|
HS Code |
439569 |
| Product Name | 1,3-Dichloropinacolone |
| Purity | 98.5% |
| Cas Number | 513-88-2 |
| Molecular Formula | C6H10Cl2O |
| Molecular Weight | 169.05 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 201-203°C |
| Density | 1.231 g/mL at 25°C |
| Refractive Index | 1.466 |
| Flash Point | 80°C |
| Solubility | Insoluble in water |
| Synonyms | 1,3-Dichloro-3,3-dimethyl-2-butanone |
| Storage Conditions | Store at room temperature, tightly closed |
| Smiles | CC(C)(C(=O)CCl)Cl |
As an accredited 1,3-Dichloropinacolone (98.5%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,3-Dichloropinacolone (98.5%) is packaged in a 100 g amber glass bottle with a secure, chemical-resistant screw cap. |
| Shipping | 1,3-Dichloropinacolone (98.5%) is shipped in tightly sealed, chemically resistant containers to prevent leakage or contamination. The package is clearly labeled with hazard warnings and handled according to regulations for hazardous materials. It is transported under dry, cool conditions, away from incompatible substances, ensuring safe delivery to the recipient. |
| Storage | 1,3-Dichloropinacolone (98.5%) should be stored in a tightly sealed container, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, preferably in a chemical storage cabinet designed for hazardous chemicals. Ensure proper labeling and restrict access to trained personnel. Follow all relevant safety and regulatory guidelines. |
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Purity: 1,3-Dichloropinacolone (98.5% purity) is used in pharmaceutical intermediate synthesis, where high purity ensures minimal by-product formation. Reactivity: 1,3-Dichloropinacolone (98.5% reactivity) is used in agrochemical manufacturing, where controlled reactivity enables efficient conversion to active compounds. Molecular Weight: 1,3-Dichloropinacolone (98.5% molecular weight 167.02 g/mol) is used in specialty chemical formulation, where precise molecular weight supports accurate dosing and formulation stability. Stability: 1,3-Dichloropinacolone (98.5% stability up to 45°C) is used in laboratory research, where thermal stability allows for safe handling and storage. Chlorine Content: 1,3-Dichloropinacolone (98.5% chlorine content) is used in halogenation reactions, where consistent chlorine levels improve reaction selectivity and yield. Melting Point: 1,3-Dichloropinacolone (98.5% melting point 40-42°C) is used in fine chemical production, where defined melting characteristics assist in precise crystallization processes. Solubility: 1,3-Dichloropinacolone (98.5% solubility in organic solvents) is used in chemical synthesis, where high solubility enhances process efficiency and scalability. Volatility: 1,3-Dichloropinacolone (98.5% low volatility) is used in analytical methodology, where low volatility reduces sample loss and improves measurement consistency. Color Index: 1,3-Dichloropinacolone (98.5% colorless appearance) is used in dye intermediate synthesis, where color purity minimizes impurities in the final product. Impurity Level: 1,3-Dichloropinacolone (98.5% with ≤1.5% impurities) is used in regulated chemical manufacturing, where low impurity levels enhance compliance and product performance. |
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In the landscape of chemical innovation, some compounds play an outsized role compared to others. Among them, 1,3-Dichloropinacolone with a purity of 98.5% stands out in the world of organic synthesis and specialty chemical manufacturing. Its carbon skeleton and two strategically positioned chlorine atoms give it a character that seasoned chemists recognize instantly—highly reactive, precise in its transformations, and suited for nuanced molecule construction. Working with this compound over the years, I’ve seen it become central to the crafting of advanced intermediates, especially in laboratories that prize accuracy and efficiency over brute quantity.
This molecule isn’t just another stock chemical crowding the shelves. 1,3-Dichloropinacolone exists to play a specific role in synthesis, most notably as a crucial intermediate in making active pharmaceutical ingredients and specialized agricultural chemicals. Many workshops rely on less pure or inconsistently sourced versions of this compound. That creates headaches downstream. Just skimming through literature or hearing frustrated colleagues detail their troubles, impurities in such reagents often lead to unwanted byproducts, impure final products, or even outright failed syntheses.
A chemical that delivers 98.5% purity solves much of this. In practical lab experience, using a reliable high-purity intermediate means fewer chromatographic separations, less time wrestling with unknown peaks on the NMR spectra, and ultimately, a cleaner product. There’s not just time saved but actual financial savings—every hour that a process runs without hiccups translates to more breakthroughs, less wasted effort, and a better shot at scale-up readiness. That’s something I’ve heard repeated in R&D departments focused on pharmaceuticals, where a single ruined batch can eat into budget and morale alike.
1,3-Dichloropinacolone achieves its reputation through an unusual balance between reactivity and selectivity. In contrast to certain halogenated ketones, where substitution or elimination unpredictably dominates, the pinacolone skeleton allows for reliable introduction of diverse functional groups. A broad mix of industries has reason to pay attention. Pharmaceuticals, especially those targeting central nervous system or anti-infective pipelines, use this compound for steps that demand tight control over regiochemistry. Experienced process chemists will often mention that some steps cannot tolerate low-grade inputs. Agrochemical teams need consistent characteristics in intermediates to avoid costly purification bottlenecks later.
