Palladium Oxide Suppliers USA
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Product | Description | |
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Palladium Oxide Nanoparticle Dispersion Quick inquiry Where to buy Suppliers range | Palladium Oxide Nanoparticle Dispersion. Product ID: ACMA00019871. Mole weight: 122.42. IUPAC Name: oxygen(2-); palladium(2+). Appearance: Liquid. EC Number: 215-218-3. Boiling Point: Varies by solvent. Melting Point: Varies by solvent. Density: Varies by solvent. SMILES: O=[Pd]. InChI: InChI=1S/O.Pd. InChIKey: HBEQXAKJSGXAIQ-UHFFFAOYSA-N. | |
Palladium(II) oxide Quick inquiry Where to buy Suppliers range | Palladium(II) oxide. Group: Palladium Complexes. Alternative Names: Palladium monoxide. Grades: 98%. CAS No. 1314-08-5. Product ID: ACM1314085-3. Molecular formula: Opd. Mole weight: 122.42. Appearance: Brown to black powder. SMILES: O=[Pd]. | |
Palladium (II) Oxide Quick inquiry Where to buy Suppliers range | PALLADIUM (II) OXIDE, ANHYDROUS, 99.9% pure, -20 mesh, (Synonym: Palladium Monoxide), Formula: PdO. CAS No. 1314-08-5. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
Palladium (II) Oxide, anhydrous Quick inquiry Where to buy Suppliers range | Palladium (II) Oxide, anhydrous. Grades: 99.9% Extremely High (>=99%). CAS No. 1314-08-5. Order Number: 2815. | www.prochemonline.com |
Palladium(II) oxide hydrate Quick inquiry Where to buy Suppliers range | Palladium(II) oxide hydrate. Group: Metal & Ceramic Materials. Alternative Names: PALLADIUM OXIDE; PALLADIUM(+2)OXIDE; PALLADIUM(II) OXIDE HYDRATE;Palladium(II) oxide monohydrate;Palladium(II) oxide hydrate, 99.9+%;PALLADIUM (II) OXIDE, 99.9% (METALS BASIS), PD 75.3% MIN;Palladium(II) oxide monohydrate, 99.9% (metals basis), Pd 73% min;P. CAS No. 64109-12-2. Molecular formula: OPd. Mole weight: 122.42 (anhydrous basis). | |
Reduced Graphene Oxide Powder, decorated with Palladium Nanoparticles Quick inquiry Where to buy Suppliers range | Reduced Graphene Oxide (RGO) Powder decorated with Palladium Nanoparticles is graphene-metal hybrid material composed of reduced graphene oxide (r-GO) and a broad distribution of nanoscale palladium particles. Applications include electron microscopy imaging and as a catalyst material in fuel cells. Uses: Electrocatalyst. Field-effect transistors. Sensors. Lithium ion batteries. Supercapacitors. Group: Catalysts. Alternative Names: RGO-Pd, reduced graphene oxide nanosheets decorated with Pd NPs. Product ID: ACMA00018474. Molecular formula: CxOzyHz. Appearance: Powder. | |
1,1?-Bis(di-isopropylphosphino)ferrocene palladium dichloride Quick inquiry Where to buy Suppliers range | red crystalline powder. Uses: Palladium-catalyzed P-C bond formation between diphenylphosphine and ortho-substituted aryl bromides. Deoxygenation of pyridine N-oxides by palladium-catalyzed oxidation of trialkylamines Air-stable catalyst useful in challenging Suzuki coupling reactions. Group: Palladium series catalysts. Alternative Names: PdCl2(dippf). Grades: Pd >17.5%. CAS No. 215788-65-1. Molecular formula: C22H36Cl2FeP2Pd. Mole weight: 595.64. IUPAC Name: cyclopentyl-di(propan-2-yl)phosphane;dichloropalladium;iron. Exact Mass: 594.00500. Melting Point: 282-287 °C. SMILES: CC(C)P([C]1[CH][CH][CH][CH]1)C(C)C. CC(C)P([C]1[CH][CH][CH][CH]1)C(C)C. Cl[Pd]Cl. [Fe]. InChIKey: UXOSTJATWDHIKQ-UHFFFAOYSA-L. | |
1,2-bis(diphenylphosphino)ethane palladium dichloride, Pd : 18.5 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: This product is widely used in catalyzing the hydrogenation of olefins, the hydrogenation reduction of nitrobenzene, the oxidation of olefins, the carbonylation of olefins with carbon monoxide, and the coupling of Grignard reagents and halogenated hydrocarbons. Group: Colloidal Catalysts. CAS No. 19978-61-1. Molecular Weight: 575.74 g/mol. SMILES: Cl[Pd]Cl. C (CP (c1ccccc1)c2ccccc2)P (c3ccccc3)c4ccccc4. InChI: LDJXFZUGZASGIW-UHFFFAOYSA-L. Boiling Point: 360 °C. Flash Point: 99 %. | |
1,2-Bis(phenylsulfinyl)ethane palladium(II) acetate Quick inquiry Where to buy Suppliers range | 1,2-Bis(phenylsulfinyl)ethane palladium(II) acetate. Uses: Catalyst for allylic oxidation. Catalyst for oxidative Heck reactions. Catalyst for allylic alkylation. Catalyst for allylic amination. Alternative Names: KS-000013IV; CTK5F5938; 2- (benzenesulfinyl) ethylsulfinylbenzene; 1,2-Bis(phenylsulfinyl)ethane Palladium(II) Diacetate; 858971-43-4; White Catalyst; TR-026796; palladium(2+). CAS No. 858971-43-4. Molecular formula: C18H20O6PdS2. Mole weight: 502.892g/mol. IUPAC Name: 2- (benzenesulfinyl) ethylsulfinylbenzene; palladium (2+) ; diacetate. Rotatable Bond Count: 5. Exact Mass: 501.974g/mol. SMILES: CC (=O)[O-]. CC (=O)[O-]. C1=CC=C (C=C1)S (=O)CCS (=O)C2=CC=CC=C2. [Pd+2]. InChI: InChI=1S/C14H14O2S2.2C2H4O2.Pd/c15-17(13-7-3-1-4-8-13)11-12-18(16)14-9-5-2-6-10-14;2*1-2(3)4;/h1-10H,11-12H2;2*1H3,(H,3,4);/q;;;+2/p-2. InChIKey: SNNYSJNYZJXIFE-UHFFFAOYSA-L. H-Bond Acceptor: 8. Monoisotopic Mass: 501.974g/mol. | |
