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HS Code |
684619 |
| Name | 3,5-Dihydroxybenzonitrile |
| Chemical Formula | C7H5NO2 |
| Molecular Weight | 135.12 g/mol |
| Cas Number | 500-83-4 |
| Appearance | Off-white to light beige solid |
| Melting Point | 211-215 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.38 g/cm³ (approximate) |
| Smiles | C1=C(C=C(C=C1O)O)C#N |
| Inchi | InChI=1S/C7H5NO2/c8-4-5-1-6(9)3-7(10)2-5/h1-3,9-10H |
| Storage Conditions | Store at room temperature, tightly sealed, in a dry place |
As an accredited 3,5-Dihydroxybenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3,5-Dihydroxybenzonitrile is packaged in a 25-gram amber glass bottle with a secure screw cap and label. |
| Shipping | 3,5-Dihydroxybenzonitrile is shipped in tightly sealed containers, protected from light and moisture. It should be handled with care, using appropriate personal protective equipment. The chemical is typically shipped by ground or air as a non-dangerous good, in compliance with local and international chemical transport regulations. Safety documentation accompanies all shipments. |
| Storage | 3,5-Dihydroxybenzonitrile should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances like strong acids or oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Properly label the container and ensure limited access to authorized personnel only. Avoid sources of ignition and store away from food or beverages. |
Applications of 3,5-Dihydroxybenzonitrile in Industrial ManufacturingAs the direct manufacturer of 3,5-Dihydroxybenzonitrile, we supply this specialty intermediate to advanced chemical processors and OEMs across several high-value sectors. Below, we detail specific industrial applications supported by technical compliance, process, and formulation insights drawn from real-world downstream use. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis3,5-Dihydroxybenzonitrile functions as a core intermediate in multiple API manufacturing routes within custom synthesis and generic small-molecule drug facilities. It undergoes further functionalization, including amination and condensation steps, allowing for the construction of complex aromatic scaffolds employed in several therapeutic categories such as antihypertensives and anti-inflammatories. Each batch must conform to critical purity and trace impurity requirements, especially in regulated offshore and domestic API plants. Our production ensures lot-to-lot uniformity for consistent downstream yield in multistep organic synthesis workflows. Industry compliance standards
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2. Advanced Agrochemical SynthesisMany advanced crop protection and pesticide actives require a resorcinol-type aromatic core, making 3,5-Dihydroxybenzonitrile a preferred intermediate for selected active ingredient syntheses. Agrochemical companies integrate it into pathways for constructing novel fungicides, herbicides, and insecticides, favoring its dual hydroxy-cyano reactivity for further halogenation, alkylation, or amide formation. Consistency in input chemistry supports large-scale campaigns for bulk technical material destined for formulation or further processing in downstream premix facilities. Routine traceability and batch retrievability ensure regulatory alignment for international product registrations. Industry compliance standards
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3. Dye and Pigment Intermediate ProductionManufacturers of high-performance dye intermediates incorporate 3,5-Dihydroxybenzonitrile within key condensation and oxidative coupling steps, particularly in synthetic routes for azo and anthraquinone dye precursors. The hydroxy and nitrile moieties enable direct functionalization, producing stable chromophoric structures suited for water-soluble and solvent-soluble dye end-use markets. Batch color strength and purity must meet established QC for downstream pigment dispersion and textile finishing. Close control at the primary synthesis stage ensures reproducibility across large commercial dye lots, supporting value chain integration at colorant producers worldwide. Industry compliance standards
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4. High-Performance Polymer Modifier SynthesisDownstream polymer manufacturers and compounding facilities apply 3,5-Dihydroxybenzonitrile as a monomeric modifier to produce specialty polyaryletherketone and polyarylethernitrile resins, enhancing thermal stability and flame-retardant properties. The difunctional groups permit controlled copolymerization and offer points for crosslinking, supporting custom-formulated polymers used in advanced electronic components, automotive under-hood parts, and chemical-resistant coatings. Purity and trace contaminant control directly impact resulting polymer performance, with precise pre-mixing and continuous addition required for batch-to-batch reproducibility at scalable volumes. Industry compliance standards
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At our manufacturing site, we handle diverse aromatic compounds every day, but 3,5-Dihydroxybenzonitrile often draws attention among chemists and purchasers with its versatility. We hear a lot of questions about this hydroxybenzonitrile. With our years of experience synthesizing and purifying it in bulk, we have witnessed the varied demands that different industries bring to this single product.
We produce 3,5-Dihydroxybenzonitrile in a controlled environment to ensure the highest purity. The product typically appears as a pale off-white crystalline powder. Experienced eyes can distinguish a quality batch by its clean appearance and the sharpness of its melting point, which signals solid control over synthesis and drying. We understand the pressures in pharmaceuticals, dyes, and specialty chemicals where a few tenths of a percent in impurity can alter reaction outcomes or product quality. To deliver what our customers expect, each lot undergoes stringent inspection with HPLC, NMR, and moisture content tests. We regularly ship with assay levels above 99%, but we always invite client-side checks because real-world verification prevents unpleasant surprises.
