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HS Code |
888736 |
| Cas Number | 39591-98-5 |
| Molecular Formula | C8H11NO |
| Molecular Weight | 137.18 g/mol |
| Iupac Name | 3,5-dimethyl-2-(hydroxymethyl)pyridine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 259.5 °C at 760 mmHg |
| Density | 1.06 g/cm³ |
| Solubility | Soluble in organic solvents; slightly soluble in water |
| Smiles | CC1=CC(=NC=C1C)CO |
| Synonyms | 2-(Hydroxymethyl)-3,5-dimethylpyridine |
| Refractive Index | 1.535 (approximate) |
| Flash Point | 126.3 °C |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Pubchem Cid | 265770 |
As an accredited 3,5-Dimethyl-2-Pyridinemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical “3,5-Dimethyl-2-Pyridinemethanol,” 25 grams, is supplied in a sealed amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | 20′ FCL: Drums tightly packed on pallets, net weight 12,000 kg per container, moisture-protected, with appropriate hazardous chemical labeling. |
| Shipping | **Shipping Description:** 3,5-Dimethyl-2-Pyridinemethanol is shipped in tightly sealed containers, protected from light and moisture. The chemical is transported according to local, national, and international regulations for laboratory chemicals. Proper labeling is ensured. Typically handled as non-hazardous, but care is taken to avoid spills or direct contact during shipping and handling. |
| Storage | Store 3,5-Dimethyl-2-pyridinemethanol in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep the storage area clearly labeled and restrict access to trained personnel. Avoid moisture and ensure proper grounding if storing in large quantities, as with most organic compounds. |
| Shelf Life | 3,5-Dimethyl-2-pyridinemethanol is stable under recommended storage conditions; shelf life is typically 2-3 years in a cool, dry place. |
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Purity 99%: 3,5-Dimethyl-2-Pyridinemethanol with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Molecular weight 137.19 g/mol: 3,5-Dimethyl-2-Pyridinemethanol with a molecular weight of 137.19 g/mol is used in fine chemical manufacturing, where it enables accurate stoichiometric calculations and consistent product quality. Melting point 48°C: 3,5-Dimethyl-2-Pyridinemethanol with a melting point of 48°C is used in organic synthesis reactions, where it allows for controlled phase transition and ease of handling. Viscosity grade low: 3,5-Dimethyl-2-Pyridinemethanol of low viscosity grade is used in liquid formulation blending, where it contributes to improved mixability and homogeneous distribution. Stability temperature up to 120°C: 3,5-Dimethyl-2-Pyridinemethanol stable up to 120°C is used in heat-assisted catalytic processes, where it maintains chemical integrity under elevated temperatures. Particle size less than 50 µm: 3,5-Dimethyl-2-Pyridinemethanol with particle size below 50 µm is used in catalyst carrier preparation, where it provides enhanced surface area and uniform dispersion. Water content <0.2%: 3,5-Dimethyl-2-Pyridinemethanol with water content below 0.2% is used in moisture-sensitive polymerization, where it prevents hydrolysis and maintains reaction efficiency. Color index ≤10 APHA: 3,5-Dimethyl-2-Pyridinemethanol with color index ≤10 APHA is used in transparent resin systems, where it assures product clarity and aesthetic quality. Residual solvent ≤100 ppm: 3,5-Dimethyl-2-Pyridinemethanol with residual solvent below 100 ppm is used in active pharmaceutical ingredient development, where it meets regulatory safety standards. Enantiomeric excess >98%: 3,5-Dimethyl-2-Pyridinemethanol with enantiomeric excess greater than 98% is used in chiral synthesis, where it guarantees high selectivity and purity of enantiomerically enriched products. |
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Long days in the lab teach people lots about what works and what simply gets in the way. Out of many reagents and building blocks, 3,5-Dimethyl-2-Pyridinemethanol finds a place on the shelf not because it’s flashy, but because it brings a balance between stability and reactive possibility that a good chemist knows to appreciate. Its structure—a pyridine ring carrying two methyl groups at the 3 and 5 positions, along with a hydroxymethyl group on the second carbon—changes how it acts when placed under different conditions. Instead of only reading off a spec sheet, people notice the real difference it makes in repeatable synthesis and reliability during scale-up. Anyone serious about results and not just filling space in the reagent cabinet understands why this specific compound earns respect.
This compound, recognized for its formula C8H11NO, lands in the hands of professionals who care about narrow melting range, low water content, and authentic purity levels. These aren’t just numbers to write down—water in the wrong place can ruin a batch, and a trace impurity can waste weeks. Typical bottles come with HPLC and NMR sheets backing up the purity, not because of marketing, but because trust is built on evidence. Whether a chemist is doing catalytic studies or designing a bioactive molecule, clean starting material means fewer surprises. Reliable suppliers stick to transparency, offering documentation for every batch, so if something goes sideways, users can track it back with confidence.
