574732
Acetonitrile solution
suitable for HPLC, contains 0.1 % (v/v) trifluoroacetic acid
Synonyme(s) :
ACN, Cyanomethane, Ethyl nitrile, Methyl cyanide
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A propos de cet article
Formule linéaire :
CH3CN
Numéro CAS:
Poids moléculaire :
41.05
NACRES:
NA.03
PubChem Substance ID:
UNSPSC Code:
12190000
EC Number:
200-835-2
MDL number:
Beilstein/REAXYS Number:
4124158
Grade:
HPLC grade
Technique(s):
HPLC: suitable
Bp:
81-82 °C
Vapor pressure:
72.8 mmHg
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Acetonitrile solution, contains 0.1 % (v/v) trifluoroacetic acid, suitable for HPLC
grade
HPLC grade
Quality Level
vapor density
1.41 (vs air)
vapor pressure
72.8 mmHg
form
liquid
contains
0.1 % (v/v) trifluoroacetic acid
expl. lim.
8 %
technique(s)
HPLC: suitable
bp
81-82 °C
mp
-48 °C
density
0.782 g/mL at 25 °C
application(s)
food and beverages
format
mixture
SMILES string
CC#N
InChI
1S/C2H3N/c1-2-3/h1H3
InChI key
WEVYAHXRMPXWCK-UHFFFAOYSA-N
General description
The product is an acetonitrile solution containing 0.1%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 volatile acid that forms hydrophobic negatively charged trifluoroacetate ion.
Application
- Preparation and characterization of stationary phase gradients on C8 liquid chromatography columns.: This study explores the development and analysis of stationary phase gradients on C8 columns, crucial for optimizing chromatographic separations in analytical chemistry (Cecil et al., 2024).
- Metal-cation-induced shifts in thiolate redox and reduced sulfur speciation.: Investigates the impact of metal cations on the redox behavior of thiolates, a key area in understanding redox processes in various chemical systems (Seo et al., 2024).
- A Phosphine-Oxide Cobalt(II) Complex and Its Catalytic Activity Studies toward Alcohol Dehydrogenation Triggered Direct Synthesis of Imines and Quinolines.: Describes the catalytic role of a cobalt(II) phosphine-oxide complex in synthesizing imines and quinolines from alcohols, a significant contribution to synthetic organic chemistry (Khatua et al., 2024).
- [Simultaneous determination of 31 banned veterinary drugs during egg-laying period in poultry eggs by ultra performance liquid chromatography-tandem mass spectrometry].: This Chinese study presents a method for detecting multiple veterinary drugs in eggs, highlighting advancements in food safety and analytical methodologies (Zhu et al., 2024).
- Probing Isolated Water Molecules in Aqueous Acetonitrile Solutions Using Oxygen K-Edge X-ray Absorption Spectroscopy.: Focuses on the molecular dynamics of water in acetonitrile solutions, providing insights that are crucial for understanding solvent effects in various chemical environments (Nagasaka, 2024).
Packaging
M-Bottle for Solvents
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Preparation Note
Product filtered through a 0.2 μm filter
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Classe de stockage
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)
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 574732-18L | 04061837479274 |
| 574732-20L | 04061832628080 |
| 574732-4L | 04061832628097 |
| 574732-4X4L | 04061832628103 |