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HS Code |
444687 |
| Cas Number | 872-00-6 |
| Iupac Name | 1-isoquinolinemethanol |
| Molecular Formula | C10H9NO |
| Molar Mass | 159.19 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 84-88 °C |
| Boiling Point | 324 °C |
| Density | 1.22 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | OCc1ncccc2ccccc12 |
| Inchi | InChI=1S/C10H9NO/c12-7-10-8-3-1-2-6-9(8)4-5-11-10/h1-6,12H,7H2 |
| Pubchem Cid | 186252 |
| Refractive Index | 1.678 |
| Logp | 1.2 |
| Synonyms | 1-(Hydroxymethyl)isoquinoline |
As an accredited 1-Isoquinolinemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Isoquinolinemethanol is supplied in a 25g amber glass bottle with a secure screw cap and tamper-evident seal. |
| Shipping | 1-Isoquinolinemethanol should be shipped in tightly sealed containers, compliant with local and international chemical transport regulations. Protect from heat, moisture, and direct sunlight. Label packages with appropriate hazard information and handle with care. Use compatible cushioning and secondary containment to prevent leaks or spills during transit. Suitable for ground or air shipment. |
| Storage | 1-Isoquinolinemethanol should be stored in a tightly sealed container, away from light, heat, and moisture. Keep it in a cool, dry, well-ventilated area, separate from oxidizing agents and incompatible substances. Store at room temperature and label the container clearly. Use appropriate safety measures, including secondary containment, to prevent accidental release or exposure. |
Applications of 1-Isoquinolinemethanol in Industrial ManufacturingAs a trusted manufacturer specializing in advanced chemical intermediates, we supply 1-isoquinolinemethanol to industrial clients operating across several critical synthesis sectors. Below, we provide a detailed overview of authentic downstream applications, compliance, usage protocols, integration procedures, and target formulations currently implemented within regulated manufacturing environments. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)Our material supports multi-step synthesis workflows in API manufacturing, especially for beta-blockers and CNS agents with isoquinoline scaffolds. Process engineers integrate 1-isoquinolinemethanol in N-alkylation or secondary hydroxylation stages, relying on its purity for consistent batch quality. Tight controls ensure conformance with specific drug monographs and reduce impurity profiles to meet global submission standards. Production-scale reactors use analytically-verified feedstock for direct conversion into pharmacologically active intermediates, enabling reliable timeline management for commercial scale-up and regulatory filings. Industry compliance standards
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2. Agrochemical Intermediate SynthesisAgrochemical contract manufacturers utilize this substance as a core modifier in forming heterocyclic herbicide and pesticide intermediates. Processing occurs in closed-system reactors under regulatory containment, often following a Grignard or Friedel-Crafts protocol. Blending precision affects the structural integrity and substitution efficiency. QC teams track in-process purity to ensure compliance with agrochemical registration dossiers, while scalable batch processes allow fine-tuning of input material based on route-of-synthesis and specific active ingredient development. Industry compliance standards
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3. Specialty Dye and Pigment ProductionDownstream manufacturers in the specialty dye sector leverage 1-isoquinolinemethanol for synthesis of nitrogen-containing pigment cores. Production protocols integrate the material during key ring-closure or methylation stages, which are essential for tailoring chromatic and solubility properties specific to demand in textile, ink, and plastics coloration. Inline spectroscopy and advanced analytical methods confirm proper incorporation, tackling quality assurance needs for consistency in color index registration and environmental safety standards. Industry compliance standards
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4. Research and Development for Analytical ReagentsProducers of analytical reagents and chemical standards rely on high-purity batches for new reagent development and structure-activity studies. The primary use involves conversion to reference substances or photometric agent precursors with well-characterized spectra. Our strict QC dovetails with ISO 17025 laboratory accreditation requirements, with material introduced to synthesis lines under controlled temperature and moisture conditions. Downstream, researchers employ the compound as a calibration standard or derivatization agent for analytical method development in regulated analytical laboratories. Industry compliance standards
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5. Fine Chemical Custom SynthesisCustom synthesis operations engage our 1-isoquinolinemethanol in the production of advanced building blocks with valuable N-heterocyclic motifs. The raw material enters project-specific synthesis at defined insertion steps, often serving as a nucleophile or ring-modifying group for further elaboration. Our supply chain supports procedures under well-documented ISO 9001 frameworks, and each custom campaign includes specification sheets and analytical data traceability to guarantee consistency for partners in material sciences and performance chemical design. Industry compliance standards
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Over the years, our team in the plant has poured a lot of effort into refining the synthesis routes for isoquinoline derivatives. We’ve found 1-Isoquinolinemethanol to be one of those compounds that really rewards attention to detail. It usually attracts chemists looking for a precise combination of aromatic structure and functional group flexibility. This isn’t just another heterocyclic alcohol — its molecular formula, C10H9NO, and the arrangement of the hydroxymethyl group at the 1-position, put it in a different category from many simple alcohols or standard benzylic alcohols.
