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Chlorphenesin

    • Product Name Chlorphenesin
    • Alias Chlorphenisin
    • Einecs 202-784-8
    • 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

    612401

    Name Chlorphenesin
    Chemical Formula C9H11ClO3
    Molecular Weight 202.64 g/mol
    Cas Number 104-29-0
    Appearance White crystalline powder
    Solubility Slightly soluble in water, freely soluble in alcohol
    Melting Point 77-81°C
    Usage Preservative in cosmetics and pharmaceuticals
    Mechanism Of Action Muscle relaxant and antimicrobial agent
    Storage Conditions Store in a cool, dry place away from light
    Ph Range 4.0 - 6.0
    Synonyms 3-(4-Chlorophenoxy)-1,2-propanediol

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

    Packing & Storage
    Packing Chlorphenesin is supplied in a sealed, amber glass bottle containing 100 grams, labeled with product name, purity, batch number, and safety warnings.
    Shipping Chlorphenesin is shipped in tightly sealed containers, protected from light, moisture, and heat. It should be labeled as a chemical substance, with transport following local regulations for non-hazardous chemicals. Handle with care to avoid spills, and store in a cool, dry, well-ventilated area during transit to maintain stability and quality.
    Storage Chlorphenesin should be stored in a tightly closed container, protected from light and moisture. It must be kept at room temperature, ideally between 15°C and 30°C (59°F to 86°F), away from incompatible substances such as strong oxidizing agents. Ensure the storage area is well-ventilated, cool, and dry, and restrict access to authorized personnel only.
    Application of Chlorphenesin

    Applications of Chlorphenesin in Industrial Manufacturing

    As a primary producer of Chlorphenesin, we supply this preservative-grade chemical to key industrial customers whose downstream sectors require trusted microbial control and strict regulatory compliance. Below are the main sectors where this material achieves specific performance, with clear dialogue to international standards, formulation guidelines, processing routes, and finished product types.

    1. Personal Care and Cosmetic Formulation

    Cosmetic and personal care producers value Chlorphenesin as a globally recognized preservative that helps prevent gram-positive and gram-negative bacterial contamination during both manufacturing and shelf life. Its use ensures compliance with a patchwork of international standards, and correct dosage must account for the full spectrum of a formulation’s water phase and the presence of other preservatives. Thorough dispersion occurs during the aqueous blending stage prior to emulsification, supporting stable, finished cosmetics such as facial creams, lotions, and colored makeup where consumer safety and product integrity remain critical.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No. 1223/2009 Annex V – Preservatives
    • US FDA 21 CFR 700.3 and CIR Safety Assessment – Preservatives in Cosmetics
    • China Cosmetic Supervision and Administration Regulation (CSAR)
    • ASEAN Cosmetic Directive (ACD)

    Typical usage ratio

    • 0.3% to 0.5% w/w; dosage may decrease when used with synergistic multifunctional ingredients, and should not exceed 0.3% in the EU for leave-on products in line with Annex V.

    Downstream process integration

    • Dissolve into water phase during bulk manufacturing; stabilize prior to emulsion formation to ensure homogeneous distribution and preservative function throughout the matrix.

    Final product types

    • Face creams, moisturizers, liquid foundations, sun care lotions, toners, micellar waters, mascaras.

    2. Topical Pharmaceutical and OTC Preparations

    Manufacturers in the pharmaceutical sector utilize Chlorphenesin in over-the-counter topical dermal products, especially where the regulatory monographs permit non-antibiotic preservation. It acts as an adjunct safeguard against microbial proliferation during both bulk manufacturing and secondary packaging. Integrators must validate addition points and concentrations to ensure consistent distribution and full compliance with strict pharmacopoeial requirements, enabling stable gels and creams that must be sterile or present minimal bioburden for end-user safety.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) Preservative requirements
    • USP–NF (United States Pharmacopeia–National Formulary) for non-sterile topical dosage forms
    • ICH Q6A Specifications – Test Procedures and Acceptance Criteria for New Drug Substances and New Drug Products
    • Current Good Manufacturing Practice (cGMP) for finished pharmaceuticals

    Typical usage ratio

    • 0.1% to 0.3% w/w; actual content specified per topical drug master file and adjusted depending on active pharmaceutical ingredients, dosage form, and product packaging.

