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2-Methyl-4-Propyl-1,3-Oxathiane

    • Product Name 2-Methyl-4-Propyl-1,3-Oxathiane
    • Alias 2-Methyl-4-n-propyl-1,3-oxathiane
    • Einecs 441-420-8
    • 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

    861691

    Chemicalname 2-Methyl-4-Propyl-1,3-Oxathiane
    Molecularformula C8H16OS
    Molecularweight 160.28 g/mol
    Casnumber 55290-63-2
    Iupacname 2-methyl-4-propyl-1,3-oxathiane
    Pubchemcid 15536651
    Appearance Colorless liquid
    Smiles CCC[C@H]1COC(S1)C
    Inchi InChI=1S/C8H16OS/c1-3-4-7-5-10-8(2)6-9-7/h7-8H,3-6H2,1-2H3
    Synonyms 2-methyl-4-propyl-oxathiane

    As an accredited 2-Methyl-4-Propyl-1,3-Oxathiane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL amber glass bottle with airtight screw cap, labeled with chemical name, hazard warnings, and batch number for 2-Methyl-4-Propyl-1,3-Oxathiane.
    Shipping 2-Methyl-4-Propyl-1,3-Oxathiane should be shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Use appropriate hazard labeling and cushioning to prevent leaks. Ship via a carrier authorized for chemical transport, complying with all relevant regulations regarding flammable or hazardous substances. Include safety data sheets (SDS) with the shipment.
    Storage 2-Methyl-4-Propyl-1,3-Oxathiane should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and use secondary containment to prevent leaks or spills. Store in a designated chemical storage area compliant with local regulations.
    Application of 2-Methyl-4-Propyl-1,3-Oxathiane

    Applications of 2-Methyl-4-Propyl-1,3-Oxathiane in Industrial Manufacturing

    2-Methyl-4-Propyl-1,3-Oxathiane has developed into a valued specialty intermediate in several tightly regulated downstream manufacturing sectors. As the original producer and direct technical partner to industrial users, we detail the following key application segments where this molecule plays a functional role, with each scenario specified by its sector’s compliance landscape, controlled use rates, placement within proprietary process steps, and the profile of finished goods delivered to market.

    1. Scent Modulation in Fine Fragrance Compounding

    Major fragrance houses rely on this specialty oxathiane as a unique modifier to impart long-lasting, subtly fruity and sulfuric notes unattainable from standard alicyclics. Its structure allows for controlled release and stability in complex perfumery bases, expanding olfactory palettes for market-differentiating perfumes.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards and Amendments
    • EU REACH Annex XVII for fragrance ingredients
    • EU CLP Regulation (EC) No 1272/2008 labeling requirements
    • US Food and Drug Administration (FDA) 21 CFR 172.515 (Indirect Flavoring Agents)

    Typical usage ratio

    • 0.005–0.05% in finished perfume concentrate, with upper limits tailored based on olfactory impact studies and IFRA dermal thresholds

    Downstream process integration

    • Added during the base note formulation phase, post-head and heart blend assembly, under inert gas and cooled conditions to preserve stability; mixed into premium absolute blends using jacketed stainless reactors

    Final product types

    • Eau de parfum
    • Luxe parfum extracts
    • High-end scented personal care bases (select deodorants and lotions)
    • Room scenting concentrates for diffusers

    2. Sulfur-Based Flavor Additive in Savory Food Ingredient Manufacturing

    Industrial flavor formulators use this compound as a specialty sulfur note for authentic, detectable nuances in processed foods such as savory snacks, broths, and seasoning blends. Its molecular profile provides an intense flavor boost at micro-dose levels, with controlled reactivity during cooking and extrusion operations.

