{"title":"Palladium Compounds [C-H Activation]","description":"\u003cp\u003e\u003cstrong\u003ePalladium Compounds [C-H Activation]\u003c\/strong\u003e — mencakup kompleks paladium pada berbagai bilangan oksidasi dan ligan seperti fosfina, asetonitril, serta ligan bidentat fosfin-fosfin atau sulfoksida yang berperan sebagai katalis pada reaksi pembentukan ikatan karbon-karbon dan karbon-heteroatom. Kelompok ini menjadi inti dari metodologi aktivasi ikatan C-H dalam kimia organologam.\u003c\/p\u003e\u003cp\u003eKompleks paladium ini digunakan dalam reaksi kopling silang seperti Suzuki, Negishi, dan Buchwald-Hartwig, serta reaksi fungsionalisasi C-H langsung untuk merakit molekul kompleks secara efisien. Kimiawan sintesis organik dan peneliti katalisis organologam memilih ligan dan bilangan oksidasi paladium tertentu (Pd(0) atau Pd(II)) sesuai mekanisme siklus katalitik yang diinginkan.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t302354536\"\u003eTCI T3023 68569-14-2 Tetrakis(acetonitrile)palladium(II) Bis(trifluoromethanesulfonate)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b619913024\"\u003eTCI B6199 905459-27-0 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t218453481\"\u003eTCI T2184 51364-51-3 Tris(dibenzylideneacetone)dipalladium(0)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b632713173\"\u003eTCI B6327 172418-32-5 trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t135052487\"\u003eTCI T1350 14221-01-3 Tetrakis(triphenylphosphine)palladium(0)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c273417591\"\u003eTCI C2734 1375325-71-5 Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b540012034\"\u003eTCI B5400 113173-22-1 Bis(1,10-phenanthroline)palladium(II) Bis(hexafluorophosphate)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d260422885\"\u003eTCI D2604 12107-56-1 Dichloro(1,5-cyclooctadiene)palladium(II)\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan bilangan oksidasi paladium, jenis ligan pendamping (fosfina, fenantrolin), serta kandungan pelarut residu pada kompleks karena memengaruhi stabilitas dan aktivitas katalitik dalam reaksi. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah C-H Activation [Catalysis], sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-rhodium-catalysis-and-inorganic-chemistry\"\u003eRhodium [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-transition-elements-catalysis-and-inorganic-chemistry\"\u003eTransition Elements [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-metallic-salts-catalysis-and-inorganic-chemistry\"\u003eMetallic Salts [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-nitrogen-donor-ligands-catalysis\"\u003eNitrogen-Donor Ligands [Catalysis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-main-group-elements-catalysis-and-inorganic-chemistry\"\u003eMain-group Elements [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-cross-coupling-reaction-using-transition-metal-catalysts-c-c-bond-form\"\u003eCross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-c-h-activation-catalysis\"\u003eC-H Activation [Catalysis]\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b619913024","title":"TCI B6199 905459-27-0 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6199 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride is a palladium(II) NHC catalyst specifically developed for C–H bond activation reactions. This catalyst enables direct functionalization of carbon–hydrogen bonds, streamlining synthetic pathways in organic chemistry. It is widely employed in C–H arylation, alkylation, and alkenylation reactions for the synthesis of pharmaceuticals, agrochemicals, and advanced functional materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085924249818,"sku":"TCI2510B619913024","price":4105000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085924282586,"sku":"TCI2510B619913025","price":14053000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085924315354,"sku":"TCI2510B619913026","price":47778000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6199_8fb24a5d-0ce1-4fc9-b0bc-4be9be705d27.jpg?v=1767864859"},{"product_id":"tci2510b632713173","title":"TCI B6327 172418-32-5 trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6327, trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II), is a highly active palladacycle-based dimeric palladium(II) catalyst optimized for C-H activation and cross-coupling reactions. It exhibits excellent thermal stability and broad substrate compatibility in Heck, Suzuki, and Sonogashira coupling reactions, as well as direct C-H functionalization of aromatic systems. This catalyst is widely employed in academic and industrial laboratories for the synthesis of pharmaceutical intermediates, agrochemicals, and advanced functional materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085930770650,"sku":"TCI2510B632713173","price":1546000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085930803418,"sku":"TCI2510B632713174","price":5341000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085930836186,"sku":"TCI2510B632713175","price":18663000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6327.jpg?v=1768193647"},{"product_id":"tci2510c273417591","title":"TCI C2734 1375325-71-5 Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2734 1375325-71-5 Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) is a specialized chemical compound used in catalytic reactions for carbon-hydrogen (C-H) activation. This compound plays a critical role in laboratory settings where complex chemical syntheses require precise and efficient catalytic