    Downstream process integration

    • Added to the aqueous phase during compounding under controlled temperature; fully solubilized before gelation, cream, or ointment formation, followed by batch QC for preservative challenge.

    Final product types

    • Topical analgesic creams, external antifungal gels, medicated ointments (hydrogel and emulsion types), pharmaceutical cleansing foams.

    3. Wet Wipe and Hygiene Textile Impregnation

    In the production of pre-moistened wipes, Chlorphenesin plays a role as a preservative that extends the microbial safety window during storage and end-use. It functions against contaminating bacteria in both manufacturing tanks and the final packed format. Producers calibrate levels based on substrate absorption and packaging type, with strict documentation to meet international hygiene certification. Processing incorporates the preservative into the moistening solution which then saturates nonwoven fabric via automated dosing and impregnation lines prior to flow-pack sealing.

    Industry compliance standards

    • ISO 22716 (Cosmetic GMP) and ISO 9001 Quality Management for hygiene textiles
    • US CTFA (Cosmetic, Toiletry, and Fragrance Association) guidelines for wipes
    • EU Regulation (EC) No. 1223/2009 for cosmetic wipes
    • KFDA (Korea Food and Drug Administration) Non-Pharmaceutical Wet Wipes Regulation

    Typical usage ratio

    • 0.2% to 0.4% in total moistening solution; final concentration adjusted based on substrate weight, ambient temperature sensitivity, and shelf-life targets (3–24 months).

    Downstream process integration

    • Measured addition to the moisturizing liquid; thorough mixing before continuous in-line impregnation and real-time QC sampling prior to bulk filling and sealing.

    Final product types

    • Facial wipes, baby wet wipes (non-rinse), personal hygiene cloths, makeup remover pads, travel towelettes.

    4. Hair Care and Scalp Treatment Products

    Industrial-scale hair care formulators incorporate Chlorphenesin in water-rich hair tonics and leave-on scalp treatments to prevent bacterial contamination, particularly where rinse-off is not part of normal use. With volatility in regional regulations, manufacturers must document specific preservative control per formula and batch size, maintaining clarity with finished product labeling. The preservative dissolves in the water phase before the addition of surfactants or active herbal extracts, ensuring effectiveness until the consumer’s final use.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No. 1223/2009, Annex V
    • Japanese Standards for Cosmetics (Ministry of Health, Labour and Welfare - Notification No. 331)
    • Health Canada Cosmetics Ingredient Hotlist
    • CTFA/PCPC Guidelines (INCI adoption)

    Typical usage ratio

    • 0.15% to 0.3% by weight in the finished formula; dosage fine-tuned for presence of botanical actives and pH sensitivity of secondary additives.

    Downstream process integration

    • Dissolved under agitation in the main aqueous tank before surfactant addition or polymer dispersion; mixed until fully clear and checked for compatibility during batch pilot validation.

    Final product types

    • Anti-dandruff scalp solutions, hair tonics, non-rinse conditioners, leave-on treatment serums, herbal scalp sprays.

    5. Water-Based Decorative Paints and Emulsion Coatings

    Some manufacturers of waterborne paints and emulsion-based wall coatings specify Chlorphenesin as a bacterial and fungal contamination safeguard, especially for controlled markets where other traditional preservatives face regulatory scrutiny. Integration requires precise proportioning relative to polymer solids and evaporation profiles, and all batch records must reflect labeling and safety documentation under regional chemical management frameworks. Addition occurs right after dispersion of pigments and fillers, before the final letdown, to protect storage tanks and extend the product’s marketable shelf life.

