Merck
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639133

Supelco

Acetonitrile solution

contains 0.1 % (v/v) ammonium hydroxide

Fórmula lineal:
CH3CN
Número de CAS:
Peso molecular:
41.05
Beilstein:
4124158
Número MDL:
ID de la sustancia en PubChem:

densidad de vapor

1.41 (vs air)

Nivel de calidad

100

presión de vapor

72.8 mmHg

formulario

liquid

contiene

0.1 % (v/v) ammonium hydroxide

lim. expl.

8 %

bp

81-82 °C

mp

-48 °C

densidad

0.782 g/mL at 25 °C

SMILES string

CC#N

InChI

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

InChI key

WEVYAHXRMPXWCK-UHFFFAOYSA-N

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Descripción general

The product is an acetonitrile solution containing 0.1%v/v ammonium hydroxide that can be employed for HPLC and UHPLC (Ultra High performance Liquid Chromatography) techniques. 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.

Nota de preparación

Product filtered through a 0.2 μm filter

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Más documentos

Quotes and Ordering

Acetonitrile, the polarity chameleon.
Zarzycki PK, et al.
Analytical and Bioanalytical Chemistry, 397(3), 905-908 (2010)
Eagleson M.
Concise Encyclopedia Chemistry, 6-6 (1994)
Maria de la Paz Celorio-Mancera et al.
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More than half of the proteome from mandibular glands in caterpillars is represented by chemosensory proteins. Based on sequence similarity, these proteins are putative transporters of ligands to gustatory receptors in sensory organs of insects. We sought to determine whether
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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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