We manufacture 1-Isoquinolinemethanol in quantities ranging from pilot-scale kilograms for R&D labs to larger industrial batches. Control at every step matters a lot more for this product than people sometimes realize. Minor impurities at the purification stage compromise its role in asymmetric transformations or target compound synthesis. We keep our purity levels tightly within 98-99% by weight, and routinely check for isomeric contamination — not something that can be skipped if you want reliable performance in the lab or plant.
The compound appears as a white to off-white crystalline solid, distinguished from many liquid or darkly colored quinoline derivatives. Because we insist on thorough drying and storage under inert atmosphere conditions, users don’t run into stability issues that could compromise sensitive reactions.
Direct feedback from our customers in pharmaceutical research shows that this molecule stands out as a synthetic intermediate for several alkaloids and active pharmaceutical ingredients. It nucleates well for downstream transformations — especially when labs move from isoquinoline to functionalized alcohols, ethers, or amides. In the hands of medicinal chemists, its structure often opens up new analog series for SAR (structure-activity relationship) studies. Unlike isomers or related heterocycles with different alkyl group positions, 1-Isoquinolinemethanol brings both the reactivity of a benzylic alcohol and the mild nucleophilicity offered by the pyridine-like nitrogen.
This is not a commodity-grade product. In our experience, using poorly controlled material creates more headaches than any procurement savings can justify. Uncontrolled synthesis leads to colored residues, altered melting points, and unpredictably reactive side products. Our customers often share that their downstream coupling reactions are sensitive to trace amine, aldehyde, and related contaminants. That's why we continue to enforce high-performance liquid chromatography (HPLC) and gas chromatography (GC) specs tailored to this molecule, far beyond what’s seen in basic chemical supply chains.
At our production site, making 1-Isoquinolinemethanol isn’t like turning out simple aliphatic alcohols. We start from fully characterized isoquinoline bases that need to meet stringent starting material profiles. This keeps trace impurities — especially isomeric and over-alkylated byproducts — from building up batch after batch. Reduction and functionalization steps work best under controlled hydrogenation conditions, and we focus on consistent catalyst reactivation protocols.
Handling the hydroxymethylation step demands a careful balance between conversion rate and selectivity. Overheating not only produces unwanted side chains, but also leads to material loss due to decomposition. Running the aqueous work-up and downstream drying through a closed system minimizes oxidative degradation. Most producers mark this compound as tricky because controlling water content is tougher than sales brochures make out. We’ve invested in dedicated glass-lined reactors and real-time moisture analyzers to consistently hit Karl Fischer results below 0.2%.
After isolation, crystallization requires matching solvent polarity curve to batch composition — a point learned the hard way by anyone who’s had a solidification disaster on the filtration line. Our plant operators use decades of know-how in cooling curves and seeding to yield the kind of crystalline product that facilitates downstream handling, limits fines, and ensures reproducible solubility.
