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HS Code |
543891 |
| Chemical Name | Pyridine-2-carboximidamide hydrochloride |
| Synonyms | 2-Pyridinecarboximidamide hydrochloride |
| Cas Number | 7154-56-7 |
| Molecular Formula | C6H8ClN3 |
| Molecular Weight | 157.6 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 209-215°C |
| Solubility | Soluble in water |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Inchi | InChI=1S/C6H7N3.ClH/c7-6(8)5-3-1-2-4-9-5;/h1-4H,(H4,7,8);1H |
| Smiles | C1=CC=NC(=C1)C(=N)N.Cl |
As an accredited Pyridine-2-carboximidamide hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White crystalline powder, sealed in a 25g amber glass bottle with a secure screw cap and desiccant; labeled with product details. |
| Container Loading (20′ FCL) | 20′ FCL container holds Pyridine-2-carboximidamide hydrochloride securely packed in 25kg drums or bags, maximizing volume, ensuring safe international shipping. |
| Shipping | Pyridine-2-carboximidamide hydrochloride is shipped in tightly sealed containers, protected from moisture and light. It is packed with appropriate cushioning inside robust outer packaging to prevent leaks or breakage. The shipment complies with chemical transport regulations, includes clear hazard labeling, and is accompanied by relevant safety documentation and Material Safety Data Sheet (MSDS). |
| Storage | Pyridine-2-carboximidamide hydrochloride should be stored in a tightly closed container, protected from moisture and light, at room temperature (15–25°C). Keep it in a well-ventilated area, away from sources of ignition, strong acids, and oxidizing agents. Ensure proper labeling and secure storage to avoid accidental exposure. Follow all local regulations regarding chemical storage and handling. |
| Shelf Life | Pyridine-2-carboximidamide hydrochloride typically has a shelf life of 2-3 years when stored in a cool, dry, and sealed container. |
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Purity 98%: Pyridine-2-carboximidamide hydrochloride with a purity of 98% is used in pharmaceutical intermediate synthesis, where high chemical yield and minimal impurities are ensured. Molecular weight 156.63 g/mol: Pyridine-2-carboximidamide hydrochloride with molecular weight 156.63 g/mol is used in ligand design for coordination chemistry, where precise stoichiometry and reliable interaction profiles are achieved. Melting point 205°C: Pyridine-2-carboximidamide hydrochloride featuring a melting point of 205°C is used in high-temperature reaction systems, where thermal stability ensures consistent processing. Particle size <50 µm: Pyridine-2-carboximidamide hydrochloride with particle size less than 50 µm is used in formulation of fine chemical reagents, where rapid dissolution rates and uniform distribution are obtained. Stability temperature up to 80°C: Pyridine-2-carboximidamide hydrochloride stable up to 80°C is used in storage-sensitive research applications, where preservation of structural integrity over time is critical. Water solubility 20 mg/mL: Pyridine-2-carboximidamide hydrochloride with water solubility of 20 mg/mL is used in aqueous bioassay preparations, where complete solubilization enables accurate dosing and analysis. |
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For those of us focused on pharmaceutical development and chemical synthesis, Pyridine-2-carboximidamide hydrochloride stands out as a compound we return to repeatedly in the lab. Years on the manufacturing floor have shown that every batch requires the same close attention, from raw material selection through to final packaging. This hydrochloride salt, with its CAS number 17156-73-1, often goes by 2-pyridinecarboximidamide hydrochloride. Our model 2PCIH is produced at a consistent assay greater than 98%, keeping strict control over both trace contaminants and moisture, since these factors impact downstream reactivity.
Chemists trust this molecule for its unique position within heterocyclic chemistry. The 2-position substitution on the pyridine ring gives the amidine group a direct orientation for hydrogen bonding and nucleophilic reactions. In our production, controlling particle size proves critical. We refrain from micronizing too finely, since lumps can clump during shipment and excess fines can lead to dusting or loss, especially troublesome for formulation blending or custom synthesis.
At the bench, most professionals working with Pyridine-2-carboximidamide hydrochloride seek robust intermediates for pharmaceutical discovery or industrial dye synthesis. The amidine functionality sits ready to form guanidines, amidrazones, or serve as a key building block for heterocycle construction. We see recurring orders from teams designing kinase inhibitors, antiparasitic candidates, and certain ligands tailored for metal catalysis. Academic teams appreciate our ability to tailor the batch size—scaling production runs from kilograms to pilot lots—without shifting the analytical fingerprint of the finished salt.
Our experience suggests that chemical stability during storage and transportation matters just as much as purity. The hydrochloride salt form resists ambient hydrolysis and oxidation, preserving both solubility and reactivity when dissolved in methanol, ethanol, or water. For those requiring silica column purification or in-situ derivatization, the hydrochloride version of pyridine-2-carboximidamide provides improved handling compared to the free base or alternative salts. Repeated hands-on testing with thermal gravimetric analysis and HPLC quality checks ensures we catch rare degradation risks before anything goes into a drum or bottle.
