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HS Code |
630119 |
| Chemical Name | 2-Benzylpyridine |
| Cas Number | 3438-00-6 |
| Molecular Formula | C12H11N |
| Molecular Weight | 169.22 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 292-294 °C |
| Melting Point | -20 °C |
| Density | 1.052 g/cm³ at 25 °C |
| Refractive Index | 1.610 |
| Solubility | Insoluble in water; soluble in organic solvents |
| Smiles | c1ccc(Cc2ccccn2)cc1 |
| Inchi | InChI=1S/C12H11N/c1-2-6-11(7-3-1)9-10-12-5-4-8-13-12/h1-8H,9H2 |
As an accredited 2-Benzylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with tamper-evident cap, labeled “2-Benzylpyridine, 100g,” including hazard symbols, chemical formula, and supplier details. |
| Shipping | 2-Benzylpyridine is typically shipped in tightly sealed containers made of compatible materials, such as glass or HDPE, to prevent leaks or contamination. The packages are clearly labeled according to chemical safety regulations and kept away from heat and strong oxidizers, with documentation provided for safe handling and transport, in compliance with relevant shipping regulations. |
| Storage | 2-Benzylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition. Protect from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. Ensure that the storage area is clearly labeled and complies with applicable safety regulations to prevent accidental exposure or spills. |
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Purity 98%: 2-Benzylpyridine of purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting Point 53°C: 2-Benzylpyridine with a melting point of 53°C is utilized in organic reaction protocols, where it enables precise process control and reproducibility. Molecular Weight 183.25 g/mol: 2-Benzylpyridine with molecular weight 183.25 g/mol is applied in ligand design for coordination chemistry, where it delivers predictable stoichiometry and binding efficiency. Stability Temperature 80°C: 2-Benzylpyridine stable up to 80°C is used in high-temperature condensation reactions, where it maintains structural integrity and minimizes byproduct formation. Particle Size <100 μm: 2-Benzylpyridine with particle size less than 100 μm is used in catalyst formulation, where it improves dispersion and reactivity in heterogeneous systems. UV Absorbance 260 nm: 2-Benzylpyridine with UV absorbance at 260 nm is employed in analytical reference standards, where it guarantees accurate calibration and quantification. Water Content <0.2%: 2-Benzylpyridine with water content less than 0.2% is used in moisture-sensitive synthesis, where it minimizes hydrolysis and unwanted side reactions. Density 1.083 g/cm³: 2-Benzylpyridine at a density of 1.083 g/cm³ is used in specialty solvent blends, where it provides optimal miscibility and solubility characteristics. |
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At our facility, 2-Benzylpyridine occupies a critical spot among the specialized pyridine derivatives that feed high-value industrial and research processes. Chemists who handle heterocycles in their syntheses usually reach a crossroads where standard methylpyridines or simple pyridines no longer do the job — they want selectivity, stability, or a certain compatibility in their targets. This is where 2-Benzylpyridine, with its unique molecular skeleton, stands out. Our operation has run this compound through the wringer of daily quality checks, repeated scale-ups, and collaborative development with clients who push the boundaries of organic chemistry and downstream manufacturing.
This compound features a benzyl group at the second position on the pyridine ring, which immediately marks it as distinct from the isomeric 3- or 4-position analogs. At the bench, this arrangement shifts reactivity in a way we can measure and reproduce. Each batch of our 2-Benzylpyridine leaves analysis with a minimum GC purity of 99%. The color runs from clear to pale yellow, a sign of absence of significant decomposition or post-reaction residues from synthesis — a small but critical quality control point for us.
We produce this material in quantities ranging from gram-scale for R&D projects up to multi-metric-ton orders for commercial implementation. Packaging most often involves amber glass for smaller volumes and lined steel drums for bulk shipment, reducing the risk of light-initiated decomposition or leaching. Each container receives a tamper-evident seal, serving the dual purpose of customer trust and our own process verification.
When we synthesize 2-Benzylpyridine, we look for control at every stage, especially during alkylation and purification. The most common pitfall in pyridine chemistry – formation of regioisomers or benzylic oxidation byproducts – receives special scrutiny by our in-line monitoring systems. Over the years, experience has taught us which solvents to avoid, how to probe catalyst choices, and what's needed to steer the selectivity. These details matter most when the compound heads out to destinations in pharmaceutical development or fine chemical manufacture.