Our analytical lab follows validated methods for identifying trace byproducts, using both NMR and mass spectrometry. The most common requests revolve around guaranteeing the position of the -CH2OH group on the isoquinoline ring. We use 1H and 13C NMR to show both the aromatic pattern and the unique chemical shift of the benzylic alcohol signal. The robustness of these tests makes it easy for researchers to confirm they’re working with the right substance, not just something “close enough”.
Melting point checks regularly fall between 62°C and 65°C, which lines up with literature values and lets us weed out unwanted impurity clusters. GC testing shows the main peak with minimal splitting, and HPLC puts our typical lots above 99% area normalization. For most research and process chemistry teams, that’s the difference between a successful synthetic milestone and a week chasing down a source of error.
Unlike many bulk heterocyclic compounds, 1-Isoquinolinemethanol’s moderate solubility in both polar and nonpolar organic solvents presents a real advantage during process design. We ship most lots in vacuum-sealed, amber glass to block moisture and UV exposure, thus allowing customers to use the entire batch without worrying about spontaneous yellowing or decomposition. Stability under controlled storage means a longer shelf life with less product lost to re-crystallization or caking.
Chemists sometimes try to substitute isoquinolinyl alcohols with their quinoline or pyridine counterparts. This shortcut almost never pays off. The unique reactivity profile of 1-Isoquinolinemethanol — especially the resonance effect from the nitrogen atom in the right position — simply isn’t available in alternative rings. Take 2-isoquinolinemethanol or its quinoline analog: their electron density and steric demand deviate just enough to throw off downstream reactions, whether it’s an O-alkylation, protective group introduction, or cross-coupling.
Our internal R&D group has run split-batch tests alongside commercial partners. In Suzuki and Buchwald-Hartwig couplings, 1-Isoquinolinemethanol shows higher conversion and less tar formation under identical conditions, all thanks to predictable nucleophilicity and base compatibility. Attempting the same sequence with isomeric benzylic alcohols invariably cuts yield and complicates purification — a pattern also seen with other non-isoquinoline heterocycles.
As a manufacturer, we deliberately avoid building production schedules for generic benzylic alcohols when customers specify this compound. The strict regulatory and quality needs for high-purity isoquinoline products are incompatible with multipurpose, low-purity lines. In fact, a lot of headaches in scale-up chemistry trace back to mistaken substitutions or the misapplication of commodity-level reagents to specialized targets like 1-Isoquinolinemethanol.
From the factory floor, one point stands out: users see most value in fields such as pharmaceutical building blocks, advanced agrochemical intermediates, and custom ligand development for metal-catalyzed processes. As a nucleophilic component, 1-Isoquinolinemethanol remains indispensable in synthesizing complex alkaloids and bridging motifs for biologically active molecules. Its aromatic platform and hydroxymethyl functional group enable a broad suite of downstream elaborations — such as etherification, oxidation, halogenation, and formation of chiral centers adjacent to the ring.
Process chemists in our partner companies often use it for scalable routes toward tetrahydroisoquinoline derivatives or regioselective heterocyclic scaffolds impossible to derive from less-finely tuned reagents. Due to its favorable leaving-group potential when protected or converted, large-scale reactions suffer fewer issues with side reactions compared to less substituted analogs.
Academic groups sometimes ask about its use as a model compound in mechanistic studies. The well-defined chemical shifts and reaction profile make it a reliable partner for exploring new reaction mechanisms or catalyst screenings. Even the physical form — free-flowing crystal versus oily solid — plays a role in high-throughput applications. We always keep communication lines open with technical leads who want to push the boundaries of how this building block gets deployed in synthesis.
In advanced manufacturing, traceability and documentation carry more weight than many imagine. For the pharmaceutical and regulated industries, we keep comprehensive batch records, spectral libraries, and impurity profiles dating back years. Our technical and compliance staff follow Good Manufacturing Practice (GMP)-inspired protocols, ensuring that specification drift or contamination events are extremely rare. Product recalls simply haven’t happened because we rigorously vet logistics, transportation containers, and storage temperature ranges.
