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HS Code |
990197 |
| Productname | 3-Hydroxy-4-Methylbenzoic Acid |
| Casnumber | 700-11-4 |
| Molecularformula | C8H8O3 |
| Molecularweight | 152.15 |
| Appearance | White to off-white solid |
| Meltingpoint | 163-166°C |
| Solubility | Slightly soluble in water |
| Density | 1.381 g/cm3 |
| Pka | 4.14 |
| Smiles | CC1=C(C=CC(=C1)O)C(=O)O |
| Iupacname | 3-hydroxy-4-methylbenzoic acid |
| Pubchemcid | 14408 |
As an accredited 3-Hydroxy-4-Methylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, labeled “3-Hydroxy-4-Methylbenzoic Acid, 25g”; features hazard warnings, product code, and storage guidelines. |
| Shipping | 3-Hydroxy-4-Methylbenzoic Acid is shipped in tightly sealed containers to prevent contamination and moisture uptake. Packaging complies with regulatory guidelines for chemicals, ensuring safe transit. It is transported at ambient temperature, away from incompatible substances, and accompanied by relevant documentation like the Safety Data Sheet (SDS). Handle with appropriate protective equipment upon receipt. |
| Storage | Store 3-Hydroxy-4-Methylbenzoic Acid in a tightly closed container, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure chemical is stored at room temperature and properly labeled. Keep out of reach of unauthorized personnel and dispose of according to local regulations. |
Applications of 3-Hydroxy-4-Methylbenzoic Acid in Industrial Manufacturing3-Hydroxy-4-Methylbenzoic Acid serves as a critical intermediate in specialty chemical synthesis across multiple value chains. As a direct manufacturer, we support downstream partners with consistent supply for high-value end products, ensuring technical compatibility with regulated processes and advanced formulations. 1. Pharmaceutical Intermediate SynthesisThis molecule acts as a key starting material in the multi-step synthesis of specific nonsteroidal anti-inflammatory drugs and active pharmaceutical ingredient (API) derivatives. Chemical engineers use it for amide coupling or esterification reactions, where its stable aromatic framework enables targeted side-chain modifications for increased pharmacological performance. Integrators favor its consistent purities to reduce side process impurities and support regulatory filings for new drugs under stringent global guidelines. Industry compliance standards
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2. Agrochemical Building BlockIn crop protection chemistry, this compound is employed as a building block for active ingredient synthesis, especially in preparing selective herbicides and fungicide backbone molecules. Its precise substitution enables the development of high-activity, low-toxicity compounds. Agrochemical formulators leverage the molecule's compatibility with chlorination and sulfonation, which establishes the base for downstream modifications leading to patent-protected actives. Industry compliance standards
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3. Polymer Modifier in Advanced MaterialsPolymers industry users incorporate this acid as a modifier and chain-terminator, especially in high-performance polyesters and liquid crystalline polymers (LCPs) where thermal resistance and mechanical properties are critical. The precise addition of this monomer introduces tailored branching or end-group functionalities, enabling enhanced dimensional stability and unique melt-flow characteristics in engineering plastics manufacturing. Industry compliance standards
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4. Specialty Dye and Pigment SynthesisDye manufacturers utilize this compound as a coupling agent or precursor for azo and anthraquinone dyes. Its specific hydroxy and methyl substitutions facilitate targeted chromophore construction via controlled diazotization or coupling reactions. This enables precise shade development, wash fastness improvement, and acid/base compatibility in the dye formulation process. Quality control experts track batch uniformity to support textile, ink, and leather coloration markets subject to global chemical safety requirements. Industry compliance standards
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5. Specialty Aromatic Compound SynthesisChemical manufacturers apply this compound in multi-step syntheses to produce specialty aromatic derivatives used in fragrance, flavor intermediates, and high-purity laboratory reagents. The hydroxy-methyl pattern serves as a functional handle for selective esterification, alkylation, or nitration, with downstream partners appreciating the purity consistency for batch-to-batch process reliability. These aromatics often require full compliance with environmental and food-safety directives, especially when destined for downstream cosmetic or ingestible uses. Industry compliance standards
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Working in chemical manufacturing, certain compounds stand out for the advantages they offer formulators in seeking consistent results and safer alternatives. 3-Hydroxy-4-Methylbenzoic Acid, often recognized by its CAS number 619-74-7, is no exception. Our facility synthesizes this compound using methods that focus on purity and repeatability. Over years of meeting both lab-scale and industrial-scale orders, we've observed how clients across pharmaceuticals, fine chemicals, and materials science benefit directly from its properties and behavior.