processes. It is particularly valuable in organic and inorganic chemistry for its ability to facilitate reactions without altering the fundamental structure of the substrate. Its application extends to various research fields, making it an essential tool for scientists working on advanced chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its high reactivity and stability, which are attributed to its complex structure involving palladium and phosphine ligands. These properties enable it to act as an efficient catalyst in C-H activation reactions, enhancing reaction efficiency and reducing the need for excess reagents. Its formulation ensures compatibility with a wide range of reaction conditions, making it adaptable to different experimental setups. The combination of stability and reactivity makes it a reliable choice for both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic and inorganic chemistry research, especially in catalysis and the synthesis of complex molecules. Its availability and adherence to international quality standards make it a preferred choice for researchers aiming to achieve high-quality results. The compound supports scientific innovation by enabling more efficient and effective chemical processes, contributing to the advancement of chemical research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this compound’s ability to activate C-H bonds, enabling the formation of complex molecular structures with high selectivity.\u003c\/li\u003e\n\u003cli\u003eInorganic chemistry experiments utilize its catalytic properties to facilitate reactions that require precise control over reaction pathways and intermediates.\u003c\/li\u003e\n\u003cli\u003eC-H activation studies rely on its stability and reactivity to explore new reaction mechanisms and improve synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003eAdvanced catalytic research applications take advantage of its efficiency in reducing reaction times and reagent consumption.\u003c\/li\u003e\n\u003cli\u003eIndustrial-scale chemical processes benefit from its consistent performance in maintaining reaction efficiency and product purity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1375325-71-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize any potential risks associated with its use. The compound should not be stored near incompatible materials to avoid any chemical interactions. Proper labeling and storage practices are essential to ensure safe handling and long-term usability in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086194389210,"sku":"TCI2510C273417591","price":7646000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2734.jpg?v=1767098705"},{"product_id":"tci2510d260422885","title":"TCI D2604 12107-56-1 Dichloro(1,5-cyclooctadiene)palladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2604 Dichloro(1,5-cyclooctadiene)palladium(II) is an organopalladium complex in which a 1,5-cyclooctadiene diene ligand is bound to palladium together with two chloride ligands. In catalysis laboratories, this compound serves as a highly practical palladium catalyst precursor: the cyclooctadiene ligand binds firmly enough to keep the complex stable during storage, yet remains labile enough to be displaced by other ligands such as phosphines, N-heterocyclic carbenes, bipyridine, or other nitrogen donor ligands when an active catalyst needs to be formed in situ. For that reason, this reagent has become a flexible starting point for many palladium-based catalytic systems.\u003c\/p\u003e\n\u003cp\u003eThe properties that make it a widely chosen reagent are the ease of ligand exchange and the clearly defined palladium content in the +2 oxidation state. Researchers can design catalysts with ligands of their own choosing without having to prepare palladium complexes from raw metal, so stoichiometry is better controlled and reaction outcomes are more reproducible. Because the complex is supplied as a solid, it is also easier to weigh and measure out than a precursor solution, while remaining straightforward to store under ordinary laboratory conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on catalysis and synthetic organic chemistry, particularly in studies of C–H bond activation and related transformations. Its solid form suits laboratories that prepare catalyst systems batch by batch on a small scale, where accurate weighing and predictable ligand substitution behaviour matter more than bulk handling. It fits naturally into method development work in which several ligand sets are screened against the same palladium source.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC–H bond activation studies: the complex delivers a well-defined palladium(II) source whose labile diene ligand can be exchanged for the directing ligand required by the activation system under investigation.\u003c\/li\u003e\n\u003cli\u003eIn situ catalyst generation: researchers combine the precursor with phosphines or N-heterocyclic carbenes directly in the reaction vessel, forming the active palladium species without isolating an intermediate complex.\u003c\/li\u003e\n\u003cli\u003eLigand screening in method development: a single palladium source can be paired with many different donor ligands, allowing systematic comparison of catalytic performance while keeping the metal input constant.\u003c\/li\u003e\n\u003cli\u003eCoordination chemistry teaching and research: the straightforward substitution of 1,5-cyclooctadiene by nitrogen donor ligands such as bipyridine illustrates ligand exchange behaviour clearly for synthesis and characterisation exercises.