    Industry compliance standards

    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012) for in-can preservatives
    • China GB 18582-2020 Limits of Harmful Substances of Interior Wall Coatings
    • US EPA List N – In-Can Preservatives for Paints and Coatings
    • REACH Regulation (EC) No. 1907/2006 – Chemical registration requirements

    Typical usage ratio

    • 0.1% to 0.2% by wet weight of total formulation; adjusted according to binder type, in-can pH, and shelf-life expectation in diverse climates.

    Downstream process integration

    • Post-dispersion dosing during grind or letdown; mixed with defoamers and thickeners in batch mixers equipped for high-shear to ensure uniform preservative action.

    Final product types

    • Interior wall emulsion paints, decorative water-based topcoats, primer sealers, children’s room odorless paints.
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    Certification & Compliance
    More Introduction

    Chlorphenesin: Manufacturer’s Insights on a Trusted Ingredient

    Introduction to Chlorphenesin and Our Experience

    At our facility, we’ve manufactured Chlorphenesin for years and followed its journey across pharmaceuticals, personal care, and specialized technical fields. Our line includes both standard and customized grades—from pharmaceutical to cosmetic. Every batch starts with high-purity raw materials, controlled by rigorous sourcing to keep heavy metals and bioburden low long before downstream testing kicks in.

    Chlorphenesin answers everyday needs for safety and preservation. In cosmetics, it stands as an antimicrobial agent, keeping water-based products from spoiling and supporting safety over shelf life. In pharmaceuticals, it acts as a mild muscle relaxant, mostly used in topical preparations. These aren’t just applications from a datasheet—we’ve worked alongside small-volume and bulk customers building these formulations, troubleshooting cloudiness, pH drift, and extraction behaviors.

    Chemical Nature and Production Advantages

    Many users recognize Chlorphenesin as a white crystalline powder, easy to handle and with a characteristic faint odor. Chemically, it’s defined as 3-(4-chlorophenoxy)-1,2-propanediol. The technical details make a difference. Unlike complex macromolecules or preserved blends, pure Chlorphenesin offers a straightforward molecular signature. Each production run follows the same synthesis, then crystallization under cooled, closed systems to limit impurities.

    We constantly test for byproducts—chlorinated aromatics, residual solvents—using liquid chromatography. By running our own in-house analytics, we address concerns fast, without waiting for third parties to confirm stability or spot-check off-spec. This hands-on oversight means each batch carries full traceability. This kind of diligence supports customer claims and regulatory filings; our own team writes the batch statements and keeps samples archived for years. It’s not about checking boxes; it’s about answering real questions from partners on five continents.

    Models, Specifications, and Practical Details

    We supply multiple models tailored for use in different sectors. The most requested specification by our downstream clients is our pharmaceutical grade Chlorphenesin, which features a high assay, typically not less than 98.5%, and impurity profiles well below current pharmacopoeial limits. Cosmetic manufacturers often request a grade with particularly low residual solvents, as measured by headspace GC. Both versions run through the same quality control team that checks moisture content, melting point, and final packaging procedures.

    For finished product developers, particle size can matter. We maintain grinding and sieving lines inside clean rooms to deliver standard or fine powders, based on the target application. No one wants grit in a lotion or a suspension prone to sedimentation in a topical medication. Our teams validate these processes with optical microscopy to confirm batch consistency.

    Shelf stability matters once Chlorphenesin leaves our loading docks. We store in HDPE-lined fiber drums under nitrogen, extending usable life. Each drum is laser-marked and fitted with tamper-evident caps. We control our warehouse humidity and temperature round the clock, reflecting lessons learned from partners whose old stocks suffered caking and absorbance of minor volatiles. Nothing is more frustrating, on the customer’s end, than seeing a year’s work ruined by compromised raw material.

    Usage in Personal Care and Cosmetics

    Decades ago, cosmetic preservation often relied on parabens, formaldehyde donors, or combination systems featuring methylisothiazolinone. These options raised health and regulatory questions. Chlorphenesin came forward as a milder alternative, providing broad-spectrum activity against fungi and bacteria, without the pronounced sensitivity reactions or labeling burden associated with older preservatives.