Manufacturers sometimes offer the free base or other salts for certain amidine compounds, yet our own work demonstrated that hydrochloride brings two direct benefits: greater shelf stability and a tighter melting range. The hydrochloride salt form withstands everyday temperature swings during transportation, so the consistency during storage beats the free base, which may absorb atmospheric CO₂ or release ammonia. Whenever a client encountered color changes, pH drift, or stickiness after a few months, the culprit inevitably turned out to be an alternate salt or an unbuffered sample.
We have always encountered fewer issues with caking and deliquescence with our hydrochloride batches than with their nitrate or acetate counterparts. This difference comes down to stronger lattice energy and denser packing in the crystalline state. Recrystallized hydrochloride needs less silica drying or extra filtration. Shelf-life data from our own storage trials backs this up: 2PCIH stays bright white and flows smoothly for more than 24 months under sealed conditions. By contrast, competing salts often yellow or clump up within six to twelve months.
Even in direct synthetic applications, hydrochloride’s improved water solubility makes aqueous phase or biphasic extractions much smoother. Several times, custom synthesis projects hit a snag with unwanted emulsification when technicians attempted to use the free base or acetate. These bottlenecks disappeared after switching to our hydrochloride material, which dissolved quickly and left subsequent phases crystal clear.
From firsthand perspective, every step of making pyridine-2-carboximidamide hydrochloride demands discipline and patience. Handling hazardous reagents—especially during the amidination step—requires trained staff and robust ventilation. Our manufacturing team has implemented rigorous pre-drying and purification regimens, not simply as a regulatory checkbox but as a result of observing real-world impact on product consistency. After years of adjusting batch speeds, tweaking solvent systems, or swapping filter aids, the process now delivers a reproducible material every time.
What technicians and project leaders often ask is where this compound slots in among related substances—say, 4-pyridinecarboximidamide, or aminoguanidine derivatives. Our own experience highlights that the 2-position offers better site-directed reactions on the pyridine backbone, thanks to adjacency to the ring nitrogen. Tautomeric stability does not introduce any ambiguous peaks in NMR, so structural assignments for downstream products rarely generate doubts. For research groups aiming for highly pure, easily traceable intermediates, this detail makes a difference—especially in regulated process development or push-button kilo-scale synthesis.
Quality control at the point of production sets apart real manufacturers from repackaging operations. We devote active time and resources to in-line monitoring using FTIR and automatic titration. Years ago, we found that relying solely on endpoint testing led to bottlenecks and missed chances to catch early trends. By shifting to near-continuous observation, batches requiring adjustment could be tuned in real time—long before drying or crystallization. As a result, lots display less than 1% moisture by Karl Fischer method, and we keep metallic impurities well below typical market averages.
End users in pharmaceutical research tell us they notice when compound arrives visibly free of dust or yellowing, without sticky residue on the packaging. This doesn’t happen by accident. Direct oversight means we pack only after confirming milligram-to-kilo consistency across test lots. In situations where clients requested larger drums for plant-scale campaigns or microbottles for high-throughput screening, our fill team has adjusted labeling and stacking protocols, always reviewing batch records before release.
Some manufacturers reduce all chemicals to interchangeable commodities, but those who use pyridine-2-carboximidamide hydrochloride for complicated multi-step syntheses know how reagents made with care lead to smoother reactions and less troubleshooting. Reputations in this field grow or wither based on whether chemists get reliable results week after week. We have received direct feedback that switching to our material reduced purification steps in imidazopyridine or pyrimidine projects, with fewer byproducts resulting from cleaner parent material.
Scale-up specialists favor this compound for pilot and early phase production, where avoiding batch-to-batch variability saves time and budget. Our team keeps application records not out of formality, but from experience troubleshooting for partners in real-time. Whether batch size shifts from 500 g to 20 kg, process steps involving our hydrochloride avoid the guesswork and trial-and-error common with less consistent alternatives. Analytical support includes HPLC retention data, impurity profiles, and customized COA packages where required. When working on tight delivery schedules, these small assurances become decisive.
Handling and shipping pyridine-2-carboximidamide hydrochloride does raise health and regulatory questions. In our own operations, we keep the intake air rate high in production suites and train workers thoroughly on spill containment. Hydrochloride dust remains irritating, so our staff wear proper masks and use anti-static mats. By following guidelines and ensuring trace solvents meet pharmacopeial standards, the risk of cross-contamination or hazardous decomposition events remains minimal.
