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2-Thiophen-2-Yl-Benzaldehyde

    • Product Name 2-Thiophen-2-Yl-Benzaldehyde
    • Alias 2-thienyl benzaldehyde
    • Einecs 630-834-9
    • 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

    199796

    Product Name 2-Thiophen-2-Yl-Benzaldehyde
    Cas Number 60404-99-3
    Molecular Formula C11H8OS
    Molecular Weight 188.25 g/mol
    Appearance Yellow to orange solid
    Melting Point 50-53°C
    Density 1.19 g/cm³ (estimated)
    Solubility Soluble in organic solvents such as ethanol, DMSO, and chloroform
    Smiles C1=CC=C(C=C1)C=O.C2=CC=CS2
    Inchi InChI=1S/C11H8OS/c12-8-9-3-1-2-4-10(9)11-6-5-7-13-11/h1-8H
    Storage Conditions Store in a cool, dry place, away from light and moisture

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

    Packing & Storage
    Packing Amber glass bottle, 25g, sealed with tamper-evident cap, labeled with chemical name, structure, hazard symbols, and manufacturer details.
    Shipping 2-Thiophen-2-Yl-Benzaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is handled according to hazardous chemical regulations, with appropriate labeling and documentation. Standard shipping includes protective packaging to prevent leaks or damage, ensuring compliance with local, national, and international transport safety guidelines for chemicals.
    Storage 2-Thiophen-2-yl-benzaldehyde should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, and segregate it from strong oxidizers and acids. Store at room temperature and ensure proper chemical labeling. Use appropriate personal protective equipment when handling the substance.
    Application of 2-Thiophen-2-Yl-Benzaldehyde

    Applications of 2-Thiophen-2-Yl-Benzaldehyde in Industrial Manufacturing

    2-Thiophen-2-Yl-Benzaldehyde serves a key role across multiple specialty chemical industries due to its well-defined reactivity and distinct aromatic structure. As direct manufacturers with extensive technical expertise, we have extensive experience supporting end-users in diversified downstream fields, ensuring compatibility with complex industrial quality systems and precise processing parameters.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize this compound as a core building block in the synthesis of heterocyclic drug intermediates, particularly for anti-inflammatory and central nervous system (CNS) active agents. Its unique thiophenyl moiety offers essential options for medicinal chemists developing molecules focused on receptor selectivity and metabolic stability. During the multi-step synthesis, this aldehyde most often undergoes condensation or cyclization reactions with amines, hydrazines, or secondary aromatic substrates under carefully controlled conditions. Batch records and validation protocols require precise dosing, strict impurity control, and full traceability from receipt through to the final API.

    Industry compliance standards

    • ICH Q7: GMP for Active Pharmaceutical Ingredient Manufacture
    • USP/NF and European Pharmacopoeia Monograph Cross-References (for intermediate class compounds)
    • FDA 21 CFR Part 211: Finished Pharmaceuticals
    • ISO 9001:2015 Certified Quality Management Systems

    Typical usage ratio

    • 0.9–1.2 equivalents relative to the amine or hydrazine co-reactant
    • Charge quantities adjusted based on overall step yield and impurity profile

    Downstream process integration

    • Added during intermediate stage condensation or ring closure transformation
    • Subject to in-process HPLC/GC purity monitoring and residual solvent analysis post reaction

    Final product types

    • API intermediates for non-steroidal anti-inflammatory drugs (NSAIDs)
    • CNS-active compound scaffolds
    • Custom pharmaceutical research intermediates
    • Precursor molecules for peptidomimetic drugs

    2. Organic Light-Emitting Diode (OLED) Material Precursors

    In the advanced materials sector, 2-Thiophen-2-Yl-Benzaldehyde acts as a core precursor in the synthesis of thiophene-based organic semiconductors. Leading OLED manufacturers modify this aldehyde via Knoevenagel condensation and Suzuki couplings to produce conjugated materials with controlled energy gaps and charge mobility vital for modern display panels. Production batches require rigorous trace-metal control, pre-polymerization purification, and specification-level characterizations by NMR and UV-vis spectrometry.

