Products

1,2,3,6-Tetrahydrobenzaldehyde

    • Product Name: 1,2,3,6-Tetrahydrobenzaldehyde
    • Alias: Cyclohex-3-ene-1-carbaldehyde
    • Einecs: 210-034-6
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    290570

    Name 1,2,3,6-Tetrahydrobenzaldehyde
    Cas Number 4984-85-4
    Molecular Formula C7H8O
    Molecular Weight 108.14 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 197-199°C
    Melting Point -31°C
    Density 1.03 g/cm³
    Refractive Index 1.521
    Flash Point 81°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Odor Aromatic, almond-like
    Pubchem Cid 11443

    As an accredited 1,2,3,6-Tetrahydrobenzaldehyde 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, with hazard labeling for 1,2,3,6-tetrahydrobenzaldehyde; compliant with chemical safety standards.
    Shipping **Shipping Description for 1,2,3,6-Tetrahydrobenzaldehyde:** Ship 1,2,3,6-tetrahydrobenzaldehyde in tightly sealed, chemical-resistant containers. Store upright and clearly label as hazardous. Protect from heat, direct sunlight, and incompatible materials. Follow all applicable local, national, and international regulations for hazardous chemicals. Ensure shipping documentation includes compound name, hazard warnings, and emergency contact information.
    Storage 1,2,3,6-Tetrahydrobenzaldehyde 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. Protect from moisture and direct sunlight. Proper labeling is essential. Store in a flammable liquids cabinet and ensure secondary containment to prevent spills or leaks. Use appropriate personal protective equipment when handling.
    Application of 1,2,3,6-Tetrahydrobenzaldehyde

    Applications of 1,2,3,6-Tetrahydrobenzaldehyde in Industrial Manufacturing

    As a dedicated manufacturer of 1,2,3,6-tetrahydrobenzaldehyde, we supply material for industry-scale synthesis across key sectors. We maintain strict control over purity, quality, and traceability, supporting compliant use in diverse chemical value chains. Below are several specialized applications where our product provides distinct functional benefits.

    1. Intermediate in Agrochemical Synthesis

    Agrochemical production frequently relies on 1,2,3,6-tetrahydrobenzaldehyde as an intermediate to construct heterocyclic scaffolds required for selective herbicides and fungicides. Our material reacts in controlled condensation and cyclization steps to build hydrogenated aromatic rings, which form critical parts of bioactive ingredients. Downstream partners integrate this aldehyde during early-stage synthesis to control final molecule stereochemistry and achieve batch-to-batch consistency in active agrochemical compounds.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH regulation (EC) No 1907/2006, Annexes II/VI/VII
    • OECD Guideline for Testing of Chemicals (purity and residue limits)
    • GLP (Good Laboratory Practice) certification for agrochemical R&D

    Typical usage ratio

    • Used at 0.1 to 5.0 molar equivalents depending on target molecule and desired yield optimization. Final ratio set according to specific route and stoichiometry in synthetic pathway.

    Downstream process integration

    • Added during the first or second condensation stage for ring construction.
    • Used in enamine or imine formation before cyclization steps.
    • Integrated under inert atmosphere to minimize side reactions during alkylation.

    Final product types

    • Selective herbicide active ingredients
    • Fungicidal intermediates
    • Pesticide pre-cursors with hydrogenated benzene rings
    • Crop protection molecule scaffolds

    2. Synthesis of Fragrance and Flavor Ingredients

    Producers in the aroma chemicals industry use 1,2,3,6-tetrahydrobenzaldehyde for the synthesis of specialty odorants. The aldehyde's cyclohexyl-based structure serves as a building block for fresh, green notes in fine fragrance composition and functional perfumery. Manufacturers convert it through controlled Grignard or Wittig reactions, followed by hydrogenation and acetylation, to yield finished aroma molecules with tailored volatility and substantivity for personal care or home fragrance markets.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards (current Amendment)
    • Cosmetic Ingredient Review (CIR) safety assessments
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • ISO 9235:2013 (Aroma Chemicals – Terminology)

    Typical usage ratio

    • 0.3 to 3.0% by weight as a reaction feedstock, typically controlled by the yield and purity requirements in the finished aroma chemical synthesis.

