|
HS Code |
272665 |
| Chemical Name | 4-Chloro-3-pyridinecarboxylic acid |
| Cas Number | 877-24-7 |
| Molecular Formula | C6H4ClNO2 |
| Molecular Weight | 157.55 |
| Appearance | White to off-white solid |
| Melting Point | 187-190°C |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Synonyms | 4-Chloronicotinic acid |
| Storage Conditions | Store at room temperature, in a tightly closed container |
| Smiles | C1=CN=CC(=C1Cl)C(=O)O |
| Inchi | InChI=1S/C6H4ClNO2/c7-5-1-2-8-3-4(5)6(9)10/h1-3H,(H,9,10) |
| Hazard Statements | Irritant |
As an accredited 4-CHLORO-3-PYRIDINECARBOXYLIC ACID factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Chloro-3-pyridinecarboxylic acid, 25g, supplied in a sealed amber glass bottle with tamper-evident cap, labeled for laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12 metric tons packed in 480 fiber drums, each drum containing 25 kg of 4-CHLORO-3-PYRIDINECARBOXYLIC ACID. |
| Shipping | 4-Chloro-3-pyridinecarboxylic acid is typically shipped in tightly sealed, labeled containers to prevent moisture ingress and contamination. It should be transported as a solid under ambient conditions, following all relevant chemical regulations. Proper documentation, including Safety Data Sheets (SDS), must accompany the shipment to ensure safe and compliant handling during transit. |
| Storage | 4-Chloro-3-pyridinecarboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible substances such as strong oxidizing agents. Protect from light and store at room temperature unless otherwise specified. Ensure proper labeling, and restrict access to trained personnel to maintain chemical stability and safety. |
| Shelf Life | 4-Chloro-3-pyridinecarboxylic acid has a typical shelf life of 2-3 years when stored tightly sealed, cool, and dry. |
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Purity 99%: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures consistent yield and minimizes impurities in final products. Melting point 174°C: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with a melting point of 174°C is used in solid-state formulation processes, where the defined melting point supports controlled crystallization and processing stability. Molecular weight 158.55 g/mol: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with molecular weight 158.55 g/mol is used in agrochemical development, where accurate molecular mass allows precise dosing and formulation calculations. Stability temperature up to 120°C: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with a stability temperature up to 120°C is used in heated reaction conditions, where thermal stability prevents compound degradation and ensures reaction integrity. Particle size ≤50 microns: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with particle size ≤50 microns is used in fine chemical blending, where fine granularity enables uniform mixing and improved dissolution rates. Assay ≥98%: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with assay ≥98% is used in active ingredient calibration, where high assay guarantees accurate quantification and consistent product performance. Water content ≤0.5%: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with water content ≤0.5% is used in moisture-sensitive syntheses, where low water content prevents hydrolysis and ensures reaction reliability. Residual solvent <0.2%: 4-CHLORO-3-PYRIDINECARBOXYLIC ACID with residual solvent below 0.2% is used in GMP-compliant productions, where minimal residues support regulatory compliance and safety. |
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I’ve seen a lot of specialty chemicals come and go in the fine chemicals trade, but 4-chloro-3-pyridinecarboxylic acid stands apart for its reliability. Across lab benches and production floors, this compound keeps finding its way into researchers’ hands and overseas purchase orders for a reason. With its CAS number 877-24-7, it finds itself called for in medicinal chemistry circles, crop science R&D, and even the design of custom electronic materials. Its model sits squarely in the middle of a well-established family of pyridinecarboxylic acids, but the presence of the 4-chloro group gives it a unique reactivity and profile.
From years working alongside synthetic chemists, I know purity makes or breaks a batch. 4-chloro-3-pyridinecarboxylic acid comes off reputable lines as a pale powder, usually registered at purities ranging from 98% upwards. Its molecular formula, C6H4ClNO2, fits within a niche application range but also allows it to be picked up for straightforward transformations. The carboxylic acid group offers a convenient handle for modification – methylation, amidation, and chain extension are all common routes. Its melting point hovers in manageable territory (usually between 170-173°C) and those working at scale know that a consistent melting point signals low levels of undesirable isomers or byproducts.
In my own work, analytical spot checks — TLC, HPLC, NMR — rarely turn up surprises on quality lots of this acid. That’s worth mentioning because small hiccups in material quality send whole projects off track. Looking at a typical COA, the chloride content and residual solvents almost always fall well below critical thresholds, lending further confidence to anyone blending or modifying this molecule.