(1,5-Cyclooctadiene)rhodium(I) chloride dimer Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·Catalysts for the coupling of 1,3-dienes with activated hydrocarbons and the preparation of chiral complexing agents; ·Rhodium-catalyzed oxidative addition to terminal alkynes to synthesize esters, amides and carboxylic acids; ·Efficient and selective catalysts for asymmetric synthesis. Group: Colloidal Catalysts. CAS No. 12092-47-6. Molecular Weight: 493.08 g/mol. SMILES: Cl[Rh]. Cl[Rh]. C1CC=CCCC=C1. C2CC=CCCC=C2. InChI: QSUDXYGZLAJAQU-MIXQCLKLSA-L. Boiling Point: 243 °C (dec.) (lit.). Flash Point: 98 %. | |
(1E,2E)-1,2-Bis(2,6-Diisopropylphenylimino)ethane Quick inquiry Where to buy Suppliers range | (1E,2E)-1,2-Bis(2,6-Diisopropylphenylimino)ethane. Uses: Reactant in preparation of derived ruthenium olefin metathesis catalysts 1 N-cyclic carbene ligand 2 Catalyst in: Palladium-catalyzed aerobic alc. oxidn. supported by a-diimine ligands 3 Regioselective alkylation in presence of ruthenium-bisimine catalytic precursors 4 N-arylation of aromatic amines 5 Preparation of ruthenium nitrosyl alpha-diimine and iminoketone complexes as catalysts for transfer hydrogenation of ketones and atom transfer radical polymerization reactions. Alternative Names: N,N'-Bis(2,6-diisopropylphenyl)ethanediimine; AKOS004909627; 1,2-bis(2,6-diisopropylphenylimino)ethane; RL04839; AKOS030229349; ZINC252616095; Glyoxal bis(2,6-diisopropylanil); J-502081; AJ-63795; (1E,2E)-N1,N2-bis[2,6-bis(propan-2-yl)phenyl]ethane-1,2-diimine. CAS No. 74663-75-5. Molecular formula: C26H36N2. Mole weight: 376.588g/mol. IUPAC Name: N,N'-bis[2,6-di(propan-2-yl)phenyl]ethane-1,2-diimine. Rotatable Bond Count: 7. Exact Mass: 376.288g/mol. SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N=CC=NC2=C (C=CC=C2C (C)C)C (C)C. InChI: InChI=1S/C26H36N2/c1-17(2)21-11-9-12-22(18(3)4)25(21)27-15-16-28-26-23(19(5)6)13-10-14-24(26)20(7)8/h9-20H,1-8H3. InChIKey: JWVIIGXMTONOFR-UHFFFAOYSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 376.288g/mol. | |
(1S)-1-Amino-2-methyl-1-phenylpropan-2-ol Quick inquiry Where to buy Suppliers range | (1S)-1-Amino-2-methyl-1-phenylpropan-2-ol can be used as reactant/reagent in stereoselective preparation of diaryl carbonyl compounds via palladium-catalyzed enantioselective redox-relay oxidative Heck arylation of arylboronic acids and homoallylic alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 110480-86-9. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H15NO, Molecular Weight: 165.23. US Biological Life Sciences. | Worldwide |
2,2?-Bis(diphenylphosphino)-1,1?-biphenyl Quick inquiry Where to buy Suppliers range | 2,2?-Bis(diphenylphosphino)-1,1?-biphenyl. Uses: Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones. Useful ligand for palladium-catalyzed amination and Kumada cross-coupling reactions Useful ligand for palladium-catalyzed synthesis of butatrenes. Useful ligand for iridium-catalyzed C-C cross-coupling of allenes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of dienes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation. Useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes. Ruthenium-catalyzed synthesis of indoles. Ruthenium-catalyzed oxidative cyclization. Rhodium-catalyzed boron arylation. Mole weight: 522.56. | |
2,2'-Bis(diphenylphosphino)biphenyl Quick inquiry Where to buy Suppliers range | 2,2'-Bis(diphenylphosphino)biphenyl. Uses: Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones. Useful ligand for palladium-catalyzed amination and Kumada cross-coupling reactions Useful ligand for palladium-catalyzed synthesis of butatrenes. Useful ligand for iridium-catalyzed C-C cross-coupling of allenes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of dienes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation. Useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes. Ruthenium-catalyzed synthesis of indoles. Ruthenium-catalyzed oxidative cyclization. Rhodium-catalyzed boron arylation. Group: Organic Phosphine Compounds. Alternative Names: BIPHEP; MFCD03094574; AKOS015911364; DB-009479; 1,1'-[[1,1'-BIPHENYL]-2,2'-DIYL]BIS[1,1-DIPHENYL]-PHOSPHINE; CTK3J1519; SCHEMBL1120987; 2,2'-Bis(diphenylphosphino)biphenyl; 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl; FT-0657577. CAS No. 84783-64-2. Molecular formula: C36H28P2. Mole weight: 522.568g/mol. IUPAC Name: [2-(2-diphenylphosphanylphenyl)phenyl]-diphenylphosphane. Rotatable Bond Count: 7. Exact Mass: 522.167g/mol. SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P (C5=CC=CC=C5)C6=CC=CC=C6. InChI: InChI=1S/C36H28P2/c1-5-17-29(18-6-1)37(30-19-7-2-8-20-30)35-27-15-13-25-33(35)34-26-14-16-28-36(34)38(31-21-9-3-10-22-31)32-23-11-4-12-24-32/h1-28H. InChIKey: GRTJBNJOHNTQBO-UHFFFAOYSA-N. Monoisotopic Mass: 522.167g/mol. | |
