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Merck

60004

Acetonitrile

≥99.5% (GC)

Synonim(y):

ACN, Cyanomethane, Ethyl nitrile, Methyl cyanide

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Informacje o tej pozycji

Wzór liniowy:
CH3CN
Numer CAS:
Masa cząsteczkowa:
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)
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Nazwa produktu

Acetonitrile, ≥99.5% (GC)

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 ( 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

Quality Level

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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.
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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

Klasa składowania

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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
Divya Subramonian et al.
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
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
Mareike Bongers et al.
Microbial cell factories, 14, 193-193 (2015-11-28)
High-throughput screening methods assume that the output measured is representative of changes in metabolic flux toward the desired product and is not affected by secondary phenotypes. However, metabolic engineering can result in unintended phenotypes that may go unnoticed in initial
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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