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2-Hydroxy-3-Methylbenzaldehyde

    • Product Name 2-Hydroxy-3-Methylbenzaldehyde
    • Alias o-Vanillin
    • Einecs 225-083-2
    • 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

    535805

    Name 2-Hydroxy-3-Methylbenzaldehyde
    Cas Number 3470-21-9
    Molecular Formula C8H8O2
    Molecular Weight 136.15 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 62-65 °C
    Boiling Point 273 °C (estimated)
    Density 1.16 g/cm³ (at 25 °C, estimated)
    Solubility In Water Slightly soluble
    Synonyms 3-Methylsalicylaldehyde
    Smiles CC1=C(C=CC(=C1)C=O)O
    Inchi InChI=1S/C8H8O2/c1-6-4-2-3-7(9)8(6)10/h2-5,10H,1H3

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, screw cap sealed, labeled with chemical name, structure, CAS number, hazard warnings, and supplier details.
    Shipping 2-Hydroxy-3-Methylbenzaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. It should be transported at ambient temperature with appropriate hazard labeling. Handle with care as it may cause irritation. Shipping complies with regulatory requirements for chemicals, ensuring safety during transit and storage. Consult the Safety Data Sheet (SDS) for details.
    Storage 2-Hydroxy-3-Methylbenzaldehyde should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep separate from incompatible substances such as strong oxidizing agents and acids. Ensure the storage area is equipped with appropriate spill containment and is clearly labeled. Follow all relevant safety guidelines and local regulations.
    Application of 2-Hydroxy-3-Methylbenzaldehyde

    Applications of 2-Hydroxy-3-Methylbenzaldehyde in Industrial Manufacturing

    2-Hydroxy-3-methylbenzaldehyde serves key roles in several specialized manufacturing processes across the chemical, pharmaceutical, and fine chemical industries. Our production focuses on high-purity batches designed for critical downstream integrations where quality, traceability, and compliance drive operational value. The following are major application areas supported by industry standards and technical validation.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Widely used as a critical building block in synthesizing specialty APIs for anti-inflammatory and anti-infective drugs, our material ensures reliable reactivity and purity for regulated pharmaceutical synthesis. During Grignard and aldol condensation steps, precise input quality and traceability support compliance with stringent pharmacopeial requirements. Its narrow impurities profile supports API route development, impurity profiling, and final product validation phases.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia - National Formulary)
    • European Pharmacopoeia (Ph. Eur.) Monographs for intermediates
    • Chinese Pharmacopoeia (ChP) guidelines for API intermediates

    Typical usage ratio

    • Ranges from 0.5 molar equivalents to 2.0 equivalents relative to core substrate; precise loading adjusted by target API synthesis yield, desired impurity profile, and downstream purification step.

    Downstream process integration

    • Introduced during initial condensation or cyclization stages of API multi-step synthesis.
    • Dosed into reaction vessel under controlled temperature and inert atmosphere to ensure full conversion.
    • Feeds directly to subsequent protection or reduction steps before API isolation and purification.

    Final product types

    • Non-steroidal anti-inflammatory APIs
    • Quinolone antibiotic cores
    • Synthetic antipyretics
    • Intermediates for oncology drugs

    2. Fragrance and Flavor Intermediate

    Used by aroma chemical manufacturers, 2-hydroxy-3-methylbenzaldehyde functions as a key structural component for synthesizing complex flavor and fragrance molecules. Its ortho-substitution pattern forms the functional base for musk, vanilla, and floral compositions. Producers require exacting consistencies in isomer purity to meet regulatory limits on trace contaminants in food and cosmetic applications, with tight control on batch-to-batch reproducibility to satisfy large-volume compounding runs.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • EU Regulation (EC) No 1334/2008 for Flavorings
    • US FDA 21 CFR Part 172 for Food Additives
    • ISO 9235:2013 (Aromatic Natural Raw Materials Vocabulary and Standards)

    Typical usage ratio

    • Usually introduced at 0.1 – 1.0% w/w of precursor mixture for fine fragrance or flavor intermediate synthesis; final ratio defined by target odor threshold and regulatory residue guidelines.

    Downstream process integration

    • Dosed at the condensation or etherification step in aroma molecule synthesis.
    • Reacts with aliphatic ketones or alcohols under mild acid catalysis, then undergoes distillation and fractional purification.
    • QC monitoring for organoleptic properties and trace impurity conformance before release to compounding plants.

