685461
Acetonitrile solution
suitable for HPLC, contains 10.0% acetone, 40.0% 2-propanol, 0.05% formic acid
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Synonym(s):
ACN, Cyanomethane, Ethyl nitrile, Methyl cyanide
Linear Formula:
CH3CN
CAS Number:
Molecular Weight:
41.05
Beilstein/REAXYS Number:
4124158
MDL number:
UNSPSC Code:
12190000
PubChem Substance ID:
Recommended Products
vapor density
1.41 (vs air)
Quality Level
vapor pressure
72.8 mmHg
form
liquid
contains
0.05% formic acid
10.0% acetone
40.0% 2-propanol
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
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General description
The product is an acetonitrile solution containing 40.0% 2-propanol, 0.05% formic acid, 10.0% acetone. This pre-blended solvent is of high purity that reduces time-consuming preparation and prevents instrument downtime because of impure mobile phases. Acetonitrile (MeCN), an organic solvent has low viscosity, high elution strength and is UV transparent at low wavelength.
Application
- Preparation and characterization of stationary phase gradients on C8 liquid chromatography columns.: This research discusses the preparation of stationary phase gradients on C8 columns using acetonitrile solutions, enhancing chromatographic resolution and efficiency, pivotal for the analytical chemistry field (Cecil et al., 2024).
- Metal-cation-induced shifts in thiolate redox and reduced sulfur speciation.: Highlighting a study on the redox behavior of thiolates influenced by metal cations, where acetonitrile solutions were crucial for maintaining reaction environments, crucial for developing new catalytic and sensor applications (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.: This paper presents the synthesis of a novel cobalt(II) complex using acetonitrile solution, which showed significant catalytic activity in synthesizing bioactive molecules, illustrating the solvent′s role in facilitating complex chemical reactions (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].: Demonstrating the use of acetonitrile solutions in sample preparation for high-throughput UPLC-MS/MS analysis, this study significantly contributes to food safety and drug residue analysis (Zhu et al., 2024).
- Probing Isolated Water Molecules in Aqueous Acetonitrile Solutions Using Oxygen K-Edge X-ray Absorption Spectroscopy.: This research utilizes acetonitrile solutions to study the interaction of water molecules at the molecular level, providing insights critical for understanding solvation dynamics and mixture behaviors (Nagasaka, 2024).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
wgk_germany
WGK 2
flash_point_f
closed cup
flash_point_c
closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Eagleson M.
Concise Encyclopedia Chemistry, 6-6 (1994)
Acetonitrile, the polarity chameleon.
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Seung-Ho Shin et al.
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Congenital cholesteatomas are epithelial lesions that present as an epithelial pearl behind an intact eardrum. Congenital and acquired cholesteatomas progress quite differently from each other and progress patterns can provide clues about the unique origin and pathogenesis of the abnormality.
Fang Xu et al.
The Plant cell, 27(5), 1547-1562 (2015-05-15)
Nod-like receptors (NLRs) serve as immune receptors in plants and animals. The stability of NLRs is tightly regulated, though its mechanism is not well understood. Here, we show the crucial impact of N-terminal acetylation on the turnover of one plant
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