You see this compound pop up in medicinal chemistry research. It’s a frequent starting point for synthesizing kinase inhibitors, anti-infectives, and small-molecule probes. Its structure lends itself to straightforward Suzuki couplings, amidations, and reductions, so chemists reach for it when they want a pyridine ring with just the right mix of electron density and steric bulk. I’ve watched it become the nucleus for modified pyridines used in agrochemical actives — those herbicides and growth regulators farmers rely on for crop protection. Because the 4-chloro substituent steers selectivity and changes metabolic routes in the field, small adjustments here can mean a world of difference once a molecule moves from R&D to a farm plot.
Beyond medicines and crop science, this acid’s role in material science grows each year. It provides an aromatic backbone essential for synthesizing advanced liquid crystals and certain specialty polymers. These aren’t products that turn up on grocery shelves, but they power the phone screens in your pocket and the high-contrast panels in new electric cars.
In the warehouse, 4-chloro-3-pyridinecarboxylic acid stores easily. It’s stable at room temperature and isn’t known for excessive hygroscopicity, so the typical chemical packaging — fiber drums with liners or foil-laminated pouches — gets the job done. I’ve seen those who try to cut corners on packaging regret it, though. Airtight seals preserve not only purity but peace of mind for anyone who values reproducibility. Nobody wants an unexpected whiff of degradation products after weeks in storage.
From a logistics perspective, this acid avoids the complications that haunt more sensitive reagents. I’ve handled drums in humid climates from India to the Gulf Coast of the US without caking or significant color change. It travels safely as long as handlers follow basic chemical precautions. There’s no need for refrigerated transport, which is always a relief for shipping teams working to simplify costs and customs paperwork.
More than once, someone has tried to swap in a different pyridinecarboxylic acid mid-project — usually to save a few dollars or speed up sourcing. Through direct experience, that’s a risky bet. 4-chloro substitution on the pyridine ring changes its reaction pathways and interaction with catalytic metals. While the 3-position remains open to derivatization, the 4-chlorine atom steers the chemistry down its own road. For example, hydrogenation, palladium-catalyzed couplings, or nucleophilic aromatic substitution yield far cleaner products here than you’ll see with 3-pyridinecarboxylic acid or 3,5-dichlorinated analogs.
There’s another real-world difference — the environmental profile. Regulatory teams run data on degradation and environmental fate. Compared with some other substituted pyridines, the 4-chloro-3-pyridinecarboxylic acid breaks down more predictably under typical field and laboratory conditions. This isn’t just a talking point; faster, more reliable degradation means less regulatory headache for engineered molecules that reach the environment.
Anyone who’s spent time at a bench knows that even minor purity slips can wreck synthetic yields or laboriously optimized routes. With 4-chloro-3-pyridinecarboxylic acid, consistency hinges on sourcing. I never take vendor claims at face value. Instead, labs should rely on third-party testing, including updates on residual solvents, trace metals, and isomer ratios. Over the years, I’ve noticed that tighter supply chains — often direct relationships with fewer intermediaries — support more reliable deliveries. Working closely with your supplier, requesting fresh batch COAs, and performing in-house NMR verification on first deliveries has saved my colleagues and me more than a few headaches.
Realistically, the gap between technical grade and high-purity material can mean the difference between a stalled project and a lead molecule hitting scale-up. In one project focusing on antifungal agents, I watched a research team spend months optimizing a route, only to be tripped up by an unseen side product stemming from a subpar lot of starting acid. A quick switch to a vetted, high-purity supply resolved the anomaly and got the development timeline back on track. The lesson is clear: transparency with suppliers counts just as much as technical skill at the bench.
Ask any medicinal chemist or process development scientist about their bench toolkit, and you’ll start to sense the importance of reliable building blocks. 4-chloro-3-pyridinecarboxylic acid isn’t the kind of compound that makes splashy news, but its impact runs deep. Every time a new herbicide reaches market, or a promising kinase inhibitor reports a bump in selectivity, odds are good that compounds like this acid played a behind-the-scenes role. Its affordability relative to more complex heterocycles also makes it accessible for cash-strapped academic and startup labs, broadening the pipeline of innovation.
That reach extends beyond chemicals: think about the time resource — scientists work faster and more confidently when baseline materials perform. I’ve seen research groups turn months-long syntheses into weeks because their route started with a high-confidence, high-purity acid. In fields where patent races and licensing deals hinge on rapid cycles, speed and reliability translate to real-world success.