2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl Quick inquiry Where to buy Suppliers range | 2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl. Uses: Exceptional ligands for Pd-catalyzed amination and amidation of aryl sulfonates. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling reaction and carbonyl enolate coupling. Ligand used for the chemoselective amination of aryl chlorides. Ligand used for the Pd-catalyzed borylation of aryl chlorides, for the formation of trifluoroborates. Ligand used for the Pd-catalyzed amination of vinyl halides and triflates. Ligand used for the Pd-catalyzed three-component synthesis of indoles. Ligand used for the Pt-catalyzed regioselective hydrosilylation of functionalized terminal arylalkynes. Ligand used for the Pd-catalyzed synthesis of carbazoles. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling of aryl chloride and NHC-boranes. Ligand used for the direct arylation of picoline N-oxide. Ligand used for the Negishi coupling of 2-heterocyclic organozinc reagents. Catalyst for a phosphine-catalyzed Heine reaction. Ligand used for the palladium-catalyzed oxidative coupling of indoles and heteroarenes. Ligand used for the silver-catalyzed hydrogenation of aldehydes. Ligand used for the palladium-catalyzed cyanation of heterycyclic halides. Group: Organic Phosphine Compounds. Alternative Names: dicyclohexyl[2-(2,4,6-triisopropylphenyl)phenyl]phosphane; ING0003480; 2,4,6-triisopropyl-2'-(dicyclohexylphosphino)biphenyl; X7076; 2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1' biphenyl; 100122-EP2289877A1; X-Phos; dicyclohexyl[2',4',6'-tris(propan-2-yl)-[1,1'-biphenyl]-2-yl]phosphane; AC-1757; 2-(dicyclohexylphosphino)-2',4',6'-triisopropyl-biphenyl. CAS No. 564483-18-7. Molecular formula: C33H49P. Mole weight: 476.729g/mol. IUPAC Name: dicyclohexyl-[2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Rotatable Bond Count: 7. Exact Mass: 476.357g/mol. SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=CC=CC=C2P (C3CCCCC3)C4CCCCC4)C (C)C. InChI: InChI=1S/C33H49P/c1-23(2)26-21-30(24(3)4)33(31(22-26)25(5)6)29-19-13-14-20-32(29)34(27-15-9-7-10-16-27)28-17-11-8-12-18-28/h13-14,19-25,27-28H,7-12,15-18H2,1-6H3. InChIKey: UGOMMVLRQDMAQQ-UHFFFAOYSA-N. Monoisotopic Mass: 476.357g/mol. | |
2-(Dicyclohexylphosphino)biphenyl Quick inquiry Where to buy Suppliers range | 2-(Dicyclohexylphosphino)biphenyl. Uses: Ligand used in the palladium-catalyzed synthesis of aromatic amines from aryl chlorides, bromides and triflates. Ligand employed in Suzuki coupling reactions involving aryl chlorides, bromides and triflates. Useful ligand for the Pd-catalyzed oxidation of alcohols in the presence of chlorobenzenes. Useful ligand for the Pd-catalyzed amination with ammonia equivalents. Ligand for the gold(I)-catalyzed intramolecular [4+2] cycloadditions involving 1,3-enynes and arylalkynes with alkenes. Ligand used in the palladium-catalyzed borylation of aryl bromdies. Ligand used in the palladium-catalyzed siliylation of aryl chlorides. Group: Organic Phosphine Compounds. Alternative Names: FT-0084457; 2-(dicyclohexylphosphino) biphenyl; 14110-EP2298767A1; ANW-25534; S-2169; 2-(dicyclohexylphosphanyl)biphenyl; A25272; dicyclohexylphosphino biphenyl; 2-(dicyclohexyl phosphino)biphenyl; 2-(dicylcohexylphosphino)biphenyl. CAS No. 247940-06-3. Molecular formula: C24H31P. Mole weight: 350.486g/mol. IUPAC Name: dicyclohexyl-(2-phenylphenyl)phosphane. Rotatable Bond Count: 4. Exact Mass: 350.216g/mol. EC Number: 480-030-2. SMILES: C1CCC (CC1)P (C2CCCCC2)C3=CC=CC=C3C4=CC=CC=C4. InChI: InChI=1S/C24H31P/c1-4-12-20(13-5-1)23-18-10-11-19-24(23)25(21-14-6-2-7-15-21)22-16-8-3-9-17-22/h1,4-5,10-13,18-19,21-22H,2-3,6-9,14-17H2. InChIKey: LCSNDSFWVKMJCT-UHFFFAOYSA-N. Monoisotopic Mass: 350.216g/mol. | |
2-Mercaptopyridine N-Oxide Sodium Salt Quick inquiry Where to buy Suppliers range | 2-Mercaptopyridine N-oxide sodium salt is a bidentate complexing agent used to chelate transition metals at a pH range of 0.7-7.4. 2-Mercaptopyridine N-oxide sodium salt is also used as a selective absorptiometric reagent in the determination of palladium. Group: Biochemicals. Grades: Highly Purified. CAS No. 3811-73-2. Pack Sizes: 2.5g, 10g. Molecular Formula: C5H4NNaOS, Molecular Weight: 149.15. US Biological Life Sciences. | Worldwide |
[ (2Z) -2- [ (3S, 5R) -3, 5-Bis [ [ (1, 1-dimethylethyl) dimethylsilyl] oxy] -2-methylenecyclohexylidene] ethyl] diphenylphosphine Oxide Quick inquiry Where to buy Suppliers range | The biphenyl-P-oxide compound, widely applied in biomedicine such as drug discovery, serves as a palladium-catalyzed cross-coupling reaction ligand. This compound presents tremendous versatility in its usability as it is instrumental in the oligonucleotide synthesis and the production of numerous bioactive molecules. Synonyms: [3S- (1Z, 3α , 5β ) ] - [2- [3, 5-Bis [ [ (1, 1-dimethylethyl) dimethylsilyl] oxy] -2-methylenecyclohexylidene] ethyl] diphenylphosphine Oxide; Phosphine oxide, [2- [3, 5-bis [ [ (1, 1-dimethylethyl) dimethylsily] oxy] -2-methylenecyclohexylidene] ethyl] diphenyl-, [3S-(1Z,3α,5β)]-; Tert-butyl-[(1R,3S,5Z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane; ( (Z) -2- ( (3S, 5R) -3, 5-bis ( (tert-butyldimethylsilyl) oxy) -2-methylenecyclohexylidene) ethyl) diphenylphosphine oxide. Grades: 95%. CAS No. 81522-68-1. Molecular formula: C33H51O3PSi2. Mole weight: 582.90. | |
