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2-Isopropyl-2-Phenylacetic Acid

    • Product Name 2-Isopropyl-2-Phenylacetic Acid
    • Alias 2-phenyl-2-propanoic acid
    • Einecs 202-705-0
    • 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

    733076

    Chemical Name 2-Isopropyl-2-Phenylacetic Acid
    Molecular Formula C11H14O2
    Molecular Weight 178.23 g/mol
    Cas Number 38186-75-1
    Appearance White to off-white solid
    Melting Point 70-74°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 1.07 g/cm³ (approximate)
    Purity Typically >98%
    Smiles CC(C)C(C1=CC=CC=C1)C(=O)O
    Inchi InChI=1S/C11H14O2/c1-9(2)11(10(12)13)8-6-4-3-5-7-8/h3-7,9,11H,1-2H3,(H,12,13)
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 2-Phenyl-2-isopropylacetic acid; alpha-Isopropyl-alpha-phenylacetic acid

    As an accredited 2-Isopropyl-2-Phenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "2-Isopropyl-2-Phenylacetic Acid, 100g," with hazard symbols, lot number, and tightly sealed screw cap.
    Shipping 2-Isopropyl-2-Phenylacetic Acid should be shipped in tightly sealed containers, clearly labeled, and protected from moisture, heat, and direct sunlight. Transport according to local, national, and international regulations for chemicals. Ensure compliance with all safety guidelines, and include a safety data sheet (SDS) with the shipment for handling and emergency reference.
    Storage 2-Isopropyl-2-Phenylacetic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Store separately from acids, bases, and oxidizing agents. Ensure containers are properly labeled, and avoid exposure to moisture. Follow appropriate chemical safety guidelines and local regulations during storage and handling.
    Application of 2-Isopropyl-2-Phenylacetic Acid

    Applications of 2-Isopropyl-2-Phenylacetic Acid in Industrial Manufacturing

    As a manufacturer of 2-Isopropyl-2-Phenylacetic Acid, we supply this intermediate for use in several specialized industrial segments. Our expertise includes supporting Europe, North America, and Asia-Pacific customers in regulated markets requiring strict documentation and process control.

    1. Pharmaceutical API Synthesis – Antihistamine Production

    Major pharmaceutical producers employ this acid in the manufacture of certain first-generation antihistamines, especially those derived from diphenylmethane structures. The compound serves as a key carboxylic acid building block during the Friedel-Crafts acylation step, where it introduces the isopropyl-phenylacetyl moiety to the core structure. Downstream synthesis requires GMP conditions, in-process HPLC checks, and rigorous isolation of the acid chloride or the amide intermediate before progressing to API crystallization and purification.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP Annex 8 for Starting Materials
    • USP–NF and European Pharmacopoeia monograph requirements
    • Regulatory filings: DMF (Drug Master File), ASMF (Active Substance Master File)

    Typical usage ratio

    • 0.90–1.10 molar equivalents relative to the amine base; adjustment according to batch scale and yield requirements

    Downstream process integration

    • Acylation agent introduced post-amine synthesis, followed by chlorination and amidation steps toward API core formation
    • Solvent and reagent recovery setup to minimize contamination in multi-step synthesis

    Final product types

    • Antihistamine bulk APIs (e.g., Mequitazine, related phenothiazines)
    • Sterile active ingredient powder
    • Film-coated antihistamine tablets
    • Oral syrup formulations

    2. Fragrance and Aroma Chemical Manufacturing

    Fragrance ingredient plants use this acid to synthesize musky and woody aromatic compounds, particularly those for fine perfumes and high-end personal care. The material acts as an acyl donor in esterification or alcohol-protection routes. Process engineers optimize reaction conditions under REACH and IFRA guidelines, often carrying out continuous distillation to yield high-purity esters or alcohols for blending into concentrated fragrance bases.

    Industry compliance standards

    • REACH (EC No 1907/2006) Registration and Safety Assessment
    • IFRA Standards for Fragrance Material Purity and Allergen Control
    • ISO 9001:2015 for Quality Management Systems
    • GMP for Cosmetic Ingredients (ISO 22716)

    Typical usage ratio

    • 5–15% by weight in synthetic aroma chemical reactions, typically adjusted according to target ester chain length or alcohol/acid reactant balance

    Downstream process integration

    • Esterification or alcohol condensation reactors fed batchwise or continuously
    • Use of in-line monitoring (GC-MS/GC-FID) to achieve required fragrance note and minimize byproducts

    Final product types

    • Fine fragrance bases for perfumes and eau de toilettes
    • Personal care fragrance blends (shampoos, lotions)
    • Specialty aroma chemicals (e.g., synthetic musks)
    • Functional perfumery ingredients for home care

    3. Agrochemical Synthesis – Herbicide Intermediates

    Agrochemical companies deploy this material as an intermediate to construct key side chains on certain selective herbicide molecules. During the industrial process, technicians couple the acid with heterocyclic core structures via acid chloride formation and subsequent amide linkage, adhering to strict control over residual solvents and isomeric content as outlined by international agrochemical approval authorities. The starting material’s purity and chiral integrity maintain the final herbicide’s crop selectivity and environmental safety profile.

    Industry compliance standards

    • FAO World Health Organization Pesticide Specifications
    • Chemical Data Reporting under TSCA (US Environmental Protection Agency)
    • OECD Principles of Good Laboratory Practice (GLP) for active substance synthesis
    • ISO 17025 Accredited Quality Control Testing

    Typical usage ratio

    • 0.75–1.25 equivalents per mole of principal heterocycle; ratio fine-tuned according to stereo-selectivity and yield

    Downstream process integration

    • Pre-coupling to key intermediates via acid chloride activation
    • Isolation and refining of herbicide precursor prior to formulation

    Final product types

    • Technical grade herbicide concentrates
    • Water-dispersible granules and suspensions
    • Pre-emergence crop protection blends
    • Herbicide-tolerant seed treatment agents

    4. Fine Chemical Intermediate for Custom Synthesis

    Custom synthesis providers and fine chemical integrators select this acid to build bespoke intermediates for specialty chemical pipelines, such as complex ligands, advanced materials, or development-stage drugs. Integration occurs at early steps, either through dicyclohexylcarbodiimide (DCC)-mediated coupling or acylation of N-protected amino compounds. Compliance focuses on controlling metallic and organic impurities and full traceability of the molecular origin, as required for high-purity and low-throughput production units commissioned for confidential customer projects.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Custom Synthesis
    • Customer-specific Supplier Qualification and Audit Protocols
    • FDA 21 CFR Part 211 Subpart D (if cGMP project)
    • SOCMA ChemStewards® for Industrial Chemical Producers

    Typical usage ratio

    • 0.85–1.00 equivalents or as specified by customer synthetic route; ratios determined by stoichiometric efficiency and impurity profile

    Downstream process integration

    • Deployed during coupling, condensation, or protection steps to construct target molecules
    • Additional purification by preparative HPLC or fractional crystallization matched to customer deliverable requirements

    Final product types

    • Specialty research intermediates
    • Custom-ordered ligands for catalysis
    • Building blocks for pilot-scale pharmaceutical candidates
    • Proprietary intermediates for development-stage agrochemicals
    Free Quote

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