    Final product types

    • Musk fragrance ingredients
    • Vanillin derivatives for food
    • Fine perfumery bases
    • Flavoring agents for beverages and confectionery

    3. Organic Dye and Pigment Precursor

    Dye and pigment manufacturers incorporate this compound as a controlled precursor for synthesizing high-color-strength, stable azo dyes and anthraquinone derivatives. Its hydroxyl and methyl functional groups enable unique coupling reactions, producing tailored chromophores for textile, paper, and specialty coatings. The presence and quality of the ortho-aldehyde group are critical to color performance and resistance profiles after industrial application.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for chemical input safety
    • EN 71-3: Safety of toys – migration of chemical elements (for pigment application in children’s goods)
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • GHS Classification for dye manufacturing safety data

    Typical usage ratio

    • Standard input 0.5 – 3.0% by weight of total dye batch, determined by desired color intensity and substrate compatibility; adjustments based on reaction conversion efficiency.

    Downstream process integration

    • Charged at primary condensation or diazotization stage of pigment synthesis.
    • Follows with coupling to aromatic amines or phenols, with inline monitoring to verify complete incorporation.
    • Filtration, washing, and drying steps validate purity before blending or granulation.

    Final product types

    • Disperse and azo textile dyes
    • Synthetic organic pigment pastes
    • Paper and ink colorants
    • Specialty pigments for industrial coatings

    4. Fine Chemical Synthesis for Ligand and Chelate Production

    Research and industrial labs utilize 2-hydroxy-3-methylbenzaldehyde as a specialized starting material for manufacturing bidentate ligands and chelating agents. Chemists exploit its ortho-hydroxyl-aldehyde structure for Schiff base formation, controlling stoichiometry to engineer metal-complexing properties important in catalysis, analytical chemistry, and extraction. High-purity supply supports downstream metal ion selectivity and stability required by advanced material and catalyst industries.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for laboratory chemicals)
    • ACS Reagent Grade or Analytical Reagent Standards
    • GHS chemical labeling and documentation standards
    • Materials Safety Data Sheet (MSDS) requirements for handling and storage

    Typical usage ratio

    • Stoichiometric ratios typically 1:1 molar with primary amine or hydrazide, tailored by intended ligand structure and chelating performance metrics.

    Downstream process integration

    • Condensation with selected diamine or hydrazine compounds under controlled pH and temperature to form Schiff base ligands.
    • Isolation, crystallization, and structural analysis (NMR/IR) for final QC confirmation prior to metal complexation.
    • Bulk product batches subjected to trace metal impurity analysis to meet downstream application requirements.

    Final product types

    • Laboratory and industrial chelating agents
    • Coordination complex catalysts
    • Metal sensor probes
    • Extraction reagents for analytical chemistry
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    Certification & Compliance
    More Introduction

    2-Hydroxy-3-Methylbenzaldehyde: Our Practical Approach to Fine Chemicals

    What Sets 2-Hydroxy-3-Methylbenzaldehyde Apart

    Our team has worked with various aromatic aldehydes over the years, but 2-Hydroxy-3-Methylbenzaldehyde stands out for a reason. This compound, known among lab veterans as HMBA or by its CAS number 703-79-5, carries a special arrangement: a hydroxyl group and a methyl group both tagging along with the benzaldehyde core. In practice, this seemingly minor shift in molecular character changes a lot—the way it dissolves, reacts, and builds into bigger, more complex molecules. From a manufacturer's perspective, mastering the details of this compound opens doors to advanced organic syntheses and downstream innovation, while some products with similar names don't offer the same routes to value-added products.

    Our Focus on Quality and Purity

    Since we started refining our approach to HMBA, we've learned the market doesn't forgive shortcuts. Impurities from careless synthesis or poor storage can ruin yield and consistency during downstream use, especially in research or medicine. That's why every batch we ship is checked rigorously. We usually bring HMBA to market as a crystalline solid, running a typical purity above 99% as measured by HPLC. Any moisture or side impurities lower the compound's reactivity and can complicate further reactions. Customers in pharmaceutical R&D or polymer design rely on this consistency—the wrong batch, or the wrong impurity profile, bogs down workflow, increases purification costs, or leads to failed reactions.

    How 2-Hydroxy-3-Methylbenzaldehyde Actually Gets Used

    Over the years, we’ve seen this material flowing into a range of end uses, but a few stand out. One recurring application pops up in the building of specialty ligands for metal-catalyzed reactions, where the ortho-hydroxy and meta-methyl groups are more than decoration—they steer the way metals and organics lock together in the catalytic pocket. Chemists have shown how even slight changes in these positions lead to better selectivity or reactivity in asymmetric synthesis, which is a big deal when scaling from grams to multi-kilo lots.