    Downstream process integration

    • Reacted with organometallic reagents in batch reactors to introduce specific side chains.
    • Undergoes selective reduction/hydrogenation to modulate intensity and stability.
    • Serves as core substrate in multi-step synthetic aroma ingredient formation.

    Final product types

    • Green note perfume raw materials
    • Aliphatic and cycloaliphatic musk components
    • Fine fragrance specialties
    • Functional household scenting ingredients

    3. Pharmaceutical Marker and Reference Compound Synthesis

    Pharmaceutical research and active ingredient development utilize 1,2,3,6-tetrahydrobenzaldehyde to build frameworks for bioactive molecular scaffolds. Its structure enables the controlled construction of chiral centers and fused rings for use as intermediates in the preparation of central nervous system (CNS) drugs and synthetic reference compounds. Major pharma and contract manufacturers require high-purity grades for integration into multi-step medicinal chemistry routes, focusing on process reproducibility and analytical traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • Ph. Eur. (European Pharmacopoeia) - impurity limits
    • 21 CFR Part 211 US FDA GMP requirements
    • USP General Chapters <467>, <232> (residual solvents, elemental impurities)

    Typical usage ratio

    • 0.05 to 1.2 molar equivalents, defined by structure–activity relationship and targeted figure for process yield or intermediate purity.

    Downstream process integration

    • Enters as key condensation or cyclization agent in stage two or three of API synthesis.
    • Used for derivatization in scaffold hopping and lead compound modification.
    • Provides aldehyde function for further pharmaceutical transformations—amide bond formation, reduction, or functionalization.

    Final product types

    • CNS agent intermediates
    • Reference standard markers
    • Synthetic building blocks for lead optimization
    • Research-scale analogues for pharmacological screening

    4. Production of Functional Polymer Modifiers

    Advanced polymer manufacturers use 1,2,3,6-tetrahydrobenzaldehyde as a modifier to introduce aldehyde groups to specialty polymers. The material functions as a controlled-reactivity cross-linker or chain-terminator in production of cycloaliphatic resins, enhancing flexibility, impact resistance, or adhesion properties for adhesives, coatings, and engineered plastics. Process engineers dose it precisely at specified stages in reactive extrusion or solution polymerization to tune the polymer’s mechanical and surface properties.

    Industry compliance standards

    • REACH (EC) No 1907/2006, Title IV & VII
    • ISO 9001:2015 Quality Control
    • ISO 14001:2015 Environmental Management
    • FDA 21 CFR 175.300 for indirect food contact applications (if used as a resin modifier)

    Typical usage ratio

    • Added at 0.2 to 2.5% by polymer mass; ratio set according to end-use application and mechanical property targets.

    Downstream process integration

    • Dosed during chain-extension or post-polymerization modification step.
    • Co-reacted in melt extrusion or solution reactors with polyurethanes, polyesters, or polyolefins.
    • Introduced pre- or post-polymerization for targeted functionalization.

    Final product types

    • Modified plastics for automotive and electronics
    • High-performance adhesive raw materials
    • Functional binder or coating bases
    • Polar-modified resin intermediates

    5. Fine Chemical Building Block for Dye and Pigment Synthesis

    Certain dye manufacturers require 1,2,3,6-tetrahydrobenzaldehyde as an aromatic precursor for synthesizing colorants based on reduced aromatic systems. Its ring structure enters key condensation and coupling reactions to give intermediates for specialized pigment and dye molecules, especially those with unique absorptivity or shade stability. This step demands rigorous material purity and precise feed rates to ensure batch reproducibility and color uniformity in textile and ink formulations.

    Industry compliance standards

    • ISO 9001:2015 for colorant production controls
    • OEKO-TEX Standard 100 for restricted substances in dyes
    • Restricted Substances Lists (RSL) of major textile brands and associations
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)

    Typical usage ratio

    • 0.5 to 5.0 molar equivalents as dictated by dye type and coloration intensity target; optimized through pilot-scale process validation.

