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2-N-Propylthiophene

    • Product Name 2-N-Propylthiophene
    • Alias 2-Propylthiophene
    • Einecs 246-404-9
    • 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

    381021

    Cas Number 26419-66-5
    Molecular Formula C7H10S
    Molecular Weight 126.22
    Iupac Name 2-propylthiophene
    Appearance Colorless to pale yellow liquid
    Boiling Point 161-163°C
    Melting Point -65°C
    Density 0.939 g/cm³ at 25°C
    Flash Point 44°C
    Refractive Index 1.5100 at 20°C

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

    Packing & Storage
    Packing 2-N-Propylthiophene is packaged in a 100 mL amber glass bottle, sealed, with a tamper-evident cap and labeled with safety data.
    Shipping 2-N-Propylthiophene is typically shipped in tightly sealed containers made of compatible materials such as glass or high-density polyethylene. It should be stored and transported in a cool, well-ventilated area, away from sources of ignition. Labeling must comply with local chemical regulations, and handling should minimize exposure and prevent leaks or spills.
    Storage 2-N-Propylthiophene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep away from direct sunlight and moisture. Store in a flammable liquid storage cabinet if available, and ensure appropriate labeling and secondary containment to prevent spills or leaks.
    Application of 2-N-Propylthiophene

    Applications of 2-N-Propylthiophene in Industrial Manufacturing

    We supply 2-N-Propylthiophene to industrial producers requiring a high-purity heterocycle for advanced synthesis in specialized sectors. Derived through controlled thiophene ring alkylation, this compound meets strict benchmarks for critical downstream integrations, supporting complex chemical development across defined markets. Below, we present certified application scenarios reflecting where end customers incorporate this material within compliant, high-value manufacturing processes.

    1. Pharmaceutical Intermediate Synthesis

    Leading pharmaceutical synthesis units incorporate 2-N-Propylthiophene in the construction of active pharmaceutical ingredient (API) scaffolds, especially those targeting novel heterocyclic drug candidates. Its unique asymmetric ring structure enables selective functionalization on scalable routes, frequently during the formation of thiophene-linked therapeutic backbones or as a pivotal building block in anti-inflammatory or oncologic drug research. Our material maintains batch traceability from incoming QC through final custom synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) when used in API precursors
    • European Pharmacopoeia (Ph. Eur.) monographs as applicable
    • REACH Annexes related to API intermediates

    Typical usage ratio

    • Employed as a core structure, typically ranging from 0.8%–6% by weight in total batch, depending on the target molecule’s synthetic step and yield requirements; optimization based on reaction scale-up and downstream purification efficiency.

    Downstream process integration

    • Introduced during the initial heterocycle construction or functional group introduction stage, entering the reaction vessel immediately after base ring assembly but before further derivatization or cross-coupling steps. Controlled addition allows for subsequent catalytic modification in closed-system reactors used for pharmaceutical synthesis.

    Final product types

    • Small-molecule hematology agents
    • Investigational oncology drugs utilizing substituted thiophenes
    • Anti-inflammatory compound libraries
    • Pharma-grade thiophene-based intermediates for contract synthesis

    2. Flavors and Fragrance Ingredient Synthesis

    Specialty fine chemical manufacturers use 2-N-Propylthiophene to create high-impact aroma compounds with a characteristic sulfur note, contributing to pyrazinic, roasted, or truffle-like profiles. Its functionalization in controlled aromatic substitution or oxidation/reduction steps yields flavor molecules that meet global food safety certification for further compounding into commercial fragrances or flavoring bases, such as complex savory blends or high-grade truffle aroma analogs.

    Industry compliance standards

    • US FDA 21 CFR § 172.515 (Synthetic flavoring substances and adjuvants, for non-direct food use in fragrance ingredients)
    • IFRA Standards (International Fragrance Association) for restricted or permitted usage
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients
    • ISO 9235 definition for natural and synthetic aroma chemicals

    Typical usage ratio

    • 0.03%–0.15% in intermediate synthesis blends, with final flavor compound concentrations determined by finished application and end-user organoleptic panels; adjustment strictly tested for sensory threshold and compliance with food additive regulations.

