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HS Code |
286585 |
| Chemicalname | 1-Indanone Oxime |
| Casnumber | 2432-46-2 |
| Molecularformula | C9H9NO |
| Molecularweight | 147.18 |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 128-131°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | 1-Indanone, oxime |
| Smiles | C1CC2=CC=CC=C2C1=NO |
| Inchi | InChI=1S/C9H9NO/c11-10-9-5-7-3-1-2-4-8(7)6-9/h1-4,9H,5-6H2 |
| Storagetemperature | Store at room temperature |
As an accredited 1-Indanone Oxime factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Indanone Oxime, 25 grams, is packaged in a sealed amber glass bottle with a secure screw cap and chemical hazard labeling. |
| Shipping | 1-Indanone Oxime is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Standard packaging includes high-density polyethylene (HDPE) or glass bottles, cushioned for transit. Shipments comply with relevant chemical transport regulations, ensuring labeling, secure containment, and documentation for safe handling and delivery. |
| Storage | 1-Indanone oxime should be stored in a tightly sealed container, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers and acids. Store it in a cool, dry, well-ventilated area at room temperature. Ensure proper labeling and restrict access to trained personnel. Follow all relevant safety protocols and regulatory requirements for chemical storage. |
Applications of 1-Indanone Oxime in Industrial Manufacturing1-Indanone Oxime serves as a key intermediate in several industrial sectors, where its consistent quality, reliable purity, and process suitability enable downstream manufacturers to address specific formulation, regulatory, and production requirements. Our manufacturing processes ensure each batch meets the demanding specification profiles set by our partners in chemical synthesis, agrochemical formulation, electronics, and specialty polymers. Below, we detail substantiated application scenarios reflecting real market practice. 1. Synthesis of Indanone-Based HerbicidesCommercial herbicide manufacturers utilize 1-Indanone Oxime as a precursor in the synthesis of selective pre-emergence weed control compounds, such as those based on the indanone core structure. The raw material enters the catalytic oximation stage, which precedes cyclization and chlorination. Accurate concentration control during scale-up helps avoid unwanted byproducts, supporting CYCLUS and similar product families. Continuous process validation maintains consistent output for regulatory submissions and mass production. Industry compliance standards
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2. Pharmaceutical Intermediate for Cardiovascular APIsLeading pharmaceutical synthesis companies incorporate 1-Indanone Oxime into the production pipeline for cardiovascular active pharmaceutical ingredients where an indanone skeleton acts as the pharmacophore. The oxime participates in a controlled reduction and rearrangement step, prior to coupling and further derivatization. Batch-to-batch consistency and contaminant control are critical, as the material contributes directly to the core structure of target molecules scheduled for EU GMP and US FDA audit trails. Industry compliance standards
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3. Photoinitiator Precursor for Electronics and UV-Curable CoatingsManufacturers of photoinitiators for UV-cured electronic coatings and photoresist materials depend on 1-Indanone Oxime as a strategic raw material. The compound enters the early-stage reaction with substituted benzaldehydes to create individualized oxime-ether photoinitiators. Strict control over moisture and trace metals at the oximation stage is required to achieve high reactivity for downstream curing efficiency and minimal device contamination, critical in microelectronics and optical applications. Industry compliance standards
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4. Specialty Polymer Synthesis for Impact-Resistant PlasticsProducers of high-performance impact-resistant polymers use 1-Indanone Oxime as a nucleophile in the chain extension or crosslinking stages of specialty resin synthesis, particularly where tailored mechanical flexibility and transparency are required. The oxime introduces structural modifications, enhancing the toughness and resilience of polycarbonate and copolyester blends. The timing of oxime addition and compatibility with chosen catalysts defines the properties of the polymer, enabling compliance with advanced application standards in electronics and automotive segments. Industry compliance standards
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5. Intermediate in Organic Pigment ProductionModern pigment manufacturing incorporates 1-Indanone Oxime into azo and indanone-based pigment synthesis, where it reacts with diazonium salts and couplers to form stable chromophores. Facilities maintain precise oxime input at the coupling phase, ensuring narrow distribution of particle size and optimal pigment dispersion properties. The selection of oxime grade and strict documentation of process parameters support regulatory conformance and batch reproducibility on scale-up. Industry compliance standards
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Chemists and process engineers working with oximes in large-scale production know how even small differences in structure or raw material purity can impact final applications. 1-Indanone oxime stands out for those who focus on the creation of specialized intermediates, especially in agrochemicals and pharmaceuticals. This compound’s defining structure, built around the indanone skeleton, delivers unique reactivity that makes synthesis more selective and repeatable.