    Downstream process integration

    • Undergoes initial condensation with amine or ketone reagents in colorant synthesis-stage one.
    • Serves as a precursor for further oxidative coupling, often under controlled pH and temperature.
    • Integrated before final purification or crystallization of pigment dye intermediates.

    Final product types

    • Specialty textile dyes
    • High-purity pigments for inkjet applications
    • Hydrogenated colorant intermediates for plastics
    • Saturated tone pigments for automotive paints

    Free Quote

    Competitive 1,2,3,6-Tetrahydrobenzaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: admin@ascent-chem.com

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    1,2,3,6-Tetrahydrobenzaldehyde: Direct from the Source

    Our Perspective as the Manufacturer

    Every product tells a story, but few bring the steady reliability that 1,2,3,6-Tetrahydrobenzaldehyde offers across both established and emerging industries. Our years working on the synthesis and scaling of tetrahydrobenzaldehyde have shown us what customers truly expect who depend on fine chemicals as the backbone of their products and research. High consistency, easy integration, and minimal disruptions during downstream reactions matter as much as any list of technical specs. We have developed our approach with full control over the entire production line, so each order reflects not only chemical purity, but also a level of process transparency that builds trust with long-term clients.

    Why We Focus on Tetrahydrobenzaldehyde

    We have watched this material move from niche use within specialized laboratories to wider adoption throughout fine chemicals, fragrances, and pharmaceutical industries. The molecule’s cyclohexenecarbaldehyde skeleton brings specific reactivity and a characteristic aromatic nuance, driving its popularity in synthesis and as a starting block for complex organic transformations. Our feedback from partners shows that slight variations during its preparation have noticeable impacts on final results, especially in catalysis, downstream condensing steps, or even olfactory profile. This prompted us to invest not only in precision equipment, but also continuous staff training centered on active monitoring of isomeric distribution and impurity profiles.

    Our Product Model and Unique Specifications

    We have set a dedicated production route for this compound, giving us control over every variable. Each batch receives GC and NMR verification to ensure that we consistently exceed industry baselines—purity routinely surpasses 99%. Controlled moisture management prevents side-reactivity, important for users in sensitive synthesis. Our specifications have evolved over time as we incorporated lessons from each scale-up and customer feedback loop; for instance, we fine-tuned solvent choices and optimized column parameters to further lower residuals. We have also refined storage conditions at our site and during transit, ensuring the batch you receive matches the properties we report down to the smallest detail.

    Beyond Technical Data: User Experience Matters

    It’s tempting to reduce any fine chemical to numbers on a safety data sheet, but those numbers only come alive as you use the material in your process. The reality of industrial-scale chemistry often means unexpected adjustments to account for subtle shifts in feedstock or reactant performance. We’ve seen many customers switch to us after running into bottlenecks with previous suppliers—the main issues are rarely headline failures but rather incremental losses in yield or inconsistent reactivity. Our team is familiar with these headaches. Our direct line of communication with production and R&D allows us to troubleshoot alongside partners, exchanging actual results in real time rather than passing blame back and forth.

    Consider an example from one of our long-time clients in the fragrance industry. They noticed small but critical differences in aroma profile when switching lots from different global suppliers. By tracing back the process variables, we pinpointed that minor solvent variations in the final run caused off-notes, which were picked up only by trained noses even though standard analytical methods showed all samples to be "within spec". Together, we refined our finishing and handled final washing under stricter controls, leading to better and more reproducible product for them—and for anyone else with similar needs.

    Comparisons to Related Aldehydes

    It’s common for new clients to ask why one should choose 1,2,3,6-Tetrahydrobenzaldehyde over chemically similar aldehydes. The best answer lies in its ring structure—this molecule bridges the flexibility and reactivity of saturated rings with the controlled reactivity that benzaldehyde and its derivatives afford. We see more predictable downstream reactions, particularly when performing Grignard additions or selective oxidations. Other saturated or partially aromatic aldehydes often bring uncontrollable side reactions or polymerization issues. Feedback collected from a range of pharmaceutical and agrochemical clients confirms that downstream intermediates from our batches tend to perform more reliably, often reducing time spent purifying products of the next step.