    Industry compliance standards

    • IEC 62341: Standards for OLED Panels
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001: Environmental Management for Electronic Chemical Processes
    • REACH Regulation (EC) No 1907/2006 for material registration and reporting

    Typical usage ratio

    • Stoichiometric: 1.0 mol per coupling monomer in OLED polymer synthesis
    • Varied loading in small-molecule host/guest matrix (0.5–2.5 wt.%), customized to emission profile

    Downstream process integration

    • Introduced at the initial monomer formation stage prior to oligomerization or polymerization
    • Requires solvent switching, vacuum drying, and spectroscopic purity verification before device application

    Final product types

    • Polymeric and small-molecule OLED emitter layers
    • Semi-conductive thin films for display backplanes
    • Electroluminescent device development kits
    • Prototype and commercial OLED display modules

    3. Fine Fragrance and Aroma Intermediate

    Fragrance compound producers use 2-Thiophen-2-Yl-Benzaldehyde for manufacturing specialty aroma chemicals providing sulfurous-green and floral notes. The aromatic aldehyde introduces complexity to high-end perfumery bases and functional fragrances for personal care and household applications. This compound typically undergoes controlled condensation, followed by reduction, acetalization, or incorporation into accord-building molecules, with stringent attention to cosmetic allergen regulations and contaminant screening.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredient Safety
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9001 Quality Management in Aroma Chemical Manufacturing
    • RIFM Monographs for Risk Assessment and IFRA Transparency Lists

    Typical usage ratio

    • 0.1–2.0 wt.% in aroma concentrate, according to olfactory profile target
    • Adjusted as trace note in complex fragrance compositions

    Downstream process integration

    • Used as key intermediate in fragrance building-block preparation step
    • Undergoes blending with fixatives and co-distillation prior to final formulation

    Final product types

    • Specialty odorant chemicals for fine perfumery
    • Functional fragrances for detergents and cleaning products
    • Cosmetic aroma bases
    • Complex scent accord intermediates

    4. Advanced Polymer Synthesis Additive

    Polymers and resins manufacturers incorporate 2-Thiophen-2-Yl-Benzaldehyde as a reactive additive to introduce sites for cross-linking and post-functionalization in specialty resin designs. Its presence modifies thermal and photophysical properties, supporting the engineering of coatings, adhesives, and elastomers that must withstand harsh environments. Downstream users require analytical batch documentation for additive concentration, thermal history, and residual monomer levels to meet performance and safety approvals.

    Industry compliance standards

    • ISO 9001:2015 for resin and polymer manufacture
    • ASTM D638 for Tensile Properties of Plastics
    • UL 94 Flammability for Polymeric Materials
    • EU Regulation (EC) No 1935/2004 for polymers in food contact (where applicable)

    Typical usage ratio

    • 0.2–1.8 mol% relative to main monomer composition
    • Varies by application, higher inclusion for UV protection or thermal modification

    Downstream process integration

    • Introduced during pre-polymer mixing phase, prior to catalyst or curing agents
    • Requires melt blending or solvent-based dispersion for uniform distribution

    Final product types

    • Cross-linked epoxy and polyurethane resins
    • Weather-resistant elastomeric coatings
    • Specialty pressure-sensitive adhesive films
    • Functionalized engineering plastics

    5. Agrochemical Discovery Intermediates

    R&D departments in agrochemical companies employ 2-Thiophen-2-Yl-Benzaldehyde as a scaffold for the development of novel fungicide and herbicide candidates. Its thiophenyl structure allows rapid assembly of diverse libraries via imine formation and heterocycle construction for biological screening. Laboratory-scale and pilot synthesis must comply with environmental health and safety regulations, robust documentation, and strict analytical characterization before scale-up.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025 Accreditation for Analytical Verification
    • REACH (EC) No 1907/2006 Registration Requirements
    • ISO 14001 Environmental Management for industrial pilot operations

    Typical usage ratio

    • 0.8–1.5 equivalents in combinatorial reaction protocols
    • Alternated based on targeted library diversity and bioactivity parameters

    Downstream process integration

    • Added at early-stage intermediate step in combinatorial synthesis
    • QC confirmation by LC-MS and NMR, with focus on high-throughput screening throughput

    Final product types

    • Agrochemical lead compound libraries
    • Chemical building blocks for fungicides
    • Precursor structures for selective herbicide candidates
    • Proprietary intermediates for crop protection R&D
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    Certification & Compliance
    More Introduction

    2-Thiophen-2-Yl-Benzaldehyde: Practical Insights from the Manufacturing Floor

    Introduction to a Precise Chemical Building Block

    Few substances perform quite like 2-Thiophen-2-Yl-Benzaldehyde in synthetic chemistry labs. As manufacturers, we appreciate this compound not for its textbook appeal, but for the way it stands out as a precise and reliable building block. Out on the production floor, our engineers and chemists watch each batch move from raw intermediates to finished aldehyde with a sharp eye for purity and repeatability. CAS number 5720-07-0, and a molecular formula of C11H8OS—these numbers matter, but for those of us who turn powder into value, it’s the day-to-day experience that sets expectations and shapes our approach.