Talk to those working in synthetic chemistry, and patterns soon appear. 3,5-Dimethyl-2-Pyridinemethanol shows up in lots of protocols for ligand design, especially in reactions needing a nudge toward selectivity. People building up frameworks for catalysts, or heading into medicinal scaffolding synthesis, often find that the extra methyl groups tweak electronic properties in a helpful way. The secondary alcohol group tends to open up new directions in functionalization—ethers, esters, oxidations—all of which chemists use to build complexity without detours. The pyridine backbone gives the molecule a knack for metal-chelation, which explains why transition metal catalysis studies keep coming back to this compound. The small tweaks in structure let it fill a gap that more basic or more crowded pyridines can’t.
On paper, it’s sometimes lumped in with other pyridinemethanols, but real-world benchwork says otherwise. The difference stands out when a transformation runs clean at mild conditions, with fewer side products and easier purification. Working late into the night—when one more column might mean missing the morning—you really start to appreciate subtle, but crucial, improvements in reagent quality and behavior.
Plenty of pyridine derivatives promise performance, but experience shows not every option actually delivers when the tubes and flasks come out. The two methyl groups at the 3 and 5 positions in 3,5-Dimethyl-2-Pyridinemethanol do more than crowd the ring—they alter electron density enough to produce real differences in how the molecule interacts with acids, electrophiles, nucleophiles, and metals. Chemists see this shift in both yield and selectivity, particularly in reactions that are unforgiving to side pathways.
It’s not just a matter of brute force or higher reactivity. Some competing products, either with no methyls or with their groups stacked differently on the ring, lack the fine-tuned reactivity that the 3,5-dimethyl arrangement brings. Less optimized analogs might be cheaper by the gram but end up costing hours in optimization or troubleshooting. People who have slogged through those endless TLC plates and reruns develop a keen sense of what makes a practical intermediate, and many land on this specific structure for a good reason.
Purity and handling properties become important fast, especially when working with sensitive transformations. 3,5-Dimethyl-2-Pyridinemethanol doesn’t turn waxy, sticky, or volatile under standard bench conditions. Opening a bottle doesn’t fill the air with choking vapors like some analogs do. It dissolves steadily in common organic solvents—THF, dioxane, ethanol—without persistent clumping or slow mixing. This saves time and prevents frustration, which might sound minor until repeated over dozens of reactions.
Storage doesn’t present special hurdles. As with most organics, keeping it in amber glass and away from moisture is best practice, but unlike certain more delicate pyridines, it doesn’t break down or form problematic byproducts after only a few months. Among research groups and process chemists, that kind of stability is worth paying a little extra. Nobody likes walking in on Monday to find out their compound grew crystals of some mystery impurity over the weekend, or worse, corroded a storage vessel. This experience gives teams confidence in both planning and scaling, especially when repeat batches are required.
While some labs stick to using base pyridinemethanol or try cost-saving alternatives, those who push for precision—developing pharmaceuticals, tuning ligands, or advancing coordination chemistry—soon recognize that not every variant offers the same control. Methyl substitution at the 3 and 5 positions changes both solubility and electronic character, which plays out in every stage from initial reaction to purification. Routine shortfalls of less optimized compounds manifest as low selectivity, nagging coproducts, or demand for harsh reagents to drive completion. Real progress on tricky transformations has made people notice these drawbacks the hard way, and word spreads quickly among colleagues.
With 3,5-Dimethyl-2-Pyridinemethanol, the modest shifts caused by structural tweaks often turn frustrating procedures into more straightforward work. It’s not a universal fix, nor is it magic—but in a field where small details turn into big wins or losses, the right building block brings shared relief across the team.
Opinions shaped by years of trial and error have a different flavor from catalog copy. After seeing too many batches of generic reagents spoil at the most inconvenient moment, people start to value material they can count on. 3,5-Dimethyl-2-Pyridinemethanol draws its following from real-world reliability—reacting as expected, storing without drama, behaving consistently at every scale. Friends across different labs mention that time after time, it saves them a headache on substitution and metal-binding protocols.
Having seen both the failures and the successes that stem from switching intermediates mid-project, I can say that the money saved on a cheaper option rarely makes up for the cost in lost time. No one remembers the few dollars pocketed in the short term, but every chemist remembers the night that a trusted supply ran out and the backup batch kept failing—or made the NMR assignments a nightmare. Selecting a better-performing variant like this pays off in traceable, long-term ways.
Seeing a certificate of analysis attached to a shipment feels reassuring—provided it’s backed by solid, batch-specific data. In a space where one contaminated flask can derail weeks of planning, reputable dealers of 3,5-Dimethyl-2-Pyridinemethanol go further than minimum requirements, providing thorough spectral and chromatographic verification. End users compare these results with their own in-house controls, and the match is rarely off. If a question arises, responses are timely, and documentation includes details down to analytical method and reference standards.
This trust becomes critically important when working under GMP or compliance-heavy settings. Traceability back to raw material source, as well as transparent records of each lot’s production and handling, give buyers peace of mind. Having realistic expectations about batch-to-batch uniformity helps everyone—not only avoiding costly missteps, but protecting the integrity of the research. Pure material alone doesn’t guarantee a good result, but it lays the foundation that all serious chemistry relies on.
