|
HS Code |
108202 |
| Iupac Name | 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine |
| Molecular Formula | C17H20BNO2 |
| Molecular Weight | 281.16 g/mol |
| Cas Number | 910869-16-0 |
| Appearance | White to off-white solid |
| Melting Point | 159-162°C |
| Smiles | CC1(C)OB(B2=CC=C(C3=CC=NC=C3)C=C2)OC1(C)C |
| Inchi | InChI=1S/C17H20BNO2/c1-17(2)21-16(20-17)18-15-8-6-14(7-9-15)13-4-10-19-11-5-13/h4-11,16H,1-2H3 |
| Solubility | Soluble in common organic solvents (e.g., dichloromethane, THF) |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store in cool, dry place; under inert atmosphere |
| Purity | Typically ≥98% (commercial) |
As an accredited Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25 grams of Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl] sealed in an amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-: Securely packed, moisture-controlled, labeled drums/pails, maximizing space, ensuring safe transport and compliance with chemical safety regulations. |
| Shipping | This chemical, Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, must be shipped in tightly sealed containers under dry, cool conditions. Ensure proper labeling and packaging in accordance with relevant hazardous material regulations. Avoid exposure to moisture, heat, and incompatible substances. Consult the SDS for specific transport classifications and emergency procedures. |
| Storage | Store Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- in a tightly sealed container in a cool, dry, well-ventilated area away from moisture, heat sources, and incompatible substances such as strong oxidizers and acids. Protect from direct sunlight. Handle under inert gas (such as nitrogen or argon) if sensitive to air or moisture. Follow standard laboratory safety protocols. |
| Shelf Life | Shelf life of Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- is typically 2-3 years when properly stored. |
|
Purity 98%: Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- with a purity of 98% is used in Suzuki coupling reactions, where it ensures high coupling efficiency and minimal byproduct formation. Molecular Weight 321.25 g/mol: Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- possessing a molecular weight of 321.25 g/mol is used in pharmaceutical intermediate synthesis, where it optimizes molecular compatibility for downstream processing. Melting Point 142°C: Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- with a melting point of 142°C is used in solid-phase organic reactions, where it provides thermal stability during reaction conditions. Moisture Content <0.5%: Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- featuring moisture content less than 0.5% is used in organometallic synthesis, where it minimizes hydrolysis risks and preserves reagent reactivity. Stability Temperature 120°C: Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- stable up to 120°C is used in heated reaction systems, where it maintains structural integrity throughout extended synthesis protocols. |
Competitive Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- 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!
As a chemical manufacturer, daily life means constant interaction with molecules that end up shaping pharmaceuticals, advanced materials, and novel research frontiers. Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- holds a key place among these building blocks. In our facilities, we treat this organoboron compound not as a mere reagent but as a bridge connecting traditional aromatic chemistry to modern cross-coupling strategies.
This molecule enters our reactors as carefully weighed raw materials, subjected to rigorous process control across each batch. Each lot goes through a sequence designed to deliver a clean, crystalline solid fit for Suzuki-Miyaura couplings and related applications. We manage purity at each stage—removing unreacted starting material and isomeric byproducts, checking for moisture ingress, confirming the absence of metals from catalytic residues, and ensuring the boronic ester core stays intact.
Other pyridine derivatives often end up as ligands or building blocks, but few combine the electronic contributions of a pyridine ring and the reactivity of a pinacol boronate. That union shapes both stability in storage and reliability in downstream coupling procedures, especially in settings where reproducibility turns into cost savings and troubleshooting risk drops.
Instead of stopgap descriptions, our team relies on lived experience: batches of this molecule must dissolve smoothly in anhydrous solvents, not just sit on the shelf waiting for an order. Real-world lab feedback fuels our conversation around sand-like powders versus glossier crystalline material—a difference that shows up during weighing, transfer, and dissolution.
We aim for material free-flowing enough to dose precisely, without caking from moisture pickup. Small differences in bulk density and granule hardness can snowball across upstream and downstream steps, causing pipetting headaches or wasted product. Commitment to process, monitoring, and batch adjustment was born from seeing material performance bottleneck entire chemistries. No theoretical description replaces lab techs scrutinizing powder texture or chemists reporting an unusually “sticky” lot.
