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4'-(Tert-Butyl)Acetanilide

    • Product Name 4'-(Tert-Butyl)Acetanilide
    • Alias N-(4-(tert-butyl)phenyl)acetamide
    • Einecs 282-536-0
    • 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

    347501

    Chemical Name 4'-(Tert-Butyl)Acetanilide
    Molecular Formula C12H17NO
    Cas Number 34562-31-7
    Appearance White to off-white solid
    Melting Point 142-145°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Synonyms N-(4-tert-Butylphenyl)acetamide
    Storage Conditions Store at room temperature, away from light and moisture
    Smiles CC(C)(C)c1ccc(NC(=O)C)cc1
    Inchi InChI=1S/C12H17NO/c1-9(14)13-10-6-8-11(7-10)12(2,3)4/h6-8H,1-4H3,(H,13,14)
    Usage Intermediate for organic synthesis

    As an accredited 4'-(Tert-Butyl)Acetanilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package features a white, tightly sealed HDPE bottle, labeled with chemical name, hazard symbols, lot number, and handling instructions.
    Shipping 4'-(Tert-Butyl)Acetanilide is shipped in tightly sealed containers to prevent contamination and moisture exposure. It is typically packed in compliance with chemical safety regulations, labeled with appropriate hazard information, and stored at room temperature. Shipping follows all local and international transport guidelines for non-hazardous laboratory chemicals.
    Storage 4'-(Tert-Butyl)acetanilide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature and ensure proper labeling. Use appropriate safety precautions and avoid contact with skin and eyes during handling.
    Application of 4'-(Tert-Butyl)Acetanilide

    Applications of 4'-(Tert-Butyl)Acetanilide in Industrial Manufacturing

    As an established manufacturer of 4'-(Tert-Butyl)Acetanilide, we supply high-purity material to well-defined industrial sectors where its functional properties directly enhance specific production processes. The following application scenarios reflect genuine, large-scale use cases in chemical synthesis and industrial processing where this raw material has proven value in downstream workflows. Each application is presented with explicit details on compliance, formulation ratios, integration points, and typical finished goods.

    1. Synthesis of Selective Herbicide Intermediates

    This chemical is widely adopted in the agrochemical sector, especially as an essential building block in the multi-step synthesis of certain acetanilide-class selective herbicide intermediates, where controlled substitution patterns influence herbicidal activity and environmental profile. Its inclusion improves physicochemical properties for further derivatization and the design of advanced crop protection compounds.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Ingredients
    • REACH Registration (EC 1907/2006) compliance for intermediates
    • ISO 9001:2015 Quality Management System for chemical manufacturing
    • GHS Safety and Labeling (UN Globally Harmonized System)

    Typical usage ratio

    • Used at 0.8–1.2 mole equivalents relative to coupling substrates, based on targeted intermediate yield and desired substitution pattern optimization during syntheses

    Downstream process integration

    • Charged at the key aromatic substitution or amidation step in batch or continuous-flow synthesis lines; directly reacts with chlorinated precursors, followed by downstream purification and crystallization before formulation of technical herbicide

    Final product types

    • Active ingredient intermediates for acetanilide-type selective herbicides (e.g., butachlor, pretilachlor families)
    • Pre-formulated technical concentrates for subsequent formulation into finished crop protection agents

    2. Formulation of Specialty Industrial Dye Precursors

    In dye manufacturing, 4'-(Tert-Butyl)Acetanilide serves as a protected aromatic amine source for the synthesis of specific azo and anthraquinone dye precursors, where steric blocking and electron-donating properties fine-tune colorfastness and solubility. The material’s compatibility with diazotization and coupling stages supports development of colorants for high-performance textiles and plastics.

    Industry compliance standards

    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) for input chemicals
    • Oeko-Tex Standard 100 banned amines compliance for dyestuff precursors
    • EU REACH Annex XVII restrictions for aromatic amines in azo dyes
    • ISO 14001 Environmental Management for chemical dye synthesis

    Typical usage ratio

    • Entrained at 5–15% by weight relative to the main aromatic amine component in multi-component coupling mixtures, with adjustments depending on target chromophore and hue

    Downstream process integration

    • Introduced in the synthetic pathway following diazotization, where it couples to aromatic or heterocyclic partners to build colorant intermediates prior to final sulfonation, isolation, and standardization steps

    Final product types

    • Azo dye intermediates with improved lightfastness for polyester and nylon applications
    • Anthraquinone dye derivatives for high-performance plastics coloring
    • Specialty colorants for technical fibers in automotive and upholstery textiles

    3. Fragrance and Aroma Intermediate Manufacturing

    This compound functions as a structurally defined masking agent and intermediate in the synthesis of fragrance chemicals, where its tert-butyl group imparts both volatility modulation and olfactory profile tuning. It supports manufacturing of musk analogs and certain aroma chemicals used in large-scale home and personal care product formulation.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Guidelines
    • EU Cosmetic Regulation (EC) No 1223/2009 for raw materials in fragrances
    • Good Manufacturing Practice (GMP), ISO 22716 certification for fragrance intermediates
    • US TSCA chemical inventory compliance for fragrance precursors

    Typical usage ratio

    • Included at 1–3% by weight in fragrance precursor synthesis batches, as determined by final aroma intensity and fixative requirements of the olfactory composition

    Downstream process integration

    • Added to the alkylation or acylation stage, followed by cyclization or oxidation to build the target musk or aroma ester, with continuous in-process gas chromatography for quality control before downstream compounding

    Final product types

    • Musk fragrance intermediates for detergents and cleaning products
    • Aroma compound building blocks for fine fragrance oils
    • Technical aroma intermediates for air care, candles, and personal care products

    4. Polymer Additive and Stabilizer Synthesis

    As a monoprotic acetanilide derivative with tert-butyl substitution, this material is utilized in the manufacture of specialized stabilizer and UV absorber intermediates for plastics, where its chemical structure provides steric bulk and improved process stability. Downstream producers employ these properties to enhance the service life and appearance of finished polyolefin and engineering resin products.

    Industry compliance standards

    • UL 94 flammability testing of plastic additives
    • FDA 21 CFR 177.1520 for polymer additive safety in food contact plastics (where applicable)
    • EU Regulation (EC) No 1907/2006 (REACH) registration for polymer ingredients
    • ISO 9001:2015 for additive manufacturing processes

    Typical usage ratio

    • Formulated at 0.1–0.5% total polymer base weight, with specific dosage tailored to target UV stability, thermal color resistance, and regulatory migration limits for each resin system

    Downstream process integration

    • Fed as an intermediate in the condensation or transesterification reactors to generate stabilizer or UV absorber molecules, which are then incorporated via compounding into masterbatches or directly into resin lines

    Final product types

    • Stabilizer masterbatches for polyethylene and polypropylene films
    • UV absorber concentrates for automotive interior plastics
    • Technical resin additives for polycarbonate, ABS, and engineering thermoplastics
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