|
HS Code |
453009 |
| Chemical Name | 2-Chloro-6-methyl-3-pyridinecarbonitrile |
| Molecular Formula | C7H5ClN2 |
| Molecular Weight | 152.58 g/mol |
| Cas Number | 6640-26-2 |
| Appearance | White to light yellow solid |
| Melting Point | 58-60°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CC1=NC=C(C#N)C(Cl)=C1 |
As an accredited 3-pyridinecarbonitrile, 2-chloro-6-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 100 grams of 3-pyridinecarbonitrile, 2-chloro-6-methyl-, labeled with hazard symbols. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Drums or bags, 12–14 metric tons net per container, packed securely to prevent spillage or contamination. |
| Shipping | Shipping of 3-pyridinecarbonitrile, 2-chloro-6-methyl- requires secure, labeled packaging according to hazardous material regulations. The chemical should be stored in airtight containers, protected from light, moisture, and incompatible substances. Ensure compliance with local and international transport guidelines, including documentation of hazard classification and safety data sheet (SDS) provision. |
| Storage | 3-Pyridinecarbonitrile, 2-chloro-6-methyl- should be stored in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and properly labeled. Store in original or compatible chemical containers, protected from direct sunlight and moisture, and follow all relevant safety and regulatory guidelines. |
| Shelf Life | Shelf life of 3-pyridinecarbonitrile, 2-chloro-6-methyl-: Typically stable for 2-3 years if stored cool, dry, and tightly sealed. |
|
Purity: 3-pyridinecarbonitrile, 2-chloro-6-methyl- with 99% purity is used in pharmaceutical intermediate synthesis, where enhanced yield and reduced impurity formation are achieved. Molecular Weight: 3-pyridinecarbonitrile, 2-chloro-6-methyl- of 150.59 g/mol is used in agrochemical development, where accurate formulation and consistency in bioactivity are ensured. Melting Point: 3-pyridinecarbonitrile, 2-chloro-6-methyl- with a melting point of 58°C is used in fine chemical production, where uniform processing and material handling are facilitated. Solubility: 3-pyridinecarbonitrile, 2-chloro-6-methyl- with high solubility in organic solvents is used in catalyst research, where rapid dissolution improves reaction kinetics. Thermal Stability: 3-pyridinecarbonitrile, 2-chloro-6-methyl- with stability up to 180°C is used in high-temperature synthesis routes, where degradation rates are minimized. Particle Size: 3-pyridinecarbonitrile, 2-chloro-6-methyl- with a particle size below 50 microns is used in advanced material composites, where improved dispersion and uniformity are maintained. |
Competitive 3-pyridinecarbonitrile, 2-chloro-6-methyl- prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Our job in chemical manufacturing means getting to grips with molecules that don't just perform, but deliver consistency that our customers can trust from one shipment to the next. 3-pyridinecarbonitrile, 2-chloro-6-methyl-, with a catalog model of 2-chloro-6-methyl-3-cyanopyridine, belongs to a class of pyridine derivatives that underpin modern organic synthesis. Through years of hands-on production, we've come to respect the value of compounds like this when it comes to offering solid performance in pharmaceutical intermediates, crop protection research, and specialty chemicals development.
From a manufacturing standpoint, a compound's true value shows through the feedback from our customers who run sensitive reactions that leave little room for error. 2-chloro-6-methyl-3-cyanopyridine brings something to the table that some basic pyridine nitriles just can't match: a stable chlorine handle at the 2-position and a methyl group at the 6-position. This tailored structure enables selective reactivity in cross-coupling, nucleophilic substitution, and heterocycle expansion. Downstream chemists appreciate how these unique groups streamline route scouting and scale-up, saving both time and cost.
We focus on delivering the product in a form that does what lab work demands. From the outset, we invest in raw material selection, reactor temperature control, and crystallization steps that drive batch purity upward. Pure 3-pyridinecarbonitrile, 2-chloro-6-methyl- doesn't just mean fewer headaches down the line, it means smoother process development, less cleanup, and clear analytical signals. The pale solid or crystalline powder we supply passes through rigorous inspection, built on analytical methods—HPLC, NMR, GC-MS—proven in industrial settings.
Customers approach us with real challenges: downstream intermediates must hit quality targets, reaction yields need to justify investment, and regulatory standards push much of the pressure onto raw ingredient sourcing. We've learned that a published assay of over 99% isn't just a selling point—it's a must for any process that can't tolerate byproduct interference.
