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Hydrocinnamoyl Chloride

    • Product Name Hydrocinnamoyl Chloride
    • Alias 3-Phenylpropanoyl chloride
    • Einecs 204-409-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    735522

    Chemical Name Hydrocinnamoyl Chloride
    Synonyms 3-Phenylpropionyl chloride
    Molecular Formula C9H9ClO
    Molar Mass 168.62 g/mol
    Cas Number 645-45-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 124-125 °C at 20 mmHg
    Density 1.14 g/cm³
    Flash Point 117 °C
    Solubility Reacts with water, soluble in organic solvents
    Storage Conditions Store under inert gas, cool and dry place

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

    Packing & Storage
    Packing Hydrocinnamoyl Chloride is supplied in a 250g amber glass bottle, tightly sealed, with hazard labels and chemical identification details.
    Shipping Hydrocinnamoyl Chloride is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous material, compliant with DOT and IATA regulations, and typically packed in glass bottles or corrosion-resistant drums with secondary containment to prevent leaks. Shipping documents include safety data and hazard labeling.
    Storage Hydrocinnamoyl chloride should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. It should be kept away from incompatible substances such as strong bases, oxidizers, and alcohols. Proper labeling and secondary containment are recommended to prevent leaks and accidental exposure. Use only in a chemical fume hood.
    Application of Hydrocinnamoyl Chloride

    Applications of Hydrocinnamoyl Chloride in Industrial Manufacturing

    Hydrocinnamoyl Chloride serves as a specialized intermediate in fine chemicals manufacturing, with application across several targeted downstream sectors. As the original manufacturer, we provide consistent bulk quality suitable for regulated environments, ensuring precise compliance and performance in each industrial segment below.

    1. Pharmaceutical Intermediates Synthesis

    Pharmaceutical manufacturers use hydrocinnamoyl chloride to introduce hydrocinnamoyl moieties in complex molecule synthesis, such as in the acylation of active pharmaceutical ingredients (APIs) and advanced intermediates. This application demands controlled conditions to maintain impurity profiles, reproducibility, and traceability. The material must meet pharmacopeial requirements and enter the process during selective functional group modification stages. These steps control the physicochemical attributes critical to pharmacological activity, with documented batch recipes supporting audit and cGMP inspection.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • United States Pharmacopeia (USP) and European Pharmacopeia (EP) reference monographs
    • FDA 21 CFR Part 210/211 audit trail requirements
    • ISO 9001:2015 QMS traceability mandates

    Typical usage ratio

    • 0.5%–2.5% by weight as acylating agent, calculated relative to starting substrate; adjusted to ensure complete conversion and byproduct minimization

    Downstream process integration

    • Stagewise addition for Friedel-Crafts or Schotten–Baumann acylation; typically added after completion of key protection or activation steps; controlled feed based on real-time HPLC monitoring

    Final product types

    • Nonsteroidal anti-inflammatory drug intermediates
    • CNS-active molecule fragments
    • Amide, ester, or other hydrocinnamoyl-linked API intermediates
    • Chiral building blocks for peptide synthesis

    2. Agrochemical Active Ingredient Manufacturing

    Hydrocinnamoyl chloride functions as a key starting reagent in agrochemical formulation, particularly within selective herbicide, fungicide, and plant growth modulator syntheses. Downstream companies rely on our controlled impurity profile and consistent assay to maintain environmental safety and regulatory registration. The material enters production via nucleophilic substitution or amidation steps, where it forms pivotal active ingredient backbones. Use rates often reflect active’s registration dossier and local field trial data, optimizing for efficacy while limiting off-target risk.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • OECD Good Laboratory Practice (GLP) for batch records
    • REACH Regulation (EC) No 1907/2006 for European market
    • EPA FIFRA standards for US agrochemical registration

    Typical usage ratio

    • 1.0%–3.0% by total reaction mass, titrated based on target molecule’s molar requirements and in-process analytical checks

    Downstream process integration

    • Dosed during acylation of heterocyclic ring systems or in amidation with primary amines; process flow generally includes inert atmosphere and post-reaction work-up under regulated waste disposal

