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2-Acetylphenothiazine

    • Product Name 2-Acetylphenothiazine
    • Alias 2-Acetyl-10H-phenothiazine
    • Einecs 223-621-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    584200

    Cas Number 2571-06-8
    Molecular Formula C14H11NOS
    Molecular Weight 241.31
    Appearance Yellow solid
    Melting Point 148-151°C
    Solubility Slightly soluble in water
    Purity Typically >98%
    Smiles CC(=O)c1cc2N(c3ccccc3Sc2cc1)
    Storage Temperature Store at 2-8°C
    Pubchem Id 83315

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled "2-Acetylphenothiazine, 10g." Features hazard symbols, batch number, and manufacturer details.
    Shipping 2-Acetylphenothiazine is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with chemical safety regulations, including appropriate hazard labeling. It is transported as a non-dangerous good under standard shipping conditions, with prompt delivery ensured to maintain product integrity. Proper documentation accompanies each shipment for regulatory compliance and traceability.
    Storage 2-Acetylphenothiazine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from light and moisture. Store at room temperature and avoid excessive heat. Ensure the area is equipped with proper spill containment and that all personnel are trained in safe chemical handling procedures.
    Application of 2-Acetylphenothiazine

    Applications of 2-Acetylphenothiazine in Industrial Manufacturing

    As the direct manufacturer of 2-Acetylphenothiazine, we supply this specialty intermediate to several technical sectors. Our in-depth industry cooperation ensures strict quality controls and traceability from synthesis to shipment. The following downstream applications highlight proven manufacturing use-cases, each with precise integration techniques, industry compliance practices, and formulation expertise.

    1. Pharmaceutical Synthesis: Phenothiazine-Based APIs

    Major pharmaceutical firms employ 2-Acetylphenothiazine as a key building block during the synthesis of phenothiazine-derivative active pharmaceutical ingredients (APIs), such as antipsychotic medications and antihistamines. Batch production environments use it during designated intermediate stages, where the acetyl group provides targeted substitution on the phenothiazine backbone. Manufacturers carefully monitor the purity via HPLC and enforce limits on residual solvents and impurities in compliance with pharmacopeial standards. Scale-up protocols demand controlled reaction profiles for reliable downstream coupling or ring closure steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters: Residual Solvents & Impurities
    • European Pharmacopoeia (Ph. Eur.) monographs
    • Chemical Registration for API intermediates (China DMF, EU CEP)

    Typical usage ratio

    • 0.10–0.30 molar equivalents in stepwise synthesis, adjusted based on yield targets and required downstream functionality
    • Dosage determined by specific API structure and multi-step conversion yield analysis

    Downstream process integration

    • Fed into condensation or coupling reactions with halogenated benzene derivatives
    • Utilized during controlled acetylation or amidation stages in GMP reactor trains
    • Integrated within closed-system handling to manage off-gassing during acyl transfer

    Final product types

    • Antipsychotic agent APIs (e.g., acetophenothiazine, promazine derivatives)
    • Antihistamine molecule intermediates
    • Chemical reference standards for pharmaceutical quality control

    2. Agrochemical Intermediate Production

    Agricultural chemical manufacturers use this raw material as a core intermediate for synthesizing select phenothiazine-derived insecticidal and fungicidal agents. The acetyl functional group on the thiazine ring enhances the activity spectrum of the active ingredient, yielding crop protection molecules with improved resistance profile. Operators introduce it at fixed conversion ratios in pilot and commercial reactors, optimizing atmosphere and temperature to prevent decomposition and maximize downstream reaction yield.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agrochemical Manufacturing
    • REACH Regulation (EC) No 1907/2006 substance tracking and safety
    • Local environmental permitting for chemical processing waste

    Typical usage ratio

    • 2–5% by weight of the initial batch, varying with the design of the synthetic pathway and targeted purity
    • Reaction stoichiometry verified by titration in each process run

    Downstream process integration

    • Added during initial heterocycle assembly or late-stage acetyl functionalization
    • Used in closed reactor synthesis under inert gas to control exothermicity
    • Purified via solvent extraction prior to downstream chlorination or oxidation

    Final product types

    • Phenothiazine-derived insecticides
    • Fungicide precursors for seed treatment formulations
    • Analytical reference substances for batch traceability

    3. Dye and Pigment Intermediate Synthesis

    Manufacturers of specialty dyes and pigments rely on this compound to introduce acetyl-phenothiazine chromophores into colorant molecules used for technical textiles, printing inks, and specialty coatings. It serves as an intermediate for producing stable structures with tailored lightfastness and shade depth. Quality assurance laboratories continually test input material for color strength and trace contaminants to guarantee reliable dispersion performance in the customer’s final products.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemical inputs
    • ZDHC Manufacturing Restricted Substances List for dyes
    • EU Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
    • ISO 14001:2015 Environmental Management for dye houses

    Typical usage ratio

    • 0.5–3% by mass relative to the total dye batch
    • Adjusted to target chromophore density, dependent on the depth of shade and substrate

    Downstream process integration

    • Condensation reactions with diazonium salts for azo dye synthesis
    • Phase transfer catalysis for pigment preparation
    • Used before final sulfonation or carboxylation stage in disperse dye production

    Final product types

    • Technical textile dyes with acetyl-substituted thiazine rings
    • Specialty printing ink pigments
    • Stable dispersed pigments for plastics and coatings

    4. Photoinitiator and Photochemical Research Applications

    Manufacturers operating in advanced photoinitiator and photochemical research sectors utilize this compound for developing light-sensitive agents used in photographic plates, specialty imaging compounds, and technical photoresist formulations. Its phenothiazine core, modified with an acetyl group, enables custom absorption profiles and radical generation for exposure-driven polymerization. Downstream customers perform extensive spectral analysis and purity confirmation prior to integrating it into high-value batches, supporting both R&D and volume production.

    Industry compliance standards

    • ISO 3664:2009 for color and photometric properties in graphic technology
    • ISO 10993 for cytotoxicity (when used in medical imaging compounds)
    • ANSI IT2.39-1991 for photographic chemicals
    • Responsible Care® certification in advanced chemical R&D

    Typical usage ratio

    • 0.2–2% by weight in laboratory-scale formulations, refined by photoreactivity and spectral characteristics
    • Modifications based on polymer matrix and desired UV absorption band

    Downstream process integration

    • Chemical precursor in synthesis of custom photoinitiators for UV-curable applications
    • Fed into photoresist formulation as a spectral sensitizing agent
    • Employed in batch irradiation setups to characterize photochemical properties

    Final product types

    • Photoresist compounds for PCB and semiconductor etching
    • Photopolymer imaging plates for industrial printing
    • Light-activated compounds for technical R&D and analytical standardization
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