4-Formylphenylboronic acid Quick inquiry Where to buy Suppliers range | Reagent used for: Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water ; Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides ; Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids ; Triethylamine-catalyzed three-component Hantzsch condensations ; Copper-catalyzed nitrations ; Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta ; Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides ; Palladium-catalyzed aerobic oxidative cross-coupling reactions Reagent used in Preparation of; Sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells; A novel protein synthesis inhibitor active against Gram-positive bacteria. Synonyms: Boronic acid, (4-formylphenyl)-; 4-Boronobenzaldehyde; p-formylphenylboronic acid; MFCD00151823; 4-benzaldehyde boronic acid; 4-(Dihydroxyboryl)benzaldehyde; CHEMBL140254. Grades: 95 %. CAS No. 87199-17-5. Molecular formula: C7H7BO3. Mole weight: 149.94. | |
4-Vinylaniline Quick inquiry Where to buy Suppliers range | 4-Vinylaniline (4-VAn) is a primary amine surfactant. Uses: 4-VAn undergoes graft copolymerization with poly(tetrafluoroethylene) (PTFE) and Si surface, followed by oxidative copolymerization with aniline. Thus, it renders PTFE and Si surface conductive. 4-VAn is coupled with hydrogen terminated Si surfaces for electroless metal and synthetic metal deposition. Palladium(II) schiff base complexes derived from Allylamine and vinylaniline has been reported. It also acts as a second surfactant for coating nanomagnetic particles. It is used in functionalization of single-walled carbon nanotube through solvent free functionalization. Group: CHN Containing Functional Groups. Alternative Names: 4-Aminostyrene. CAS No. 1520-21-4. Molecular Weight: 119.16. Molecular Formula: H2C=CHC6H4NH2. SMILES: Nc1ccc(C=C)cc1. Flash Point: 97%. | |
4- (Vinyloxymethyl) cyclohexanemethanol Quick inquiry Where to buy Suppliers range | 4- (Vinyloxymethyl) cyclohexanemethanol is used as a reagent in the synthesis of acetic acid esters by catalytic oxidation of vinyl ethers with aqueous H2O2 solutions in the presence of palladium catalysts having phosphine ligands and amines. Also used in the synthesis of Si-containing monomers and 4-substituted cyclohexane carbaldehydes. Group: Biochemicals. Grades: Highly Purified. CAS No. 114651-37-5. Pack Sizes: 1g, 10g. Molecular Formula: C10H18O2, Molecular Weight: 170.25. US Biological Life Sciences. | Worldwide |
5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine palladium(II) Quick inquiry Where to buy Suppliers range | 5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine palladium(II) is a phosphorescent dye that is a derivative of palladium(II). It can be used as a singlet oxygen sensitizer due to the presence of fluorine atoms. It provides photostability and is resistant to oxidation. Uses: It can be used as a porphyrin dye with a high quantum yield for use in the fabrication of oxygen sensors. Group: Palladium Complexes. Alternative Names: Pd(II)meso-tetra(pentafluorophenyl) porphine. Grades: 98%+. CAS No. 72076-09-6. Product ID: ACM72076096-2. Molecular formula: C44H8F20N4Pd. Mole weight: 1078.9. IUPAC Name: palladium(2+);5,10,15,20-tetrakis(2,3,4,5,6-pentafluorophenyl)porphyrin-22,24-diide. SMILES: C1=CC2=C (C3=NC (=C (C4=CC=C ([N-]4)C (=C5C=CC (=N5)C (=C1[N-]2)C6=C (C (=C (C (=C6F)F)F)F)F)C7=C (C (=C (C (=C7F)F)F)F)F)C8=C (C (=C (C (=C8F)F)F)F)F)C=C3)C9=C (C (=C (C (=C9F)F)F)F)F. [Pd+2]. | |
Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate), 99% Quick inquiry Where to buy Suppliers range | Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate), 99%. Uses: This dimeric palladium complex is used in the chemoselective oxidation of polyols. Alternative Names: MFCD28411662;Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate); 959698-19-2. CAS No. 959698-19-2. Molecular formula: C32H30N4O4Pd2+2. Mole weight: 747.456g/mol. IUPAC Name: 2, 9-dimethyl-1, 10-phenanthroline; palladium(2+); diacetate. Exact Mass: 748.034g/mol. SMILES: CC1=NC2=C(C=C1)C=CC3=C2N=C(C=C3)C. CC1=NC2=C(C=C1)C=CC3=C2N=C(C=C3)C. CC(=O)[O-]. CC(=O)[O-]. [Pd+2]. [Pd+2]. InChI: InChI=1S/2C14H12N2.2C2H4O2.2Pd/c2*1-9-3-5-11-7-8-12-6-4-10(2)16-14(12)13(11)15-9;2*1-2(3)4;;/h2*3-8H,1-2H3;2*1H3,(H,3,4);;/q;;;;2*+2/p-2. InChIKey: XNKIUDQGRLENPA-UHFFFAOYSA-L. H-Bond Acceptor: 8. Monoisotopic Mass: 746.034g/mol. | |
Allyl[1, 3-bis (2, 6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium (II) Quick inquiry Where to buy Suppliers range | Allyl[1, 3-bis (2, 6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium (II). Uses: Catalyst for the cross-coupling of aryl chlorides or bromides with aromatic amines. Catalyst for the α-arylation of ketones. Catalyst for anaerobic alcohol oxidation. Group: Heterocyclic Organic Compound. Alternative Names: ALLYLCHLORO[1,3-BIS(2,6-DI-I-PROPYLPHENYL)-4,5-DIHYDROIMIDAZOL-2-YLIDENE]PALLADIUM (II);Allylchloro[1, 3-bis(2, 6-di-i-propylphenyl)-4, 5-dihydroimidazol-2-ylidene]palladium(II), 97%;ALLYLCHLORO[1, 3-BIS-(DIISOPROPYLPHENYL)-2-IMIDAZOLIDINYLIDENE]PALLADIUM(II). Grades: 96%. CAS No. 478980-01-7. Molecular formula: C30H43ClN2Pd. Mole weight: 573.55. IUPAC Name: Allylchloro[1,3-bis(2,6-di-i-propylphenyl)-4,5-dihydroimidazol-2-ylide. Exact Mass: 572.21500. Safty Description: 26-36/37/39. | |
Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II) Quick inquiry Where to buy Suppliers range | white solid. Uses: Catalyst for the cross-coupling of aryl chlorides with boronic acids. Catalyst for the diamination of conjugated dienes and trienes. Catalyst for the dehalogenation of aryl chlorides. Catalyst for anaerobic alcohol oxidation. Catalyst for anaerobic ketone oxidation and domino oxidation/α-arylation. Group: Organic Phosphine Compounds. Alternative Names: Palladium, [1,?3-bis[2,?6-bis(1-methylethyl)?phenyl]?-1,?3-dihydro-2H-imidazol-2-ylidene]?chloro(η3-2-propen-1-yl)?-. Grades: 98%, Pd>18.5%. CAS No. 478980-03-9. Molecular formula: C30H42ClN2Pd. Mole weight: 572.54. Symbol: GHS07. Melting Point: > 300 °C (> 572 °F). Hazard statements: H315-H319-H335. | |
Allylchloro[1,3-bis-(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium(II) Quick inquiry Where to buy Suppliers range | Allylchloro[1,3-bis-(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium(II). Uses: Amination?Buchwald-Hartwig Aminaton; Cross Coupling Reactions with Arenes?Alpha Arylation; Cross Coupling Reactions with Arenes?Dehalogenation; Cross Coupling Reactions with Arenes?Kumada Coupling Reaction; Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Cross Coupling Reactions with Arenes?Oxidation; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction. Group: Catalysts for Pharmaceutical. CAS No. 478980-04-0. Molecular Weight: 487.38. Molecular Formula: C24H29N2ClPd. Purity: Metal purity 99.95. | |
Allylchloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]palladium(II) Quick inquiry Where to buy Suppliers range | Allylchloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]palladium(II). Uses: Amination?Buchwald-Hartwig Aminaton; Cross Coupling Reactions with Arenes?Alpha Arylation; Cross Coupling Reactions with Arenes?Dehalogenation; Cross Coupling Reactions with Arenes?Kumada Coupling Reaction; Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Cross Coupling Reactions with Arenes?Oxidation; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction; Dehalogenation; Oxidation; Telomerization. Group: Catalysts for Pharmaceutical; Oxidation. CAS No. 478980-03-9. Molecular Weight: 571.54. Molecular Formula: C30H41N2ClPd. Purity: Metal purity 99.95. | |
Allylpalladium chloride dimer, Pd : 56.5 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: Application: Oxidant; Oxidation of Δ1-ene to enol acetate; Acetoxylation of aromatic hydrocarbons; Suzuki reaction, cross-coupling reaction, olefin carbonylation reaction. Group: Colloidal Catalysts. CAS No. 12012-95-2. Molecular Weight: 365.89 g/mol. SMILES: Cl[Pd]CC=C.Cl[Pd]CC=C. InChI: TWKVUTXHANJYGH-UHFFFAOYSA-L. Boiling Point: 216.3-223.7 ?. Flash Point: 98 %. | |
Allylpalladium chloride dimer, Pd : 58.2 % Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: Application: Oxidant; Oxidation of Δ1-ene to enol acetate; Acetoxylation of aromatic hydrocarbons; Suzuki reaction, cross-coupling reaction, olefin carbonylation reaction. Group: Colloidal Catalysts. CAS No. 12012-95-2. Molecular Weight: 365.89 g/mol. SMILES: Cl[Pd]CC=C.Cl[Pd]CC=C. InChI: TWKVUTXHANJYGH-UHFFFAOYSA-L. Boiling Point: 216.3-223.7 ?. Flash Point: 98 %. | |
Biotinyl-phenylboronic acid Quick inquiry Where to buy Suppliers range | Biotinyl-phenylboronic acid is the functionalized arylboronic acid of biotin used for palladium-catalyzed oxidative Heck reaction to protein-bound alkenes and Suzuki-Miyaura cross-coupling for labeling of protein bound phenylhalides in high yields and with excellent chemoselectivity. Synonyms: [3-[5-(2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl)pentanoylamino]phenyl]boronic acid. Grades: 99%. CAS No. 1661014-48-7. Molecular formula: C16H22BN3O4S. Mole weight: 363.24. | |
Bis (acetonitrile)dichloropalladium (II) Quick inquiry Where to buy Suppliers range | Bis (acetonitrile)dichloropalladium (II). Uses: Carbonylation; Cyclization; Isomerization; Oligomerization; Oxidation. Group: Palladium Complexes. Alternative Names: Palladium dichlorobis(acetonitrile). Grades: 98%. CAS No. 14592-56-4. Product ID: ACM14592564-1. Molecular formula: C4H6Cl2N2Pd. Mole weight: 259.43. Appearance: Dark yellow powder. SMILES: CC#N.CC#N.Cl[Pd]Cl. | |
Bis(dibenzylideneacetone)palladium, Pd : 18.4 wt.% Quick inquiry Where to buy Suppliers range | Bis(dibenzylideneacetone)palladium (Pd(dba)2) is an air-stable Pd0 complex. It is a reagent for the synthesis of allyl-substituted cyclopentadiene. It is a homogeneous catalyst that can catalyze the alkylation of allyl acetate by the action of various nucleophiles under mild conditions. Uses: ·Synthesis of isomer 2-aryl-2,5-dihydrofuran by Heck coupling reaction of aryl bromide with alkene using neopentylphosphine ligand; ·Heck reaction of benzyl trifluoroacetate and 2,3-dihydrofuran phosphoramidite ligand; ·Allylation of stable anions; ·Cross-coupling of allyl, alkenyl and aryl halides with organotin compounds; ·Cross-coupling of vinyl halides with alkenyl zinc compounds; ·Carbonylation of alkenyl and aryl halides; ·Efficient oxidation of alcohols to aldehydes and ketones together with cyclic thiourea ligands. Group: Colloidal Catalysts. CAS No. 32005-36-0. Molecular Weight: 575 g/mol. SMILES: [Pd]. O=C(/C=C/c1ccccc1)\C=C\c2ccccc2. O=C(/C=C/c3ccccc3)\C=C\c4ccccc4. InChI: UKSZBOKPHAQOMP-SVLSSHOZSA-N. Boiling Point: 150 °C. | |
Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) Quick inquiry Where to buy Suppliers range | Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II). Uses: Amination?Buchwald-Hartwig Aminaton; C-H Activation; Carbonylation; Cross Coupling Reactions with Arenes?Negishi Coupling Reaction; Cross Coupling Reactions with Arenes?Stille Reaction; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction; Oxidation. Group: Catalysts for Pharmaceutical; Oxidation; Amination. CAS No. 72287-26-4. Molecular Weight: 731.71. Molecular Formula: C34H28Cl2FeP2Pd. Purity: Metal purity 99.95. | |
Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) acetone adduct Quick inquiry Where to buy Suppliers range | Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) acetone adduct. Uses: Carbonylation; Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Oxidation. Group: Catalysts for Pharmaceutical; Oxidation. CAS No. 851232-71-8. Molecular Weight: 789.79. Molecular Formula: C37H34OCl2FeP2Pd. Purity: Metal purity 99.95. | |
Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) dichloromethane adduct Quick inquiry Where to buy Suppliers range | Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) dichloromethane adduct. Uses: Carbonylation; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction; Oxidation. Group: Catalysts for Pharmaceutical; Oxidation. CAS No. 95464-05-4. Molecular Weight: 816.65. Molecular Formula: C35H30Cl4FeP2Pd. Purity: Metal purity 99.95. | |
Dichloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)](3-chloropyridyl)palladium(II) Quick inquiry Where to buy Suppliers range | Dichloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)](3-chloropyridyl)palladium(II). Uses: Amination?Buchwald-Hartwig Aminaton; C-H Activation; Cross Coupling Reactions with Arenes?Kumada Coupling Reaction; Cross Coupling Reactions with Arenes?Negishi Coupling Reaction; Cross Coupling Reactions with Arenes?Oxidation; Cross Coupling Reactions with Arenes?Sonogashira-Hagihara Coupling Reaction; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction. Group: Catalysts for Pharmaceutical; Amination. CAS No. 905459-27-0. Molecular Weight: 679.47. Molecular Formula: C32H40N3Cl3Pd. Purity: Metal purity 99.95. | |
Dichloro(4,5-bis(diphenylphosphino)-9,9-dimethylxanthene)palladium(II) Quick inquiry Where to buy Suppliers range | Dichloro(4,5-bis(diphenylphosphino)-9,9-dimethylxanthene)palladium(II). Uses: Hydrogenation?Transfer Hydrogenation; Oxidation. Group: Catalysts for Pharmaceutical; Oxidation. CAS No. 205319-10-4. Molecular Weight: 755.94. Molecular Formula: C39H32Cl2OP2Pd. Purity: Metal purity 99.95. | |
Dichlorobis (triphenylphosphine)palladium (II) Quick inquiry Where to buy Suppliers range | Dichlorobis (triphenylphosphine)palladium (II). Uses: Carbonylation; Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Cross Coupling Reactions with Arenes?Sonogashira-Hagihara Coupling Reaction; Cross Coupling Reactions with Arenes?Stille Reaction; Cyclization; Oxidation; Reduction. Group: Catalysts for Pharmaceutical; Oxidation. CAS No. 13965-03-2. Molecular Weight: 701.91. Molecular Formula: C36H30Cl2P2Pd. Purity: Metal purity 99.95. | |
Dichloro (N, N, N?, N?-tetramethylethylenediamine)palladium (II) Quick inquiry Where to buy Suppliers range | Dichloro (N, N, N?, N?-tetramethylethylenediamine)palladium (II). Uses: Catalyst for: Cross-coupling reactions. Catalytic reduction reactions. Preparation of silyl ethers via reaction of silicon-hydrogen bond with alcohols. Oxidative carbonylation reactions. Group: Palladium series catalysts. Alternative Names: I14-10025; AC1L4Z7Y; AC1Q1RTB; Palladium, dichloro(N,N,N',N'-tetramethyl-1,2-ethanediamine-N,N')-, (SP-4-2)- (9CI); RL01764; Palladium, dichloro(N,N,N',N'-tetramethylethylenediamine)- (8CI); AKOS015900158; TRA0000186; dichloride. CAS No. 14267-08-4. Molecular formula: C6H16Cl2N2Pd. Mole weight: 293.528g/mol. IUPAC Name: palladium(2+);N,N,N',N'-tetramethylethane-1,2-diamine;dichloride. Rotatable Bond Count: 3. Exact Mass: 291.973g/mol. SMILES: CN(C)CCN(C)C.[Cl-].[Cl-].[Pd+2]. InChI: InChI=1S/C6H16N2.2ClH.Pd/c1-7(2)5-6-8(3)4;;;/h5-6H2,1-4H3;2*1H;/q;;;+2/p-2. InChIKey: FJOUSQLMIDWVAY-UHFFFAOYSA-L. H-Bond Acceptor: 4. Monoisotopic Mass: 291.973g/mol. | |
Dichloro (pentamethylcyclopentadienyl)rhodium (III) dimer Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·Used as a catalyst in reactions, as well as in synthetic oxidative arylation reactions with indoles, azobenzene derivatives and o-alkynylated arylalkylamines. ·As organic synthesis intermediates and pharmaceutical intermediates, mainly as phosphine ligands, it can be used in laboratory research and development processes and chemical and pharmaceutical synthesis processes. Group: Colloidal Catalysts. CAS No. 12354-85-7. Molecular Weight: 618.08 g/mol. SMILES: Cl[Rh]Cl. Cl[Rh]Cl. C[C]1[C](C)[C](C)[C](C)[C]1C. C[C]2[C](C)[C](C)[C](C)[C]2C. InChI: QNIVKTTWBMFSBR-UHFFFAOYSA-J. Boiling Point: 300 °C. Flash Point: 97 %. Density: Soluble in chloroform and acetone. Slightly soluble in tetrahydrofuran and methanol. Insoluble in water and diethylether. | |