    Most end users blend our Chlorphenesin into creams, lotions, serums, and wipes. It dissolves well in water and ethanol, so it integrates easily into both aqueous and hydroalcoholic bases. Manufacturers have expanded its use into sunscreens, after-sun products, deodorants, foundations, and even wipes, where risk of contamination runs high. We’ve supported production pilots by guiding dosage (typically between 0.1% to 0.3% total formula weight), clarifying issues tied to separation or color stability, and helping large-scale partners minimize batch rejection.

    Product safety takes priority. Our compliance team regularly monitors current thinking from cosmetic regulators in major markets. For example, while Chlorphenesin is widely approved, some markets set specific upper concentration limits or pair its use with warnings about mucosal application. Our internal R&D group keeps reference samples and updated regulatory dossiers so customer launches don’t hit a wall in customs or fall foul of changing guidelines.

    Pharmaceutical Applications: Perspectives from the Manufacturer’s Floor

    In the medicinal field, Chlorphenesin serves primarily as a topical muscle relaxant, sometimes in compounded creams for specific neuromuscular disorders. Because it’s delivered in low concentrations and is not systemically absorbed like oral actives, it’s particularly valued in pediatric and geriatric care, where minimizing drug interactions or toxicity is key. Over the years, we’ve partnered with hospitals and compounding pharmacies who need a worry-free, pure raw material with predictable solubility and reconstitution behavior.

    Manufacturing standards for this sector often outstrip those for personal care—batch records run longer, analytical trails grow thicker, and we run stability tests stretching past 24 months. Our team ensures every kilo packs a robust audit trail; injectable, parenteral, or direct skin application places much higher scrutiny on contamination and trace impurities. We meet these clinical demands by investing in extra filtration and further endpoints for heavy metal screening, reflecting our commitment to reliability in mission-critical circumstances.

    Key Differences from Other Preservatives and Actives

    Preservation isn’t one-size-fits-all. While working with formulators and quality specialists, we often discuss the strengths and weaknesses between Chlorphenesin and other agents like phenoxyethanol, ethylhexylglycerin, potassium sorbate, and parabens. Some alternatives offer stronger fungicidal action or work better in low-pH environments. Others face regulatory limits, consumer skepticism, or compatibility issues.

    Chlorphenesin usually brings a gentler profile for skin tolerability. End-users regularly report it supports sensitive skin and doesn’t generally provoke irritation at recommended concentrations. Unlike formaldehyde donors, it doesn’t break down to problematic byproducts, making it a preferred choice for natural or ‘clean label’ lines. Its broad activity window means formulators can reach for Chlorphenesin where shelf lives have stubbornly lagged or contamination is a recurring issue.

    Compared to compounds like parabens, Chlorphenesin breaks down more quickly in the environment, reducing downstream chemical persistence. This matters not just for consumers but for manufacturing wastewater handling. Over the past five years, as global demand for environmentally considered formulations has soared, our customers have leaned more heavily on Chlorphenesin to meet both performance and regulatory expectations.

    Industry Challenges and Real Solutions

    Few products stand still across decades. Customers expect steady supply, price stability, and zero interruption for mission-critical lines. Challenges persist—tightening regulations, shifting consumer perceptions about preservatives, ever-increasing documentation for allergens, traceability, and environmental safety. As a direct manufacturer, we see these pressures day in, day out.

    Reliable sourcing isn’t about chasing lowest cost. For us, it means long-term supply agreements with vetted suppliers, periodic risk audits, and a willingness to pull lots from production until we’re satisfied any question has been answered. Our industry faces ever-stronger scrutiny over contaminant metals and persistent organics. We’ve responded by running in-house metals screens with ICP-MS, tracing levels far below global thresholds.

    Transport and storage pose further headaches. Our early days saw more products affected by temperature swings and moisture ingress. Now, every export shipment rides in climate-controlled containers, and our partners appreciate our commitment to just-in-time logistics. We draw insight from shipment analytics—tracking time in transit, evaluating temperature excursions, and re-training warehouse teams to spot early warning signs of caking or container breach.