This compound’s exact substitution pattern turns the dial on how it engages in cross-coupling. The 4-position boronic ester on a para-substituted phenyl delivers balanced electron density and sterics. Changing the ring position changes the reactivity; moving the nitrogen from pyridine or substituting the boronate region leads to unpredictable yields or side products.
Older boronic acids often hydrolyze faster, generate more protodeboronation byproducts, or attract water that destabilizes entire bins over a few weeks. Pinacol-protected boronates like ours resist hydrolysis, help maintain shelf stability, and let chemists spend less time fussing about dryboxes or stabilizers. The pinacol group also increases compatibility with a wider array of ligands and catalyst systems, especially palladium, which has driven this class of compounds into the front line of arylation technology.
Traditional pyridines lack this tailored balance. They might enter reactions as nucleophiles or ligands, but without the boronic ester, they have little to offer contemporary cross-coupling chemistry. Alternatives with varied protecting groups either break down sooner or complicate purification. Our experience guiding process optimization comes from cataloging batch failures and learning that every change in protection strategy carries a ripple effect on yields, waste, and safety conditions.
We measure product quality by its ability to deliver predictable results on the scales customers actually use. Our technical staff spends time in regular communication with research labs and scale-up teams. They report flocculation problems, tricky filtration, or unexpected side reactions. We incorporate this feedback into how we control end-point purities and fine-tune storage protocols. It's not some abstract quality metric—we track how often scientists report “clean” couplings, low tar formation, or skipped recrystallization steps.
On paper, competitors offer similar nominal purities and comparable melting points. Differences become clear in how products handle moisture on long transit routes, survive summer shipping delays, or avoid microcontamination by breakdown products detectable only once the material interacts with sensitive enzymes or ligands.
We track every batch by lot and date, keep archival samples for each run, and apply lessons drawn from stability data stretching back years. Our staff cross-links feedback from medicinal chemists seeking high-throughput screening with the demands faced by process engineers tasked with running multi-kilogram syntheses. One batch showing subtle yellowing or extra fines signals an immediate investigation, not a future project.
This care pays off in low-waste, high-yield Suzuki couplings, especially as the pharmaceutical sector tunes protocols for key heteroaromatic linkages. We’ve watched innovations in process chemistry outpace catalog chemistry—there’s no substitute for chemical provenance or open conversations between our technical support and the bench. Sourcing directly from us means any deviation in yield, product color, or crystalline appearance gets addressed with every back-end record available.
Our approach draws lessons from years of adjusting protocol based on real-world environmental and safety audits. The shift from boronic acids to pinacol boronates wasn’t cosmetic; it helps minimize hazardous byproduct formation, cut down on need for specialized ventilation or scrubbing, and makes shipping safer for both people and the environment.
Disposal procedures—often overlooked until a batch goes off—factor into our product design. The pinacol group stays robust in normal storage conditions without producing volatile acids. Even end-of-life solutions integrate into broader green chemistry initiatives aimed at reducing metal leaching, excess solvent use, and processing water contamination. Material that leaves our facility carries a backup trail of documentation not to tick a regulatory box but to answer every question about source, safety, and chain of custody.
We regularly host external auditors, run internal training to maintain best practices, and respond in real-time to shifts in industry guidelines. These measures foster trust, not only within our company but throughout the supply chain, all the way to labs using our materials in clinical trial precursors or cutting-edge research.
Chemists in academic groups use our product for small-scale coupling methods, aiming for novel heterocyclic targets or combinatorial libraries. In pharmaceutical manufacturing, batches scale smoothly to larger reactors—years of collaboration taught us that only tightly specified moisture and impurity limits unlock those outcomes. We’ve seen how the overlap between aromatic and boronic ester chemistry opens up design space for kinase inhibitors, PET imaging agents, or next-generation OLEDs.