Lindlar Catalyst Quick inquiry Where to buy Suppliers range | Lindlar Catalyst. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. | |
(Oxybis(2,1-phenylene))bis(diphenylphosphine) Quick inquiry Where to buy Suppliers range | (Oxybis(2,1-phenylene))bis(diphenylphosphine). Uses: Useful as a ligand in the Pd-catalyzed formation of diaryl amines. Has been recently applied to the C3 benzylation of indoles. Has been recently applied to the monoallylation of ammonia. Ligand used in the palladium-catalyzed, aerobic oxidation coupling of acyl chlorides with arylboronic acids. Ligand used in carbonylation of aryl iodides. Ligand used in the direct C-H arylation of benzothiodiazoles. Ligand used in stereo-retentive azacyclization of propargylic carbonates. Ligand used in palladium catalyzed benzyne trimerization. Group: Organic Phosphine Compounds. CAS No. 166330-10-5. Molecular formula: C36H28OP2. Mole weight: 538.567g/mol. IUPAC Name: [2-(2-diphenylphosphanylphenoxy)phenyl]-diphenylphosphane. Rotatable Bond Count: 8. Exact Mass: 538.162g/mol. SMILES: C1=CC=C (C=C1) P (C2=CC=CC=C2) C3=CC=CC=C3OC4=CC=CC=C4P (C5=CC=CC=C5) C6=CC=CC=C6. InChI: InChI=1S/C36H28OP2/c1-5-17-29(18-6-1)38(30-19-7-2-8-20-30)35-27-15-13-25-33(35)37-34-26-14-16-28-36(34)39(31-21-9-3-10-22-31)32-23-11-4-12-24-32/h1-28H. InChIKey: RYXZOQOZERSHHQ-UHFFFAOYSA-N. H-Bond Acceptor: 1. Monoisotopic Mass: 538.162g/mol. | |
Palladium Quick inquiry Where to buy Suppliers range | Palladium and its alloys are used for hydrogen purification in fuel cells. Energy dispersive x-ray diffraction during electrochemical loading of palladium foils with hydrogen and deuterium was studied. Palladium foil was tested as a catalyst for Suzuki-Miyaura cross coupling reaction. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Group: Electrode Materials; Evaporation Slugs; High-Purity Metal Foils. Alternative Names: Palladium (powder),Palladium black,Palladium element. CAS No. 7440-5-3. IUPAC Name: palladium. Molecular Weight: 106.42. Molecular Formula: Pd. SMILES: [Pd]. | |
Palladium Quick inquiry Where to buy Suppliers range | Palladium and its alloys are used for hydrogen purification in fuel cells. Energy dispersive x-ray diffraction during electrochemical loading of palladium foils with hydrogen and deuterium was studied. Palladium foil was tested as a catalyst for Suzuki-Miyaura cross coupling reaction. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Group: Oil & Gas. Alternative Names: Palladium (powder),Palladium black,Palladium element. CAS No. 7440-5-3. IUPAC Name: palladium. Molecular Weight: 106.42. Molecular Formula: Pd. SMILES: [Pd]. | |
Palladium Quick inquiry Where to buy Suppliers range | Palladium and its alloys are used for hydrogen purification in fuel cells. Energy dispersive x-ray diffraction during electrochemical loading of palladium foils with hydrogen and deuterium was studied. Palladium foil was tested as a catalyst for Suzuki-Miyaura cross coupling reaction. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Group: Electrode Materials; Evaporation Slugs; High-Purity Metal Foils. Alternative Names: Palladium (powder),Palladium black,Palladium element. CAS No. 7440-5-3. IUPAC Name: palladium. Molecular Weight: Pd. Molecular Formula: 106.42. SMILES: [Pd]. Density: 12.02 g/cu cm. | |
Palladium(II) Chloride Quick inquiry Where to buy Suppliers range | Palladium(II) Chloride. Uses: Palladium dichloride dissolves in HCl forming tetrachloropalladate ion, PdCl2+2Cl¯? [PdCl4]2¯ The complex ion catalyzes various types of organic reactions including oxidation of ethylene to acetaldehyde in aqueous solution (the Wacker Process): PdCl42¯+ C2H4 + H2O ? CH3CHO + Pd + 2HCl + 2Cl¯ Palladium dichloride forms polymeric carbonyl complexes when the dry chloride is heated in a stream of carbon monoxide charged with methane vapor. Such complexes include [PdCl2(CO)n] and [PdCl(CO)2]n. The reaction also occurs in aqueous phase resulting in decolorization of the solution. When H2S is passed through palladium dichloride solution, it yields a brown-black precipitate of palladium monosulfide, PdS. When heated with sulfur at 450 to 500°C, palladium dichloride forms palladium disulfide, PdS2, a grey-black crystalline compound, insoluble in strong acids but soluble in aqua regia, and which converts to monosulfide, PdS, on heating at 600°C. When ammonia gas is passed through an aqueous solution of PdCl2, the product is tetrammine palladium(II) chloride, Pd(NH4)2Cl2. The same product also is obtained in dry state by passing ammonia gas over anhydrous PdCl2. Group: Metal & Ceramic Materials. Alternative Names: Palladium(II) chloride, 59% Pd; PdCl2; RTR-033694; Palladium(II) chloride, 99.999%, (trace metal basis); dichloropalladium(11); Enplate activator 440; AC-18128; NSC146183; CAS-7647-10-1; AKOS015833820. CAS No. 7647-10-1. Molecular formula: PdCl2;Cl2Pd. Mole weight: 177.32g/mol. IUPAC Name: dichloropalladium. Exact Mass: 175.841g/mol. EC Number: 231-596-2. Melting Point: 934 ° F (DECOMP) (NTP, 1992);678-680 deg C. Solubility: Soluble (NTP, 1992);Sol in water, ethanol, acetone;Readily soluble in hydrochloric acid and solutions of alkali metal chlorides. Density: 4 at 64 ° F (NTP, 1992);4.0 g/cu cm. SMILES: Cl[Pd]Cl. InChI: InChI=1S/2ClH.Pd/h2*1H;/q;;+2/p-2. InChIKey: PIBWKRNGBLPSSY-UHFFFAOYSA-L. Monoisotopic Mass: 175.841g/mol. | |
