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3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile

    • Product Name 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile
    • Alias BMTA
    • Einecs 407-060-1
    • 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

    960809

    Product Name 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile
    Cas Number 1337532-29-4
    Molecular Formula C13H10F3NOS2
    Molecular Weight 317.35
    Appearance Yellow solid
    Purity ≥98%
    Melting Point 101-104°C
    Solubility Soluble in DMSO, DMF
    Storage Temperature 2-8°C
    Smiles CCS(=C(C#N)C(=O)C1=CC(=CC=C1)C(F)(F)F)SC
    Inchi InChI=1S/C13H10F3NOS2/c1-19-13(20-2)11(7-17)12(18)8-3-4-10(5-6-8)9(14,15)16/h3-6H,1-2H3

    As an accredited 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle with a secure cap, featuring a clear chemical label and appropriate hazard warnings.
    Shipping The chemical 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile should be shipped in tightly sealed, chemical-resistant containers, under cool, dry conditions. Package and label per hazardous materials regulations, avoiding exposure to heat, moisture, and incompatible substances. Handle with care and ensure all documentation complies with relevant local and international transport guidelines.
    Storage Store **3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Properly label storage containers and ensure they remain protected from moisture and physical damage. Use appropriate personal protective equipment when handling.
    Application of 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile

    Applications of 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile in Industrial Manufacturing

    We supply 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile as a specialty raw material for advanced chemical synthesis. The following sectors represent current routes of substantial industrial consumption.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies and CMOs apply this compound as a protected building block for synthesizing selective kinase inhibitors and receptor modulators. Its unique structure enables regioselective coupling in step-growth routes, supporting assembly of advanced drug candidates in oncology and CNS research pipelines. Controlled addition into the reaction batch reduces side-product formation and allows precise downstream purification. Regulatory review demands consistent batch traceability and impurity documentation across all synthesis stages.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR 210–211 (FDA cGMP regulations)
    • USP/Ph. Eur. General Chapters on Residual Solvents and Organic Impurities

    Typical usage ratio

    • 0.05–0.15 moles per mole of target drug scaffold; ratio depends on yield optimization and impurity control in route design

    Downstream process integration

    • Fed into protected functional group introduction, followed by cyclization and deprotection steps in small-molecule synthesis

    Final product types

    • Active Pharmaceutical Ingredients (API) for investigational drugs and generics
    • Key pharmaceutical intermediates for contract manufacturing

    2. Agrochemical Synthesis (Herbicide and Fungicide Precursors)

    Leading crop science firms incorporate this compound into formulations of advanced herbicide and fungicide precursors, targeting more selective weed or pathogen control. Because it can introduce both methylthio and trifluoromethyl moieties, formulators enhance bioactivity while reducing environmental persistence. Usage requires compliance with registration dossiers and controlled toxicological evaluation.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals
    • FAO and WHO specifications for pesticide manufacturing
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.1–1.0% w/w in active ingredient manufacturing, adjusted for molecular equivalency in multi-step reactions

    Downstream process integration

    • Dosed into Grignard or cross-coupling reactions, followed by oxidation or functional group modification for staple agrochem actives

    Final product types

    • Herbicide actives (e.g., protoporphyrinogen oxidase inhibitors)
    • Fungicide precursors for cereal or vegetable crop protection

    3. Specialty Dye and Pigment Manufacturing

    Industrial colorant manufacturers use this chemical as a functionalized intermediate in high-storage-stability dyes. Its structural motifs facilitate the introduction of electron-withdrawing groups, thereby raising colorfastness and resistance to photobleaching. Integration into pigment blending occurs at the pre-condensation stage, supporting production of high-performance coatings and textiles.

    Industry compliance standards

    • EN 71-3: Migration of Certain Elements (dyes for toys and textiles)
    • ISO 105-A02: Textiles—Tests for color fastness
    • REACH (EC 1907/2006) registration for specialty chemicals

    Typical usage ratio

    • 0.5–5.0% by total mass of pigment blend; adjusted per required chromatic intensity and thermal stability

    Downstream process integration

    • Added to azo or anthraquinone dye syntheses, prior to final coupling and filtration in the pigment workflow

    Final product types

    • UV-resistant polymer colorants for automotive parts and plastics
    • Industrial textile dyes with anti-fading properties

    4. Advanced Organic Electronics Material Fabrication

    Producers of organic semiconductors and optoelectronic components employ this molecule as a key monomer for developing high-mobility molecular crystals and charge-transfer complexes. The presence of trifluoromethyl and methylthio groups allows precise tuning of HOMO-LUMO energy levels to optimize device stability and efficiency. Manufacturers introduce this raw material during the precursor-polymerization or surface functionalization stage, ensuring integration into downstream photolithography and device assembly.

    Industry compliance standards

    • ISO/TS 80004: Nanotechnologies—Vocabulary
    • RoHS Directive (2011/65/EU) for restricted substances in electronics
    • IEC 60068: Environmental Testing for electronics

    Typical usage ratio

    • 1–10 mol% of total monomer feedstock in polymeric semiconductor synthesis; ratio modified to balance charge mobility and morphology

    Downstream process integration

    • Mixed with functionalized aryl compounds in solution-phase polymerization, followed by deposition onto substrates for device fabrication

    Final product types

    • Organic Field-Effect Transistors (OFETs)
    • Flexible photovoltaic panels
    • OLED display components

    5. Custom Fine Chemical Synthesis for Contract Manufacturing

    Custom synthesis providers and toll manufacturers source this specialty molecule for producing bespoke fine chemicals, such as specialty reagents and structure-activity probes. The unique electron-donating and withdrawing functionalities enable custom reactivity patterns in multi-step organic transformations. Process engineers control process sequencing to maximize yield and reduce batch variability, meeting project-specific documentation and audit requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Responsible Care Management Framework (International Council of Chemical Associations)
    • SOCMA ChemStewards for batch record-keeping and EHS compliance

    Typical usage ratio

    • Determined per customer process; often 0.02–0.5 molar equivalents relative to main target compound

    Downstream process integration

    • Delivered as an input for custom batch reactions or as a functional handle for library generation in medicinal chemistry projects

    Final product types

    • Structure-activity relationship (SAR) probes
    • Custom-modified detection reagents for research institutes and analytical labs
    Free Quote

    Competitive 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile prices that fit your budget—flexible terms and customized quotes for every order.

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