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| Product | Description | |
|---|---|---|
| Palladium hydroxide | Palladium hydroxide. Uses: Nonpyrophoric catalyst for hydrogenolysis of benzyl-nitrogen and benzyl-oxygen bonds. Group: Salt. Alternative Names: Palladium(II)dihydoxide. CAS No. 12135-22-7. Product ID: palladium(2+); dihydroxide. Molecular formula: 140.43. Mole weight: H2O2Pd. [OH-].[OH-].[Pd+2]. InChI=1S/2H2O.Pd/h2*1H2;/q;+2/p-2. NXJCBFBQEVOTOW-UHFFFAOYSA-L. 98%. |  |
| Palladium Hydroxide (20% on Carbon) | Palladium Hydroxide (20% on Carbon). Group: Biochemicals. Alternative Names: Escat 1951; Palladium Dihydroxide; Palladium(II) Hydroxide; Pearlman's Catalyst. Grades: Highly Purified. CAS No. 12135-22-7. Pack Sizes: 1g. Molecular Formula: H2O2Pd, Molecular Weight: 140.43. US Biological Life Sciences. |  Worldwide |
| Palladium hydroxide on carbon | Palladium hydroxide on carbon. Group: Biochemicals. Grades: Highly Purified. CAS No. 12135-22-7. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: H2O2Pd. US Biological Life Sciences. | Worldwide |
| Palladium hydroxide on carbon powder | Pearlman's catalyst H2O2Pd. CAS No. 12135-22-7. Product ID: 8-01384. Mole weight: 140.43. Purity: 20 w% wet (water <50%). Properties: d 0.92 Bp 220 °C nD20 1.424-1.426 Fp 111 °C. |  |
| Palladium (II) hydroxide | Palladium (II) hydroxide. Group: Biochemicals. Grades: Reagent Grade. CAS No. 12135-22-7. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Tetraamminepalladium(II)hydroxide | Tetraamminepalladium(II)hydroxide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Tetraamminepalladium(II) dihydroxide. Product Category: Palladium series catalysts. Appearance: yellow. CAS No. 68413-68-3. Molecular formula: [Pd(NH3)4](OH)2. Mole weight: 208.56. Purity: Pd 51%. Product ID: ACM68413683. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Bis(tri-tert-butylphosphine)palladium(0) | Bis(tri-tert-butylphosphine)palladium(0) is also used in the preparation of G6P-T1 translocase inhibitors used in the treatment of diabetes. Also, its used to prepare new dibenzofulvenes. Uses: Introduced as an easier to handle pd/p(t-bu)3-based catalyst for the negishi cross-coupling of aryl/vinyl chlorides. a versatile catalyst for the cross-coupling of aryl and vinyl chlorides. catalyst for the amination of aryl chlorides and bromides using aqueous hydroxide bases. useful catalyst for the cross-coupling of heteroaromatic carboxylic acids. pd-catalyzed newnan-kwart rearrangement of o-aryl thiocarbamates. cross-coupling of silanolates and halides. elimination/isomerization of enol triflates derived from β-ketoesters. Group: Polymerization reagents. Alternative Names: palladium,tritert-butylphosphane; Pd(t-Bu3P)2. CAS No. 53199-31-8. Product ID: palladium; tritert-butylphosphane. Molecular formula: 511.064g/mol. Mole weight: C24H54P2Pd. CC(C)(C)P(C(C)(C)C)C(C)(C)C. CC(C)(C)P(C(C)(C)C)C(C)(C)C. [Pd]. InChI=1S/2C12H27P.Pd/c2*1-10(2, 3)13(11(4, 5)6)12(7, 8)9;/h2*1-9H3; : MXQOYLRVSVOCQT-UHFFFAOYSA-N. | |
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