Some customers press for modifications—alternative protecting groups, different isomer ratios, or tighter allowable impurity profiles. Our approach remains grounded in empirical validation. We run parallel stability and reactivity studies, sometimes pursuing alternate routes if a target application warrants. Every change runs face-to-face with our knowledge of how fragile some of these systems become under non-ideal handling.
Feedback from custom synthesis projects guides which impurities need stricter thresholding. Early-stage researchers often tolerate broad spec ranges, but makers of clinical trial material watch for every trace byproduct. We adjust methods: changing a quench step, washing sequence, or even the geometry of our filtration gear—all with the user’s pain points in mind.
Long-standing relationships with medicinal chemists taught us to listen closely to reports of water content, high-residue salts, or bits of side products that only emerge as chromatography surprises during scaleup. Informed manufacturing means human contact across every order and real troubleshooting help instead of formulaic responses.
Stories circulate about failed couplings, material stuck to vials, or endless purification headaches caused by minor lot-to-lot inconsistency. We view these as learning moments—each time a project manager tells us a competitor’s batch fell short, we dissect possible trace contaminants, packing flaws, or missed storage details.
Direct communication with process engineers lets us tweak drying protocols, alter packaging to resist humidity spikes, or investigate subtle energetic differences between granular forms. We don’t treat our compound just as a CAS number; it’s reflected in our QA tracking, post-shipment follow-up, and willingness to recall or replace if anything diverges from our own standards.
No two batches ever leave our floor without clear, transparent data on NMR, chromatography, and moisture content. We prepare reference spectra for every lot, storing them in accessible archives. Customers receive this documentation as a matter of course, not a paid add-on.
In the rare event that a task calls for more specialized spec—even at higher cost or extended lead time—we shift resources to meet the demand rather than pressing standard product. Scientists know us as manufacturers who respond, not as distant catalog vendors.
Investment in process improvement carries weight only when reliability shows in end use. We have run countless experiments optimizing crystallization rates, washing conditions, and packaging materials. Handling techniques change as the seasons shift or as end-user protocols pivot; we keep up by testing fresh approaches, such as improved anti-caking agents or custom fiber drums for large-quantity shipments.
With access to advanced analytical tools, we catch suspect lots earlier, minimizing costly delays downstream. Data from real-time shipping loggers helps us watch for temperature swings or transit damage. These investments keep the product’s active boronate functionality intact, even as it travels across continents or sits in international customs.
The focus remains on material that meets the same reactivity benchmarks, batch after batch. This lets research teams redirect their energies away from sourcing stress and back to building new medicines, advanced polymers, or functionalized targets.
Real learning happens at the interface of intended chemistry and lived user experience. A misbehaving batch of Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- could ripple into lost research time or missed clinical campaign windows. We log every complaint, traceback to root sources, and treat minor quality glitches with the same urgency as major returns.
Growth as a manufacturer means documenting each process tweak, cross-training staff on new analytical results, and applying those lessons with each customer case. Sometimes, it’s about catching a trace contaminant; other times, it involves adjusting delivery timelines to accommodate stricter shelf-life windows.
We view quality as an evolving target—set not only by written specs but by the accumulated expectations and pain points shared by every lab, pilot plant, or process chemist relying on this building block.
Chemical manufacturing extends past selling grams or kilograms of a compound. Each batch of Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- carries responsibilities—to people, laboratories, and industries betting research budgets and public health on reliable access. We keep supply chains transparent, audit our own environmental footprint, and incorporate the insights of hundreds of research and production partners.
Where competitors focus on short-term pricing or top-line specs, we invest in long-term partnership and active feedback loops. Our doors remain open to chemists with questions, frustrations, or special requests. We treat every batch as a link in our commitment to safe, cutting-edge, reproducible chemical technology, grounded in years of manufacturing experience.
As direct manufacturers, not intermediaries, we see Pyridine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- as more than a catalog entry or line item—it's the result of disciplined process, steady learning, and transparent partnership with the people creating tomorrow's discoveries. Each lot stands as testimony to that tradition, each improvement grows from candid conversation and trackable action. That’s what sets our chemical manufacturing apart and turns every purchase into productive chemistry.