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4-Isopropoxybenzoic Acid

    • Product Name 4-Isopropoxybenzoic Acid
    • Alias p-Isopropoxybenzoic acid
    • Einecs 249-582-6
    • 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

    920125

    Product Name 4-Isopropoxybenzoic Acid
    Cas Number 1667-92-9
    Molecular Formula C10H12O3
    Molecular Weight 180.20 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 180-183 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 1.19 g/cm3 (approximate)
    Purity Typically ≥98%
    Synonyms p-Isopropoxybenzoic acid; 4-(1-Methylethoxy)benzoic acid
    Smiles CC(C)OC1=CC=C(C=C1)C(=O)O
    Inchi InChI=1S/C10H12O3/c1-7(2)13-9-5-3-8(4-6-9)10(11)12/h3-7H,1-2H3,(H,11,12)

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

    Packing & Storage
    Packing The 500g package of 4-Isopropoxybenzoic Acid comes in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 4-Isopropoxybenzoic Acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. Packaging complies with chemical safety regulations. The product is labeled with hazard information and handled in accordance with relevant transport guidelines. Shipping is typically via ground or air transport, depending on destination, ensuring efficient and secure delivery.
    Storage 4-Isopropoxybenzoic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat and ignition. It should be kept away from incompatible substances such as strong acids, bases, and oxidizing agents. Protect the chemical from moisture and direct sunlight. Properly label the storage container and follow all local chemical storage regulations.
    Application of 4-Isopropoxybenzoic Acid

    Applications of 4-Isopropoxybenzoic Acid in Industrial Manufacturing

    4-Isopropoxybenzoic Acid is a critical intermediate in several high-value industrial sectors requiring strict regulatory compliance and advanced synthetic control. As a direct manufacturer with controlled purity and traceability, we support demanding downstream processes for pharmaceuticals, liquid crystals, polymer additives, and specialty chemical synthesis. Each application below outlines material function, regulatory context, formulation practices, and integration in the end-user process chain.

    1. Pharmaceutical Intermediates for Anti-inflammatory APIs

    Many anti-inflammatory drug manufacturing routes use 4-Isopropoxybenzoic Acid as a key building block. The molecule provides a specific aromatic backbone enabling esterification or amidation in the synthesis of non-steroidal anti-inflammatory drug (NSAID) intermediates, such as derivatives related to ibuprofen or fenoprofen analogs. Production setups demand full traceability, in-process impurity monitoring, and batch-to-batch analytical consistency to reach approval in regulated markets. Our supply enables consistent lot-scale and multi-ton batch delivery for API plants operating under validated GMP conditions.

    Industry compliance standards

    • ICH Q7 Guidelines (Current Good Manufacturing Practices for APIs)
    • USP-NF Monographs (when applicable)
    • European Pharmacopoeia Generic Chapter 5.10 guidelines
    • FDA 21 CFR Part 210/211 (for finished pharmaceuticals)

    Typical usage ratio

    • 0.7–1.2 molar equivalents per API batch, adjusted by downstream process yield and scale, typically representing 18–32% by weight in targeted step

    Downstream process integration

    • Direct charge to reactor during acylation, condensation, or amidation stages
    • Coupling or esterification with activated carboxylic acid derivatives
    • Subject to in-process HPLC/GC monitoring for residuals and conversion tracking
    • Tank and pipeline systems isolated from cross-contamination

    Final product types

    • Bulk active pharmaceutical ingredients (APIs) for human NSAIDs
    • Pharma-grade intermediates for analgesic production
    • Veterinary drug substance intermediates
    • Raw material for further downstream functionalization

    2. Monomer for High-Performance Liquid Crystal Material Synthesis

    Top-tier electronic and display manufacturers formulate specialty liquid crystals using high-purity 4-Isopropoxybenzoic Acid as a monomer. Its para-substituted, isopropyl-ether structure supports the production of rod-shaped esters with unique phase behavior, key for controlling response times, clarity, and operational temperature windows in LCD modules. Material entry requires narrow metal impurity control and strict solvent residue limits to safeguard final pixel stability and screen uniformity in consumer and industrial devices.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for electronic device materials)
    • IEC 61249-2-21 (halogen-free electronic materials)
    • Manufacturing restricted to ISO 9001 and ISO 14001 compliant sites
    • Household and Industrial Electronic Display Materials (Chinese Standard GB/T series)

    Typical usage ratio

    • Monomer loadings adjusted to 10–40 mol% in complex esterification reactions, depending on desired birefringence and phase sequence in liquid crystal mixtures

