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T72001

Trimethylacetonitrile

Name: Trimethylacetonitrile
Brand: ALDRICH

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

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24900438

EC Number:

211-133-0

Beilstein/REAXYS Number:

1361449

MDL number:

MFCD00001847

Assay:

98%

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Properties

Quality Level

100

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

Description

pictograms

GHS02,GHS06

signalword

Danger

hcodes

H225,H301 + H311 + H331

pcodes

P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

39.2 °F - closed cup

flash_point_c

4 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

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Opening up ZSM-5 Hierarchical Zeolite's Porosity through Sequential Treatments for Improved Low-Density Polyethylene Cracking.

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

Acetonitrile Ion Suppression in Atmospheric Pressure Ionization Mass Spectrometry.

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.

Novel 3'-Substituted-1',2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo.

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

Global Trade Item Number

SKU	GTIN
T72001-100G	04061836831288
T72001-25G	04061836831295