Palladium(II) chloride solution Quick inquiry Where to buy Suppliers range | Palladium(II) chloride solution. Uses: Carbonylation; Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Oxidation. Group: Catalysts for Pharmaceutical; Oxidation. CAS No. 16970-55-1. Molecular Weight: 250.24 (anhydrous). Molecular Formula: H2Cl4Pd. Purity: Metal purity 99.95. | |
Palladium monoxide Quick inquiry Where to buy Suppliers range | Palladium monoxide. Group: Nanoparticles & Nanopowders. Alternative Names: CTK4B7267; AC1NO7R7; 1314-08-5; oxopalladium; Palladium(II) oxide, anhydrous; TR-004294; RTR-004294; Palladium oxide (PdO); HBEQXAKJSGXAIQ-UHFFFAOYSA-N; ACMC-1BQVH. CAS No. 1314-08-5. Molecular formula: OPd. Mole weight: 122.419g/mol. IUPAC Name: oxopalladium. Exact Mass: 121.898g/mol. EC Number: 215-218-3. SMILES: O=[Pd]. InChI: InChI=1S/O.Pd. InChIKey: HBEQXAKJSGXAIQ-UHFFFAOYSA-N. H-Bond Acceptor: 1. Monoisotopic Mass: 121.898g/mol. | |
Palladium Nanoparticles Dispersion (Pd, Purity: 99.99%) Quick inquiry Where to buy Suppliers range | Lead is gray and easily oxidized by oxygen in the air into gray-black lead oxide, making its silvery white luster gradually dull. However, this layer of lead oxide forms a dense film that prevents further oxidation of the lead inside. Because of this, and the chemical properties of lead are relatively stable, lead is not easily corroded. Nano-lead is a gray-black liquid, with a fine and greasy feel, heavy in quality, insoluble in water and alcohol, but soluble in carbonated water and dilute nitric acid. Uses: ·For the manufacture of lead-acid batteries ·Manufacture of lead bricks or lead clothing for protection against X-rays and other radiation ·Alloy Manufacturing ·Powder metallurgy oil-free lubricant ·Pigment. Group: Metal Colloids. CAS No. 7440-5-3. Molecular Weight: 106.42 g/mol. InChIKey: 2970 °C (lit.). Boiling Point: 1554 °C (lit.). Flash Point: 99.9 %. Purity: 1.025g/mL at 25 °C. | |
Palladium on calcium carbonate Quick inquiry Where to buy Suppliers range | Palladium on calcium carbonate. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. The metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. Palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation state. When heated in air or oxygen above 350°C, palladium forms a black oxide, PdO coated over its surface. On further heating to over 790°C, the oxide decomposes back to the metal. Palladium dissolves more oxygen in molten state than in solid form. Palladium reacts with fluorine and chlorine at 500°C forming its halides, the black PdF3 and the red deliquescent solid PdCl2. Palladium is attacked by concentrated nitric acid, particularly in the presence of nitrogen oxides. The reaction is slow in dilute nitric acid. Finely divided palladium metal reacts with warm nitric acid forming palladium(II) nitrate, Pd(NO3)2. Hydrochloric acid has no affect on the metal. Reaction with boiling sulfuric acid yields palladium sulfate, PdSO4, and sulfur dioxide. Palladium readily dissolves in aqua regia forming chloropalladic acid, H2PdCl6. Evaporation of this solution yields palladium(II) chloride, PdCl2. Palladium absorbs hydrogen over 800 times its own volume over a range of temperature. By doing so, the metal swells, becoming brittle and cracked. Such absorption of hydrogen decreases the electrical conductivity of the metal. Also, such absorption activates molecular hydrogen, dissociating it to atomic hydrogen. Molecular formula: Pd. | |
Sensitizer Quick inquiry Where to buy Suppliers range | Sensitizer. Uses: Tetraamminepalladium(II) chloride monohydrate is used to prepare trans-diamminedichloropalladium(II). It is also utilized in the preparation of mesoporous carbon supporting palladium nanoparticles by using graphite oxide. It is used as catalysts, reagents, and analytical reagents. Group: Metal & Ceramic Materials. Alternative Names: Tetraamminepalladium(II) chloride monohydrate; KS-00000H5G; AKOS027250697; chloride hydrate; MFCD00151033; Palladium(2+), tetraammine-, dichloride, monohydrate, (SP-4-1)- (9CI); TETRAAMMINEPALLADIUM (II) CHLORIDE; Sensitizer; ST24050111. CAS No. 13933-31-8. Molecular formula: Cl2H14N4OPd. Mole weight: 263.459g/mol. IUPAC Name: azane;dichloropalladium;hydrate. Exact Mass: 261.958g/mol. SMILES: N.N.N.N.O.Cl[Pd]Cl. InChI: InChI=1S/2ClH.4H3N.H2O.Pd/h2*1H; 4*1H3; 1H2; /q; ; ; ; ; ; ; +2/p-2. InChIKey: WVCXSPJPERKPJS-UHFFFAOYSA-L. H-Bond Donor: 5. H-Bond Acceptor: 5. Monoisotopic Mass: 261.958g/mol. |