The details behind any batch begin with its structure: a benzene ring supporting hydroxy and methyl substituents. We produce 3-Hydroxy-4-Methylbenzoic Acid as an off-white solid, favoring either fine powder or crystalline form based on client feedback. Among our most sought-after models, the powder grade with assayed purity of 99% suits research, while high-purity crystals serve as reference standards and advanced intermediates. Shelf stability and handling are straight forward; storage under dry, ambient conditions maintains integrity for extended periods, with our QA testing confirming minimal degradation even after a year.
People working hands-on with 3-Hydroxy-4-Methylbenzoic Acid value how easily it blends into organic solvents. Thanks to the hydroxy group, it dissolves more readily in methanol, ethanol, and dimethylformamide. Water solubility remains limited, so operations often prefer hydroxylated solvents for conversions or reactions. Its melting point, clocking in between 196°C and 200°C, lets users heat and handle the material without risking early decomposition or darkening—a clear improvement over certain isomeric acids that polymerize at lower temperatures.
The uses of this acid stretch far and wide, although the real value emerges where technical requirements are strict. On our production lines and across our customer base, we see this compound largely in two types of applications: as a building block for more complex molecules and as a performance additive in specialty materials. The benzene ring and phenolic group allow the acid to participate in coupling reactions, esterifications, and amidations, building up molecular complexity for both pharma actives and advanced polymers.
No matter the sector, 3-Hydroxy-4-Methylbenzoic Acid is often brought into multi-step syntheses. Medicinal chemists rely on it for easy derivatization. The methyl group at the 4-position blocks certain reactive sites, steering chemistry toward more predictable end products—an advantage not found in simpler benzoic acids. Materials scientists use it to confer both rigidity and chemical reactivity to polymers, especially where higher temperatures or extended durability is required.
Some projects take advantage of its intermediate acidity and electron-donating hydroxy group to influence catalyst selection and reaction rate. In workups, the material handles aqueous and organic extraction cycles cleanly, helping to drive up total product yields and lower waste. In specialty resins and coatings, it grants improved resistance to ultraviolet degradation and oxidative stress, which we’ve tracked over multiple industrial trials and customer feedback cycles.
It’s one thing to provide a chemical with high purity on paper, but actual manufacturing tells the other half of the story. Over time, we’ve optimized particle size and moisture levels to minimize dusting and improve batch transfer rates. Teams formulating with 3-Hydroxy-4-Methylbenzoic Acid report the powder flows easily through standard screw feeders, and even at high concentrations, clogging or bridging events are rare.
Occupational exposure is another concern that comes up repeatedly in training. The acid has a low dust potential when handled properly, lowering inhalation risk. Standard handling protocols—basic gloves and goggles—address most assembly-line safety concerns. Bulk customers who require 25 kg fiber drums or custom-packed lots commented positively on our triple-seal liner system, which further reduces exposure risk and limits humidity ingress.
From a waste and recovery perspective, the compound breaks down through typical acidic and oxidative routes, avoiding halogenated byproducts or non-recyclable residues. We’ve advised multiple partners on selecting solvents and neutralization agents that both recover value and avoid creating new hazards. Any clean-up from spills or overbatches stays simple: sweeping the dry material directly to proper waste containers.