From a manufacturing perspective, the choice of model and grading specification reflects genuine process realities. The typical model for 1-indanone oxime, often called “technical grade,” prioritizes purity and manageable crystallinity. Most of our output reaches above 98% purity, with controlled melting points near 143 to 146°C, and water content held below 0.5%. Chemists value these numbers—high consistency lets them plan batch reactions and achieve reliable results downstream. If you’ve ever tried substituting “any” oxime into a process built for 1-indanone oxime, you will notice unusual side reactions creeping in, especially during scale-up.
Under the hood, 1-indanone oxime builds on a five-membered indan ring, making the oxime group more shielded than more open alternatives like cyclohexanone oxime or acetone oxime. This feature narrows its range of reactivity, granting finer control in nucleophilic addition or reduction; it’s a physical difference any bench chemist can see during both pilot and full-plant operations. The denser ring system imparts a subtle difference in solubility and stability, lending itself to customized formulations that stay robust at higher temperatures and in mixed solvent systems.
One area where 1-indanone oxime shines involves the synthesis of certain indole or indoline derivatives. Traditional alternatives can introduce by-products or force later purification steps that shrink final yields. Swapping in 1-indanone oxime, with its predictable response and thermal stability, makes it a backbone compound for research groups needing a certain backbone rigidity. Anyone who has scaled up heterocyclic intermediate production will appreciate a product that keeps purity where it counts: just high enough to be predictable, without wasting cost on unneeded refinement.
We have watched demand for 1-indanone oxime shift steadily upward, in response to the evolving needs of contract manufacturing organizations and formulation labs. Customers care about supplier transparency, batch records, and reproducibility—and rightly so. Our production process emphasizes closed-system synthesis, minimizing exposure and controlling moisture from start to finish. The technical team keeps an eye on upstream material selection; only starting materials with rigid QC make the first cut.
Lab users and formulators running pilot-scale campaigns call out repeatability as their highest concern. One-off results make research papers; reproducibility supports a production line. Formulation chemists who revisit older protocols from the literature featuring 1-indanone oxime often find that earlier authors assumed a level of purity or stability that modern practice can now guarantee. Where decades ago, yield drifted run-to-run, high-purity oxime ensures scalable yields and less off-spec waste.
General-purpose oximes like methyl ethyl ketone oxime or cyclohexanone oxime serve in antiskinning paints, adhesives, or even anti-corrosion primers. While these materials do the job in broad-spectrum blocking of reactive groups, their open-chain backbone limits specificity for advanced organic transformations. 1-Indanone oxime carries a built-in rigidity and resonance that alters both its physical and chemical behavior. It resists hydrolysis better, especially where clients need storage stability across seasons.
In practice, this means process chemists can keep raw stock on hand for longer storage periods, reducing inventory risk. Those developing fine chemicals or targeted pharmaceutical scaffolds welcome this distinction, as it keeps downstream impurity profiles tight and helps pass through regulatory control points with less rework or retesting.
Another critical point involves the handling of isomeric impurities. Open-chain oximes have a reputation for tautomeric forms that slowly shift with moisture, heat, or time, eroding product consistency. The fused rings of indanone oxime lock conformation and minimize these ambiguities. This difference can look trivial on paper, but in a kilo-lab or at pilot scale, it makes the vintage difference between batch acceptance and an outlier that ties up an entire reactor bay pending analysis.
From the manufacturer’s side, synthesizing 1-indanone oxime demands close monitoring at all key stages. Each year, some buyers approach us hoping to use another “generic” oxime because they believe the category behaves uniformly. In truth, subtle structural variations create wide differences in reduction methods, crystal morphology, and final product performance. Our process starts by enforcing a strict temperature curve and monitoring pH balance point-by-point. A shallow deviation in these can precipitate colored by-products or drop the purity below the thresholds process chemists require.
Melting point consistency matters to every downstream user. We monitor melting range across every shipped lot—expect any batch to fall within 143–146°C, with a sharp transition that signals product integrity. Laboratories benchmarking new analogs frequently return to this data point before preparing semi-bulk synthesis. Melting point drift can hint at slow decomposition or low-level impurity inclusion, both of which set off bells for downstream organic chemists planning sensitive coupling or rearrangement reactions.
Delivering 1-indanone oxime in bulk demands a hands-on approach, particularly around moisture management and safe transfer. We pack most shipments in double-lined bags inside fiber drums, sealed to lock out atmospheric water. Even so, we encourage customers to store their supply in cool, dry conditions, away from reactive alkalies or acids. Shipping temperature can matter more than some realize — direct sunlight or high humidity can push surface moisture outside specification, so air-conditioned storage makes a noticeable difference over a storage season.
Regulatory compliance, from the REACH registration down to regional custom documentation, requires batch-level traceability and a robust QC paper trail. Several of our downstream clients operate under cGMP or related pharma standards; they expect and receive direct access to full Certificates of Analysis, with chromatography data and batch release specifications. We adapt to these varying documentation requirements because traceability remains a primary concern wherever intermediate purity influences marketed finished product.