    As more customers shift to smaller package sizes for batch-only manufacturing, we’ve invested in line flexibility. A high-output drum filling line serves legacy partners, while smaller, vacuum-sealed packs reduce waste and contamination for niche or boutique cosmetic makers. Our main plant runs 24 hours with staggered shifts to cover both demand surges and bespoke orders.

    Quality Assurance and Product Support

    Our in-house QA labs carry out elemental and organic testing that goes beyond simple minimum thresholds. We prepare reference batches and run accelerated aging studies to mimic real world conditions, ensuring our Chlorphenesin works as promised through the product lifecycle. We’re happy to supply technical documentation, kosher/halal certifications, dual-language COAs, and periodic supply chain audits on request.

    Tech support isn’t just an afterthought; our team has resolved real-life customer issues—cloudy creams, off-odors, packaging compatibility failures—through direct, honest conversation. We’ve helped clients shifting from legacy preservatives to adjust pH, solve micro “incompatibilities” that aren’t always listed in open literature, and even guided solvent switching to restore finished product performance. This feedback cycle makes us better manufacturers and makes our partners’ launches smoother.

    Regulatory compliance follows a similar philosophy. We maintain an active watch on global changes—every market from North America through Asia and the EU upgrades ingredient guidelines, prefers new labeling standards, or narrows accepted preservatives from time to time. Our regulatory staff prepares regular client notifications, translates new data for ease of understanding, and supports filings for customer dossiers.

    Environmental and Safety Considerations

    Factory safety ranks alongside product purity. Our operators receive annual training on chemical handling, dust collection, and emergency containment. All process wastes are captured, neutralized, and sent for approved chemical disposal. We retain fully auditable data from each production run and hold relationships with local environmental authorities to maintain our operating permits.

    For end users, we recommend smart handling: dry, cool storage, and sealed containers extend the shelf life, while fast addition to water-based blends limits dusting. Most routine handling poses low risk, but as with any chemical, gloves and goggles support safe workplace practice.

    We commit to transparency rather than greenwashing. Our technical sheets map out degradation rates in various conditions, and we assist clients in understanding downstream breakdown and wastewater implications. Over the years, we’ve found that candid information enables customers to address their own sustainability agendas, avoiding surprises months down the line.

    Future Perspectives and Evolving Market Needs

    As newer preservation technologies enter the market—peptides, certain organic acids, silver-based agents—we still see Chlorphenesin play a vital role for thousands of manufacturers. Its compatibility with traditional bases, safety in finished goods, and record of regulatory acceptance gives it a strong place even as customers try “greener” or next-gen approaches.

    We attend global cosmetic and pharma expos, connecting with R&D teams exploring hybrid preservative systems. Feedback from these conversations leads us to invest in blending lines, powdered pre-mixes with synergistic boosters, and continued upgrades to analytical testing. We collaborate openly on improved solubility formats, granules for blending, and solvent-free solutions to reduce process residues.

    We don’t expect Chlorphenesin to be the only answer for every formulation. Some new markets need preservative systems that function in ultra-low pH, ultra-clean label, or challenging technical regimes. But manufacturers rely on proven tools while validating newcomers. We’re committed to maintaining open, two-way communication and evolving our product and support in line with what regulatory agencies, our partners, and the market expects.

    Direct Engagement Matters

    Our reputation builds batch by batch, through reliable product, fast answers, and clear documentation. We avoid grand claims, preferring to solve practical challenges alongside the people who use Chlorphenesin. From our team’s practical troubleshooting in the plant to late-night discussions about label clarity and compliance, we invest in the craft of manufacturing, not just in cost control.

    For us, every purchase is a partnership. By committing to consistency, transparency, and constant improvement, we deliver Chlorphenesin not just as a commodity, but as a foundation for safe, reliable, and innovative formulations around the world.