Name | Ruthenium(III)-2,4-pentanedionate |
Synonyms | Rutheniumpentanedionate Ruthenium 2,4-pentanedionate RUTHENIUM(III) ACETYLACETONATE Ruthenium(III) acetylacetonate Ruthenium(Ⅲ) 2,4-pentanedionate Ruthenium(III)2,4-pentanedionate Ruthenium iii 2,4-pentanedionate Ruthenium(III) 2,4-pentanedionate RUTHENIUM(III) 2,4-PENTANEDIONATE Ruthenium(III)-2,4-pentanedionate Tris-(2,4-pentanedionato)-ruthenium Tris(acetylacetonato)ruthenium(III) TRIS(ACETYLACETONATO)RUTHENIUM(III) Rutheniumacetylacetonateredbrownxtl Tris(acetylacetonato)ruthenium (III) Tris(2,4-pentanedionato)ruthenium(III) TRIS(PENTANE-2,4-DIONATO)RUTHENIUM(III) 2,4-PENTANEDIONE, RUTHENIUM(III) DERIVATIVE 4-pentanedionato-o,o')-tris((oc-6-11)-rutheniu ruthenium(3+) tris[(2Z)-4-oxopent-2-en-2-olate] Ruthenium(III) 2,4-pentanedionate~Tris(acetylacetonato)ruthenium(III)~Tris(2,4-pentanedionato)ruthenium(III) |
CAS | 14284-93-6 |
EINECS | 238-193-0 |
InChI | InChI=1/3C5H8O2.Ru/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3/b3*4-3- |
InChIKey | RTZYCRSRNSTRGC-LNTINUHCSA-K |
Molecular Formula | C15H21O6Ru |
Molar Mass | 398.39 |
Melting Point | 260°C (dec.)(lit.) |
Boling Point | 187.6°C at 760 mmHg |
Flash Point | 71.9°C |
Water Solubility | Soluble in most organic solvents such as acetone, chlorinated hydrocarbons, alcohols, cyclohexane and benzene. Insoluble in water. |
Vapor Presure | 0.174mmHg at 25°C |
Appearance | Red to purple powder |
Color | White |
Storage Condition | Store below +30°C. |
MDL | MFCD00000030 |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10 |
TSCA | Yes |
HS Code | 28439000 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
use | can be used to make heterogeneous catalysts. MOCVD precursor compound, homogeneous catalyst. For example, specific tritiation in the region where sodium borohydride and aromatic carboxylic acids are hydrolyzed. It can also be used as an enantioselective hydrogenation catalyst for acids such as aryl acrylic acid and aryl propionic acid. Catalytic hydrogenation of dimethyl oxalate to ethylene glycol under mild conditions. |