    Downstream process integration

    • Integrated as a starting heterocyclic component within controlled batch reactors following precursor blending. Afterward, it undergoes sulfur marshaling or catalytic partial oxidation before extraction and further refinement for high-purity flavour deliverables.

    Final product types

    • Truffle-flavor additives for gourmet food products
    • Sulfur-rich aromatic base notes in complex fragrance compositions
    • Meat mimic and savory enhancers for processed foods
    • Luxury fine perfume bases requiring trace-level heterocycles

    3. Advanced OLED and Organic Electronics Manufacturing

    Producers of organic electronic materials employ 2-N-Propylthiophene as a high-purity starting monomer for synthesizing polythiophene derivatives used as semiconducting layers in organic light-emitting diodes (OLEDs) and other printed electronics. Its well-defined alkyl substitution pattern enables precise tuning of electronic properties and film morphology. Strict electronics-grade specifications govern each lot from initial monomerization through final layer deposition, assuring stability and consistency for downstream device fabrication.

    Industry compliance standards

    • IEC 62341 for OLED device performance requirements
    • RoHS EU Directive 2011/65/EU, controlling use of hazardous substances in electronics
    • ISO 9001 Quality Management System for material traceability
    • IEC 60068 for environmental testing of electronic components

    Typical usage ratio

    • 0.5%–3% relative to other thiophene monomers in copolymerization recipes for semiconducting polymer formation; concentration tailored to target bandgap and layer thickness in device design.

    Downstream process integration

    • Fed into controlled Suzuki, Kumada, or Stille coupling protocols to generate π-conjugated polythiophenes with carefully regulated chain length and dispersity. Material typically enters after initial halogenation and prior to catalyst introduction for step-growth polymerization.

    Final product types

    • OLED emitter and transport layers for display technologies
    • Printed organic photovoltaic cells
    • Flexible circuit sensor modules using polythiophene derivatives
    • Organic field-effect transistor (OFET) substrate coatings

    4. Agrochemical Intermediate Manufacturing

    Agrochemical processors use 2-N-Propylthiophene as a core structural motif for designing new-generation crop protection agents, often as a precursor in the synthesis of thiophene-substituted fungicides or insecticides. The compound’s chain configuration supports functionalization in sulfonylation, chlorination, or acylation routes. Industrial-scale deployment adheres to regulated procedures, from closed-system weighing to waste capture, in line with agricultural chemical laws and end-product registration protocols.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • US EPA toxicological and residue limit requirements for pesticide intermediates
    • ISO 9001 for quality assurance and environmental, health, and safety (EHS) protocols

    Typical usage ratio

    • Usually 0.6%–5% as an intermediate reacting component, with specific loading determined by downstream target molecule and process yield optimization; ratio modulated through kinetic studies and reaction scale calculations.

    Downstream process integration

    • Reaction begins with batch introduction into a jacketed vessel equipped for inert atmosphere operations, proceeding to functionalization via selective oxidation, sulfonation, or halogen substitution pathways, prior to final purification and solid formulation.

    Final product types

    • Fungicidal active ingredients based on thiophene derivatives
    • Systemic insecticide intermediates
    • Seed treatment precursor blends
    • Stabilized agricultural adjuvant formulations
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    Certification & Compliance
    More Introduction

    Understanding 2-N-Propylthiophene: Experience from the Manufacturing Floor

    Working with 2-N-Propylthiophene: What It Is and How It Performs in Real Operations

    Over the years at our chemical plant, we’ve come to know every wrinkle of 2-N-Propylthiophene. This compound stands out among substituted thiophenes, both for the characteristics it brings to advanced synthesis and for its consistent reliability in long production runs. Our daily process has shaped not just how we think about the product but how we engineer it to address the needs chemists and researchers encounter on their end.

    Producing with Purity and Precision

    Getting to know 2-N-Propylthiophene starts with the basics: clear colorless liquid, subtle sulfur odor, with a molecular formula of C7H10S. Quality isn’t a point on a specification sheet for us; it’s a matter of outcome and repeatability at scale. Most customers ask for ≥99% purity, and our processes—distillation under inert gas, leak-checked transfer lines, high-vacuum drying, and in-line GC sampling—hit that target batch after batch. After hundreds of cycles, we’ve found that patient control of reaction atmospheres preserves structure and shines in end-use performance, especially where sulfur stability matters.

