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| | AMMONIUM TETRAPHENYLBORATE Basic information |
| Product Name: | AMMONIUM TETRAPHENYLBORATE | | Synonyms: | AMMONIUM TETRAPHENYLBORATE;TETRAPHENYLBORON AMMONIUM;Ammonium tetraphenylborate 99%;Ammoniumtetraphenylborate,99%;Ammonlum tetraphenylborate;azanium:tetraphenylboranuide;Ammonium tetraphenyl boron | | CAS: | 14637-34-4 | | MF: | C24H24BN | | MW: | 337.27 | | EINECS: | | | Product Categories: | | | Mol File: | 14637-34-4.mol |  |
| | AMMONIUM TETRAPHENYLBORATE Chemical Properties |
| Melting point | 220 °C (dec.)(lit.) | | storage temp. | Store at room temperature, keep dry and cool | | Appearance | White to off-white Solid | | BRN | 3799683 | | InChI | InChI=1S/C24H20B.H3N/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;1H3/q-1;/p+1 | | InChIKey | ZWFYDLYRTYMBIL-UHFFFAOYSA-O | | SMILES | [B-](C1C=CC=CC=1)(C1C=CC=CC=1)(C1=CC=CC=C1)C1C=CC=CC=1.[NH4+] |
| | AMMONIUM TETRAPHENYLBORATE Usage And Synthesis |
| reaction suitability | core: boron
reagent type: catalyst | | Purification Methods | Dissolve it in aqueous Me2CO and allow crystallisation to proceed slowly; otherwise very small crystals are formed. No trace of Me2CO is left in the crystals after drying at 120o [Davies & Staveley Trans Faraday Soc 53 19 1957]. Also, the salt can be precipitated from a dilute AcOH solution of sodium tetraphenylborane in the presence of NHions. After standing for 5minutes, the precipitate is filtered off onto a sintered porcelain crucible, washed with very dilute AcOH and dried at room temperature for at least 24hours [Vendlandt Anal Chem 28 1001 1956]. Alternatively a solution of sodium tetraphenylborane (5% excess) in H2O is added to NH4Cl solution. After 5minutes the precipitate is collected, washed several times with H2O and recrystallised from aqueous Me2CO. [Howick & Pflaum Analyt Chim Acta 19 342 1958, Beilstein 16 IV 1625.] |
| | AMMONIUM TETRAPHENYLBORATE Preparation Products And Raw materials |
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