    We also hear from polymer scientists and fine fragrance blenders. They find the compound’s scent signature, neither aggressively green nor overly resinous, lends a subtlety difficult to achieve with straightforward benzaldehyde. Attempts to replace it with open-chain analogs or higher polycyclic variants seldom bring the same balance, frequently battling either volatility or a lack of robustness in the final blend. This is a direct consequence of the molecule’s semi-cyclic backbone—a feature we learned not to compromise during process changes. If anything, our experience points toward the value of strict adherence to synthesis best practices over quick attempts at process shortcuts.

    The Challenge of Consistency in Bulk Production

    Lab-scale batches look impressive on a technical report but often mask the risks of full-scale runs. We have encountered issues in the past: temperature management, off-gassing, even oil and water phase separation in early crystallization attempts. By sticking with a hands-on philosophy—where production and QC teams collaborate closely—we’ve overcome those hurdles. Careful adjustment of reaction time, not just relying on monitored temperature but also in-process sampling, helped us stabilize yields above 95% across consecutive large batches. Our chemists often share practical notes internally, recording minute details such as slight shifts in input reagent moisture content, which can have an outsized impact on crystallization time and final clarity.

    We don’t hide problems; open discussion is a big part of refining both product and skillset. Some of our strongest internal breakthroughs come directly from the batch floor rather than senior management or consultants. We learned, for instance, to avoid certain monomodal filtration steps that look efficient on paper but invariably led to an extra round of micro-filtration later. Each small change, documented by chemists and operators, led directly to the current state of our process—a state defined by reliability rather than idealized specification tables.

    Role in Research and New Applications

    Academic groups and industrial R&D labs alike continue finding new uses for 1,2,3,6-Tetrahydrobenzaldehyde. Some approach us pursuing specialty ligands for catalysis, others pursue bioactive heterocycles where the aldehyde acts as a versatile building block. Because we are the manufacturing source, we share not just lots but also application-specific advice based on process history and customer feedback. A recent project involved an international pharmaceutical firm aiming to customize a cyclohexene-based intermediate. Early runs showed yield loss and some by-product formation. Sharing our own insights about controlling exothermic points and staging catalyst dosing helped them raise their yield from below 80% to nearly 90%, with less waste disposal required.

    Requests for specialty packaging and solvent-free isolations have increased as both pharma and food tech clients move to greener processes. We maintain flexibility in how we prepare and bottle each order—often working under nitrogen, dry-ice, or inerted atmospheres to preserve stability—without adding unnecessary cost. Our on-site logistics team has developed routines for short-notice shipments and can even prepare mixed orders when required by a client with changing needs. Our philosophy: if a process tweak helps a partner get results, and doesn’t compromise safety or product quality, we figure out how to make it work.

    Detailing the Differences: Applications and Challenges Set Us Apart

    We face the question of “What sets your product apart from others?” almost weekly. Rather than restate abstract buzzwords, we share the specifics drawn from practice. Some competitors, for instance, blend lots from different reactors or even off-site sources. Variability shows not only in purity, but also in crystal habit, color, and ambient stability. Our batch records and in-house analytical checks create a chain of accountability rare in the sector. More than once we’ve noticed divergences in refractive index and residual solvent readings that alerted us to minor equipment drift, which we caught before delivery.

    Clients working in scale-up reactions often point out that, though two samples look similar by HPLC or GC, one can trigger unwanted side reactions or uneven product separation. Root causes usually trace back to trace impurities, stabilized by incomplete workup or exposure to airborne moisture. Our investment in workflow mapping and detailed SOPs aims to minimize these events. Every improvement—from drying protocols to rapid stabilization after isolation—came from on-the-ground experience, not theory alone.

    Many users draw distinctions between this tetrahydrobenzaldehyde and linear aldehydes, or those with alternative ring substitutions. In practice, our product gives more consistency in reactions such as cyclizations and enamine formation, compared to those alternatives. Open-chain analogs might bring erratic reaction times and side-chain instability. Highly aromatic versions risk faster oxidation or decrease the selectivity in coupling reactions. We encourage customers to consult us not just for chemical properties, but also real usage tips—whether using a fresh supply or considering storage for extended campaigns.