Some users request extremely tight specifications for their syntheses, particularly when downstream derivatization or API production comes into play. A standard batch from our plant carries these characteristics: melting point in the expected range of 191-194°C, potent nitrile odor indicating intact functionality, and low residual solvent content. Our process consistently avoids contamination by aromatic amines, which sometimes creep in with less robust setups. For fine chemical houses, small differences in trace metals or isomeric content could mean costly setbacks; we review our raw material inputs and process control logs for each lot before release. Moisture pickup during transit presents another key concern, so we seal our packaging in foil-lined drums, topped with desiccant packs. Field reports have proven that proper sealing makes a real difference in laboratory and pilot plant reproducibility.
Years ago, our production team supplied this intermediate mainly to dye manufacturers, where hydroxybenzonitriles help to introduce specific hues and high stability. Since then, demand has shifted thanks to progress in medicinal chemistry. Academic and industrial inquiries for 3,5-Dihydroxybenzonitrile have increased, especially for coupling reactions and heterocycle formation. Its dual hydroxyls and a strongly electron-withdrawing nitrile group give it unique reactivity among its isomers. In practice, this means faster conversions, cleaner reactions, and fewer side products when constructing more complex building blocks—something several clients in API and material science research have confirmed after switching from ortho or para hydroxybenzonitriles.
During a process transfer to a pharmaceutical client, we observed that their previous supplier’s ortho isomer promoted undesired coupling and gave broad, tailing peaks in chromatography. By introducing our 3,5-Dihydroxybenzonitrile, the team saw narrower peaks and eliminated a purification step, saving both time and money. This type of feedback has shaped our own raw material selection and purification strategy. Every kilogram that leaves our plant benefits from these real-world lessons.
Not all sources of hydroxybenzonitrile behave the same way. Some factories using legacy synthetic routes produce batches with yellowish tints and sticky powder texture, indicating residual byproducts or incomplete washing. At one point, a customer approached us after finding that another supplier’s product picked up humidity in storage, causing clumping that threw off dosing in their reactor feeds. In our plant, drying, sieving, and careful handling have reduced this risk. We have always favored filtration and crystallization stages that provide batch-to-batch physical consistency—powder should pour, not cake.
Some users look for material free from particular solvents or metal traces, especially when scaling up for regulated industries. For example, we keep solvents like dimethylformamide and toluene below detectable limits, as their presence could trip up downstream regulatory checks or interfere with analytical work. If a customer flags a new impurity or hardship in their process, we look at our own procedures together and troubleshoot until the root cause is clear.
It’s one thing to list potential uses, but what we see day-to-day shapes our opinion. In dye synthesis, the site-selective hydroxyl groups speed up azo coupling and generate more intense color shades. After shifting to our product, one pigment plant reported a 12% yield bump over their older meta isomer blend due to lower byproduct formation. Our batches allowed their process engineers to reduce base loads and shave minutes off each batch—practical improvements that make real operational differences.
Life science companies, especially those developing phenolic antibiotics and kinase inhibitors, value the strong electron-withdrawing nitrile group in the molecule. We worked with one research group struggling to maintain selectivity in their enzyme assays. Our high-purity 3,5-Dihydroxybenzonitrile improved their baseline, highlighting how a well-made building block avoids false positives from impurities or unpredictable breakdown products. That isn’t always obvious from a technical data sheet, but it becomes clear in repeated experimental runs.
Material scientists focus on the potential for functionalization. Introducing electron-rich hydroxy functionalities and an electrophilic nitrile opens synthetic doors to polyaromatic compounds and resins. Our product showed easy incorporation in a multi-step polymerization for an R&D customer, due to clean reaction runs free from traces of metals and byproducts that would otherwise poison the catalyst.
Sourcing chemicals looks straightforward, but those with lab experience know the pain of product variability. In busy production months, we’ve seen how the consistency of 3,5-Dihydroxybenzonitrile influences downstream efficiency and cost. It’s tempting to compare only price-per-kilogram across the market, though time and again, clients confirm that paying a little more for consistently pure lots avoids much costlier setbacks later. We dedicate real resources to repeated lab-scale and pilot plant evaluation, troubleshooting, and even customizing micronization or packaging when users face unique challenges in their reactors.
Years of scaling production have led us to standardize packaging, minimize headspace in drums, and keep product exposure to humidity minimal. We don’t just ship off-the-shelf boxes; our team adjusts pack sizes and container types based on actual feedback from plant techs handling multi-tonne reactors or kilo-scale research. It might seem minor, but overpacking or undersizing can clog material feeds, spill onto working surfaces, or confound inventory management—practical considerations that shape our operational choices.
Feedback from real users shaped our product evolution. Initial shipments went to a handful of dye factories and R&D labs, but as word spread, more technical teams started to specify custom grind sizes, lower moisture content, or even specific expiry dates. Some buyers needed drum lots for continuous production, while others bought small-scale packs for early-stage research. We learned to listen, adapting process steps and storage logistics to meet these requests, rather than relying on templated datasheet claims. Those actual use cases clarified which specifications mattered to whom.
