Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales6@sinochem-nanjing.com
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P-Cymene

    • Product Name P-Cymene
    • Alias 1-Methyl-4-(1-methylethyl)benzene
    • Einecs 202-796-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    801621

    Chemical Name p-Cymene
    Cas Number 99-87-6
    Molecular Formula C10H14
    Molecular Weight 134.22 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 177 °C (351 °F)
    Melting Point -68 °C (-90 °F)
    Density 0.857 g/cm³ at 20 °C
    Solubility In Water Insoluble
    Flash Point 50 °C (122 °F)
    Odor Aromatic, pleasant, mild citrus odor

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

    Packing & Storage
    Packing P-Cymene is packaged in a 500 mL amber glass bottle with a secure screw cap, labeled with safety and handling instructions.
    Shipping P-Cymene is typically shipped in tightly sealed containers, such as drums or bottles, made of materials compatible with aromatic hydrocarbons. It should be stored and transported in a cool, well-ventilated area, away from sources of ignition and incompatible substances. Proper labeling and adherence to local and international transport regulations are required.
    Storage P-Cymene should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and incompatible substances such as oxidizing agents. Keep the container tightly closed and clearly labeled. Protect from direct sunlight and moisture. Store in a chemical storage cabinet designated for flammable liquids, ensuring proper grounding and bonding to prevent static discharge.
    Application of P-Cymene

    Applications of P-Cymene in Industrial Manufacturing

    P-Cymene serves as a key aromatic hydrocarbon intermediate for multiple chemical sectors, supporting the synthesis and formulation of advanced materials and bulk specialty chemicals. Its unique structure and high purity grade make it suitable for integration in various regulated industrial processes, from monomer synthesis to agrochemical production.

    1. Intermediate for Agrochemical Synthesis

    Agrochemical manufacturers use P-Cymene as a precursor in the production of herbicides and fungicides, where its methyl and isopropyl-substituted aromatic structure provides high chemical stability for downstream transformation. The material reacts under controlled Friedel-Crafts alkylation and oxidation protocols, supporting the synthesis of crop protection agents such as cymoxanil and related benzoic acid derivatives. Consistent product traceability and compliance with environmental guidelines are critical during scale-up and formulation.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • EU Plant Protection Products Regulation (EC) No 1107/2009
    • ISO 9001:2015 Quality Management Systems
    • US EPA Toxic Substances Control Act (TSCA)

    Typical usage ratio

    • 10–25% by mass as aromatic intermediate in multi-step synthesis
    • Exact ratio depends on required target molecule and conversion yield
    • Adjustable to minimize by-product formation in catalytic alkylation processes
    • Strict monitoring for residual aromatic hydrocarbon in final formulation

    Downstream process integration

    • Introduced at initial aromatic alkylation/reactive distillation stage
    • Feeds into oxidation or amination reactors for active ingredient synthesis
    • Supports solvent-based extraction and crystallization of technical-active material
    • Follows with formulation blending before packaging at agrochemical plant

    Final product types

    • Herbicide active compounds (e.g., cymoxanil)
    • Fungicidal benzoic acid derivatives
    • Formulated crop protection blends
    • Bulk agrochemical intermediates for export

    2. Monomer and Resin Manufacturing

    Manufacturers of specialty monomers and resins utilize P-Cymene as a building block for synthetic polymers, phenolic resins, and alkyd resins, leveraging its aromatic moiety for rigidity and process compatibility. Large-scale polymerization plants incorporate it in alkylation or condensation reactions to modify polymer backbone properties and tailor thermal stability for industrial coatings and molded plastics.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • EN 13980:2002 Equipment and Protective Systems intended for use in Potentially Explosive Atmospheres (ATEX)
    • ASTM D3576 (Standard Test Methods for P-Cymene Content in Industrial Chemicals)
    • OSHA Process Safety Management (PSM)

    Typical usage ratio

    • 5–20% by weight in monomer/resin precursor formulations
    • Levels adjusted according to crosslinking requirements and end-use durability
    • Lower end of range for flexible coating resins, higher for rigid plastics
    • Usage determined by downstream viscosity and curing protocols

    Downstream process integration

    • Added to mixing vessel with phenol, formaldehyde or phthalic anhydride
    • Enters resinification/condensation step for backbone structuring
    • Continues with neutralization and filtration post-polymerization
    • Direct feed into extrusion or casting unit as intermediate resin

    Final product types

    • Industrial phenolic resins (for brake linings, abrasives)
    • Modified alkyd resins for protective industrial coatings
    • Polymerized molding compounds
    • High-performance adhesives and laminates

    3. Fragrance and Flavors Ingredient Manufacture

    The aroma and volatility profile of P-Cymene supports its use in the synthesis of fragrance bases and food-grade flavoring additives. Downstream facilities transform it through catalytic oxidation or cyclization processes to yield compounds such as p-cresol, thymol, and carvacrol, essential for perfumery, flavor, and aromatic therapeutic oils. Compliance with stringent food-grade safety and allergen standards governs its use throughout these processes.