    Quality Control—No Gaps Between Claims and Reality

    Our QC journey started with traditional spot testing. Very quickly, it became clear that spot checks alone can’t capture the consistency this market demands. Now, each outgoing batch carries a full GC-MS and NMR dossier, including minor impurity mapping and identification. Such extensive controls may seem time-consuming, but they root out subtle batch-to-batch fluctuations that otherwise cascade into trouble during client use. We have developed a feedback cycle that allows customer labs quick access to analytical data, so they can compare incoming products against their process performance and flag anything abnormal before it disrupts their output.

    We also test physical traits such as melting point, density, and even changes to product appearance under clean-room conditions. Our staff understands the value of a transparent error-reporting pathway; mistakes happen, but immediate reporting and open documentation prevent small defects from turning into lost investment for a customer. We take pride in rapid batch recall and traceability. In almost a decade of supplying this material, not a single customer has complained of delayed proactive communication or trouble retrieving batch-specific data.

    Insight from Solving Real Problems

    Several years ago, a pharmaceutical client experimented with scaling up one of their core intermediates using our tetrahydrobenzaldehyde. Midway through, they encountered an unexpected change in product viscosity and color. Instead of evasive answers, our technical specialist visited, looked through their batch records, and quickly traced the issue to an unintended temperature spike during addition of an amine reactant. Since we had seen similar scenarios internally, we suggested specific agitation rates, cooling profiles, and premix ratios—practical solutions grounded in first-hand knowledge rather than distant literature data. The client not only salvaged the batch, but also improved their next run, reducing waste and maximizing product value.

    Such collaborations remind us that chemical manufacture extends far past making a pure compound. It’s about anticipating those real-world variables that cropped up for us time and again—waste disposal, unexpected odors, storage stabilities during hot seasons, or compatibility with bulk packaging. A one-size-fits-all solution never fits tightly enough. That’s why our staff answers with context, practical science, and genuine investment in each case.

    Supporting Innovation Through Responsiveness

    Chemistry demands quick answers and adaptability. Over time, our direct-to-customer approach has saved both us and our partners many lost hours. One research group reduced their scale-up cycle by days by relying on our advice for best solvent systems, after sharing chromatograms and side-product data. Another fragrance developer credited our flexibility in providing non-standard shipments for their internal sensory panel, allowing real-world testing with their team. Whether a client wants technical depth or just a fast resupply, we value each relationship and keep the communication lines open—no pretense, just practical support using real-world results.

    The Future: Continuous Improvement Rooted in Manufacturing Experience

    Innovation occurs not just at the laboratory bench, but at every step from sourcing raw material to final batch shipping. For us, commitment to improvement means keeping our process documentation open and incorporating suggestions directly from batch operators, QC chemists, and our most involved customers. We invest in training and analytical upgrades, clear in our belief that staying ahead of common pitfalls means fewer surprises downstream. Sustainability and responsible waste management play into every operating decision—not merely because of regulatory trends, but to provide clients with the peace of mind that comes from alignment with best industry practices.

    Based on more than a decade of direct manufacturing experience, we see success following the chemical from daily operator walk-throughs all the way to customer product testing lines. Delivering 1,2,3,6-Tetrahydrobenzaldehyde isn’t about a one-off sale. It is about ongoing partnerships, reliable performance, and a willingness to share what actually works across a range of industries.

    Invitation to Collaborate

    We invite new and returning customers to ask about our approaches and see the results for themselves. Our factory and technical teams remain available to discuss application-specific guidance, from synthetic route planning all the way to finished product testing or unexpected field challenges. As both a manufacturer and a partner, we recognize that every improvement begins with shared knowledge and mutual trust. By keeping production, quality, and customer support under one roof, we aim to provide more than just a chemical—we deliver a solution informed by years of trial, growth, and direct feedback from those who rely on us most.

    Top