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Merck

574724

Acetonitrile solution

suitable for HPLC, contains 0.05 % (v/v) trifluoroacetic acid

Synonym(s):

ACN, Cyanomethane, Ethyl nitrile, Methyl cyanide

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About This Item

Linear Formula:
CH3CN
CAS Number:
Molecular Weight:
41.05
NACRES:
NA.03
PubChem Substance ID:
UNSPSC Code:
12190000
EC Number:
200-835-2
MDL number:
Beilstein/REAXYS Number:
4124158
technique(s):
HPLC: suitable
bp:
81-82 °C (lit.)
vapor pressure:
72.8 mmHg

Product Name

Acetonitrile solution, contains 0.05 % (v/v) trifluoroacetic acid

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

form

liquid

contains

0.05 % (v/v) trifluoroacetic acid

expl. lim.

8 % (lit.)

technique(s)

HPLC: suitable

bp

81-82 °C (lit.)

mp

-48 °C (lit.)

density

0.782 g/mL at 25 °C

format

mixture

Quality Level

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General description

The product is an acetonitrile solution containing 0.05%v/v trifluoroacetic acid. This pre-blended mobile phase solvent is of high purity that reduces time-consuming preparation and prevents instrument downtime because of impure mobile phases. Trifluoroacetic acid/acetonitrile mobile phase system is generally employed for peptide separation. Acetonitrile (MeCN), an organic solvent has low viscosity, high elution strength and is UV transparent at low wavelength. Trifluoroacetic acid (TFA) is commonly used as a mobile phase additive. It is a UV transparent, volatile acid that forms hydrophobic negatively charged trifluoroacetate ion.

Preparation Note

Product filtered through a 0.2 μm filter

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

42.8 °F - closed cup

flash_point_c

6 °C - closed cup

ppe

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


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Optimum concentration of trifluoroacetic acid for reversed-phase liquid chromatography of peptides revisited.
Chen Y, et al.
Journal of Chromatography A, 1043(1), 9-18 (2004)
Eagleson M.
Concise Encyclopedia Chemistry, 6-6 (1994)
Acetonitrile, the polarity chameleon.
Zarzycki PK, et al.
Analytical and Bioanalytical Chemistry, 397(3), 905-908 (2010)
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
Kangmin Chon et al.
Water research, 81, 388-397 (2015-07-05)
In this study, the changes in UV absorbance at 254 nm (UVA254) and electron donating capacity (EDC) were investigated as surrogate indicators for assessing removal of micropollutants and bromate formation during ozonation of wastewater effluents. To measure the EDC, a novel

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