    Final product types

    • Pre-emergence and selective herbicide actives
    • Benzylamide-based fungicides
    • Plant growth regulator intermediates
    • Custom pesticide active ingredient scaffolds

    3. Flavor and Fragrance Intermediate Production

    Major fragrance and flavor compound houses incorporate hydrocinnamoyl chloride into the synthesis of aromatic esters and alcohol derivatives used in perfumery and food additives. The material’s consistent reactivity and purity support predictable downstream chromatographic profiles. Manufacturers utilize this intermediate in the introduction of hydrocinnamoyl groups to core molecules, which impart distinctive olfactory notes and modify volatility. Formulation ratios and conditions reflect IFRA and food additive safety requirements, and QA release must confirm absence of prohibited trace impurities.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards for restricted substances
    • EU Regulation (EC) No 1334/2008 on flavorings
    • FDA 21 CFR Part 182 (Generally Recognized as Safe – GRAS) for food applications
    • ISO 17025 certified analytical methods validation

    Typical usage ratio

    • 0.1%–1.2% relative to total batch mass; selection guided by targeted fragrance intensity or chromatogram requirements

    Downstream process integration

    • Loaded as acylating agent in esterification or amidation reactors after alcohol or amine substrate charging; monitored by GC-MS or NMR analysis; subsequent purification yields finished intermediate

    Final product types

    • Luxury fine fragrance compounds
    • Natural-identical food flavor enhancers
    • Synthetic musk and spicy aroma agents
    • Aromatic ester and alcohol intermediates for perfumery blending

    4. Polymer and Resin Modifier Synthesis

    In specialty resin and polymer industries, hydrocinnamoyl chloride supports the synthesis of modified polyesters, polyamides, and alkyd resins that demand precise control of polarity, glass transition, and cross-linking behavior. Resin formulators value this intermediate for introducing hydrophobic or aromatic character, which impacts compatibility and end-use film properties. Material introduction occurs within controlled reactors where stoichiometry and reaction runtime impact final molecular weight distribution. Quality assurance depends on achieving tightly specified acid value and residual chloride thresholds.

    Industry compliance standards

    • ISO 9001:2015 process control for specialty chemicals
    • RoHS Directive 2011/65/EU (where used in coatings for electronics)
    • REACH substance registration and reporting for EU resin markets
    • ASTM D1652 for ester/acid value testing in resin blending

    Typical usage ratio

    • 3.0%–8.0% by polymer backbone mass; reaction ratio optimized by targeted Tg and flexural properties in the downstream application

    Downstream process integration

    • Charged post-polyol or diacid addition, typically in batch or semi-continuous reactors; fed during polyesterification or polyamidation with process pressure and temperature logged for each lot; residual chloride removed during work-up filtration

    Final product types

    • Modified alkyd resins for industrial coatings
    • Functionalized polyamide stabilizers
    • Aromatic polyester segments for specialty plastics
    • Structural adhesives and electronics encapsulants

    5. UV Stabilizer and Antioxidant Component Manufacturing

    Producers of high-performance UV absorbers and phenolic antioxidants rely on hydrocinnamoyl chloride to build specific chemical structures enhancing polymer stability, especially for automotive and outdoor applications. The material is dosed in aromatic substitution and esterification reactions to yield stabilizer molecules with customized hydrophobicity or thermal resistance. End-use compliance depends on absence of unreacted acid chlorides and accurate stoichiometry. Final products support demanding QA documentation for downstream plastic, rubber, or coating manufacturers.

    Industry compliance standards

    • EN 71-3 safety for use in toys and consumer goods
    • ISO 178:2019 for polymer UV resistance
    • UL 94 flame retardancy in coatings/plastics
    • REACH Annex XVII restrictions where applicable

    Typical usage ratio

    • 0.8%–1.5% based on final molecular design; batch adjustment depends on substitution degree and HPLC endpoint verification

    Downstream process integration

    • Added following polynuclear aromatic or phenol substrate charging, with continuous pH and temperature monitoring; reaction vessels fitted with acid scrubbing and solvent recovery modules

    Final product types

    • UV stabilizer masterbatches for plastics extrusion
    • High-performance hindered phenol antioxidants
    • Weather-resistant surface protection additives
    • Automotive coating stabilizer blends
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