Typical batches reach this bar, with water content kept below 0.3%. Our packaging team works with moisture-proof liners, because even brief exposure during transfers can let moisture undermine sensitive synthesis. A standard packaging unit comes in 25kg fiber drums, but we scale up for bulk orders in appropriate containers, reflecting years of experience moving sensitive powders for fine-chemical clients.
From batch sampling, we've observed a melting point tight around 64–67 degrees Celsius for pure lots. Many process chemists ask about this figure since even a degree or two can signal contamination or unexpected equilibrium. Though melting point can vary with pressure and local impurity load, we give honest, batch-specific data because transparency brings repeat business and keeps development teams focused on real variables.
Pyridine rings offer remarkable versatility, but the ortho-chlorine and para-nitrile combo here allows for transformation steps that less substituted pyridines struggle with. Many of our pharma and crop-science customers lean on 3-pyridinecarbonitrile, 2-chloro-6-methyl- for ease in Suzuki and Buchwald couplings, not to mention efficient introduction of amides, amidines, or other heterocycles by displacing the chloride under mild conditions.
We’ve observed start-ups aiming for unique kinase inhibitors and agrochemical firms developing novel insecticides reach for this molecule because it bridges the gap between pure building block and reactive intermediate. With the 6-methyl’s electron-donating effect and nitrile’s activating nature, they gain a platform that's reactive enough to move chemistry along without risking uncontrolled side reactions.
It’s easy to underestimate the number of variables in pyridine chemistry. Control over reaction conditions, quench technique, and drying parameters all show up in the product’s downstream value. Our in-house team maintains a semi-continuous synthesis route, monitoring by-product load at multiple stages. We calibrate analytical checkpoints along the way so final material shows a single major peak by HPLC and confirms structure by both 1H and 13C NMR.
Year-to-year process optimization has paid off. Five years ago, our plant saw up to 0.7% cumulative unidentifieds with some older reactor setups; we've since replaced agitators and fine-tuned the addition sequence to cut this down below 0.2% for our dedicated lots. Customers have responded with better yields in their own hands, and we've received repeat feedback confirming that less purification means faster time to market. Chemical manufacturing is never static, so we adjust as the market and technology shift.
As a manufacturer, we pay attention to where our chemicals get put to work. In the pharma sector, 2-chloro-6-methyl-3-cyanopyridine makes for an excellent early-stage intermediate. Its combination of halide, methyl, and nitrile leaves multiple handles open for elaboration while showing good bench stability. Contract research organizations favor this compound when screening series of candidate molecules for lead development.
In crop protection, the molecule’s reactive sites translate into new scaffolds for fungicides and insecticides. Several multinational clients have let us know the methyl group aids environmental persistence tuning, while the nitrile improves binding characteristics. Since the capture of patent territory often rides on just such substitutions, having a ready batch with traceable QA history has tipped the scales for more than a few contracts.
Custom synthesis players approach us for specialized variants. We’re always ready to explore custom manufacture, including isotopically labeled or alternate halide versions, since our setup allows flexible starting materials and route control. Many competitor products on the market either lack clear traceability or offer inconsistent specifications—both of which can set development projects back weeks or months. We’ve built our business by not cutting those corners.
If someone asks what sets this compound apart from closely related nitrile pyridines, the answer often lies in synthetic flexibility. More basic pyridinecarbonitriles, without substitution at 2 or 6, generally perform with less selectivity in cross-coupling and tend to suffer from regioisomer formation or off-pathway reactions. The 2-chloro-6-methyl version we make lets users leverage the ortho and para reactivity for more controlled outcomes.
From direct experience, we’ve seen a far lower rate of product loss on downstream HPLC with substituted versions like this, compared to unsubstituted analogues. The difference shows up most starkly in late-stage functionalization, where competing positions on the pyridine ring confuse catalysts or promote poor selectivity. Our track record with 3-pyridinecarbonitrile, 2-chloro-6-methyl- proves that the right substitution pattern minimizes post-reaction purification and increases isolated yield.
Some projects do call for smaller or bulkier groups in the 2 or 6 position, yet the methyl group here balances electron effects and steric profile. This fine-tuning proves vital when the molecule operates as a scaffold for biological target engagement. Years of customer feedback have reinforced that our controlled substitution brings both predictable yields and good downstream processability.
Generic product claims don’t help the chemist running reactions on tight timelines or budgets. Instead, we concentrate on translating practical experience into tangible value: stable crystalline form, easy sampling, and clear analytical documentation for every batch. We train our operations staff with a strong focus on material handling, running sample splits through both internal and third-party labs, so nothing leaves our plant with question marks over its identity or purity.