    What Sets 2-Thiophen-2-Yl-Benzaldehyde Apart in Synthesis

    This compound does not try to replace broad-spectrum reagents or act as a “one size fits all” aldehyde. What it brings to the bench is specific: the thiophene ring fused to a benzaldehyde core. Year after year, customers in specialty pharma and advanced materials research specify 2-Thiophen-2-Yl-Benzaldehyde when a unique combination of electron structure and aromatic behavior is required. They point out that reactions involving this molecule often avoid problematic polymerization seen in some analogs. We see fewer side reactions and more yield, particularly in Suzuki and Heck-type couplings, where side chain integrity matters.

    Specification and Quality Matters

    Our manufacturing process follows strict standards that go beyond internal protocols and meet independently audited benchmarks. Achieving high purity, which we guarantee above 98 percent by GC, requires tight control at each stage of the synthesis. Storage and handling must not compromise this threshold. Moisture, temperature, and cross-contamination with other aromatic aldehydes receive constant attention, not just during drying and packaging, but at every checking point between equipment and storage. Staff know from routine experience that even a small deviation in process temperature can push the impurity profile well outside acceptable ranges.

    Why Chemists Request This Aldehyde—Direct Feedback from Our Partners

    We make regular rounds with the researchers and scale-up teams who rely on 2-Thiophen-2-Yl-Benzaldehyde. They care less about grand claims and more about reliability batch after batch. In fields such as medicinal chemistry, the differences may show up subtly—in total synthesis, a single step that proceeds smoothly or not comes down to things like the electron-donating character of that thiophene ring. Teams working on OLED materials report sharper and more predictable emissions profiles when using this precursor, compared with similar aldehydes missing the sulfur heteroatom.

    Several partners have noted that using this reagent, rather than typical benzaldehyde or other thiophene-functionalized aldehydes, improves downstream selectivity. During a major project last year, a research group noticed cleaner separations and easier purification—saving them both labor and solvent use. That kind of practical difference is harder to put in a sales sheet, but it’s what drives loyalty among experienced users.

    No Substitute for Tight Process Control—How We Ensure Consistency

    We started scaling up this synthesis route over ten years ago, guided by trial, error, and serious troubleshooting. Intermediates require precise temperature zones—our reactors carry real-time monitoring on each run. No shortcuts. The reactivity inherent in the molecule’s fused ring system can lead, if even a slight excess of oxidant is applied, to undesirable side products. Training operators on reaction exotherms and expected visual cues remains part of our protocol.

    Post-processing matters just as much. During final purification, we apply both column chromatography and recrystallization. This dual purification narrows the impurity bandwidth and assists our customers with analyses like HPLC or NMR—nobody wants to trace spurious signals back to their starting material. Over time, we’ve refined these procedures not just by automating steps, but also by documenting and learning from the inevitable runs that show lower-than-usual yields or fail clarity tests. It’s an iterative approach, anchored in years of ground-level chemical work.

    Meeting the Needs of Research and Industry—Not Just Theory

    The wide world of benzylic aldehydes features many choices. 2-Thiophen-2-Yl-Benzaldehyde sits in a different niche than typical benzyl or furyl aldehydes. Chemists focused on sulfur heterocycles gravitate to this product because it brings distinctive reactivity to cross-coupling and condensation reactions, including those targeting pharmaceutical intermediates or specialty dyes. We’ve participated hands-on in pilot programs aiming to scale up precursor synthesis for bioactive molecules. In each case, the fact that our product does not bog down columns with intractable byproducts means real savings—less downtime, less media replacement, and more throughput.