We dedicate multiple steps of analytical QC — GC-MS, HPLC, NMR — before signing off on a finished batch. In one instance, feedback from a long-term partner pointed to trace unknowns in the effluent, so we recalibrated column conditions and identified a rare co-elution artefact. That ran us through a week of adjustment, but our customers noticed the difference in downstream yield and separation ease.
Laboratories seeking intermediates for agrochemical or pharmaceutical synthesis rarely want a one-size-fits-all solution. In our experience, the demand for 2-Benzylpyridine arises mostly from two groups: medicinal chemistry teams trying to design novel bioactive motifs, and process chemists who need a pivot point — where the benzyl group acts as both a directing group and a protective anchor.
Our contacts in academic research often utilize 2-Benzylpyridine as a ligand precursor, or as a scaffold that can undergo further transformation via functional group manipulation. The benzyl substituent at the C2 position directs reactivity in cross-coupling and selective hydrogenation steps. Notably, we've collaborated with several pharmaceutical manufacturers to develop routes where the benzyl group is later cleaved, yielding a tailored pyridine core for highly specific applications.
For those building up N-heterocycles, the C2-defined benzyl exposure sets the stage for cyclization, halogenation, and borylation reactions. The starting purity and profile of trace metals have a noticeable impact on catalyst turnover, so our customers depend on us to limit those elements consistently below 5 ppm in finished product.
With every new inquiry, one of the first questions we answer centers on the difference between 2-Benzylpyridine and related isomers or simple pyridine derivatives. In practical terms, the position of the benzyl group skews both the electronic landscape of the ring and the steric environment around sites poised for further elaboration. For synthetic chemists and process engineers, that means reactions behave differently, even under nearly identical conditions.
We’ve tested batches of 3- and 4-Benzylpyridine alongside our 2-isomer under standard Suzuki couplings, and the outcomes diverge significantly; the C2 location supports more selective ortho-functionalization and manages to suppress unwanted N-alkylation. Our production notes from a multi-year catalyst project with an agrochemical company highlight this — yields using 2-Benzylpyridine reached over 92%, while comparable reactions with the 3-isomer lagged by at least 15% due to competitive side reactions.
Physical handling also differs. 2-Benzylpyridine carries a melting range slightly higher than some N-alkylpyridines, making it less prone to unwanted volatilization at room temperature. For formulators and technicians in the plant, this translates to a solvent choice with less headache and easier handling, both in weighing and transfer. Product stability, especially during long-term storage, becomes a manageable variable. We’ve responded to customer observations favoring 2-Benzylpyridine for multi-step syntheses, where even a single degree-shift in stability could interrupt a days-long reaction run.
Far from being a bench curiosity, 2-Benzylpyridine has found a place in several commercial product streams. Across our client portfolio, pharmaceutical companies look to this molecule to scaffold receptor-binding units, while materials scientists rely on it to introduce both rigidity and tunability in specialty polymers. The list extends to advanced dyes, select agrochemicals, and even as a building block for ionic liquids with unusual solubility and conductivity profiles.
For practitioners focusing on custom herbicide synthesis, the selective alkylation and subsequent functionalization offered by 2-Benzylpyridine streamlines multi-step processes. We have seen this molecule deployed as an intermediate for constructing extended aromatic systems, where the need for both stability in storage and predictable behavior in scale-up become critical. Our technical support teams have engaged in several troubleshooting sessions to optimize customers' purification methods, including solid phase extraction, crystallization, and column chromatography – each time, input from production and R&D feeds back into the process to push out trace impurities.
Another notable sector that takes advantage of 2-Benzylpyridine’s properties is the catalysts community. Several metal-catalyzed transformations leverage the electron-donating properties of the benzyl group for enhanced selectivity, especially when coupling with aryl halides or when activating the pyridine nitrogen for downstream ring functionalization.
Delivering high-purity 2-Benzylpyridine involves more than routine process control. Our long-term investment in analytical equipment enables us to move quickly when raw material specification changes ripple through the process. On several occasions, minor fluctuations in the aldehyde feedstock purity were traced down to seasonal changes from upstream suppliers. Each event triggered an internal review, rapid retesting, and ultimately process tweaks that held finished product within specification – preventing expensive product recalls or downstream process failures for end users.
