Skip to Content
Merck

60004

Acetonitrile

≥99.5% (GC)

Synonym(s):

Methyl cyanide, Anhydrous ACN, Dry MeCN

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

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:
≥99.5% (GC)
Technique(s):
GC/GC: suitable
Bp:
81-82 °C (lit.)
Vapor pressure:
72.8 mmHg ( 20 °C)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Level

vapor density

1.41 (vs air)

vapor pressure

72.8 mmHg ( 20 °C)

assay

≥99.5% (GC)

form

liquid

autoignition temp.

973 °F

expl. lim.

16 %

technique(s)

GC/GC: suitable

impurities

≤0.1% water (Karl Fischer)

refractive index

n20/D 1.344 (lit.)

bp

81-82 °C (lit.)

mp

−45 °C (lit.)

density

0.786 g/mL at 25 °C (lit.)

format

neat

SMILES string

CC#N

InChI

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

InChI key

WEVYAHXRMPXWCK-UHFFFAOYSA-N

Application


  • Modified QuEChERS method combined with ultra-performance liquid chromatography-tandem mass spectrometry: This research utilizes acetonitrile′s excellent solvent properties for the detection of cyclopiazonic acid in feeds. The method enhances the efficiency and accuracy of chemical analyses in food safety, demonstrating acetonitrile′s pivotal role in ensuring the quality of agricultural products (Peng et al., 2024).

  • Liquid Chromatographic Enantioseparation of Newly Synthesized Fluorinated Tryptophan Analogs: Highlighting its use in pharmaceutical research, acetonitrile is employed in the chromatographic enantioseparation of complex amino acids, essential for drug development and molecular pharmacology studies (Tanács et al., 2024).

  • Synthesis and Application of 1,8-Naphthalimide Derivatives Fluorescent Probe: Acetonitrile′s versatility is showcased in the synthesis of fluorescent probes for environmental monitoring. Its application in detecting and measuring environmental pollutants highlights its significant impact on ecological research and safety (Negi et al., 2024).

Other Notes

The article number 60004-4X2.5L will be discontinued. Please order the single bottle 60004-2.5L which is physically identical with the same exact specifications.


Still not finding the right product?

Explore all of our products under Acetonitrile


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

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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
Hélène Hall et al.
Brain : a journal of neurology, 137(Pt 9), 2493-2508 (2014-07-27)
The neuropathological substrate of dementia in patients with Parkinson's disease is still under debate, particularly in patients with insufficient alternate neuropathology for other degenerative dementias. In patients with pure Lewy body Parkinson's disease, previous post-mortem studies have shown that dopaminergic
Elke H J Krekels et al.
Clinical pharmacokinetics, 53(6), 553-563 (2014-02-06)
From a previously validated paediatric population pharmacokinetic model, it was derived that non-linear morphine maintenance doses of 5 μg/kg(1.5)/h, with a 50 % dose reduction in neonates with a postnatal age (PNA) <10 days, yield similar morphine and metabolite concentrations