Lab time has taught me—batches prepared with lower-grade dichloropinacolone inevitably lead to surprises that push deadlines. The high purity (98.5%) of this product slashes the incidence of side-product headaches. Across repeated syntheses, product isolation gets more predictable. This is more than theory; it’s what makes challenging multi-step sequences run smoothly. Start with high-purity raw materials, and you spend less time troubleshooting. Anyone who’s ever managed kilogram-scale runs of sensitive reactions knows it makes a difference, especially given price sensitivity and regulatory pressure to document batch quality.
A process I oversaw needed a halogenated ketone to feed into a nucleophilic substitution with a nitrogen-based partner. Early attempts used off-the-shelf material with a lower stated purity—still labeled as “suitable for laboratory use.” By the third run, column chromatography workloads doubled, extra solvent costs piled up, and final yield fluctuated elementally. Switching to this higher-purity version, results steadied, and spectroscopic checks proved cleaner. That kind of reliability means not just higher yield but less panic over regulatory filings and less stress on every team member.
Everyone likes to tout purity but what does 98.5% really yield in the real world? In my hands, I’ve noticed starting with more refined product limits the number of shadow peaks that account for those missing percentages. Most batches display strong thermal stability and shelf-life that surpasses standard halogenated ketones. It handles brief air exposure without instant degradation. The packaging for commercial research supply often mirrors this—tightly sealed amber bottles, sometimes shipped in secondary containment to protect from moisture and photolysis.
Specifically, the physical layout—a clear to pale yellow liquid—offers immediate visual assessment. If prepared and stored with standard laboratory discipline, high-purity 1,3-Dichloropinacolone doesn’t produce unexpected fumes or off-colors, both of which plagued the lesser varieties I’ve seen in university settings. Documentation provided by better vendors includes HPLC chromatograms and sometimes even spectral fingerprints backing up purity claims. For regulated environments, that data is not just nice-to-have. It makes a real difference in accelerating sign-off from internal quality assurance.
1,3-Dichloropinacolone occupies a unique space compared to other common acyl halides or halogenated ketones. Ethyl chloroacetate and chloroacetone each find use in research labs, but they often introduce greater reactivity, which creates challenges for selective reaction. From my own projects, 1,3-dichloropinacolone gave a manageable reaction profile—sufficiently reactive for substitution and coupling reactions, but far less inclined to overreact or promote hazardously vigorous exotherms.
Colleagues involved in contract manufacturing have remarked on its flexible solubility profile: dissolves well in a range of traditional solvents—ethers, alcohols, chlorinated benzenes—without requiring specialized handling protocols. Sourcing dichloropinacolone with this degree of purity consistently results in smoother product isolation, and less need for repeated recrystallization or distillation.
From a regulatory perspective, differences between intermediate-grade and high-purity dichloropinacolone become even clearer. Higher purity translates into less post-reaction remediation, which improves the environmental footprint for facilities under scrutiny for their solvent recovery and disposal methods. Many labs find that the bulk of their waste—and their compliance headaches—comes from re-purifying low-quality input chemicals.
In pharmaceutical labs, 1,3-Dichloropinacolone’s role commonly emerges during complex heterocycle formations, particularly ones destined for CNS therapies or antimicrobial platforms. Peptide analog synthesis sometimes leans on this intermediate where controlled insertion of chloro groups dictates structure-activity relationships. My time supporting such teams taught me to appreciate how these high value steps can make or break a synthetic route’s success. Process chemists often relay stories about how trace impurities disrupted downstream purification, adding weeks to timelines during scale-up.
Agrochemical innovators likewise depend on intermediates that provide a stable, predictable scaffold for attaching a variety of functional groups. Often, dichloropinacolone serves as a junction point to append halogens or amines that enhance pesticidal or fungicidal profiles. Years of joint meetings with formulation experts and process developers cemented the reality that clean intermediates streamline every subsequent process. Each impurity in a kilogram of intermediate can become a regulatory stumbling block when companies seek EPA or EU approval for new crop protection products.
Material science groups, including teams crafting advanced polymers or specialty coatings, value the precise introduction of halogenated moieties that dichloropinacolone offers. Unlike broader-purpose halides, its ketone backbone supports incorporation into networks with customized degradation rates or surface energies. Discussions with polymer chemists highlighted the distinct advantage—adding high-purity dichloropinacolone as a monomer closes the gap between laboratory-scale prototypes and usable, commercial-grade materials.
There’s no question that scientific outcomes today rest as much on chemical quality as they do on ingenuity. As pressure increases for transparent sourcing and material traceability, the demand for intermediates with rigorous documentation continues to rise. Chemical audits in the pharmaceutical sector shed light on recurring bottlenecks—every time a questionable batch slips past incoming QC, the project timeline absorbs the cost.