Any chemical deserves respect — I’ve learned caution from old-timers working with less modern safety gear. 4-chloro-3-pyridinecarboxylic acid, like many organohalogens, benefits from basic personal protective equipment. Nitrile gloves, lab coats, and effective local ventilation head the list. Its fine dust can irritate the respiratory system, so open containers under a hood. Good safety data backs up most companies’ handling recommendations, and I haven’t seen evidence linking this compound to outsize risk compared with others in its class.
In terms of environmental release, careful process control during washing, disposal, and clean-up prevents accidental loading to wastewater. Many companies now deploy closed-loop systems or activated carbon treatment to capture trace organochlorines, something worth investing in for labs and pilot plants. Integrated safety protocols and basic hazard training stop most issues before they start.
In talking to colleagues at trade shows and watching sourcing cycles over the past decade, it’s obvious that demand for 4-chloro-3-pyridinecarboxylic acid tracks closely with pharma and crop protection cycles. Fluctuations in Asian output, logistics crunches, or regulatory shifts create periodic shortages. Experienced buyers keep a reserve in place, and larger firms sometimes hedge by dual-sourcing across continents.
Cost trends tell a story of gradual upward pressure on specialty acids tied to raw material availability and environmental controls. Workhorse plants run continuous campaigns to ensure they can meet global demand. At the same time, tensions in energy prices and local environmental regulations apply extra costs. Flexible end users now consider alternate synthetic routes in case market volatility spikes or one supply chain region faces disruption. I’ve seen more research groups form consortia to pool demand and negotiate steady supply contracts, protecting themselves from spot shortages and pricing swings.
More than ever, academic journals and industrial clients scrutinize data on batch reproducibility, trace contaminants, and supplier transparency. After watching a promising synthetic route go sideways due to an undetected impurity in input acid, most chemists rightly grow cautious. Routine spectroscopic analysis (NMR, IR, and mass spec) and chromatography help catch problems before they become disasters. High-quality lots deliver clean TLC spots and sharp NMR signals, keeping scale-up on solid footing.
Process chemists also demand updated certificates of analysis that include expanded impurity profiles, not just minimum threshold data. I’ve seen customers reject shipments for failing to declare relevant heavy metal content or trace halogenated impurities. Long-term, setting tighter internal quality standards — and, if possible, harmonizing requirements across all projects using this acid — reduces internal friction and drives up the overall quality in downstream products.
Several recurring challenges come up in handling and sourcing 4-chloro-3-pyridinecarboxylic acid. Quality drift — slippage in purity or unexpected byproducts — trips up users at smaller scales without the means to test every incoming lot. Partnering with analytical labs, pooling resources to perform joint QC runs, or leveraging central university facilities solves this for many smaller firms. For larger buyers, contractual arrangements specifying routine third-party verification bring peace of mind.
Waste minimization also takes center stage, especially for groups running substantial campaigns where chlorinated organics can mean costly disposal. Plant engineers often turn to user-friendly solvent recycling equipment, and on the R&D side, greener methods that avoid chlorinated solvents altogether are gaining ground. Some synthetic chemists now design routes to minimize halogenated waste, employing modern coupling techniques or telescoping steps to cut the process footprint.
Sustainability pressures, both regulatory and reputational, encourage suppliers to invest in continuous process improvements. It’s encouraging to see more manufacturers publish lifecycle data and carbon footprint assessments for their product lines — a shift that supports better decision-making for end users trying to meet increasingly tough sustainability standards.
Mixing personal insight and years of industry observation, the continued value of 4-chloro-3-pyridinecarboxylic acid lies in its balance of reliability, reactivity, and accessibility. It might not garner headlines, but it underpins some of the most impactful advances in health, agriculture, and materials science. Where chemists, agronomists, and engineers demand both performance and predictability, this acid’s proven profile — from its defined melting point to its clear reaction pathways — ensures it remains a sought-after specialty material.
Ongoing dialogue between suppliers and users means evolving standards for quality and sustainability. As markets shift and application requirements grow ever more demanding, I expect this acid’s role to expand — new uses, improved synthetic routes, and increasingly transparent value chains. If experience is any guide, researchers and sourcing teams that treat this versatile compound with the respect it deserves — careful quality checks, sustainable handling, and a standpoint rooted in scientific rigor — will keep pushing the boundaries of what this basic chemical building block can help accomplish.