Our collaborative work with downstream users highlights how end-to-end control avoids production stoppage, invalid batch results, or regulatory concerns during audits. Synthetic chemists in GMP settings recognize the benefit of having a documented, reproducible supply of high-purity 1-Isoquinolinemethanol. This level of reliability helps avoid multi-month project delays or emergency reformulations, a lesson that smaller producers often learn only after costly errors.
Waste management is another area where actual manufacturer experience sets the standard. Our team integrates reclaiming streams for spent solvents and water, reducing environmental impact and cutting operational costs. We keep staff well trained in handling, labeling, and disposing of waste — not just because regulations demand it, but because it preserves plant safety and long-term viability for everyone.
End-users today request not only purity and specification assurances, but also clarity on residual metals, solvent additives, and other trace ingredients. We voluntarily provide extended COAs covering everything from trace solvent quantification by headspace GC to residual catalyst metal levels determined by ICP-OES. Our internal QA team pushes for method validation by cross-checking with customer labs, working to align on detection limits and reproducibility well below regulatory maximums.
Working in a plant means “zero defect” isn’t a simple slogan; it drives every operational and maintenance protocol. Due diligence goes well beyond batch checks. Maintenance crews regularly inspect vessels for corrosion, residue build-up, or cross-contamination, while QA tracks even small shifts in product color, crystal form, or melt profile. If a customer flags even a small deviation in NMR, we investigate root causes and close the feedback loop before the next lot leaves the warehouse.
Product safety and transparency factor into shipping decisions as well. Our logistics team monitors transport temperature and humidity to ensure the solid arrives without transition or caking. Technical documentation includes recommended handling precautions, though most users find the low volatility and moderate toxicity profile make it easier to work with than many lower-boiling isoquinoline derivatives. Eye and skin protection remain standard, as do good ventilation and process hygiene, particularly when scaling beyond bench quantities.
We work directly with researchers, process development teams, and multinationals to troubleshoot and co-design new synthetic routes utilizing 1-Isoquinolinemethanol. Our continued investment in application support and tailored analytical packages is really driven by years of cumulative learning rather than formulaic customer service. Whether a customer is working through route scouting for a new intermediate or automating a multi-step synthesis at scale, our chemists offer practical, experience-based guidance.
In collaborative projects, early data-sharing accelerates root-cause analysis of unexpected results. For instance, a recent partnership with a specialty agrochemical group yielded a more robust protocol for site-selective O-alkylation, thanks in part to a shared analytics package that tracked byproduct formation in real time. Other clients have leveraged our isolation and purification expertise to drive down impurity levels for high-throughput screening, with real cost and reliability benefits.
This hands-on support continues in the form of technical training, troubleshooting visits, and regular feedback loops. By treating each batch as part of a long-term relationship, not simply a line item, we both grow with client needs and keep pace with the rapid evolution of modern process development.
1-Isoquinolinemethanol’s role keeps expanding as more industries recognize the strategic potential of high-purity, well-characterized ISO-quinoline intermediates. Advances in targeted therapeutics, next-generation crop protectants, and catalysis platforms all depend on well-behaved and traceable starting materials. By stressing every aspect of production from sourcing, reaction monitoring, and crystallization to shipping and documentation, we deliver more than a commodity — we enable real progress in lab and plant.
Real manufacturing experience brings an understanding of the subtleties involved at every scale. Safe handling, waste minimization, and continuous batch analytics maintain both operator safety and product quality. Suppliers without integrated, experience-driven controls often struggle to match the confidence that precise, reproducible molecules like 1-Isoquinolinemethanol deliver for advanced research.
As a manufacturer steady in this specialized chemical space, we continue improving processes and keeping pace with demanding applications. Our approach never substitutes convenience for reliability. Instead, we bring the same hands-on attention to every lot, benefitting long-term partners and pushing new boundaries across specialty, pharma, and fine chemical fields. 1-Isoquinolinemethanol isn’t just another intermediate — it’s a product built on decades of hard-won experience, scientific collaboration, and ongoing refinement.