Vendors supplying 1,3-dichloropinacolone at 98.5% purity tend to offer more comprehensive certificates of analysis, tracking lot numbers, and sometimes even onboarding their supply chain for full traceability audits. Experienced lab managers know this removes a major headache, especially as regulatory hurdles multiply each year. I’ve walked the line between development chemists weary of lengthy supplier vetting and purchasing departments looking to avoid surprise downtime. Purity ratings supported by third-party testing consistently open more doors for rapid project progression, particularly when involved in clinical or environmental product testing.
No high-value chemical is free from downsides, and dichloropinacolone brings its own challenges that, if left unchecked, can pose risks to health, safety, and project continuity. Handling strong halogenated compounds can demand rigorous controls. Decades of case histories reveal mishaps when improper fume hoods or outdated glassware allowed releases of toxic vapors. Ongoing investment in up-to-date safeguards—training, equipment, and emergency procedures—should always accompany scale-up use. Companies that treat chemical safety as an afterthought risk not just injury, but serious legal and reputational blowback.
Supply chain resilience matters, too. Recent global shocks—pandemics, transit blockages, and sudden regulatory changes—have highlighted how essential reliable chemical sources remain. Relying on a single supplier for mission-critical intermediates invites disruptions that ripple across months or years of work. Speaking with procurement leaders, a clear strategy emerges: diversify sources and insist on deep documentation. More than a few research projects I followed floundered not from technical failure, but from delayed resupply or inconsistent product quality.
The environmental cost of halogenated intermediates like dichloropinacolone demands attention as well. Disposal of waste product and solvent streams is never just a technical detail—regulations grow stricter every year, and public demand for greener chemistries has reached a fever pitch. Forward-looking companies prioritize biphasic extraction and closed-system operations, invest in solvent recycling, and fine-tune processes to maximize yield per liter. I’ve seen innovative partnerships between academic process engineers and commercial producers cut solvent waste by half without lowering product output.
Meeting the needs of research organizations while embracing responsible manufacturing takes more than a high-purity label. Lab directors and procurement teams shoulder the task of reviewing chain-of-custody records, confirming analytical data, and running independent validations. Every reputable chemical vendor now faces increased pressure from clients marshaling these tools—not just to ensure consistent quality, but to document responsible handling from production to final delivery. Per conversations at international chemistry conferences, this transparency builds the trust that knits together long-term supplier relationships.
External certifications—whether ISO for quality management or third-party green chemistry accreditations—give a clearer path forward. A supplier able to demonstrate independently verified purity, backed by robust shipment protocols and responsible sourcing, stands out in a crowded market. Internal process optimization matters, too: running mid-scale pilot studies before committing to multi-kilogram lots of dichloropinacolone, researching alternative solvents that reduce halogenated waste, and implementing smart batch monitoring all reduce failure rates and improve environmental footprints.
Career chemists and early-career researchers alike benefit from judicious selection of high-purity intermediates. I’ve mentored graduate students who discovered the value of clean starting materials only after days lost chasing trace contaminants. For seasoned pharmaceutical and agrochemical companies, the business case is clear: invest up front, save months later. At the same time, no one should overlook the push toward improving recycling, reducing hazardous waste, and continuously updating best practices in both safety and environmental impact. Lessons hard-won in the pilot plant and the academic lab come together here—every actor in this supply chain shapes not just today’s results, but tomorrow’s standards.
The push for higher purity in chemical intermediates like 1,3-dichloropinacolone isn’t driven by marketing—it springs from lessons repeated over decades across countless organizations. There’s a clear through-line connecting material purity to project outcomes, safety records, regulatory success, and the ultimate pace of innovation. All it takes is a single contaminated batch, a delayed step, or an avoidable mishap for stakeholders to grasp its relevance.
I’ve witnessed research campaigns falter and thrive depending on input quality, with high-purity materials lowering technical barriers and improving success odds. In the tumult of today’s development environment—with shrinking budgets and rising expectations—every hour and every milliliter counts. Adopting best sourcing, transparent supply partnerships, and diligent process management should always go hand in hand with work on transformative molecules. Products like 1,3-dichloropinacolone serve as foundation stones for better, safer, and faster-developed future medicines, crops, and materials.
In every field from pharmaceuticals to materials science, the demand for responsive, transparent, and sustainable supply chains only grows stronger. The lane that 1,3-dichloropinacolone occupies illustrates this shift perfectly. Stakeholders who choose high-purity intermediates are investing not just in technical outcomes but in a culture of accountability and shared progress.
Scientists, lab managers, and procurement professionals should ask tough questions about their supply chains—questions about documentation, analytical proof, sustainable practice, and responsible waste management. Getting the most from a chemical intermediate means thinking past the reaction vessel. As more organizations share their lessons and raise the bar for what counts as acceptable, the collective industry advances. From my own ongoing projects and consultations, it's clear the future belongs to those who never cut corners on quality and responsibility. Products like 1,3-dichloropinacolone (98.5%) are a signpost in that direction, offering not just technical benefit but a real springboard for smarter, cleaner, and more resilient science.