Our QC team conducts lot-release analysis using HPLC and NMR methods to benchmark every batch. Product acceptance focuses on identity confirmation, residual moisture, and per-lot particulate size. Surface area differences, though subtle, can direct filter clogging and agitation requirements for fine chemical users, so granulometry remains part of our screening checklist. Chromatographic fingerprints verify identity and flag minor impurities typical of early reaction stopping points.
We also focus on odor contaminants and volatile residuals; 1-indanone oxime’s faint aromatic note makes a reliable negative indicator of process cleanliness. Every batch gets headspace GC screening before release. Material handling and plant cleanliness play just as big a role as reaction optimization in our product’s consistent performance.
Among its applications, 1-indanone oxime finds a reliable home in the synthesis of specialty intermediates, especially in producing building blocks for agricultural and pharmaceutical compounds. Research teams exploring new synthetic routes favor it for its fine-tuned reactivity and predictable selectivity. Routine feedback from synthetic chemists shows a reduction in side-product formation compared to more open-ringed or alkyl-substituted oximes. This feature gives users a stronger starting position, cutting both time and solvent waste in subsequent purification stages.
In the broader chemical industry, the need for reliable specialty intermediates has grown sharply. Sourcing managers and R&D teams alike look for suppliers who can offer both technical expertise and long-term consistency. We have found that regular direct communication with customers—be they new entrants or established global firms—helps keep specifications practical for every unique production line. If a customer requires tailored crystallinity or batch-to-batch tightness, we respond with lab-scale trial production and stability testing as a matter of course.
Comparing 1-indanone oxime with more widely used relatives like cyclohexanone oxime, one sees significant differences in reduction side-reactions and hydrolytic stability. While both carry the oxime group featuring the N–OH bond, the indanone framework resists ring opening and N–O bond cleavage better under both acidic and basic conditions. This means extended shelf life and less decomposition during heating or mixing; anyone who has dealt with product breakdown after weeks of storage will recognize this advantage immediately.
For users in research and process development, the choice often comes down to desired selectivity. The aromatic-fused ring structure generates less tautomerism, making it a favorite for work requiring precise hydrazone or amide formation. These characteristics save time during post-reaction workup and reduce the risk of forming phenolic or aldehydic by-products.
Less structurally complex oximes demonstrate faster but less predictable reactivity, resulting in more by-products or harder-to-remove contaminants. Any workflow needing a well-behaved starting material for advanced ring-closure, especially for biotech or bioactive compound development, will benefit from indanone oxime’s controlled reaction profile.
One real-world challenge with any specialty intermediate like 1-indanone oxime is maintaining batch-to-batch consistency over extended production cycles. Variations in raw materials, plant humidity, or even seasonal changes in water content threaten uniformity. Our approach involves strict supplier qualification, real-time process monitoring, and reserve batch testing. We schedule overlapping production campaigns to allow side-by-side comparison of output, holding back a reference sample from each lot as a baseline.
Managing end use, especially for pharmaceutical applications, drives us to invest in staff training and laboratory infrastructure. We regularly host process audits and invite customer QA teams to review in-process records and analytical logs. This level of transparency reduces friction for customers applying for regulatory approval of new compositions or filing documentation with authorities worldwide.
For large-scale end users, handling and dissolving 1-indanone oxime presents specific requirements, especially regarding solvent choice and dispersion. The product dissolves readily in typical polar solvents such as methanol or ethanol, but shows poor compatibility with highly non-polar media. Customers running continuous reactors or fast-charging dissolution tanks set agitation and temperature points based on real-use data, not theoretical tables. We openly share experience and receive ongoing feedback to refine these operating points. Every piece of learning cycles back into our production guidance.
1-Indanone oxime’s market continues to respond to the pressure for higher-purity chemical building blocks that deliver not only on specification but in actual process performance. Sustainable growth in pharmaceutical intermediates and advanced agricultural agents keeps demand steady, as does the trend toward more controlled, safer production practices worldwide. Our work involves more than filling orders; we partner with users to troubleshoot, optimize, and innovate as applications evolve.
Real feedback from the bench and the plant floor shapes every aspect of our operation. Many end users transfer lab-scale procedures to commercial production with minimal loss in yield—a testament to the stability and reliability that 1-indanone oxime brings to modern chemical synthesis. As regulatory scrutiny and end-use sophistication expand, the demand for predictable, high-quality intermediates like this one will only deepen.
For users intent on simplifying supply chain management, reducing risk, and supporting new research directions, 1-indanone oxime offers a well-understood, robust platform for both incremental improvement and breakthrough innovation. Our focus remains clear—deliver materials that improve workflow, streamline compliance, and help colleagues in the field create value from the molecular level up.