    Downstream process integration

    • Esterification with biphenol or cyclohexanol derivatives in inert solvent media
    • Crystallization and ultra-fine filtration before final formulation
    • Analysis via POM, DSC and gas chromatography throughout blending
    • In-line drying and atmosphere-controlled transfer into fill lines for LCD manufacturing

    Final product types

    • Standard TN, STN and IPS mode liquid crystal mixtures
    • High-stability LCD panels for smartphones and flat-panel displays
    • Electronic paper and industrial display media
    • Advanced temperature-resistant liquid crystal glass applications

    3. Precursor for Aromatic Polyester Synthesis

    Aromatic polyesters engineered for high-heat resistance and dimensional stability incorporate 4-Isopropoxybenzoic Acid as a rigid diacid monomer. These polyesters serve in electronics, specialty films, and high-performance fiber sectors. The acid moiety reacts with glycols or bisphenols, imparting increased glass transition temperature and mechanical strength. Industrial users evaluate residual acid content and perform reactivity adjustments based on melt index and molecular weight targets.

    Industry compliance standards

    • ISO 9001:2015 for quality systems in polymer production
    • REACH Regulation (EC) No. 1907/2006 for chemical safety
    • ISO 14001:2015 for environmental management in plastics plants
    • ASTM D3418 for differential scanning calorimetry of polymers

    Typical usage ratio

    • 5–18 wt% of total diacids in proprietary resins, customized to end-use mechanical performance and processing window

    Downstream process integration

    • Fed to continuous polycondensation reactors with other aromatic diacids and alkylene glycols
    • Functional group ratio monitored by NMR and endpoint titration
    • Polymer output pelletized and dried for further transformation
    • QC sample retention according to traceability protocols

    Final product types

    • High-performance thermoplastic polyesters
    • Melt-processable engineering resins
    • Specialty packaging films and multilayer barrier sheets
    • Injection-molded housings for electrical and automotive sectors

    4. Intermediate in Fine Fragrance Ester Synthesis

    The unique aromatic profile of 4-Isopropoxybenzoic Acid supports synthesis of fine esters and aromatic ethers, widely used by global fragrance and aroma compound producers. These specialty esters find application in premium perfume blends, personal care formulations, and luxury soaps. Downstream partners verify raw material history, allergen status, and CMR-free declaration for global market registration, with focus on reliable purity and batch traceability.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • Cosmetics Regulation (EC) No. 1223/2009 for ingredient safety
    • Allergen disclosure per Annex III of EU Cosmetics Regulation
    • ISO 22716 for Cosmetic Good Manufacturing Practice (GMP)

    Typical usage ratio

    • Typically reacts as 1:1 molar equivalent with selected alcohols, dosage depending on formulation strength, batch volumes from 5–250 kg scale

    Downstream process integration

    • Fed to batch esterification reactors under controlled pH and temperature
    • Post-reactor stripping and filtration after primary conversion
    • Organoleptic and GC–MS batch validation pre-delivery
    • Trace documentation for allergens, synthesis condition, and safety

    Final product types

    • Base-stock fragrance esters for perfumer use
    • Aromatic ethers for luxury hand creams and personal care
    • Impact notes in high-end eau de perfume blends
    • Scent carriers in premium skincare and bath soaps

    5. Building Block for UV-Filter and Specialty Sunscreen Ingredients

    Cosmetic and sunscreen material producers employ 4-Isopropoxybenzoic Acid in the synthesis of custom UV-absorbing molecules and light-stabilizing agents. The aromatic and alkoxy substituents yield esters and ethers with defined absorption spectra, improving photostability and broadening UVA/UVB protection in formulations. Downstream integration demands validated specification for trace solvents, heavy metals, and absence of banned photoinitiators, supporting international compliance and consumer safety.

    Industry compliance standards

    • Regulation (EC) No. 1223/2009 Annex VI (for UV-filters in cosmetics)
    • FDA 21 CFR Part 352 (sunscreen drug products in USA)
    • ISO 16128 (guidelines for natural and organic cosmetic ingredients)
    • ISO 22716 (GMP for cosmetics manufacturing)

    Typical usage ratio

    • Material input typically at 8–25 wt% in specialty filter intermediates; process engineers adjust based on target UV absorption profile and finished formulation batch size

    Downstream process integration

    • Synthesized via controlled esterification and alkylation reactions
    • Purification and phase separation under nitrogen blanketing
    • Analytical verification using UV–Vis spectrometry and purity assays
    • Material delivered in sealed, light-proof drums to avoid degradation

    Final product types

    • Novel UV-filter actives for broad-spectrum sunscreens
    • Light-stabilizer components for haircare and skin protection
    • Photostable sunscreen ingredient pre-mixtures
    • Cosmetic bases for global beauty and sun-care brands
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