    Suppliers without experience handling sulfur-containing aromatics may struggle to keep air and light exposure under control. Through direct experience, we know that packaging this material requires air-tight, light-resistant containers, and shipment arranged to avoid long storage in uncontrolled environments. Material stored improperly, even for a couple of weeks, can arrive with yellowing or dimming that warns seasoned chemists of compromised performance. Returning batches for reprocessing costs far more than correct handling the first time around. We take satisfaction in hearing from clients that our delivered product stays stable from arrival through final use.

    User Experience: Purity and Handling Really Count

    A lab manager at one of our key customer sites explained the headaches that come from using off-spec aldehyde. In one case, a shipment from another supplier produced a persistent ghost peak in NMR spectra. Weeks later, it traced back to a low-level benzothiophene contaminant. That single impurity stalled their drug candidate’s progress. Our process, which draws on over a decade’s accumulated “problem batches,” keeps such setbacks in mind. We use dedicated glassware and isolate runs to head off cross-contamination, running full QA on each batch before shipping.

    Customers also comment on how easy the product is to dissolve, compared with similarly structured aldehydes on the market. The crystalline form improves both weighing accuracy and solution homogeneity, traits that are often overlooked except by those who work with hundreds of grams at a time. It’s small details like these that earn repeat business far more than broad claims about general “versatility.”

    Specification Details from a Manufacturer’s Perspective

    Chemists often request: “Send your lot specifications and a recent COA.” We supply these regularly, with full disclosure of GC analysis, melting point, moisture (Karl Fischer), and color. Typical melting range sits at 58 to 62°C. Product purity remains above 98 percent, and daily checks confirm that no persistent residual solvents linger beyond detection limits. The sulfur atom in the thiophene supports UV-Vis characterization—an aspect appreciated by those developing optoelectronic materials.

    Shipping matches customer workflow. Deliveries arrive in high-integrity, tamper-evident bottles with batch labeling for traceability. We carry out all labeling in line with global regulatory requirements, but also with practical guidance for safe bench handling. What’s often left unsaid is how much work goes into keeping contaminant profiles transparent and honest. Good producers know that “98 percent pure” means nothing if the remaining 2 percent includes a problematic byproduct.

    Practical Uses and Real-World Scenarios

    Across our customer base, uses concentrate on medicinal and materials chemistry. Research teams running heterocycle syntheses say that the electron-rich nature of the thiophene ring stabilizes intermediates, especially where electron flow affects coupling or condensation outcomes. Several pharmaceutical groups choose this molecule to construct scaffolds for drug discovery, highlighting selectivity that’s hard to replicate with a simple benzaldehyde.

    In the world of chromophores and dyes, the fused system excites interest because of the interaction between sulfur and the aromatic system. Developers cite increased brightness and sharper absorption features, especially in blue and green wavebands. Dye makers highlight how the aldehyde’s ease of functionalization supports custom modifications that cannot be easily managed with other aromatic precursors. In our own trials, we’ve confirmed that copper-catalyzed couplings proceed cleanly and that product isolation is carried out with high recovery—even at larger scales.

    Direct Comparison: What Makes This Product Different

    Chemists ask: “Why not other substituted benzaldehydes?” Answers come down to molecular structure and process behavior. Compared to 4-methoxybenzaldehyde, which lacks a sulfur component, 2-Thiophen-2-Yl-Benzaldehyde brings the added dimension of electron density variation arising from the thiophene ring. This difference is crucial in metal-catalyzed cross-couplings or cyclization reactions. We’ve seen this demonstrated in projects pushing the boundaries on drug-like heterocycles, where yields and selectivity gain real improvements.

    Comparing with furyl-substituted aldehydes, some projects attempted to substitute furan for thiophene, only to encounter excessive oxidation or instability at the required temperatures. Our experiences echo published findings: the sulfur atom imparts not just stability but also better solubility in common organic solvents. This feature drives differences in extraction and purification downstream.

    Practical Challenges: Storage, Transport, and Reliability

    Handling aromatic aldehydes with reactive heterocycles teaches hard lessons in logistics. Not all freight options maintain required conditions. We have invested in dedicated packaging and storage solutions to hold up under variable warehouse conditions and prevent photooxidation or hydrolysis. Standard packaging for this product includes amber glass with inert gas backfill. Regular clients receive advice on how to store opened bottles under anhydrous conditions to avoid yellowing, loss of reactivity, or buildup of off-odors.