    Industry compliance standards

    • FCC (Food Chemicals Codex) for flavor ingredient purity
    • IFRA (International Fragrance Association) Standards
    • ISO 22000 Food Safety Management Systems
    • 21 CFR Part 172 (US FDA Approved Food Additives)

    Typical usage ratio

    • 3–12% in flavor intermediate synthesis
    • 1–8% in essential oil preparation, depending on volatility and aroma strength required
    • Trace residual limits according to food and fragrance regulations
    • Purity and dilution rate strictly controlled to match formulation guidelines

    Downstream process integration

    • Introduced at oxidation and demethylation stage to form target aroma chemicals
    • Undergoes cyclization to generate specific terpene derivatives
    • Blended into concentrated perfume oil or diluted into spirit base for end-use applications
    • Finished materials pass through GC-MS purity verification and allergen screening

    Final product types

    • Fragrance intermediates (e.g., carvacrol, thymol)
    • Food flavorings and enhancers
    • Essential oil blends for aromatherapy
    • Personal care products with aromatic additives

    4. Fine Chemical Derivatives and Solvent Formulation

    Producers of fine chemical intermediates and solvent mixers use P-Cymene as a reactant or diluent for specialty organic synthesis, providing high-boiling solvent properties and aromatic ring orientation for selective chemical transformations. The chemical’s physicochemical stability ensures consistent process parameters in nitration and sulfonation reactions, which are necessary for manufacturing antioxidants and specialty dyes.

    Industry compliance standards

    • GMP for Pharmaceutical Excipients (ICH Q7)
    • ISO 9001:2015 Quality Management for Fine Chemicals
    • UN Recommendations on the Transport of Dangerous Goods
    • European Pharmacopoeia (Ph. Eur.) Annexes for chemical purity

    Typical usage ratio

    • 5–18% by volume in fine chemical manufacture
    • 2–15% as a co-solvent in specialty dye synthesis
    • Proportions adjusted for reactivity and downstream solubility
    • Specific dosing set by required end-product residue limits

    Downstream process integration

    • Added at reaction initiation with controlled temperature and inert gas blanket
    • Supports substrate dissolution before sulfonation or nitration
    • Remains in solution for separation or purification post-reaction
    • Recovered by fractional distillation for circular production use

    Final product types

    • Antioxidant additives for lubricant blends
    • Specialty dyes for plastics and fibers
    • Pharmaceutical fine chemical intermediates
    • Custom industrial solvent mixtures

    5. Extraction Aid in Natural Product Isolation

    Some phytochemical and natural products facilities deploy P-Cymene as an auxiliary extraction solvent, particularly during the isolation of complex terpenoids and essential oil fractions from botanical sources. Its capacity to selectively dissolve specific organic constituents improves yield and efficiency, under validated process conditions to avoid cross-contamination and maintain product naturality claims, in line with global natural extract standards.

    Industry compliance standards

    • ISO 9235: Aromatic Natural Raw Materials — Vocabulary
    • US FDA GRAS (Generally Recognized As Safe) for solvent residues
    • European Pharmacopoeia natural extract monographs
    • EFSA Scientific Opinions on Extraction Solvents

    Typical usage ratio

    • 2–10% by volume of total extraction medium, depending on botanical matrix
    • Reduced ratios for low-resin content or volatile-rich substrates
    • Final ratio set by recovery step and solvent residue specification
    • Strict limit tests for final solvent traces in isolated extract

    Downstream process integration

    • Employed at solvent-assisted extraction during initial plant material maceration
    • Integrates with hexane, ethanol, or supercritical CO2 protocols for efficiency
    • Removed by vacuum distillation or rotary evaporation prior to standardization
    • Quality check for solvent carryover before product blending and bottling

    Final product types

    • Standardized essential oils (e.g., oregano, thyme)
    • Botanical extracts for food supplements
    • Natural perfume base concentrates
    • Plant-derived health ingredients for functional foods
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