    Another major route uses HMBA as a feedstock in fragrance and flavor synthesis. Its unique comfort—hard to put into words for people who haven’t sniffed the product, but definitely recognizable—plays a role in middle and base notes for specialty blends. We keep track of volatility and oil compatibility because perfume houses can be picky, and consistency wins repeat business. Industrial labs sometimes ask about food grade, and we have to clarify: while structurally related to flavoring agents, our batches focus on industrial and research criteria.

    Comparing to Related Benzaldehydes

    Chemists might lump HMBA together with plain vanilla benzaldehyde, or even 2-hydroxybenzaldehyde (salicylaldehyde), but experience has shown us how their behaviors differ on the benchtop. Salicylaldehyde, with no methyl group, often reacts faster in condensation and coupling reactions, producing different yield and selectivity outcomes. The extra methyl group in HMBA slows down certain nucleophilic attacks, opening up milder routes for sensitive transformations. That’s become useful in multi-step total syntheses, especially when fragile moieties can’t handle aggressive conditions.

    Our team also watches trends with 3-methylbenzaldehyde (no hydroxyl group). Without the phenolic hydroxyl, it won’t participate in typical chelation or hydrogen bonding that drives many coordinate-based transformations. After fielding several requests from customers who tried non-hydroxyl analogs and saw inconsistent results, we started offering technical support to help them transition to a more reliable process using HMBA. It’s an instructive example: tiny changes in substitution can multiply out into major downstream effects, and only hands-on production experience brings out these differences.

    Specifying Product Performance

    From a producer viewpoint, specification is all about reliability, not paperwork. HMBA holds a melting point between 96 and 99 Celsius. It’ll dissolve smoothly in most polar organics—ethylene glycol, DMSO, THF—though solubility shifts sharply with local temperature and water content. Our operations department tests solubility ranges regularly, because we know a soap-like intermediate from uneven solubilization can ruin a batch in dispersion polymerizations. We even had one run years back where a dried, poorly milled lot produced clumps during scaling. After revising both our drying and comminution steps, we locked in the crystalline habit so that what leaves our plant disperses easily and enables accurate weighing and dosing.

    Keeping moisture controlled matters too. This aldehyde loves to pull in water over time thanks to the ortho-hydroxy group. If it sits open to humid air, the product cake can clump or even kick off slow degradation. Every shipment includes a controlled-moisture container and we advise repackaging in dry compartments once received; customers with ongoing issues often solve them by swapping out their storage approach rather than blaming the chemistry.

    Making the Product Right, from Raw Material to Delivery

    Scaling up from lab-scale synthesis to production is where most projects trip up. We tackle raw material quality scrap by going upstream—perennial issues like hydrolysis-prone intermediates mean our team scrutinizes each barrel or drum before green-lighting the reactor load. In those early years, slow-reacting precursors led to inconsistent color or purity, so we now run a two-step filtration cleanup at the end, followed by low-residue crystallizations from tailored solvents. That means batches match spectroscopic benchmarks every time.

    Our packaging operation does more than slap a label. Many of our customers complained about caking or difficult transfers in the past, and we responded by sourcing tight-head, moisture-proof pails, with tamper marks so clients can confirm integrity at a glance. Our own QA/QC team verifies each outbound unit— getting feedback directly from returned containers (customers sometimes send them back if unexpected residue shows up) has improved our moisture control over the years, proving how close collaboration brings stronger products to market.

    Supporting the People Who Use It

    Technical support isn’t just a nice-to-have, it’s a necessity. Several industries rely on this aldehyde, and their needs keep shifting. One of our biggest challenges comes from academic researchers, who sometimes try to apply procedures from salicylaldehyde directly to HMBA and get frustrated by sluggish or unexpected results. Explaining the role of that methyl group often clears up the confusion—over and over, experience on the shop floor trumps what the textbooks claim.

    Fragrance customers tend to ask about long-term stability, oil compatibility, and batch-to-batch variance. We run stress tests under heat and light, monitoring yellowing or volatility losses that could shift a perfume’s profile. Each time we improve, we update our run books and share practical tips with formulating chemists—an approach that’s earned trust far more reliably than flashy spec sheets.

    Environmental and Safety Realities

    We pay close attention to handling requirements. HMBA does feature the aldehyde functional group, which means it should be kept away from amines and oxidizers during storage. We recommend standard PPE for all plant operations, but we also equip our lines with dedicated extraction and containment on account of the material’s volatility and reactive aroma. Over the years, we’ve found that simple practices—well-labeled storage, mandatory ventilated handling—reduce risk and build stronger habits in new staff.