    Application Insights: Synthetics, Electronics, and Pharmaceuticals

    Lab teams have walked the floors and brought us field data showing just how 2-N-Propylthiophene holds up under various conditions. Synthetics houses rely on it as a starting material for further transformations—uregular alkylations, heterocyclic fusions, and cross-couplings. Some of the biggest boosts come from its core role as a building block in high-performance organic materials. Thin-film transistors and flexible display coatings need high-purity thiophenes with minimal trace byproducts—the sort of thing we monitor chromatographically before the tankers leave the site. Pharmaceuticals look to this molecule for its adjustable reactivity; small tweaks around the thiophene ring open doors to analogs that simply can’t be reached with either the bare or overly substituted rings.

    Why the N-Propyl Group Changes the Game

    Across our process development team, one thing became clear. Not all thiophenes deliver the same in target applications. Where many stick with methyl or ethyl at the 2-position, our trials pointed to a performance edge with the propyl variant: a higher boiling point, smoother distillation curves, and noticeably reduced volatility losses. In packed-bed reactor setups, that means less vapor-phase loss and a tighter mass balance every time.

    We ran parallel tests comparing 2-N-Propylthiophene to its shorter-chain cousins. The conclusion matched customer feedback: side reactions drop, especially in metal-catalyzed couplings. Propyl gives a slightly bulkier profile on the ring, slowing down undesired overreaction and providing a steadier pace for stepwise syntheses. When electronics clients trial new semiconducting polymers, they appreciate the consistent chain extension and improved solubility compared to methyl- and ethylthiophene analogs.

    Specifying the Product: Real-World Characteristics

    What matters in the field comes down to two things: purity and reproducibility. Our team’s standard cut on 2-N-Propylthiophene passes GC and NMR checks, with sulfur and hydrocarbon impurities held well below application thresholds. Water content gets tracked and minimized using molecular sieves; we know that even a fraction of a percent will show up downstream in performance testing. In microelectronic applications, residual acidity must be managed, so there’s a focus on careful storage and cleanroom transfer.

    Hazard profile deserves respect. Thiophene derivatives, including the n-propyl version, call for proper fume handling thanks to that sharp sulfur note. Over time, we’ve optimized bottle closure systems and packing for smooth downstream transfer. Techs prepping pilot-scale reactions regularly talk about clear pour consistency and fast layering, noting the difference from denser, stickier analogs.

    Problems That Matter: From Shelf Stability to Scale-Up

    The gap between small-bottle batches and bulk drum handling brings its own risks and headaches. A product like 2-N-Propylthiophene, with reasonable vapor pressure and sensitivity to oxidation, won’t forgive leaks or lax storage. Early on, we identified incidents where ambient oxygen or stray water vapor would cloud the clarity or dull reactivity. After listening to the shop floor, we switched to nitrogen-purged containers, invested in vacuum-sealed transfer systems, and cut nearly all spoilage complaints.

    Another pain point came to light at the bottling line: rate of demand swings. Unlike some mass-volume solvents, 2-N-Propylthiophene goes to specialist buyers who place irregular, high-quality orders on short notice. Our warehouse team, led by veteran handlers, designed a just-in-time holding protocol—shorter shelf times, real-time status updates to production, and small pilot lots to pre-check the next drum’s purity before packing.

    Supported Applications: Stories from Our Customers

    Research chemists often circle back with updates on pilot projects. In one batch synthesis of new conjugated polymers for solar cell applications, a major difference emerged between propyl and ethyl thiophenes. Charge mobility measurements jumped by over 15%. This boost helps explain why the propyl derivative gets top billing in advanced electronics and optoelectronics applications.

    Colleagues in pharmaceutical manufacturing pointed out a secondary benefit: improved intermediate yields in Suzuki and Stille coupling reactions. The longer side chain resists unwanted backbone rearrangements, and overall throughput climbs as a result. A recurring insight from field reports has been enhanced separation during product washing; the slightly heavier propyl group makes for clearer phases compared to lighter thiophene analogs.

