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4-Methyl-3-Penten-2-One

    • Product Name 4-Methyl-3-Penten-2-One
    • Alias mesityl oxide
    • Einecs 211-234-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    945995

    Cas Number 141-79-7
    Molecular Formula C6H10O
    Molecular Weight 98.15 g/mol
    Iupac Name 4-methylpent-3-en-2-one
    Synonyms Mesityl oxide
    Appearance Colorless to pale yellow liquid
    Boiling Point 130-132 °C
    Density 0.857 g/cm³ at 20 °C
    Melting Point -41 °C
    Flash Point 28 °C (closed cup)
    Solubility In Water Moderate (4.2 g/100 mL at 20 °C)
    Vapor Pressure 12 mmHg at 20 °C

    As an accredited 4-Methyl-3-Penten-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500 mL amber glass bottle, tightly sealed, labeled with hazard warnings for 4-Methyl-3-Penten-2-One, including concentration and safety symbols.
    Shipping 4-Methyl-3-Penten-2-One is shipped in tightly sealed containers made of compatible materials, typically glass or metal, to prevent leakage and contamination. Containers are labeled with hazard warnings, stored upright in cool, well-ventilated areas, and protected from ignition sources. Transport complies with local hazardous material regulations to ensure safe handling.
    Storage 4-Methyl-3-penten-2-one should be stored in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances like oxidizing agents. Keep the container tightly closed and properly labeled. Use corrosion-resistant containers and store away from flammable or combustible materials. Avoid exposure to moisture, and ensure proper grounding and bonding if stored in large quantities to prevent static discharge.
    Application of 4-Methyl-3-Penten-2-One

    Applications of 4-Methyl-3-Penten-2-One in Industrial Manufacturing

    We supply 4-Methyl-3-Penten-2-One to diverse downstream sectors. As the original manufacturer, we support precise process and quality demands at scale. Below, explore the key industrial applications, compliance protocols, processing stages, compounding ratios, and end-products involving this specialty intermediate.

    1. Agrochemical Intermediate Synthesis

    Major crop protection producers use 4-Methyl-3-Penten-2-One as a key intermediate in the synthesis of selective herbicides and insecticides. Its unsaturated ketone structure enables direct condensation and alkylation reactions for building complex active molecules with high stability in field conditions. Integration occurs in multi-step processes with stringent purity monitoring, especially for synthesis routes involving heterocyclic or aromatic coupling partners.

    Industry compliance standards

    • ISO 9001:2015 QMS for agricultural chemical manufacturing
    • FAO/WHO Technical Guidelines for Pesticide Specifications and Residues
    • REACH compliance for agricultural active ingredient supply
    • GHS labeling for agrochemical raw materials

    Typical usage ratio

    • 0.5 – 1.2 molar equivalents per batch, depending on target molecule and route
    • Adjustment based on conversion efficiency and downstream yield
    • Strict mass balance control in multi-stage reactors

    Downstream process integration

    • Condensation stage in heterocycle formation
    • Alkylation step as a ketone source in side-chain elongation
    • Purification and QA prior to formulation blenders or technical concentrate tanks

    Final product types

    • Phenoxy-alkyl herbicides
    • Pyridine or pyrazole insecticides
    • Custom crop protection actives

    2. Pharmaceutical Intermediate Manufacturing

    Leading pharmaceutical ingredient producers incorporate 4-Methyl-3-Penten-2-One in the production of APIs for antihistamines and antifungal agents. The molecule serves as a carbon backbone in key Grignard or Wittig reaction steps, with full traceability and batch validation. Operators monitor residual solvents and by-product profiles to meet stringent GMP and pharmacopeial standards.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • EU GMP Annex 8 (Intermediate Controls)
    • USP and EP monograph adherence for intermediates
    • FDA 21 CFR Part 210/211 for API manufacturing

    Typical usage ratio

    • 0.8 – 1.05 molar equivalents per key condensation/coupling step
    • Adjustments for chiral selectivity, impurity profile, and yield optimization

    Downstream process integration

    • Substrate for nucleophilic addition in API backbone assembly
    • Introduced in stepwise hydrogenation and refining sequences
    • Critical for validated cleaning and cross-contamination controls

    Final product types

    • Antihistamine intermediates (e.g. loratadine precursor)
    • Imidazole antifungal API precursors
    • Fine specialty pharmaceutical actives

    3. Flavors and Fragrance Precursors

    Specialty fragrance blenders and flavor ingredient plants utilize 4-Methyl-3-Penten-2-One as a starting building block for high-impact aroma chemicals. Its conjugated unsaturated ketone enables selective hydrogenation or addition reactions to yield functionalized cyclic or acyclic ketones deployed as flavor enhancers or perfumery notes. Finished batches require compliance with global food safety and cosmetic standards, demanding rigorous risk management in sourcing and process control.