This approach stems from listening to feedback—the kind that comes in the form of urgent calls for additional documentation during regulatory submissions or a request for deeper lot history after an unexpected HPLC signal. Our philosophy is simple: chemists want what works so they can focus on discovery, scale-up, and launch. We get out of the way except to make sure the chemical supplied does exactly what was promised, with no unwelcome surprises.
At the plant level, developing a traceable history for each lot doesn’t just satisfy audits, it underpins reliable project scheduling for our clients. Our in-house batch records pair with digital spectrograph snapshots—each lot can be traced back to the precise run date, reactor, and operator. These systems help demonstrate our commitment to traceability and give our customers confidence during their own compliance reviews.
Some industry peers cut corners on documentation. We know all too well the fallout: product recalls, failed runs, opaque C of A trails. More than once, customers who tried switching to a cheaper supply have returned after seeing process failures or failed regulatory submissions. This supports our belief that robust internal controls and open traceability make a tangible difference once the compound leaves our facility.
No one can predict every challenge in today’s dynamic fine chemical marketplace. Patents shift, environmental regulations evolve, and demand for greener, more process-efficient molecules keeps rising. We respond by re-evaluating our own upstream routes, looking for ways to switch to greener solvents or cut down on hazardous byproducts. Our shift toward water and ethanol-based crystallization, for example, reduced organic waste and earned recognition under local regulatory frameworks.
We maintain dialogue with downstream innovators, because market shocks—like new import tariffs or sudden demand surges—ripple upstream fast. We’ve stood through supply chain crunches and worked overtime to meet urgent batch requests when customer projects pivoted unexpectedly. This gives us a practical viewpoint: transparency and regular updates prove more valuable than making hard promises about a "never interrupted" supply flow.
We entered the chemical industry long before "digital twin" became a buzzword, relying instead on plant data, hands-on troubleshooting, and a feedback loop with the customers who actually push molecules to market. As a result, our production of 3-pyridinecarbonitrile, 2-chloro-6-methyl- reflects not just technical skill, but steady improvement based on lessons learned at the bench and the reactor.
This means every batch we load for shipment carries not only analytical credentials but a manufacturing backstory—experiments, optimizations, failures, and hard-earned process tweaks. Each technical inquiry, whether about impurity profiles or alternate synthetic routes, gets root-level attention. We don’t shy away from sharing what went right or wrong: chemical manufacturing is as much about navigating complexity as it is about hitting numbers on a certificate.
Many established manufacturers stick faithfully to standard catalogs, yet the evolving needs of research and development push us to offer more. Increasingly, our partners seek tailored impurity profiles, specific packaging environments, or even bespoke chemical modifications integrated upstream. Our setup allows quick adaptation, whether that means installing an extra purification column or scaling a batch with unusual environmental controls.
Our research chemists keep up with trends in late-stage functionalization and green chemistry, regularly trialing alternative bases or solvent systems for this compound. Direct collaboration with key customers means we get early warnings of emerging requirements, letting us trial new approaches before they become industry standard. We value this cycle—market signals, lab trials, process updates—since it places us on the front line of meaningful product evolution.
Throughout years in this business, we’ve learned chemical manufacturing never runs on autopilot. Unexpected shifts in demand, regulatory requirements, and downstream workflows call for much more than transactional sales. We nurture partnerships—listening to real-world needs, adapting specification packages, and speeding up custom sample delivery.
Like every serious manufacturer in the sector, we stand behind our product not out of routine but because our reputation and future business rely on each delivery performing exactly as described. We pride ourselves on answering technical questions directly, supporting scale-up guidance, and keeping channels open for honest feedback.
We take pride in supplying 3-pyridinecarbonitrile, 2-chloro-6-methyl- to some of the most demanding innovators in pharmaceuticals and agrochemicals. Our approach to this compound—prioritizing traceable quality, offering honest data, and fostering adaptable, cooperative relationships—stands as our simple formula for success. As regulatory environments tighten and discovery cycles accelerate, it’s the hands-on experience and openness to feedback that truly set us apart.
For anyone developing new molecules or improving established processes, the choice of raw material partner determines not just cost, but speed and certainty. By staying true to robust quality controls, continuous improvement, and open communication, we help our customers keep their projects moving—right from the first gram up to full-scale campaigns. This is how we see our role as a manufacturer today and in the future.