    Market Dynamics, Regulatory Lessons, and Quality Management

    A major shift in the industry stems from rising purity demands for organic synthesis and electronics. While basic specs worked for classic intermediates, today’s devices—and their buyers—expect a higher bar, not just for chemistry but for documentation traceability and transparent supply chains. We’ve met audits on raw feedstocks and solvent recovery cycles, and updated our in-process controls to match global trends. Our in-house analysts and experienced lab crew now run environmental monitoring at every key handoff, keeping customers and auditors confident.

    As with all aromatic sulfur compounds, regulatory frameworks shift over time. Teams at our site keep tabs on evolving guidelines for hazardous material transport and volatile organic compound management. Safe handling instructions come directly from our process experience, not just paperwork. We’ve invested in thicker drum linings, vapor-tight closures, and marked routes within our own facility to stay ahead of emerging standards.

    Comparing 2-N-Propylthiophene to Other Thiophenes in Day-to-Day Work

    It’s in the routine steps—loading reactors, checking distillation cuts, or troubleshooting process hiccups—where the practical differences stand out. Making a straight swap from methyl or ethyl analogs to n-propyl brings immediate changes. Longer retention in vacuum stripping, slower evaporation losses on open transfer, and—most important—steadier purity retention under different temperature regimes.

    We’ve found the odor profile, while always sulfur-rich, seems less piercing with propyl attached. This makes handling easier for operators in the long haul. Better still, the slightly raised flash point offers another safety margin, an important feature when pilot chemists work round-the-clock shift rotations.

    Viscosity falls right in the zone where microdispensing or syringe transfer gives less drip and better regulator control compared to higher-mass thiophenes. During gas-phase or vapor phase synthesis, flow meters hold stability longer, helping maintain batch-to-batch analytics. Thin-film casting for electronics demonstrates improved edge definition, a frequent request from device fabricators.

    Solving Issues: What Works and What Needs More Focus

    Not every challenge in the world of 2-N-Propylthiophene submits to a checklist fix. Shelf life remains tied to careful sealing, and we’ve learned that new lined drums and single-use septa give the best shelf outcomes. For those in high-purity demand fields, best results come from smaller packaging and rapid drawdown once opened—a workflow we’ve tailored with our logistics partners.

    Process engineers noted a recurring bottleneck: residue inside filling equipment. Transitioning to fluoropolymer-lined lines and active flushing routines after every run preserves quality and reduces carryover. Our training teams also rolled out fresh safety drills; sulfur compounds need respect, but clear, prepared operators cut exposure issues to almost nil.

    Routine analytical work picks up issues before they become problems. Our protocols flag RO sample integrity and trend shifts well ahead of any customer call. Flexibility and fast course corrections make a difference between on-spec shipments and rework delays. We’re not shy about making changes if the evidence justifies the switch.

    The Real-World Value of 2-N-Propylthiophene—Beyond Data Sheets

    Across decades, our crew has learned that the real story of 2-N-Propylthiophene goes beyond purity numbers or regulatory boxes checked. This compound continues to earn its reputation where synthesis quality, electronics shelf stability, and efficient process handling carry weight. While some newcomers enter the field relying only on generic intermediates, long-time clients return for the specific performance that comes from consistent, practical manufacturing know-how.

    In every shipment, quality hangs on details: batch-to-batch uniformity, tight end-use controls, and tested logistics. We don’t leave results to hope. Field reports feed right into production tweaks, and direct conversations with R&D chemists elsewhere help sharpen our delivery.

    Adapting for the Future: Sustainability, Waste, and Innovation

    Every chemical facility knows that efficiency and stewardship rise together. Reduction of solvent waste and careful recovery of thio-residues became more than cost savings—they’re a point of pride among our production staff. Investment in closed-loop distillation recycles and energy recovery lets us meet broader sustainability goals, all while supporting consistent 2-N-Propylthiophene output.

    We stay watchful for trends calling for further purification breakthroughs or regulatory shifts that demand fast adaptation. The agility comes from veterans on the plant line who translate changes into process upgrades rather than after-the-fact fixes.

    From bench-scale research to metric ton runs, our long-term focus remains: help partners solve new problems, meet rising technical standards, and ensure every batch of 2-N-Propylthiophene delivers exactly what modern synthesis or integration calls for. Our roots are in manufacturing, but our reach is always shaped by customer goals and the next breakthrough just over the horizon.