\u003c\/li\u003e\n\u003cli\u003eReproducible small-scale synthetic work: because the palladium oxidation state is clearly defined, stoichiometry can be calculated precisely, which supports repeatable results across successive experimental runs.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 12107-56-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C–H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003eChemical name: Dichloro(1,5-cyclooctadiene)palladium(II)\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the available TCI catalogue packaging options for this product code\u003c\/li\u003e\n\u003cli\u003eStorage: store under ordinary laboratory storage conditions in a closed container\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, kept dry and protected from moisture, in a cool and well-ventilated chemical storage area away from incompatible reagents. Glass or the manufacturer's supplied container is suitable; reseal promptly after each use to limit exposure to air and humidity. Handle the solid in a fume hood using gloves, safety glasses, and a laboratory coat, and avoid generating dust when weighing. Transfer with clean, dry spatulas to prevent contamination that could affect catalytic performance. Collect residues and spent catalyst as heavy-metal chemical waste according to institutional disposal procedures, and consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086567715034,"sku":"TCI2510D260422885","price":4442000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086567747802,"sku":"TCI2510D260422886","price":17230000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2604.jpg?v=1767105066"},{"product_id":"tci2510d433324901","title":"TCI D4333 205319-10-4 Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4333, Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II), CAS 205319-10-4, is a palladium(II) complex already coordinated to the Xantphos diphosphine ligand. It belongs to the catalysis and inorganic chemistry category, specifically within C–H activation applications. In the laboratory this compound serves as a ready-to-use precatalyst: a palladium source that arrives carrying its own ligand, so researchers do not need to prepare a separate mixture of a palladium salt and free ligand before running a coupling or functionalization reaction. That single-bottle format removes a preparation step from the bench workflow.\u003c\/p\u003e\n\u003cp\u003eThe most notable advantages of this material come from the Xantphos ligand itself, a diphosphine built on a rigid xanthene backbone that is known for its large bite angle. This wide bite angle influences the geometry of the complex and generally accelerates the reductive elimination step, which makes many coupling reactions that were previously difficult far more efficient — particularly carbon–nitrogen and carbon–sulfur bond formation, as well as carbonylation chemistry. Because the material is a fully formed complex rather than an in-situ mixture, it delivers a defined metal-to-ligand ratio, so experimental results are easier to reproduce from one researcher to another and from one laboratory to another.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this kind of preformed precatalyst is typically used in synthetic organic chemistry groups at universities, in research institutes, and in industrial R\u0026amp;D units working on coupling and functionalization chemistry. The defined stoichiometry is especially valuable where several researchers share the same catalytic protocol, because it keeps loading consistent between users and reduces variability caused by weighing out palladium salt and ligand separately during method development and route-scouting work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCarbon–nitrogen bond formation: the wide bite angle of the Xantphos ligand accelerates reductive elimination, making amination couplings that are otherwise sluggish proceed more efficiently in routine synthetic work.\u003c\/li\u003e\n\u003cli\u003eCarbon–sulfur bond formation: the preformed palladium–Xantphos complex supports thioetherification-type couplings, where the ligand geometry favors the product-releasing step rather than unproductive catalyst pathways.\u003c\/li\u003e\n\u003cli\u003eCarbonylation reactions: the rigid xanthene backbone and its resulting complex geometry make this precatalyst a suitable choice for carbonylative coupling protocols described in the catalysis literature.\u003c\/li\u003e\n\u003cli\u003eC–H activation studies: as the category for this product indicates, the complex is applied in C–H functionalization chemistry where a defined palladium(II) source with a bound diphosphine is required.\u003c\/li\u003e\n\u003cli\u003eReproducible method development: the fixed metal-to-ligand ratio of the isolated complex lets groups repeat catalytic screening results across different researchers and laboratories without re-optimizing ligand loading.