Across many product comparison charts, the differences between 3-Hydroxy-4-Methylbenzoic Acid and close relatives like 3-Hydroxybenzoic Acid or 4-Methylbenzoic Acid don’t always look significant at first glance. In practice, those differences shape reaction pathways and downstream purification steps. We regularly work with clients to select 3-Hydroxy-4-Methylbenzoic Acid specifically for its regioselectivity. That methyl group at the 4-position does more than boost lipophilicity; it gives synthetic chemists a strategic handle to avoid side reactions.
Unlike unsubstituted benzoic acids, which sometimes lead to unwanted ring substitutions under harsh conditions, 3-Hydroxy-4-Methylbenzoic Acid’s substitution pattern improves selectivity in aromatic substitutions. Peers working process chemistry appreciate this distinction, especially where regulatory filings demand strict impurity profiles. During scale-up, its stability under both basic and acidic hydrolysis minimizes byproduct formation—a key reason process chemists come back to us for kilogram quantities.
Differences between this product and ortho- or meta-hydroxy analogues show up clearly in crystallization and solvent selection. The higher melting point and protectivity of the methyl group enable re-crystallization using less solvent, reducing both batch times and production costs. Analytical chemists have mentioned that HPLC resolution is typically sharper, with lower tailing and fewer co-eluting impurities—saving on both rework and consumable use.
Buyers, especially those running long-term processes or switching formulation strategies, often evaluate cost and reliability side-by-side. After many years shipping 3-Hydroxy-4-Methylbenzoic Acid to both domestic and international partners, our team sees that bulk pricing never tells the whole story. Lower variability from lot to lot means fewer surprises and tighter control over end-product quality. Our retention rates reflect this—formulators stick with us through project cycles and scale-ups.
Clients in pharma development reported smoother regulatory audits, due in part to years of uninterrupted supply and standardized specification sheets. Downstream manufacturers involved with coatings or adhesive systems have found that consistency in assay, moisture, and particle profile enables predictive modeling in new product launches. As a result, their troubleshooting time drops, and they’re more likely to avoid unexpected production stops.
From an environmental compliance standpoint, regulators favor manufacturing footprints with minimal emissions and clear records. Our experience in waste handling and solvent recovery puts us in discussions about closed-loop production models—several partners share how this supports both internal sustainability goals and external customer audits.
Our manufacturing facility frequently helps customers transition from pilot projects to routine production. Starting out, teams might require just a few hundred grams for synthetic trials and lab-scale workups. As projects advance, those requirements grow into the multi-kilogram and tonnage ranges. One practical observation: scaling up with 3-Hydroxy-4-Methylbenzoic Acid tends to involve fewer formulation headaches than many other aromatic acids. Particle morphology and batch consistency maintain their integrity right up to the bulk scale, reducing the risk of delayed launches.
Throughout scale-up, analytical support and batch history become more critical. Clients value being able to trace each batch lot and receive rapid technical guidance if minor properties shift outside expectations. To address this, we keep detailed batch records and provide on-request technical documentation for every production run, often at no extra cost. This approach, grown from requests by our most demanding partners, lowers both technical and administrative burden during critical phases.
Every new project brings unique challenges. For 3-Hydroxy-4-Methylbenzoic Acid, we’ve learned to pre-empt customer pain points by targeting root causes. Early on, clients shared experiences of inconsistent particle size leading to inaccurate dosing during automated weighing. Our response involved overhauling sieving and milling stations so that every batch meets a narrow particle size distribution. This shift not only improved blend uniformity but reduced total cycle time in customer facilities.
Moisture pickup resulting from poor packaging once impacted not just our warehousing, but also the flow ability and stability of the acid itself. Our packaging team moved to high-barrier liners paired with vacuum-sealed drums—feedback since implementation has shown far fewer reports of clumping or caking. Teams appreciate being able to dose directly from containers without breaking up solidified blocks, which can otherwise impact yield and accuracy.
