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IRON DODECACARBONYL

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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
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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)
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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
10-23
HazardClass 
6.1
PackingGroup 
II
HS Code 
29310099

MSDS

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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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