Trimethylacetonitrile, 98+%, Thermo Scientific Chemicals
Trimethylacetonitrile, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Trimethylacetonitrile, 98+%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
100 g
Catalog number A12011.14
also known as A12011-14
Price (USD)/ Each
74.65
Online exclusive
82.50 
Save 7.85 (10%)
-
Add to cart
Quantity:
25 g
Request bulk or custom format
Price (USD)/ Each
74.65
Online exclusive
82.50 
Save 7.85 (10%)
Add to cart
Trimethylacetonitrile, 98+%, Thermo Scientific Chemicals
Catalog numberA12011.14
Price (USD)/ Each
74.65
Online exclusive
82.50 
Save 7.85 (10%)
-
Add to cart
Chemical Identifiers
CAS630-18-2
IUPAC Name2,2-dimethylpropanenitrile
Molecular FormulaC5H9N
InChI KeyJAMNHZBIQDNHMM-UHFFFAOYSA-N
SMILESCC(C)(C)C#N
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Identification (FTIR)Conforms
Refractive Index1.3755-1.3795 @ 20?C
FormLiquid
Assay (GC)≥98.0%
Trimethylacetonitrile used as a solvent and as a labile ligand in coordination chemistry. It is also used as an intermediate in organic synthesis. It is used in the presence of titanium(II) chloride and zinc to undergoes reductive coupling reaction of aromatic and aliphatic ketones including acyclic aliphatic ketones to give the corresponding pinacols.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Trimethylacetonitrile used as a solvent and as a labile ligand in coordination chemistry. It is also used as an intermediate in organic synthesis. It is used in the presence of titanium(II) chloride and zinc to undergoes reductive coupling reaction of aromatic and aliphatic ketones including acyclic aliphatic ketones to give the corresponding pinacols.

Solubility
Miscible with ethanol, acetone and toluene. Slightly miscible with water.

Notes
Store in a cool place. Incompatible with strong acids, strong bases, strong oxidizing agents and strong reducing agents.
RUO – Research Use Only

General References:

  1. For in situ reaction with vinyl triflates in the synthesis of sterically hindered 2,4,6-trisubstituted pyrimidines, see: Synthesis, 881 (1990); for reaction scheme, see Trifluoromethanesulfonic acid, A1173 .
  2. Bagal, D. B.; Bhanage, B. M. Recent Advances in Transition Metal-Catalyzed Hydrogenation of Nitriles. Adv. Synth. Catal. 2015, 357 (5), 883-900.
  3. Akhtar, N.; Akhtar, W. Prospects, challenges, and latest developments in lithium-air batteries. Int. J. Energy Res. 2015, 39 (3), 303-316.