Name | Tetra-n-propylammonium perruthenate(VII) |
Synonyms | TPAP tetrapropylammonium oxido-trioxo-ruthenium TerapropylaMMoniuMperruthenate Tetrapropylammonium perruthenate TETRAPROPYLAMMONIUM PERRUTHENATE TETRA-N-PROPYLAMMONIUM PERRUTHENATE Tetrapropylammonium tetraoxoruthenate Tetra-n-propylammonium perruthenate(VII) TETRA-N-PROPYLAMMONIUM PERRUTHENATE (VII) 1-Propanaminium, N,N,N-tripropyl-, (T-4)-tetraoxoru |
CAS | 114615-82-6 |
EINECS | 628-415-8 |
InChI | InChI=1/C12H28N.4O.Ru/c1-5-9-13(10-6-2,11-7-3)12-8-4;;;;;/h5-12H2,1-4H3;;;;;/q+1;;;;-1;/rC12H28N.O4Ru/c1-5-9-13(10-6-2,11-7-3)12-8-4;1-5(2,3)4/h5-12H2,1-4H3;/q+1;-1 |
InChIKey | NQSIKKSFBQCBSI-UHFFFAOYSA-N |
Molecular Formula | C12H28NO4Ru |
Molar Mass | 351.43 |
Melting Point | ~160 °C (dec.) (lit.) |
Water Solubility | Insoluble in water. |
Solubility | Methanol (Slightly) |
Appearance | crystal |
Color | green |
Storage Condition | Inert atmosphere,2-8°C |
Stability | store cold |
Sensitive | Hygroscopic |
MDL | MFCD00074914 |
Use | Soluble, non-volatile, air-stable, mild catalysts that can be used with appropriate co-oxidants in stoichiometric terms or as catalytic applications. An oxidant used to convert N,N′-dihydroxyimidazoline into nitroxide radicals. Oxidation of hydroxyl-substituted tri-n-butylammonium trifluoroborate to aldehydes and ketones without? concomitant cleavage of the carbon-boron bond. |
Risk Codes | R5 - Heating may cause an explosion R8 - Contact with combustible material may cause fire R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S17 - Keep away from combustible material. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
UN IDs | UN 1479 5.1/PG 2 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 3-10 |
HS Code | 28439000 |
Hazard Class | 5.1 |
Packing Group | III |
use | soluble, non-volatile, air-stable mild catalyst, can be used with appropriate co-oxidizer according to stoichiometry or as catalytic use. An oxidant used to convert N,N′-dihydroxyimidazoline into nitroxide radicals. Oxidation of hydroxyl-substituted tri-n-butylammonium trifluoroborate to aldehydes and ketones without? concomitant cleavage of the carbon-boron bond. |