    Disposal, too, isn’t an afterthought. We neutralize waste streams with sodium bisulfite after each clean-up; this keeps residue aldehydes from causing persistent odors or volatilizing into lab air. Any organic facility handling benzaldehyde derivatives will understand why we push for responsible effluent controls—unmanaged byproducts can pose both health and compliance risks.

    Keeping a Close Eye on Upstream Trends

    The landscape for fine chemicals changes faster than many expect. Global supply chains bring new opportunities but also introduce uncertainty. Over the past two years, we’ve seen cost swings on key feedstocks—tolualdehyde and phenolic intermediates—forcing us to revisit contract arrangements and sometimes work through alternate suppliers to maintain our supply promise.

    We don't simply accept price spikes. Instead, our sourcing specialists have built up multi-region relationships, allowing us to hedge against shortages or shipping slowdowns that occasionally hit local markets. Being an actual manufacturer, not just a re-packer, gives us flexibility that strictly traders never enjoy. Our emergency runs and off-shift production cycles can bridge temporary gaps, keeping the product flowing to those who depend on it for their research timelines or commercial rollouts.

    Bridging the Gap Between Research and Industry

    Academia and industry sometimes view fine chemicals from totally different angles. Researchers search for a precise tool, while production chemists worry about scale, waste, and reproducibility. Over several years, we’ve partnered with university groups who first encountered batch-to-batch variation or reactivity quirks using commercial HMBA. Once we explained how the subtle interplay of moisture, crystal size, and storage impacts outcomes, professors and postdocs got reproducible results and their own students learned about the practical side of chemical logistics.

    Our belief is that open communication and transparent feedback loops foster both innovation and safety. We’ve hosted visiting chemists to walk our production floor, and these exchanges often uncover small process improvements that serve both sides. More than abstract claims, it’s direct engagement that pushes the product and the science forward.

    Common Questions and Challenges

    Some new users ask why they can’t substitute plain benzaldehyde or its 3-methyl analogs in their synthesis. After working with a wide spectrum of compounds, we can confidently highlight—each substitution changes the reaction pathway. In practical terms, HMBA's reactivity profile allows certain protected additions, and multistep syntheses, where uncontrolled condensation or side-product formation would damage yields if a less specialized aldehyde were used.

    Another question we hear surrounds scalability. Bench chemists want to know if moving from a 100-gram setup to 10-kilogram runs will disrupt outcomes. Based on our own scale-up experience, the main watch-out lies in crystallization and filtration. Variabilities emerge during cooling, with faster rates yielding small, hard-to-filter fines. Over time, we've optimized agitation rates and solvent exchange processes to lock in suitable crystal sizes—fixing problems that plagued early trial runs. Technical users benefit from these lessons, taking advantage of process parameters we share openly.

    Looking Forward with 2-Hydroxy-3-Methylbenzaldehyde

    Future applications for HMBA keep emerging. With the rise of advanced materials and novel molecules, demand from both academic and commercial sectors is climbing. We've watched the market for specialty aldehydes shift toward tighter impurity specifications and more sustainable production methods. Our team invests in greener solvent systems and low-waste processes, not out of obligation but to lower overhead, improve yield, and maintain the safety record we’ve worked hard to achieve.

    Bottom line: it takes practical shop-floor know-how to make and deliver 2-Hydroxy-3-Methylbenzaldehyde the right way. Whether it’s answering a specialist’s late-night question, refining a run to deliver on time, or troubleshooting a tricky reaction with a down-the-line partner, we back every shipment with a layer of technical knowledge that only comes from actually making the stuff. For those building new molecules or formulations, knowing their starting material comes from a source with real experience helps clear away doubts and keeps projects moving.

    Final Thoughts on Our Approach

    Chemical manufacturing, as we see it, isn’t just about selling a bag or drum of powder. It’s about solving practical problems for people in labs, pilot plants, and full-scale factories—meeting needs that shift with technology, regulation, and market tastes. Our ongoing conversations with formulators, chemists, and purchasing managers keep us grounded. We only improve by listening carefully and backing up every detail with direct production evidence, customer feedback, and years of hands-on troubleshooting.

    So, for research and industrial partners seeking a reliable source of 2-Hydroxy-3-Methylbenzaldehyde, our shop keeps pushing for higher standards—not because specs demand it, but because real-world use exposes the difference. The right version of this aromatic aldehyde turns complicated syntheses, flavor framings, and catalytic explorations into success stories, and that satisfaction carries through every step, from raw material testing to that final shipped drum.