Every experienced researcher has a drawer or two packed with the ghosts of past mistakes. Early in my own bench career, I reached for generic pyridinemethanol when building a metal complex library, thinking a methyl here or there wouldn’t make much difference. After days of muddled NMR spectra, stubborn emulsions, and reactions that never seemed to reach completion, someone wiser walked over and pointed at the structural mismatch. Swapping in 3,5-Dimethyl-2-Pyridinemethanol resolved those issues nearly overnight—a lesson that fine details in molecular design don’t just belong in textbooks but play out in the hands-on work of the lab. This story isn’t unique, and as teams grow, advice handed down takes on special weight.
Sometimes, issues arise not from the main reagent, but from a contaminated bottle or a supplier that cut corners. Outsourcing to vendors who take pride in their quality saves much chasing down stubborn contaminants or repeating purification. With 3,5-Dimethyl-2-Pyridinemethanol, well-established suppliers uphold high standards, making it easier to detect sources of error if the lab ever runs off course. This reliability builds community confidence and allows researchers to set ambitious goals, knowing their materials won’t hold them back.
Several cutting-edge research areas depend on careful selection of building blocks. In pharmaceutical development, lead optimization can turn into a marathon of synthesis and resynthesis, and every inconsistent reagent magnifies delays and regulatory headaches. Medicinal chemists lean toward 3,5-Dimethyl-2-Pyridinemethanol for its role in scaffold diversification and late-stage functionalization, both critical for tuning biological properties. Similarly, those working in ligand design—meshwork that underlie catalysis or chiral recognition—depend on structure-activity relationships informed by these subtle methyl groups.
These aren’t just scholarly pursuits. The everyday grind of building small-molecule libraries, diagnostic probes, or fine-tuned ligands for industrial processes relies on dependable molecular tools. Over the years, 3,5-Dimethyl-2-Pyridinemethanol evolved from an obscure intermediate to a go-to staple, known not by the flashiness of its catalog entry but by performance in real, demanding reactions.
Every compound, no matter how trusted, presents the chance for misadventure if skipped over details or improper storage creep in. Mishandling can undermine the reliability that users count on. Being vigilant about container hygiene and proper resealing—never scooping from open bottles or contaminating with wet spatulas—matters as much as supplier documentation.
Another challenge comes when switching up a protocol or transferring methods between labs. Subtle differences in grade, age, or even the solvent environment can shift outcomes. Open communication about sourcing, lot numbers, and perceived differences helps minimize finger-pointing and wasted effort. Teams used to sharing successes also benefit from speaking up when things go awry, tracing the issue back before small cracks become major setbacks.
Waste disposal and environmental factors can’t be ignored, either. Like most pyridine derivatives, 3,5-Dimethyl-2-Pyridinemethanol should be handled mindful of local regulations and best laboratory practices. Careful logging and compliance with hazardous waste procedures build habits that protect people, facilities, and the surrounding environment, which only increases trust across the field.
Looking back on years in research, the most expensive purchases rarely caused regret. It’s shortcuts—cheaping out on critical reagents or gambling on unproven sources—that leave the deepest scars. 3,5-Dimethyl-2-Pyridinemethanol, at a glance, might seem like a minor upgrade from generic pyridinemethanol, but once weighed against weeks of reliable progress, it justifies its place. Those who’ve learned this lesson aim to balance budgetary constraints with project-critical needs, sometimes even pooling orders to keep quality up and costs controlled.
Seasoned group leaders often share wisdom at meetings and conferences: cut cost elsewhere before downgrading chemicals that play central roles. This approach pays off through reproducible data, easier troubleshooting, and the kind of professional pride that builds strong research programs. Over time, the difference between a good year and a slog often traces back to small, thoughtful choices—like choosing the better variant.
The culture among synthetic chemists and chemical engineers naturally shifts toward sharing both wins and failures. Whether through preprints, conference talks, or casual chats in the hallway, best practices spread fast. Many who rely on 3,5-Dimethyl-2-Pyridinemethanol take the time to report both positive and puzzling results. This open dialogue helps new users sidestep costly mistakes, and brings out new uses that push the boundary of what the compound can do.
A more connected research world means issues—such as unexpected side reactions or compatibility with new catalysts—surface quicker and get solved by collective effort. Crowdsourcing solutions—swapping purification tricks or warning about a troublesome vendor—has helped keep the use of this compound clear-eyed and honest, never just relying on marketing.
Near the heart of chemical innovation, it’s not always the biggest or showiest molecules that push projects ahead. 3,5-Dimethyl-2-Pyridinemethanol proves the value of fine-tuned design and quality-focused execution. My own journey, echoed by users across the field, points to the lasting payoff from honest evaluation, responsible sourcing, and lessons passed down from one researcher to the next. As the needs of the lab keep growing more complex, and as demands on precision keep rising, compounds with proven, reliable profiles will continue to earn trust—project after project, year after year.