    Industry compliance standards

    • IFRA Standards for Fragrance Compounds
    • FEMA GRAS (Generally Recognized as Safe) Status for Flavors
    • EU Regulation (EC) No 1334/2008 on Flavourings
    • US FDA 21 CFR Part 172 (Food Additives)

    Typical usage ratio

    • 0.2 – 0.7 molar equivalents per batch for selected aroma targets
    • Ratio determined by downstream reactivity and final odor strength

    Downstream process integration

    • Enters at initial carbonyl addition or cyclization steps
    • Key for hydrogenation/isomerization in aroma building
    • Batch returns evaluated for sensory and analytical compliance

    Final product types

    • Musk ketones and macrocyclic fragrance compounds
    • Ketone-based food flavors
    • Specialty high-value aroma bases

    4. Fine Chemicals and Specialty Polymers

    Producers of high-performance specialty polymers and resins use 4-Methyl-3-Penten-2-One to introduce controlled unsaturation and carbonyl functionality. This intermediate often acts as a co-monomer or reactive plasticizer in polymerization or Michael addition mechanisms, critical for adjusting glass transition temperature, solubility, or cross-linking density in the final material. End users monitor reaction kinetics and material compatibility to optimize finished product performance.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical & resin production
    • REACH Full Registration for high-volume chemical intermediates
    • ASTM D5630 (polymer additive analytics)
    • RoHS 3 for electronic component applications

    Typical usage ratio

    • 5 – 20% by weight of total monomer input for co-polymerization
    • Levels fine-tuned for elasticity or processability targets

    Downstream process integration

    • Dosed directly into bulk or solution polymerization reactors
    • Integrated at pre-polymer preparation or curing steps
    • Managed under continuous addition or batch mode

    Final product types

    • Specialty polyurethane foams
    • Modified acrylic resins
    • Elastomeric sealing compounds

    5. Electronic Chemical Formulations

    In the electronic materials sector, process formulators use 4-Methyl-3-Penten-2-One as a reactive solvent or intermediate for photoresist and etching chemical manufacture. Its selective reactivity profile allows controlled backbone modification and crosslinking under lithographic and patterning conditions. Electronic grade processing requires advanced filtration, trace impurity monitoring, and packaging protocols to prevent microcontamination and meet industry-specific analytical standards.

    Industry compliance standards

    • SEMI C1 and C93 for electronic chemical purity
    • IATF 16949 for supply chains in automotive electronics
    • ISO 14001 for environmental control in semiconductor plants
    • RoHS and REACH compliance for microelectronic systems

    Typical usage ratio

    • 1 – 5% by weight in formulated etching or photoresist products
    • Controlled based on desired solvent power or reactivity

    Downstream process integration

    • Mixed at solvent blending or monomer derivatization stages
    • Filtered and controlled for particle/anion content
    • Packaged in cleanroom conditions for fab consumption

    Final product types

    • Positive and negative photoresists
    • Microelectronic etching agents
    • Lithographic imaging substrates

    6. Industrial Coatings and Adhesive Additive Production

    Manufacturers of performance coatings and adhesives employ 4-Methyl-3-Penten-2-One as a reactive modifier to impart adhesion, flow, or cure enhancement. Its structure allows covalent integration during crosslinker synthesis or as a functional monomer in urethane/acrylic hybrid systems. Consistent dosing and mixing controls ensure the desired balance of flexibility, hardness, and chemical resistance in the finished formulas.

    Industry compliance standards

    • ASTM D7767-11 for chemical admixtures
    • ISO 12944 for anticorrosive industrial coatings
    • EN 923 for adhesives raw materials
    • REACH and SVHC screening for workplace safety

    Typical usage ratio

    • 2 – 10% by weight relative to total polymer or crosslinker phase
    • Adjusted for target viscosity, bond strength, and application climate

    Downstream process integration

    • Reactive blending in prepolymer or hardener kettles
    • Introduced prior to filler, pigment, or catalyst addition
    • Subject to in-house cure profile and VOC emission testing

    Final product types

    • Epoxy and polyurethane industrial coatings
    • Structural construction adhesives
    • Flexible automotive sealants
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