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T72001

Sigma-Aldrich

Trimethylacetonitrile

98%

Synonym(s):

Pivalonitrile, tert-Butyl cyanide

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About This Item

Linear Formula:
(CH3)3CCN
CAS Number:
630-18-2
Molecular Weight:
83.13
Beilstein:
1361449
EC Number:
211-133-0
MDL number:
MFCD00001847
UNSPSC Code:
12352100
PubChem Substance ID:
24900438
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.377 (lit.)

bp

105-106 °C (lit.)

mp

15-16 °C (lit.)

density

0.752 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)C#N

InChI

1S/C5H9N/c1-5(2,3)4-6/h1-3H3

InChI key

JAMNHZBIQDNHMM-UHFFFAOYSA-N

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Pictograms

FlameSkull and crossbones
GHS02,GHS06

Signal Word

Danger

Hazard Statements

H225,H301 + H311 + H331

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

39.2 °F - closed cup

Flash Point(C)

4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Kevin Colizza et al.
Journal of the American Society for Mass Spectrometry, 27(11), 1796-1804 (2016-09-01)
Efforts to analyze trace levels of cyclic peroxides by liquid chromatography/mass spectrometry gave evidence that acetonitrile suppressed ion formation. Further investigations extended this discovery to ketones, linear peroxides, esters, and possibly many other types of compounds, including triazole and menadione.
Karolina A Tarach et al.
Molecules (Basel, Switzerland), 25(12) (2020-06-26)
An adequately tuned acid wash of hierarchical ZSM-5 zeolites offers a levelling up in the catalytic cracking of low-density polyethylene. Identification of crucial and limiting factors governing the activity of the zeolite was extended with studies about the accessibility of
Andrey V Markov et al.
International journal of molecular sciences, 21(10) (2020-05-21)
A series of novel 18βH-glycyrrhetinic acid (GA) derivatives containing 3'-(alkyl/phenyl/pyridin(-2″, -3″, and -4″)-yl)-1',2',4'-oxadiazole moieties at the C-30 position were synthesized by condensation of triterpenoid's carboxyl group with corresponding amidoximes and further cyclization. Screening of the cytotoxicity of novel GA derivatives

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