliable logistics routes, a heatwave can push product above its intended storage range. We switched to temperature-transmitting tags that travel inside a sample pouch with every batch. If there’s any doubt about shipping stress, we pull a retain, check physical properties, and compare it to the client’s results, proving the merits of close batch tracking and transparency.

    Why End-Use Results Matter

    Our job as chemical manufacturers is only finished when the compound performs at the customer’s line. Success is obvious on their end—a batch that blends fast, disperses clean, and holds up through the shelf life of the finished lozenge or rinse. Bottlers have called out small texture changes within finished cough drops caused by humidity shifts in our own mixing rooms. We made changes as a result, adding automated humidity control zones and recalibrated our drying process.

    Major formulators in the oral care industry describe their ideal compound in very direct terms: low odor, fast dissolution, consistent bulk density, and adherence to compendial purity. Our in-house approach—narrow lot sizes, tracked auxiliary raw materials, and batch-level investigations—keeps us running in step with those needs. About ten years ago we partnered closely with two leading mouthwash manufacturers to address their demand for extra-low-chloride lots. Their filter systems picked up even trace residues. We developed extra polisher resin applications solely for their projects, rather than push a “standard” grade and risk downtime at their plants. Feedback cycles like this keep our quality bench-marked against real, not theoretical, performance.

    Proper odor management came after repeated complaints from one key customer who reported subtle “earthy” off-notes. Investigation found a trace back-flow from one cleaning fluid used during shutdown. This story shows how direct dialogue and factory-side flexibility can solve embedded root issues that may not show up on specification sheets or in short-run lab tests.

    Compared with Other Preservatives and Antimicrobials

    The preservative market offers a long menu of options, but dichlorobenzyl alcohol has endured thanks to its balance of effectiveness and safety. Unlike benzalkonium chloride or chlorhexidine gluconate, which leave strong aftertastes or require more careful handling due to higher toxicity, our product performs well at lower concentrations with limited flavor impact. This is one reason oral care formulators still rely on it to protect flavor integrity without sacrificing protection.

    Compared with parabens, another common class of personal care preservatives, dichlorobenzyl alcohol does not bring the regulatory risks currently attracting tighter scrutiny. Long-term, we expect consumer and regulatory trends will drive even more interest in compounds that have stood up to decades of use with minimal controversy. Our customers appreciate being able to list a recognizable, accepted preservative with a straightforward safety dossier.

    We know some manufacturers look at alcohol-based antimicrobials as alternatives, but these often struggle with volatility and rapid evaporation, degrading shelf life. Dichlorobenzyl alcohol offers the solid-state stability and slow release that gels well with slow-dissolving pastilles or lozenges. In our direct trials, substitution with liquid actives introduces negative impacts on crystallization, causes shrinking or cracking in finished tablets, and reduces shelf stability.

    Some users trialed pure benzyl alcohol or simple benzylic derivatives as alternatives, only to encounter reduced spectrum of activity or increased irritation risk. Our version of dichlorobenzyl alcohol works effectively across both gram-positive and gram-negative bacteria, plus a range of fungi—while maintaining a mild user experience. This reflection is echoed in the production feedback our customers send us: fewer product recalls, fewer formulation fails, and smoother audits.

    Supply Chain, Traceability, and Customer Partnership

    With global supply chains strained in recent years, we learned that customers value reliability as much as performance. We keep stocks of critical materials, issue batch certificates tied to quality tests, and back shipments with a clear paper trail. Our sales engineers often visit customer sites directly—not just to secure the next order, but to watch our ingredients at work on foreign machines, under different humidity and mixing conditions. This loop feeds back improvements into our next manufacturing runs, making our workflow a direct partner to the users’ own realities.

    Recent years pushed all manufacturers, ourselves included, to bolster documentation and transparency. More often, finished products manufactured from our dichlorobenzyl alcohol move through global markets, with regulators demanding not just purity but source documentation, allergen risk assessments, and “clean room” records of who touched or handled each lot. We invested early in electronic batch record systems and agreed-upon reference samples held in climate-monitored archives, so both we and our customers can respond rapidly to any downstream queries.

    Packaging decisions also evolved from these partnerships. Some end users requested smaller, lined kegs to suit automated minor-ingredient feeders and reduce cross-contamination. Others needed bulk super sacks for cost-effective, large-scale blending. We respond by customizing formats, not just sending out a standard drum size, because our interests are aligned with both economic efficiency and downstream product quality.

    Continuous Improvement on Both Sides of the Drum

    We treat every customer complaint or process improvement as a trigger for internal review—cross-checking handling SOPs, sample retention cycles, and training refresher courses. Internal audits prompted by minor crystal habit changes led us to re-tune our condensation and filtration steps, resulting in higher overall product uniformity and fewer downstream issues for our clients. When feedback comes in regarding rare off-odors or longer-than-expected dissolution times, plant staff work alongside our quality team to walk through the process day-by-day, often finding subtle points of improvement.

    We run reliability testing for each lot, not just spot tests. Every operator on the floor can pull a sample and flag concerns before they become systemic. This has cut down on customer returns, and improved trust over the years. Customers now expect a short direct communication if anything unexpected arises, not a slow chain email conversation. By sharing our own internal data openly with key buyers, we equip them for regulatory audits and certification renewals, backing up every claim with fact-based results.

    In the end, dichlorobenzyl alcohol might look like just another entry in a catalog, but from the perspective of the person running the reactor or packing the drum, every lot represents dozens of checks, improvements, and feedback cycles. This hands-on approach, and our emphasis on real-world chemical manufacturing over middleman commerce, sets our product apart. Our pride in the final batch reflects the trust our customers place in the work we do every day.

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