Shipping regulations rarely cause issues for hydrochloride compared to flammable or highly toxic chemicals—this salt does not trigger Dangerous Goods labelling at common batch sizes. Our warehouse crew packages material in double-sealed, moisture-barrier bags. This approach prevents caking during sea shipment or air freight, and our records show less than a fraction of a percent product return rate—usually the result of simple mislabeling, not quality complaints.
Many new researchers ask if it matters where their pyridine-2-carboximidamide hydrochloride comes from. After years refining every production stage, we can say with certainty that reliable performance in scale-up projects or early drug development does depend on more than a matching CAS number. Small details—like using an extra precipitation step, washing crystals thoroughly, or selecting the optimal grade of hydrochloric acid—directly impact how the salt behaves in your reactions. For example, recycled solvents or off-spec bulk acids have caused yield drops over 5% in our earliest test runs. Our solution sticks with certified raw materials and redundant QC at every major handoff in the plant.
Users in specialty fields, including those developing analytical reference standards or advanced ligands, benefit from lots generated with traceable origin and full batch history. Our in-house analytical team maintains primary reference samples for up to five years post-lot. Clients have confirmed that downstream impurities rarely crop up, and when they do, we offer batch trace-back and root-cause analysis to keep projects on track.
Some of the recurring practical questions from our customers include solubility in polar and non-polar solvents, compatibility with organic oxidants, and photostability. Through direct laboratory testing, we have found that 2PCIH dissolves rapidly in water, acetonitrile, and lower alcohols. For those using strong oxidants, our data shows minor byproduct formation under standard oxidative workup, but complete recovery with antioxidant buffering. Stability to light ranks high as well—material stored in amber vials at ambient temperature remains unchanged over more than a year in our monitored environment.
Technicians pulling material for multi-gram bench-scale synthesis ask for recommendations on transfer methods. In our own labs, we suggest closed-system spatulas, since the compound’s fine crystals can disperse if open scooping is used. We keep our handling procedures adaptable, matching the real-world needs of those doing preparative or analytical work. Over the years, picking up insights through process troubleshooting helped us improve not only manufacturing but also how users interact with the compound.
True expertise in manufacturing stems from persistent effort and close communication with users. Our team regularly reviews project feedback, not just for customer satisfaction but also for insight into the practical success of our product design choices. We have tweaked crystallization flow, adopted new particle sieving geometry, and updated dessication protocols all based on issues flagged by partners in the field. Sometimes this means running side-by-side pilot batches and matching powder flow characteristics, especially for process chemists driving automation in tablet or injectable formulation. With each lesson learned, we turn immediate feedback into incremental upgrades—never from a single laboratory, but a blend of dozens of long-running collaborations.
One common story comes from partners who previously sourced generic or repackaged lots, only to face setbacks from batch-to-batch inconsistency: sluggish dissolution, unexpected clumping, or leftover process residues. After consulting with our team and switching to directly-manufactured material, these teams reported smoother workflow and reproducible analytical results. By staying close to the manufacturing process and keeping collaboration channels open, we maintain a cycle of feedback-driven improvement that outpaces routine “quality by specification.”
A detailed look at downstream use of pyridine-2-carboximidamide hydrochloride in pharmaceutical and fine chemical contexts highlights its unique contributions. In the past five years, we have supplied material for over 100 development campaigns, from preclinical proof-of-concept through to toxicology scale-up. End users report that this compound features in synthesis of pyridine-fused heterocycles, as a nucleophilic partner in guanidinylation, and as an amidine donor in targeted substitution. Reaction yields using our hydrochloride consistently come in above 90% for optimized routes, based on feedback and joint review of laboratory notebooks.
A practical illustration from a key partner: during process optimization for a potential CNS-active pharmaceutical ingredient, early lots from unidentified sources generated side reactions attributed to excess base and trace metallics. After switching to our controlled-lot hydrochloride, off-target byproducts vanished and purification steps dropped from three to one. Chromatographic purity exceeded 99%, and pilot batches maintained photostability over months, supporting the decision to advance to commercial supply.
Industrial dye teams use our hydrochloride form for nucleophilic aromatic substitution reactions. The improved solubility in polar media enables faster reactions, sharper endpoint titrations, and color product reproducibility from batch to batch. Several specialty materials clients have achieved higher selectivity during ligand preparation for coordination chemistry applications, highlighting how even a simple salt form can impact the entire process.
Our daily work with pyridine-2-carboximidamide hydrochloride has taught us that genuine quality emerges from experience, transparency, and constant willingness to listen to users. By remaining hands-on in every phase of production, QC, and customer support, we move beyond the limitations of generic alternatives and give project teams real peace of mind. The next generation of chemical and pharmaceutical breakthroughs ride on the shoulders of reliable building blocks. Through our continued commitment to direct manufacturing, process traceability, and open dialogue, we help our partners push discovery further, confident in the materials driving their research and production forward.