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCatalog code: D4333\u003c\/li\u003e\n\u003cli\u003eCAS number: 205319-10-4\u003c\/li\u003e\n\u003cli\u003eChemical name: Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II)\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C–H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's instructions on the container label and in the accompanying safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this palladium precatalyst in its original tightly closed container, in a cool, dry and well-ventilated area away from moisture, heat and incompatible materials, following the storage conditions stated by the manufacturer on the label and safety data sheet. Handle the solid in a fume hood or other suitable ventilated enclosure, using gloves, safety goggles and a laboratory coat. Avoid generating dust and avoid direct contact with skin and eyes. Keep the container closed when not in use to limit exposure to air and humidity, transfer with clean dry spatulas to prevent contamination that could affect catalytic performance, and collect residues and used catalyst as chemical waste in line with your laboratory's waste-handling procedures. Always review the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086687449306,"sku":"TCI2510D433324901","price":929000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086687482074,"sku":"TCI2510D433324902","price":3345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4333.jpg?v=1767107422"},{"product_id":"tci2510d571926693","title":"TCI D5719 85719-56-8 [(2-Dimethylamino)propyldiphenylphosphine]palladium(II) Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5719 [(2-Dimethylamino)propyldiphenylphosphine]palladium(II) Dichloride, CAS 85719-56-8, is a palladium(II) complex bound by a hybrid phosphine–amine ligand together with two chloride ligands. The bidentate ligand combines a strongly donating phosphorus atom with a tertiary amine nitrogen atom, producing a distinctive coordination environment around the palladium centre. Precatalyst complexes of this kind matter in the laboratory because they provide a well-defined, easily weighed source of palladium that does not need to be assembled from a palladium salt and free ligand at the moment of reaction, which makes experimental results easier to reproduce.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this complex attractive is the hemilabile nature of the phosphine–amine ligand. The relatively weak Pd–N bond can open temporarily to create room for a substrate and then close again to stabilise the metal centre, a pattern that is frequently advantageous in catalytic cycles involving C–H bond activation. The amine group can also act as an internal base that assists deprotonation steps, while the two phenyl groups on phosphorus supply electron donation and steric bulk that support the stability of the complex. The defined solid form makes measuring out catalyst loadings straightforward.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is used in the same way as any defined palladium precatalyst: as a weighable solid dispensed at a chosen catalyst loading rather than prepared in situ from separate palladium and ligand components. Because the complex arrives as a single defined substance, catalyst loading is set directly at the balance, and work carried out across different sessions or by different operators in the same group remains comparable and easier to repeat.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC–H activation catalysis — the hemilabile Pd–N bond can open to admit a substrate and reclose to stabilise the palladium centre, a pattern often favourable in these catalytic cycles.\u003c\/li\u003e\n\u003cli\u003eReactions requiring an internal base — the tertiary amine group of the ligand can assist deprotonation steps directly, without the coordination chemistry being assembled separately in the flask.\u003c\/li\u003e\n\u003cli\u003eReproducible catalyst screening — because the palladium and ligand arrive as one defined compound, loadings are set at the balance and repeat experiments give comparable starting conditions.\u003c\/li\u003e\n\u003cli\u003eMethod development where catalyst loading is varied — the well-defined solid form allows straightforward weighing across a series of loadings without preparing fresh palladium–ligand mixtures each time.\u003c\/li\u003e\n\u003cli\u003eWork replacing in-situ precatalyst preparation — using this complex removes the step of combining a palladium salt with free ligand at reaction time, reducing a common source of run-to-run variation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 85719-56-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePhysical form: defined solid, suitable for direct weighing\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the available packaging options for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated by the manufacturer\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, kept in a cool, dry and well-ventilated area away from moisture and from incompatible substances, and follow the storage conditions indicated by the manufacturer on the label and safety data sheet. Use clean, dry glass or otherwise chemically compatible containers and clean spatulas when transferring the solid, so that no contamination is carried into the remaining stock. Handle the compound in a fume hood with appropriate personal protective equipment, including safety glasses, gloves and a laboratory coat. 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085706244314,"sku":"TCI2510B31608948","price":7167000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085706277082,"sku":"TCI2510B31608949","price":24649000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B3160_a4c0b85c-059a-4cb6-9b5d-8c432346ca89.jpg?v=1767431571"},{"product_id":"tci2510b32929136","title":"TCI B3292 858971-43-4 1,2-Bis(phenylsulfinyl)ethane Palladium(II) Diacetate","description":"\u003cp\u003e\u003cstrong\u003e1,2-Bis(phenylsulfinyl)ethane Palladium(II) Diacetate\u003c\/strong\u003e (CAS 858971-43-4) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Used as a catalyst in cross-coupling reactions such as Suzuki, Heck, and 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