    Transport mishaps can happen. One shipment delayed for several weeks led to a batch arriving with visible color shift—prompting remediation at our expense, not the client’s. This was a wake-up call that insurance cannot replace the value of correct shipment handling. It’s not enough to manufacture to tight tolerances; maintaining those tolerances through distribution to the customer’s bench or production area completes the circle.

    Customer Collaboration: Continuous Improvement Anchored in Experience

    Our chemists keep up with customer R&D through regular call-ins and collaborative troubleshooting. We schedule feedback sessions to gather observations and improvement wish-lists. In one instance, an academic partner required support with a new synthesis involving a modified Suzuki coupling. We supplied not just a product sample but analysis on expected byproducts so their purification could be better optimized. Feedback from such cases returns to our production workflow, leading to micro-adjustments in temperature control or wash stages that make the next batches even cleaner.

    It’s only through repeated cycles of listening and adaptation that we’ve improved both product quality and customer success rates. Our QA records track not just numbers, but stories—cases where a reagent’s failure would have set a project back months. By sharing practical lessons from previous missteps, we help partners anticipate and prevent common pitfalls.

    Supporting Demanding Projects—From Milligrams to Multikilograms

    We regularly scale up output of 2-Thiophen-2-Yl-Benzaldehyde for both research labs and pilot plants. Each scale presents different hurdles. Milligram lots demand precise measurement, and attention to loss during transfer or dry down. Multi-kilogram runs need robust filtration and crystallization controls to keep particle size within client specifications. In the early years, we ironed out clumping and inconsistent drying that dogged larger orders, introducing better agitation and additional drying cycles without sacrificing throughput.

    Clients moving toward commercial scale-up expect shipment timelines that echo their production windows. Meeting those timelines means more than just holding inventory—it takes reliable documentation, flexible batch release, and transparent communication about lead times and expected delivery. Cases where unexpected surges in demand stress our capacity, we alert customers so they can adjust procurement, and where possible, we allocate reserve lots by priority and project phase. It’s this responsiveness, informed by real manufacturing logistics, that keeps partnerships resilient.

    Environmental and Regulatory Responsibility—Actions Speak Louder Than Claims

    Handling sulfur aromatics carries waste streams that can challenge compliance. For years, we struggled with disposal and minimization strategies for byproducts and wash solutions. Now, we use a solvent recovery loop and tight effluent characterization—practices driven as much by cost savings as environmental good housekeeping. Onsite audits encourage us to keep honest accounts of everything from solvent transitions to operator PPE practices. Our process achieves high recovery and tracks emissions, not just for internal metrics but to stand up to independent environmental reviews.

    Regulatory discussions deserve transparency. Customers trust us to provide documentation not only for product purity but for trace contaminants, residual solvents, and batch traceability. We stay current on safety data requirements, labeling expectations, and updated shipping classifications, forwarding all new information as soon as it is available. Clients value this clarity, especially those operating under GMP or seeking regulatory filings.

    Troubleshooting: Avoiding and Correcting Mistakes is Core to Our Operations

    Production does not move forward without regular process reviews. Our teams meet to work through issues spotted during QC—color drift, drop in melting point, or emergent impurities. We’ve learned to approach problems systematically: isolate variables, rerun suspect steps at varying scales, and confirm corrective changes with side-by-side batch comparisons. These lessons, paid for by lost output and lab hours, feed directly into long-term batch records and operating procedures.

    Customer returns are rare, but when they occur, they drive fast action. One client received a shipment with micro-crystal deviations—a defect missed by visual inspection but caught during microscopy. We changed our sieving and bagging methodology that same week. That kind of adaptability, spurred by hands-on experience rather than paperwork, is the hallmark of a producer who stands behind each lot.

    Final Word: Real Value Built on Practice, Not Hype

    2-Thiophen-2-Yl-Benzaldehyde earns its place in our long-term portfolio through technical merit and consistent day-to-day delivery. Each batch that ships reflects thousands of hours sweating process details, learning from customer needs, and adapting techniques to avoid pitfalls. Feedback loops, quality controls, and industry knowledge sharpen every kilogram that moves from our plant to your lab. It's not marketing or specification sheets, but the steady hand of experience that ensures users receive a reagent ready to meet today’s research and production demands. The product’s difference shows up in cleaner reactions, easier handling, greater reliability, and ultimately, scientific and commercial results that stand tall in a competitive world.