For manufacturers of active pharmaceutical ingredients or specialty intermediates, trace element content and purity in the low ppm range mattered most. In pigment work, storage stability and flowability topped the list. Some academic clients cared less about cosmetic appearance and more about reactivity, asking for open batch data or unusual solvent-free lots for green chemistry. We kept records of these priorities, using them to improve each cycle of production, and sharing lessons learned across teams.
Global chemical supply chains saw more turbulence in recent years than at any time in recent memory. Access to pure, on-specification 3,5-Dihydroxybenzonitrile swung wildly for many downstream users. Customers shared stories of delayed shipments, out-of-spec consignments, and unexplained color or odor deviations. We maintained buffer stocks and short production lead times to stabilize our supply, and we approached each order as a partnership with the end user.
Purity matters for another reason beyond regulatory compliance or process yield: the reputation of your finished product hinges on the quality of intermediates. It is not uncommon for a slick-looking datasheet to mask underlying solvency or transformation issues that only reveal themselves under real reaction conditions. We’ve learned that investing in raw material inspection and repeated trial batches—the kind that simulate client processes—unveils potential trouble before it reaches the customer’s site.
Chemists often pit 3,5-Dihydroxybenzonitrile against its regiochemical cousins: 2,3-, 2,4-, or 4,5-dihydroxybenzonitriles. These isomers perform differently due to subtle ring activation and steric access around the substituents. Our teams have run side-by-side comparison syntheses to offer fact-based guidance on choosing the right variant for specific transformations. For example, certain oxidative couplings require the meta-hydroxyls present in 3,5-Dihydroxybenzonitrile, letting the reaction advance cleanly and predictably. That level of selectivity distinguishes it from other hydroxybenzonitriles, which tend to bring side reactions or offer less practical functionalization points.
Physical differences also crop up. The 2,4-isomer produced at our plant comes out as a stickier powder, prone to caking, and needs more anti-caking agents during transit. In contrast, 3,5-Dihydroxybenzonitrile usually delivers granular, free-pouring product bins, reducing waste in dosing and loss from sticking to vessel walls. Lab data and user feedback have shown that minor shifts in structure can reshape not just reactivity, but also practical handling during storage, weighing, and loading.
Our years on the production side taught us one guiding principle: proactively addressing end-user concerns creates the best long-term partnerships. Many issues only appear when packing is cracked open or a batch enters a heated reactor—by then, delays can turn into costly downtime. We personally keep logs of customer reports—storage failures, color instability, hygroscopic behavior, and foaming during dissolution. This feedback flows back into our process development and packaging design.
The next generation of chemical development will draw more on green processes, scalable manufacturing, and regulatory transparency. We have already begun implementing closed-loop solvent recovery, improved traceability for all input streams, and batch-level tracking that allows us to identify and resolve points of risk before they translate to off-spec products. 3,5-Dihydroxybenzonitrile, simple as it may look on a chemical drawing, gives a perfect example of how attention to process detail delivers not just better intermediate, but more reliable outcomes.
Seasoned plant operators will confirm that chemistry is only part of the story—the rest is logistics, follow-through, and honest communication. Over the years, we have discovered that even established clients benefit from open lines for sharing application-specific concerns or upcoming project shifts. One innovation manager recently explained that their team needed assurance of backward traceability and transparent audit trails in line with newly updated European standards; we made system changes to provide this, and now offer digital access to key batch records and analysis results.
There’s a sense of pride in being able to answer these kinds of requests quickly, using our own records and expertise rather than waiting for third-party clarification. The difference shows up not just in customer satisfaction surveys, but also in repeat orders and technical referrals.
Selling chemicals involves more than fulfilling a bill of materials. The way a product moves from drum to working solution, spreads out on a weighing spoon, or even cleans up after a spill all point to manufacturing practices behind each kilogram. We have found that transparency about manufacturing, real-time resolution of complaints, and preemptive supply chain adjustments distinguish reputable producers from those who simply move boxes onto a truck.
We routinely visit client plants, observe their batch set-ups, and see firsthand how our 3,5-Dihydroxybenzonitrile batches integrate into their protocols. A pigment plant once discovered that their automated feeder clogged less frequently with our free-flowing material. Another pharmaceutical team noted that our tailored packaging cut down on time spent in material reconciliation, simply because our batch was labeled and documented down to the smallest details.
The chemistry landscape keeps evolving. Tighter regulations, higher product standards, and rapid scaling of innovations all place demands on material suppliers. As direct manufacturers, we embrace these pressures not just to meet compliance, but to create more robust and reliable products. In the coming years, we expect new synthetic applications for 3,5-Dihydroxybenzonitrile to appear—perhaps in biobased material synthesis or advanced pharmaceuticals. Our approach remains grounded in feedback-driven improvements, rigorous testing, and a direct line from our process engineers to customer technical teams.
For those sourcing hydroxybenzonitriles, real value shows up in the smoothness of your scaling, the reliability of your test results, and the confidence your own customers show in finished goods. After decades of production and hands-on support, we know that every kilogram delivered shapes not just immediate chemistry, but the reputation and success of everyone in the supply chain.