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4-Propylresorcinol

    • Product Name 4-Propylresorcinol
    • Alias 4-n-Propylresorcinol
    • Einecs 202-848-9
    • 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

    963357

    Cas Number 18979-61-8
    Molecular Formula C9H12O2
    Molecular Weight 152.19 g/mol
    Iupac Name 4-propylbenzene-1,3-diol
    Appearance White to off-white crystalline powder
    Melting Point 96-100°C
    Boiling Point 298.3°C at 760 mmHg
    Solubility In Water Slightly soluble
    Density 1.1 g/cm3 (approximate)
    Synonyms 4-Propyl-1,3-dihydroxybenzene

    As an accredited 4-Propylresorcinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Propylresorcinol comes in a 25-gram amber glass bottle, securely sealed and labeled with hazard symbols and identification details.
    Shipping 4-Propylresorcinol is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. Packages are clearly labeled according to regulatory standards. During transit, it is stored away from incompatible substances, sources of ignition, and direct sunlight. Appropriate documentation and safety data sheets (SDS) accompany each shipment for safe handling and regulatory compliance.
    Storage 4-Propylresorcinol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Proper labeling and safety precautions should be maintained to avoid accidental exposure or chemical degradation. Store it according to standard chemical safety protocols.
    Application of 4-Propylresorcinol

    Applications of 4-Propylresorcinol in Industrial Manufacturing

    4-Propylresorcinol serves as a critical active and intermediate ingredient within several tightly regulated sectors. We support production partners with best-practice technical use, backed by on-site QC and collaborative scale-up experience. See key applications below, each connected to defined downstream product lines and real operational standards.

    1. Cosmetic Skin Lightening Actives

    Dermatological and cosmetic manufacturers employ 4-Propylresorcinol as a targeted melanin synthesis inhibitor in high-performance skin lightening formulations. The industry values its effectiveness at low concentrations, supporting clear formulation requirements under cosmetic regulatory frameworks. Manufacturers must adhere to authorized ingredient lists and purity controls across global markets.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • FDA Title 21 CFR 700 Subpart B (for OTC skin lighteners, US)
    • China NMPA Cosmetic Safety Technical Specification (2021 Edition)
    • ISO 22716:2007 Cosmetics – GMP Guidelines

    Typical usage ratio

    • 0.1% to 0.5% w/w in finished emulsions and serums; adjusted by skin tolerance data and product claim.

    Downstream process integration

    • Dissolve in warm oil or water phase under nitrogen; integrate in pre-emulsification before final cooling and preservation steps for stability.

    Final product types

    • Skin brightening face creams
    • Spot corrector serums
    • Hyperpigmentation treatment creams
    • Professional dermatology ampoules

    2. Pharmaceutical Intermediates for Dermatological APIs

    Specialty drug manufacturers leverage 4-Propylresorcinol as a key intermediate in synthesis of specific APIs for medical dermatoses. Validated routes require strict documentation under active pharmaceutical ingredient guidelines, ensuring traceability and impurity control throughout synthesis and isolation steps in cGMP-compliant plants.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • WHO TRS 986 Annex 2 GMP for APIs
    • Ph. Eur. Monograph 5.10 (related substances assessment)
    • USP General Chapters for Residual Solvents and Impurity Profiles

    Typical usage ratio

    • Stoichiometric ratios per target API synthesis (e.g., 0.8 – 1.2 equivalents as a phenolic precursor), batch size and yield targets control the scaling.

    Downstream process integration

    • Charged in controlled temperature reactors as substrate, followed by step-wise addition with acylation/alkylation partners and in-process HPLC monitoring.

    Final product types

    • Medicated melasma treatments (prescription and hospital use)
    • Topical depigmenting pharmaceuticals
    • Research actives for dermatological trials

    3. Fine Chemical Intermediate in UV Absorber Synthesis

    UV filter manufacturers use 4-Propylresorcinol as an aromatic phenolic building block for producing specialty UV absorbers in polymer and coating industries. This route supports stable, light-resistant end products required in automotive and packaging films. Downstream operators demand precise impurity control to meet photostability and safety testing protocols.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006, Annex XIV (substance registration and control)
    • OECD Guidelines for Testing of Chemicals (Phototoxicity, UV Stability)
    • ISO 4892-2:2013 (Plastics – Methods of exposure to laboratory light sources)
    • ASTM D6083 (Polymer film and coating performance)

    Typical usage ratio

    • 0.4 to 2.0 equivalents depending on target UV absorber; adjusted for product-specific polymer compatibility and UV absorption peak requirements.

    Downstream process integration

    • Condensation with benzotriazole or triazine derivatives in controlled reactors; followed by solvent extraction and distillation for downstream compounding.

    Final product types

    • UV-blocking masterbatch for plastics
    • Automotive coating additives
    • Flexible packaging films
    • Weather-resistant flooring materials

    4. Analytical Reference Material Production

    Laboratory consumables producers employ 4-Propylresorcinol as a primary standard and as a component in calibration solutions for assay validation and system suitability tests. Clients require consistent, traceable lots with full impurity and stability documentation, in compliance with analytical and pharma reference requirements.

    Industry compliance standards

    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • USP Reference Standard Program Guidelines
    • ISO Guide 34 (General requirements for the competence of reference material producers)
    • OECD GLP Principles (analytical laboratories)

    Typical usage ratio

    • Typically 0.1 mg/mL to 1 mg/mL solutions in certified solvents; prepared gravimetrically according to analytical method parameters.

    Downstream process integration

    • Weighing and dissolving in controlled environments; filtered and bottled under low-light to prevent photodegradation, for shipment with full COA and traceability.

    Final product types

    • HPLC calibration standards
    • System suitability test mixes
    • Proficiency testing kits
    • Pharmacopeial reference solutions

    5. Active Ingredient in Functional Textile Finishes

    Specialist textile chemical suppliers incorporate 4-Propylresorcinol in functional coatings for technical fabrics, targeting applications where antimicrobial and anti-discoloration properties are required. Textile mills apply these formulations using precise recipe-based dosing systems and must maintain rigorous QC to confirm functional performance across repeated wash and exposure cycles.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (harmful substance limits in textile chemistry)
    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)
    • ISO 20743:2021 (Textiles – Determination of antibacterial activity)
    • ZDHC MRSL 2.0 (Manufacturing Restricted Substances List)

    Typical usage ratio

    • 0.05% to 0.3% mass fraction in aqueous finishing baths; adjusted based on target surface loading, textile substrate, and regulatory limits.

    Downstream process integration

    • Dispersed into finishing bath prior to the final dip-pad-dry-cure step; post-application wash and cure optimize fixation and functional durability.

    Final product types

    • Anti-bacterial hospital wear textiles
    • Anti-yellowing bedding and mattress fabrics
    • Fade-resistant uniform linings
    • Odor-control sportswear fabrics
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