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Merck

110086

Acetonitrile

99%, suitable for UV/Vis spectroscopy, ReagentPlus®

Synonym(s):

ACN, Cyanomethane, Ethyl nitrile, Methyl cyanide

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1 L

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About This Item

Linear Formula:
CH3CN
CAS Number:
Molecular Weight:
41.05
NACRES:
NA.03
PubChem Substance ID:
eCl@ss:
39031501
UNSPSC Code:
12191502
EC Number:
200-835-2
MDL number:
Beilstein/REAXYS Number:
741857
Assay:
99%
Technique(s):
UV/Vis spectroscopy: suitable
Bp:
81-82 °C (lit.)
Vapor pressure:
72.8 mmHg ( 20 °C)

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Product Name

Acetonitrile, ReagentPlus®, 99%

InChI key

WEVYAHXRMPXWCK-UHFFFAOYSA-N

InChI

1S/C2H3N/c1-2-3/h1H3

SMILES string

CC#N

vapor density

1.41 (vs air)

vapor pressure

72.8 mmHg ( 20 °C)

product line

ReagentPlus®

assay

99%

form

liquid

autoignition temp.

973 °F

expl. lim.

16 %

technique(s)

UV/Vis spectroscopy: suitable

refractive index

n20/D 1.344 (lit.)

bp

81-82 °C (lit.)

mp

−45 °C (lit.)

solubility

organic solvents: soluble(lit.)
water: soluble(lit.)

density

0.786 g/mL at 25 °C (lit.)

format

neat

Quality Level

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43755734851
technique(s)

UV/Vis spectroscopy: suitable

technique(s)

solid phase extraction (SPE): suitable

technique(s)

HPLC: suitable

Quality Level

100

Quality Level

200

Quality Level

100

assay

99%

assay

≥99.5%

assay

≥99.9%

solubility

organic solvents: soluble(lit.), water: soluble(lit.)

solubility

water: soluble

solubility

-

form

liquid

form

liquid

form

liquid

vapor density

1.41 (vs air)

vapor density

1.41 (vs air)

vapor density

1.41 (vs air)

Application


  • Metal-cation-induced shifts in thiolate redox and reduced sulfur speciation.: This study explores the redox behavior of thiolates affected by metal cations in acetonitrile, shedding light on sulfur speciation processes critical for developing catalytic and environmental remediation technologies (Seo et al., 2024).

  • Rational design and investigation of nonlinear optical response properties of pyrrolopyrrole aza-BODIPY-based novel push-pull chromophores.: Focused on nonlinear optics, this research uses acetonitrile as a solvent to study the optical properties of newly designed chromophores, contributing to advances in optical materials science (Kothoori et al., 2024).

  • Acetonitrile real gas phase behavior from quasi-ideal gas to nanodroplets: A microscopical view.: Providing a microscopic insight into the phase behavior of acetonitrile, this research enhances understanding of fluid dynamics at nanoscale levels, relevant for both academic studies and industrial applications (Martínez et al., 2024).

  • Crystalline CdS/amorphous Cd(OH)2 Composite for Electrochemical CO2 Reduction to CO in a Wide Potential Window.: Highlighting the role of acetonitrile in electrochemical setups, this study develops new materials for efficient CO2 reduction, potentially impacting energy conversion strategies globally (Hua et al., 2024).


Features and Benefits

ReagentPlus® solvents have a guaranteed purity ≥98.5% and are ideal for experiments and applications that need fewer specifications. They are primarily defined by assay specifications and offer suitable quality for general lab use.

General description

Acetonitrile (MeCN), an aliphatic nitrile, is a colorless liquid with a characteristic odor. MeCN has low viscosity, high elution strength and is highly miscible in water. It is widely used as a solvent and intermediate in organic syntheses and is transparent to UV-visible light, making it highly applicable in spectrophotometric and fluorimetric techniques. It also plays a major role as an extractant medium in liquid-liquid extraction, solid-phase extraction or microextraction.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup


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Eagleson M.
Concise Encyclopedia Chemistry, 6-6 (1994)
Purification of acetonitrile.
Walter M and Ramaley L.
Analytical Chemistry, 45(1), 165-166 (1973)
Timo Glatter et al.
Molecular systems biology, 5, 237-237 (2009-01-22)
Protein complexes represent major functional units for the execution of biological processes. Systematic affinity purification coupled with mass spectrometry (AP-MS) yielded a wealth of information on the compendium of protein complexes expressed in Saccharomyces cerevisiae. However, global AP-MS analysis of
Divya Subramonian et al.
Journal of proteome research, 13(9), 3905-3918 (2014-07-30)
SUMOylation is an essential posttranslational modification and regulates many cellular processes. Dysregulation of SUMOylation plays a critical role in metastasis, yet how its perturbation affects this lethal process of cancer is not well understood. We found that SUMO-2/3 modification is
Changting Xiao et al.
Diabetes, 63(7), 2394-2401 (2014-03-04)
The dipeptidyl peptidase-4 inhibitor sitagliptin, an antidiabetic agent, which lowers blood glucose levels, also reduces postprandial lipid excursion after a mixed meal. The underlying mechanism of this effect, however, is not clear. This study examined the production and clearance of

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