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| Product | Description | |
|---|---|---|
| Gold hydroxide | Gold hydroxide. Group: Electrolytes. Alternative Names: goldhydroxide(au(oh)3); Gold trihydroxide; GOLD(III) HYDROXIDE; GOLD HYDROXIDE; Gold(III) hydroxide, 99.9%; GOLD (III) HYDROXIDE, 99.9% (CL ; Gold(III) hydroxide, Au 79% min; gold trihydrate. CAS No. 1303-52-2. Molecular formula: 247.99. Mole weight: AuH3O3. Au ≥78.0%. |  |
| 1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidenegold(I) hydroxide, min. 97% | Catalyst used for the carboxylation of C-H bonds. Catalyst used for the hydrofluorination of alkynes. Gold-catalyzed synthesis of sulfinate derivatives Effective catalyst for the carboxylation/cyclization of propargylamines with carbon dioxide. Catalyst used for the polymerization of racemic β-butyrolactones. Catalyst used for the intermolecular mono and dihydroamination of activated alkenes. Group: Gold catalysts. Alternative Names: MFCD22666054;1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidenegold(I) hydroxide;1240328-73-7. CAS No. 1240328-73-7. Molecular formula: C27H38AuN2O. Mole weight: 603.581g/mol. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]imidazole;gold;hydrate. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2C=CN ([C]2)C3=C (C=CC=C3C (C)C)C (C)C. O. [Au]. Catalog: ACM1240328737. |  |
| Gold(III) hydroxide | Gold(III) hydroxide. Group: Biochemicals. Grades: Highly Purified. CAS No. 1303-52-2. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. |  Worldwide |
| Gold(III) hydroxide 99.5+%, (79% Gold content) | Gold(III) hydroxide 99.5+%, (79% Gold content). Group: Biochemicals. Grades: Reagent Grade. CAS No. 1303-52-2. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Gold (III) hydroxide, 99.9% (Cl < 100ppm) | 1g Pack Size. Group: Inorganic Chemicals, Salts. Formula: AuH3O3. CAS No. 1303-52-2. Prepack ID 23620799-1g. Molecular Weight 247.99. See USA prepack pricing. |  |
| Gold(III) hydroxide, Au(OH)3 | Gold(III) hydroxide, Au(OH)3. Group: Magnetic nanoparticles. | |
| Iron Pigment Yellow | Iron Pigment Yellow. Uses: For analytical and research use. Group: Dyes & metabolites; dyes & metabolites. Alternative Names: SunPuro Yellow C 33-9001, Iron Yellow AZ 138, S 920 (pigment), Synthetic yellow iron oxide pigment, Zh 1 (pigment), Bayferrox 3960, CTD 7201, Sicotrans Gold L 1916, 362R, Bayferrox 415, Iron oxide yellow, PY 42, YellowCap 1, L 1, Toda Yellow 48, Disperse HG 457, Puricolor Yellow PYE 42, Timbasol PW 895, YZ 1688, Trans Oxide Yellow AC 2544, Bayferrox Yellow 4920, CM 3FA70ERH, R 131CN, LB 100E172, L 1918, Anchor FY 766, Bayferrox Yellow 3905, SunPURO Yellow, Xeracolor Yellow Oxide, C 7055, Kobo Yellow WSJ 20EYAMP, Sicopharm Yellow, Pigment Yellow 42, Tarox YP 1200P, Iron hydroxide oxide yellow, Iron Oxide Yellow 313, G 313M, LL 100PD, Mapico Yellow 1050, Bayferrox Yellow 3920, Iron Oxide Orange Transparent 188VN,C.I. Pigment Yellow 42, EC 481, Cosmetic Yellow, Unipure Yellow LC 182, Bayferrox 3905, EMF Color Ochre HL, Mapico Yellow 5, Unipure LC 182, GA 7311, Burnt Sienna TY, YB 3100, E 172 Yellow, Mapico Yellow Lemon, Iron Oxide Yellow 420, Sicoflush L Yellow 1916C4, Bayferrox 3920, Pure Yellow Oxide YO 6087, G 131M, Toda Color Y 2, Unisperse Yellow Oxide M-S, Iron Yellow S 313, Ariabel Yellow 300407, LL-XLO, Syn-Ox HTR 820, Xeracolour Yellow Oxide, Bayferrox 3910, YO 2087, Bayferrox Yellow 920, Y 10M, Sicotrans Yellow L 1916, Bayferro |  |
| Tetrabutylammonium Tetrafluoroborate | Tetrabutylammonium tetrafluoroborate (TBATFB) is a phase transfer catalyst. It can be synthesized by the reaction between 30% aqueous solution of tetrafluoroboric acid and 40% aqueous solution of tetrabutylamonium hydroxide. Tetrabutylammonium tetrafluoroborate acts as an electrolyte and inhibits the self-assembly of alkylthiosulfate on gold. Group: Ammonium ionic liquids. Alternative Names: N,N,N-tributyl-1-butanaminiu tetrafluoroborate. CAS No. 429-42-5. Molecular formula: C16H36NBF4. Mole weight: 329.27 g/mol. Appearance: White to Almost white powder to crystal. Purity: >98.0%(N). IUPACName: tetrabutylazanium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F. CCCC[N+](CCCC)(CCCC)CCCC. ECNumber: 207-058-8. Catalog: ACM429425-4. | |
| Tetrabutylammonium Tetrafluoroborate | Tetrabutylammonium tetrafluoroborate (TBATFB) is a phase transfer catalyst. It can be synthesized by the reaction between 30% aqueous solution of tetrafluoroboric acid and 40% aqueous solution of tetrabutylamonium hydroxide. Tetrabutylammonium tetrafluoroborate acts as an electrolyte and inhibits the self-assembly of alkylthiosulfate on gold. Group: Electronic materials molecular conductors. Alternative Names: N,N,N-tributyl-1-butanaminiu tetrafluoroborate. CAS No. 429-42-5. Product ID: tetrabutylazanium; tetrafluoroborate. Molecular formula: 329.27 g/mol. Mole weight: C16H36NBF4. [B-](F)(F)(F)F. CCCC[N+](CCCC)(CCCC)CCCC. InChI=1S/C16H36N. BF4/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; 2-1(3, 4)5/h5-16H2, 1-4H3; /q+1; -1. NNZZSJSQYOFZAM-UHFFFAOYSA-N. >98.0%(N). | |
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