Identification | Back Directory | [Name]
Hexanoicacid,2-ethyl-,iron(3+)salt | [CAS]
7321-53-1 | [Synonyms]
52%inmineraloil Einecs 230-794-6 Iron Ethylhexanoate Iron(III) octanoate Ferric isooctanoate Ferric 2-ethylhexanoate ferrum 2-ethylhexanoate 2-ethylhexanoate:iron(3+) iron tris(2-ethylhexanoate) Quantitative analysis of iron 2-ethyl-hexanoicaciiron(3++)salt Hexanoicacid,2-ethyl-,iron(3+)sal Iron(III) 2-ethylhexanoate Liquid Hexanoicacid,2-ethyl-,iron(3+)salt Iron(III) 2-ethylhexanoate solution 2-ethyl-Hexanoic Acid Iron(3+) Salt Tris(2-ethylhexanoic acid)iron(III) salt Hexanoic acid, 2-ethyl-, iron(3+) salt (3:1) Iron(III) 2-ethylhexanoate, 52% in mineral oil Iron(III) 2-Ethylhexanoate Mineral Spirits Solution IRON (III) 2-ETHYLHEXANOATE, 52% IN MINERAL SPIRITS, FE 6% Iron(III) 2-ethylhexanoate, nominally 50% in mineral spirits Iron(III) 2-ethylhexanoate solution, 50 wt. % in mineral spirits Iron(III) 2-ethylhexanoate, nominally 50% in mineral spirits, Fe 6% Iron 2-ethylhexanoate, 6% (Fe) in Mineral spirits (99.998+%-Fe) PURATREM | [EINECS(EC#)]
230-794-6 | [Molecular Formula]
C24H45FeO6 | [MDL Number]
MFCD00014006 | [MOL File]
7321-53-1.mol | [Molecular Weight]
485.455 |
Chemical Properties | Back Directory | [Boiling point ]
400℃[at 101 325 Pa] | [density ]
0.91 | [Fp ]
41℃ | [storage temp. ]
Refrigerator | [form ]
Liquid | [Water Solubility ]
Miscible with chloroform. Immiscible with water. | [Exposure limits]
ACGIH: TWA 100 ppm OSHA: TWA 500 ppm(2900 mg/m3) NIOSH: IDLH 20000 mg/m3; TWA 350 mg/m3; Ceiling 1800 mg/m3 | [InChI]
InChI=1S/3C8H16O2.Fe/c3*1-3-5-6-7(4-2)8(9)10;/h3*7H,3-6H2,1-2H3,(H,9,10);/q;;;+3/p-3 | [InChIKey]
ULUYRVWYCIOFRV-UHFFFAOYSA-K | [SMILES]
[Fe](OC(=O)C(CC)CCCC)(OC(=O)C(CC)CCCC)OC(=O)C(CC)CCCC | [LogP]
5.59 at 20℃ | [EPA Substance Registry System]
Ferric 2-ethylhexanoate (7321-53-1) |
Hazard Information | Back Directory | [Uses]
As a catalyst, Iron(III) 2-ethylhexanoate can be used in wide range of polymerization reaction. It has been used as a mild Lewis acid catalyst for the stereoselective Diels-Alder reaction as wel as in a Ziegler-Natta type catalyst system for the polymerization of 1,3-butadiene.
|
|
|