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Trimethylacetonitrile

CAS No.
630-18-2
Chemical Name:
Trimethylacetonitrile
Synonyms
(CH3)3C-CN;Pivalonitril;PIVALONITRILE;Pivalic nitrile;Pivalonitrile>tert.-Butylcyanid;tert-Butylnitrile;TERT-BUTYL CYANIDE;Pivalinsαurenitril;Trimethylacetonitril
CBNumber:
CB9285121
Molecular Formula:
C5H9N
Molecular Weight:
83.13
MDL Number:
MFCD00001847
MOL File:
630-18-2.mol
MSDS File:
SDS
Last updated:2024-04-01 18:07:32

Trimethylacetonitrile Properties

Melting point 15-16 °C (lit.)
Boiling point 105-106 °C (lit.)
Density 0.752 g/mL at 25 °C (lit.)
refractive index n20/D 1.377(lit.)
Flash point 40 °F
storage temp. Sealed in dry,Room Temperature
form Liquid
color Clear colorless
Water Solubility Miscible with ethanol, acetone and toluene. Slightly miscible with water.
BRN 1361449
Exposure limits NIOSH: IDLH 25 mg/m3
Dielectric constant 20.09
InChI InChI=1S/C5H9N/c1-5(2,3)4-6/h1-3H3
InChIKey JAMNHZBIQDNHMM-UHFFFAOYSA-N
SMILES C(#N)C(C)(C)C
CAS DataBase Reference 630-18-2(CAS DataBase Reference)
FDA UNII N-(ISOPROPOXYCARBONYL)PIPERIDINE (89G5X4BJFC)
PIVALONITRILE (AQD7ZXJ3PR)
EPA Substance Registry System Propanenitrile, 2,2-dimethyl- (630-18-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS06
Signal word  Danger
Hazard statements  H225-H301+H311+H331
Precautionary statements  P210-P233-P280-P301+P310-P303+P361+P353-P304+P340+P311
Hazard Codes  F,T,Xi
Risk Statements  11-23/24/25-36
Safety Statements  16-36/37/39-45-26-7/9
RIDADR  UN 1993 3/PG 2
WGK Germany  3
19
Hazard Note  Irritant
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29269090
NFPA 704
4
1 0

Trimethylacetonitrile price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T72001 Trimethylacetonitrile 98% 630-18-2 25g $106 2024-03-01 Buy
Sigma-Aldrich T72001 Trimethylacetonitrile 98% 630-18-2 100g $182 2024-03-01 Buy
TCI Chemical P0463 Pivalonitrile >98.0%(GC) 630-18-2 25mL $59 2024-03-01 Buy
TCI Chemical P0463 Pivalonitrile >98.0%(GC) 630-18-2 100mL $161 2024-03-01 Buy
Alfa Aesar A12011 Trimethylacetonitrile, 98+% 630-18-2 25g $82.5 2024-03-01 Buy
Product number Packaging Price Buy
T72001 25g $106 Buy
T72001 100g $182 Buy
P0463 25mL $59 Buy
P0463 100mL $161 Buy
A12011 25g $82.5 Buy

Trimethylacetonitrile Chemical Properties,Uses,Production

Description

Trimethylacetonitrile is a colorless and transparent liquid with high polarity and solubility. Its dielectric constant varies with temperature and frequency. At room temperature, the dielectric constant of trimethylacetonitrile is approximately 37.5, which gradually decreases at high temperatures. The high dielectric constant of trimethylacetonitrile makes it widely used in the field of electrochemistry. For example, in electrochemical reactions, trimethylacetonitrile can be used as a solvent and electrolyte to improve the efficiency and rate of the reaction. At the same time, trimethylacetonitrile can also be used as a dielectric for capacitors, to store charge and energy.

Chemical Properties

CLEAR COLOURLESS LIQUID

Uses

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.

Application

Trimethylacetonitrile can be used:
As an intermediate compound, it is a product of benzopyrimidine in the preparation of 6-substituted phenanthridines[1].
As a laboratory research material for the thermodynamic correlation index determination of chemistry, spectroscopic determination and reduction reaction studies with Grignard reagents[2-4].

Purification Methods

Purify it by a two-stage vacuum distillation and de-gas by the freeze-pump-thaw technique. Store it under vacuum at 0o. TOXIC, use an efficient fume hood. [Beilstein 2 IV 875.]

References

[1] JAN PAWLAS; Mikael B. A One-Pot Access to 6-Substituted Phenanthridines from Fluoroarenes and Nitriles via 1,2-Arynes[J]. Organic Letters, 2002. DOI:10.1021/ol026197c.
[2] T. MOHAMED. Computational (DFT and MP2) and spectral interpretations, normal coordinate analysis, force constants and barriers to internal rotations of Trimethylacetonitrile[J]. Journal of Theoretical & Computational Chemistry, 2016. DOI:10.1142/S0219633616500346.
[3] EDGAR F. WESTRUM JR. Aaron R. Trimethylacetonitrile. Low-temperature heat capacity, vapor pressure, and chemical thermodynamics of the crystalline, liquid, and gaseous phases[J]. The Journal of Physical Chemistry , 1967. DOI:10.1021/j100864a006.
[4] HARRY S. MOSHER; William T M. The Reduction of Trimethylacetonitrile with Grignard Reagents1[J]. Journal of the American Chemical Society, 1951. DOI:10.1021/ja01152a114.

630-19-3
630-18-2
Synthesis of Trimethylacetonitrile from Pivaldehyde
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View Lastest Price from Trimethylacetonitrile manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	TRIMETHYLACETONITRILE pictures 2019-07-06 TRIMETHYLACETONITRILE
630-18-2
US $7.00 / kg 1kg 99% 100kg Career Henan Chemical Co
2,2-DIMETHYL-PROPANENITRILE 2,2-DIMETHYLPROPIONITRILE PIVALONITRILE TERT-BUTYL CYANIDE TRIMETHYLACETONITRILE (CH3)3C-CN 2,2-dimethyl-propanenitril 2,2-Dimethylpropionsαurenitril 2-Cyano-2-methylpropane Trimethylacetonitrile, 2,2-Dimethylpropionitrile, Pivalonitrile TriMethylacetonitrile, 98% 25ML 2,2-Dimethylpropiononitrile 2,2-Dimethylpropionitrile Trimethylacetonitrile Pivalic nitrile Pivalinsαurenitril Pivalonitril propanenitrile,2,2-dimethyl- tert.-Butylcyanid tert-Butylnitrile Trimethylacetonitril tert-Butyl cyanide~Pivalonitrile Trimethylacetonitrile,98+% Trimethyl acetaldehyde/pivalaldehyde Pivalonitrile> Tertiary butyl carbonyl cyanide High purity Trimethylacetonitrile Perfemiker]Trimethylacetonitrile,97% 630-18-2 C1 to C5 Analytical Chromatography Product Catalog Analytical Reagents Building Blocks Cyanides/Nitriles Nitrogen Compounds Organic Building Blocks Small molecule Building Blocks C1 to C5 Chemical Synthesis Cyanides/Nitriles Nitrogen Compounds Organic Building Blocks bc0001