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ChemicalBook >> CAS DataBase List >>Trimethylacetonitrile

Trimethylacetonitrile

CAS No.
630-18-2
Chemical Name:
Trimethylacetonitrile
Synonyms
PIVALONITRILE;tert-Butylnitrile;Trimethylacetonitril;(CH3)3C-CN;Pivalonitril;Pivalic nitrile;Pivalonitrile>tert.-Butylcyanid;TERT-BUTYL CYANIDE;Pivalinsαurenitril
CBNumber:
CB9285121
Molecular Formula:
C5H9N
Molecular Weight:
83.13
MDL Number:
MFCD00001847
MOL File:
630-18-2.mol
MSDS File:
SDS
Last updated:2026-05-28 06:22:50
Product description Number Pack Size Price
Trimethylacetonitrile 98% T72001 25g $116
Trimethylacetonitrile 98% T72001 100g $200
Pivalonitrile >98.0%(GC) P0463 25mL $52
Pivalonitrile >98.0%(GC) P0463 100mL $143
Pivalonitrile FP32327 100g $199
More product size

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)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Skull and Crossbones (GHS06)
GHS02,GHS06
Signal word  Danger
Hazard statements  H225-H301+H311+H331
Precautionary statements  P210-P233-P280-P301+P310-P303+P361+P353-P304+P340+P311
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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  TSCA listed
HazardClass  3
PackingGroup  II
HS Code  29269090
Storage Class 3 - Flammable liquids
Hazard Classifications Acute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Flam. Liq. 2
REACH Registrations Active
Limited Quantities 1.0 L (0.3 gallon) (liquid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
4
1 0

Trimethylacetonitrile price More Price(44)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T72001 Trimethylacetonitrile 98% 630-18-2 25g $116 2026-04-30 Buy
Sigma-Aldrich T72001 Trimethylacetonitrile 98% 630-18-2 100g $200 2026-04-30 Buy
TCI Chemical P0463 Pivalonitrile >98.0%(GC) 630-18-2 25mL $52 2026-04-30 Buy
TCI Chemical P0463 Pivalonitrile >98.0%(GC) 630-18-2 100mL $143 2026-04-30 Buy
Biosynth FP32327 Pivalonitrile 630-18-2 100g $199 2026-06-04 Buy
Product number Packaging Price Buy
T72001 25g $116 Buy
T72001 100g $200 Buy
P0463 25mL $52 Buy
P0463 100mL $143 Buy
FP32327 100g $199 Buy

Trimethylacetonitrile Chemical Properties,Uses,Production

Hydrogenation of trimethylacetonitrile

Trimethylacetonitrile is an aliphatic nitrile compound in which the α-carbon of the nitrile group lacks a hydrogen atom; it can be used in hydrogenation reactions to produce secondary and tertiary amines. The hydrogenation reaction is carried out in the liquid phase using a Pd/C catalyst, at a reaction temperature of 110 °C and a hydrogen pressure of 5 MPa. In the hydrogenation reaction of trimethylacetonitrile with lower-chain aliphatic N,N-dialkylamines (such as diethylamine), dineopentylamine (96.3 wt%) and neopen tylamine (2.8 wt%) were produced, whilst no trineopentylamine was formed.[5]

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.
[5] Jiri Krupka, Anna H., Jakub Drahonsky. (2012). Aminocarbene mechanism of the formation of a tertiary amine in nitrile hydrogenation on a palladium catalyst. Reaction Kinetics, Mechanisms and Catalysis, 108 1, 91–105. https://doi.org/10.1007/s11144-012-0497-2

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
$7.00 1kg 99% 100kg Career Henan Chemical Co
2,2-DIMETHYL-PROPANENITRILE 2,2-DIMETHYLPROPIONITRILE 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-Butyl cyanide~Pivalonitrile Trimethylacetonitrile,98+% Trimethyl acetaldehyde/pivalaldehyde Pivalonitrile> Tertiary butyl carbonyl cyanide High purity Trimethylacetonitrile Perfemiker]Trimethylacetonitrile,97% Trimethylacetonitril PIVALONITRILE tert-Butylnitrile 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
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