Storage and transport conditions do not come as an afterthought. We’ve learned not to let sealed drums stand exposed for more than a few days, especially in warm climates where traces of residual alkyl halides could accelerate yellowing. Real-life production means working with logistics partners to synchronize shipping times, limit warehouse turnover, and implement regular spot-checks upon arrival at the customer’s site. Every step paid off during incidents where careful documentation preserved the integrity of both product and reputation.
Remembering our early days, material returned for “off-smell” led to pinpointing a storage tank cleaning agent residue. Today, nothing leaves the plant unless cleared by organoleptic and instrumental analysis, giving customers confidence that what’s on our certificate of analysis matches their expectations on the bench.
Markets and applications often bring questions about regulatory status, residual solvents, and potential environmental footprint. We audit our starting materials against relevant REACH and TSCA guidelines, and work to minimize traces of halogenated solvents during washing and purification steps. For those in the pharmaceutical and biotech industries, we document and verify process residuals below accepted limits, which can be the deciding factor for approval in an API synthesis route.
On-site, we maintain robust containment and air monitoring during both synthesis and packaging. This reduces both operator exposure and batch-to-batch product variability related to ambient contamination. Customers shipping our product across regions value our documentation trail for customs clearance and audit requirements, easing the path to global distribution.
Client feedback directly shapes our protocols. Several years ago, a formulation chemist reported trace solids forming during solvent concentration runs – a rare solvate from a new supplier’s stabilizer. We adjusted our raw material selection, added a final filtration, and re-validated the method. Yield improvement and removal of that issue saved downstream operators both man-hours and cost. We see this as a recurring cycle: end usage in the field identifies the small but costly drawbacks that batch analytics could miss, and our process improves for everyone.
In industrial partnerships, learning travels both directions. As manufacturers, our ears stay open to suggestions for modified grades – for example, customers who want lower trace moisture content for sensitive coupling reactions receive customized drying and packaging. Our operations staff logs each request, and in-house chemists replicate those customer procedures with production-scale samples to verify improvements.
Experience has also shown that seasonal shifts in humidity and temperature can subtly affect handling and reactivity. Customers report their real-world findings, such as shifts in solubility or extrusion properties in manufacturing environments; in response, we maintain flexibility in supply chain and storage recommendations depending on the customer's plant configuration. Adjustments such as switching to vacuum-sealed pouches for tropical shipment routes stemmed directly from this collaboration.
For researchers mapping new synthetic routes, each choice of starting material carries consequences downstream. We have seen process chemists compare candidate pyridines for dozens of kinetic and functional criteria, from selectivity under catalytic hydrogenation to compatibility with specific solvents. Our technical team often runs pilot-scale syntheses side by side with client methods, troubleshooting on the fly, documenting minor changes in color or consistency, and adjusting protocols in response to scalability hurdles.
Several customers have used our 2-Benzylpyridine in process development timelines that stretched over multiple years, with batch consistency underpinning reproducibility. For those making gram-scale sample libraries or shifting to hundred-liter reactors, having a partnership that can adjust delivery timing and scale on short notice adds practical value. Our scheduling team works closely with production and logistics to avoid delays, because real-time R&D timelines wait for no supplier.
In complex molecules, especially those aimed for regulatory submission or pilot-scale launch, trace impurities are an unforgiving bottleneck. Preparation and downstream handling protocols are tight; one overlooked variable in pyridine impurity formation or residual solvent content can add weeks to developmental timescales. We've built our batch logs and QC traceability around those demands, providing details not only for regulatory audits but also for teams validating process transfer from lab to plant scale.
Maintaining reliable 2-Benzylpyridine production requires adapting to a changing world. Regulatory landsapes tighten, clients innovate faster, and raw material supply chains evolve in ways that challenge tradition. By keeping production methods transparent and adaptable, we minimize surprises for customers who depend on stability and performance day after day. We keep feedback loops active, invest in process analytics, and build quality improvement into every kilogram made.
Every batch that leaves our plant reflects more than routine process compliance. It represents careful attention born from collective experience, close working relationships with chemists and engineers, and a resolve to support those whose product depends on each shipment meeting stringent expectations.
2-Benzylpyridine’s utility grows alongside new applications, but its success depends on more than molecular structure. By blending technical rigor, open communication, and readiness to solve emerging challenges, industrial and research customers can derive genuine value from a partnership grounded in real-world manufacturing practice.