We have also observed that solvent selection and work-up protocols drive a huge variation in both cost and environmental impact for downstream partners. By running parallel trials in our applications lab, we can provide solvent recommendations that optimize both product recovery and minimize waste. These protocols are shared upon customer request and are regularly updated as new data comes in, building a knowledge base our clients use for process improvement.
Supply chain continuity matters for both small R&D orders and large manufacturing contracts. Disruptions can stall entire production lines. Maintaining robust supplier networks for all starting materials, keeping buffer stocks, and running multiple reaction vessels in sync lets us ensure on-time delivery, even when global logistics slow down. Additionally, our established relationships with reagent suppliers earn us preferential access for critical raw materials, helping us buffer against spikes in demand or supply gaps during spot market volatility.
3-Hydroxy-4-Methylbenzoic Acid stands out during analytical method development. Quality control labs appreciate its sharp melting point and reproducible HPLC/GC retention times. The compound’s UV-absorbing properties enable straightforward UV-based identification, reducing the layers of unnecessary complexity in verification. Thanks to the consistency of our manufacturing, reference standards for internal calibration—whether for pharma, food contact, or industrial hygiene—remain reliable over many years.
As regulatory scrutiny tightens across many sectors, the structure and stability of 3-Hydroxy-4-Methylbenzoic Acid help reduce surprises during impurity profiling. Analytical teams find it easier to meet threshold limits for related substances, since the methyl and hydroxy groups minimize side product formation during standard process chemistries. Our internal documentation and thorough batch release data let customers satisfy compliance auditors efficiently.
Some industries, particularly in Europe, have raised concerns about trace contaminant levels in aromatic acids sourced from third parties. Our experience has shown that vertical integration—controlling both key precursor input and end-stage refinement—leads to detectable reductions in contaminants like toluene, formaldehyde, or heavy metal ions. Several multi-national partners reported smoother cross-jurisdiction certifications, in part due to stable impurity profiles and well-documented change controls on our side.
Our engagement with partners continues long after initial order fulfillment. Over the past decade, open dialogue with both production managers and R&D scientists using 3-Hydroxy-4-Methylbenzoic Acid has led us to multiple real-world improvements. No chemical operates in a vacuum. We solicit troubleshooting reports, host regular technical calls, and offer lab-scale samples for process validation. Recent feedback influenced our decision to invest in a new milling system, producing even finer, more homogeneous powder—an upgrade now standard across all large-volume orders.
Collaborative development extends to sustainability concerns. Several clients on-boarding 3-Hydroxy-4-Methylbenzoic Acid for the first time raised valid questions about green chemistry routes. We have responded with life-cycle assessments and solvent recovery programs, as well as ongoing research into water-minimized processes for the next generation of aromatic acid chemistry. Partners seeking to reduce regulatory complexity in their own products look to these programs as evidence of responsible stewardship.
Multiple application areas feature crossover techniques. Our in-house specialists have supported transfer of knowledge from pharmaceutical intermediate synthesis to polymer additive research—accelerating success by sharing best practices for reaction optimization, work-up, and even downstream quality control. Whether a partner is preparing for a DMF filing or looking to improve yield in an adhesive project, our technical support and lessons learned remain readily available.
3-Hydroxy-4-Methylbenzoic Acid stands as a proven, high-value option in synthetic, analytical, and manufacturing settings. Our direct manufacturing experience proves that its unique substitution pattern offers advantages that reach well beyond the lab bench. Reliable performance, clear differentiation from other benzoic acid analogs, and responsiveness to real-world challenges drive selection among discerning formulators and production managers. Looking across long-term projects, it becomes clear that this compound rewards repeat users through supply stability, practical handling, and compatibility with emerging process technologies.
For those seeking to optimize workflow, enable sustainable practices, and extend the performance envelope in modern chemical production, 3-Hydroxy-4-Methylbenzoic Acid continues to demonstrate value borne out by evidence and experience—not just promise.