    Industry compliance standards

    • US FDA 21 CFR 172.515 for synthetic flavoring substances
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients
    • Food Chemicals Codex (FCC) 13th Edition
    • ISO 22000 food safety management systems

    Typical usage ratio

    • 0.0005–0.003% by weight in finished food products; precise dosage defined via flavor sensory panel calibration and matrix interaction studies

    Downstream process integration

    • Injected into the blender with liquid or pre-dispersed with solvents during flavor concentrate formulation; for extruded snacks, dosed immediately before extrusion under closed feed hoppers to minimize volatilization

    Final product types

    • Potato and wheat-based savory snacks
    • Dehydrated instant soup bases
    • Stock and bouillon cubes
    • Meat-flavored seasoning premixes

    3. Aromatic Intermediate in Synthesis of Pharmaceutical Actives

    In regulated pharma manufacturing, this oxathiane acts as an intermediate in multi-step syntheses for certain APIs, specifically those where a sulfur-containing heterocycle is a key motif or precursor. Its purity profile, handled under GMP, supports consistent conversion rates and downstream impurity management.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) specifications for pharmaceutical intermediates
    • US Pharmacopeia (USP) relevant general chapters
    • 21 CFR Parts 210 & 211 Current GMP for Finished Pharmaceuticals

    Typical usage ratio

    • 0.3–2.0 molar equivalents as a core reactant or ring-forming agent, adjusted by batch size and the purity requirements of subsequent intermediates

    Downstream process integration

    • Charged during protected heterocycle coupling or cyclization stages, typically under controlled temperature (<60°C) and inert atmosphere in glass-lined reactors; sampling at this stage ensures target conversion ratios before quench and extraction

    Final product types

    • Pharmaceutical intermediates containing thioether or oxathiane scaffolds
    • Small-molecule APIs with sulfur bridgehead motifs
    • Building blocks for cardiovascular drug candidates
    • Precursors for central nervous system (CNS) active agents

    4. Performance Modifier in Polymeric Coating Materials for Industrial Metalworking

    Formulators in industrial coatings incorporate this molecule as a performance enhancer to impart hydrophobicity, improved anti-corrosive properties, and flexibility in alkyd and polyurethane-based metal protective coatings. Its sulfur atom aids cross-linking with metal substrates, while the alkyl chain tunes film-forming characteristics.

    Industry compliance standards

    • ISO 12944-6 (Corrosion protection of steel structures by protective paint systems — Laboratory performance test methods)
    • ASTM D3359 (Adhesion by Tape Test)
    • REACH registration with use-specific safety data
    • RoHS Directive 2011/65/EU (if applied in electronic hardware finishes)

    Typical usage ratio

    • 0.1–0.5% by total resin solids, optimized through lab accelerated weathering tests and salt spray exposure benchmarks

    Downstream process integration

    • Added during the resin modification stage, pre-pigment milling, ensuring full dissolution and uniform distribution before solvent thinning; inline dosing systems meter the additive during continuous batch production

    Final product types

    • Anti-corrosive alkyd and polyurethane coatings
    • Heavy-duty industrial steel primers
    • Protective coatings for marine and oilfield equipment
    • Specialty coatings for metal enclosures in electrical infrastructure

    5. Specialty Odorant in Gas Leak Detection Formulations

    Utility product blenders value this compound for manufacturing sulfur-based odorants, enabling detection of flammable gases by smell at trace levels. Its volatility and distinct odor profile provide reliable, detectable signatures in gas blends supplied for public and industrial use.

    Industry compliance standards

    • EN ISO 13734:2013 (Odorization of natural gas)
    • U.S. DOT Pipeline Safety Regulations 49 CFR Part 192, Subpart L
    • National Fire Protection Association (NFPA) 58 and NFPA 54
    • EPA Clean Air Act compliance for volatile emissions

    Typical usage ratio

    • 0.01–0.045 ppm in final gas mixtures, calibrated to local regulatory odorization thresholds and matrix gas composition

    Downstream process integration

    • Injected into bulk pressurized gas streams via automated odorant dosing skids prior to cylinder filling or pipeline transfer; continuous online monitoring ensures strict dosage accuracy for trace delivery

    Final product types

    • Domestic and industrial natural gas supplies
    • Bottled LPG (liquefied petroleum gas) blends
    • Utility gas odorant concentrates
    • Trace addition for synthetic biogas distribution
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