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Di-n-butylmagnesium

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Di-n-butylmagnesium Basic information

Product Name:
Di-n-butylmagnesium
Synonyms:
  • MAGNESIUM DIBUTYL
  • DI-N-BUTYLMAGNESIUM
  • DIBUTYLMAGNESIUM
  • dibutyl-magnesiu
  • dibutyl magnesium solution
  • Dibutylmagnesium solution
  • DIBUTYL MAGNESIUM SOLUTION, ~1 M IN HEPT ANE
  • DIBUTYLMAGNESIUM, 1.0M SOLUTION IN HEPTA NE
CAS:
1191-47-5
MF:
C8H18Mg
MW:
138.54
EINECS:
214-736-7
Product Categories:
  • Materials for Hydrogen Storage
  • Materials Science
  • Organometallics
  • Grignard Reagents
  • Metal Hydrides
  • Grignard Reagent
  • Organometallic Reagents
  • Others
  • Alternative Energy
Mol File:
1191-47-5.mol
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Di-n-butylmagnesium Chemical Properties

Melting point:
-71 °C
Density 
0.749 g/mL at 20 °C
Flash point:
21 °F
storage temp. 
2-8°C
BRN 
3535184
InChIKey
ODHFJIDDBSDWNU-UHFFFAOYSA-N
CAS DataBase Reference
1191-47-5
EPA Substance Registry System
Magnesium, dibutyl- (1191-47-5)
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Safety Information

Hazard Codes 
F+,C,T,F,N
Risk Statements 
12-14/15-22-34-66-67-48/20/22-40-39/23/24/25-23/24/25-11-10-65-50/53-17-19-62-52/53-48/20
Safety Statements 
16-26-36/37/39-43-45-7/8-62-61-60
RIDADR 
UN 3399 4.3/PG 1
WGK Germany 
1
1-3-10
HS Code 
29310099

MSDS

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Di-n-butylmagnesium Usage And Synthesis

Chemical Properties

The pure substance is a waxy solid. Commercially, it is marketed as solution in?heptane. Di-n-butylmagnesium solution is a useful reagent for the synthesis of organomagnesium compounds.

Uses

Electrochemically inactive [Mg2(μ-Cl)3.6THF][C2H5AlCl3] crystal may be obtained from an electrolyte composed of Di-n-butylmagnesium and ethylaluminum dichloride. Di-n-butylmagnesium may be used in the carbon metallation of α-olefins. A study reports the possible use of the organometallic compound in the intercalation of magnesium and zinc into the layers of TiS2 or WO2Cl2. Interaction of lithium alkoxide with di-n-butylmagnesium was investigated.

Application

Di-n-butylmagnesium solution can be used as a reagent for the deprotection of aromatic and aliphatic benzyl thioethers to synthesize corresponding benzylthiols in the presence of titanocene dichloride. It can also be used as a catalyst to synthesize enantioenriched nitrogen-containing heterocyclic derivatives by the asymmetric ring-opening reaction of aziridines with substituted tetrazoles in the presence of chiral ligand.

General Description

Contains up to 1 wt. % Triethylaluminum as a viscosity reducer. stable under normal temperature and pressure, sensitive to light. contact with water releases flammable gas.

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