IRON DODECACARBONYL
IRON DODECACARBONYL Basic information
- Product Name:
- IRON DODECACARBONYL
- Synonyms:
-
- Dodecacarbonyltriiron, 95+% (Assay on dry basis), stab. with 5-10% methanol
- Triiron dodecacarbonyl, stabilized, 99%
- Iron dodecacarbonyl(Stabilized with 5-10% methanol)
- di-mu-carbonyldecacarbonyl-triangulo-triiron
- TRIIRON DODECACARBONYL, PROTECTED WITH 5 -10% METHYL ALCOHOL
- TRI-IRONDODECACARBONYL MOISTENED WITH ME THANOL(CH3OH 5-10%
- stabilisedwith5-10%methanol
- IRON DODECACARBONYL
- CAS:
- 17685-52-8
- MF:
- C12H24FeO12
- MW:
- 416.15676
- EINECS:
- 241-668-5
- Product Categories:
-
- metal carbonyl complexes
- Mol File:
- 17685-52-8.mol
IRON DODECACARBONYL Chemical Properties
- Melting point:
- 165 °C (dec.) (lit.)
- Density
- 1.99
- Flash point:
- 9℃
- storage temp.
- 2-8°C
- form
- crystal
- Specific Gravity
- 2
- color
- black
- Water Solubility
- Insoluble in water. Soluble in non polar organic solvents.
- Sensitive
- Air Sensitive
- Exposure limits
- ACGIH: TWA 1 mg/m3
NIOSH: TWA 1 mg/m3 - NIST Chemistry Reference
- Triiron dodecacarbonyl(17685-52-8)
Safety Information
- Hazard Codes
- F,Xn,T
- Risk Statements
- 11-23/24/25-36/37/38-20/22-39/23/24/25-20/21/22
- Safety Statements
- 16-26-28-33-36/37/39-45-7/9-24-36/37
- RIDADR
- UN 3175 4.1/PG 2
- WGK Germany
- 3
- F
- 10-23
- HazardClass
- 6.1
- PackingGroup
- II
- HS Code
- 29310099
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
IRON DODECACARBONYL Usage And Synthesis
Chemical Properties
black powder or crystals
Uses
It eliminates sulfur from substituted thiophene complexes, which leads to ferroles. Access to new areas of organometallic chemistry is promising using the reaction of Fe3(CO)12 with tellurium-nitrogen heterocycles such as benzoisotellurazole.
Uses
Eliminates sulfur from substituted thiophene complexes, leading to ferroles. Access to new areas of organometallic chemistry is promising using the reaction of Fe3(CO)12 with tellurium-nitrogen heterocycles such as benzoisotellurazole.
General Description
This product has been enhanced for catalytic efficiency.
Purification Methods
It usually contains 10% by weight of MeOH as stabiliser. This can be removed by keeping it in a vacuum at 0.5mm for at least 5hours. It can be sublimed slowly at high vacuum and is soluble in organic solvents. [Landesberg et al. J Org Chem 37 930 1972, Case & Whiting J Chem Soc 4632 1960, King & Stone Inorg Synth VII 193 1963.] TOXIC.
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