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Documentos Principais

60004

Sigma-Aldrich

Acetonitrilo

≥99.5% (GC)

Sinônimo(s):

ACN, Cianeto de metila, Cianometano, Etil-nitrilo

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About This Item

Fórmula linear:
CH3CN
Número CAS:
Peso molecular:
41.05
Beilstein:
741857
Número CE:
Número MDL:
Código UNSPSC:
12191502
eCl@ss:
39031501
ID de substância PubChem:
NACRES:
NA.03
Ensaio:
≥99.5% (GC)
p.e.:
81-82 °C (lit.)
pressão de vapor:
72.8 mmHg ( 20 °C)

densidade de vapor

1.41 (vs air)

Nível de qualidade

pressão de vapor

72.8 mmHg ( 20 °C)

Ensaio

≥99.5% (GC)

Formulário

liquid

temperatura de autoignição

973 °F

Lim. expl.

16 %

Impurezas

≤0.1% water (Karl Fischer)

índice de refração

n20/D 1.344 (lit.)

p.e.

81-82 °C (lit.)

pf

−45 °C (lit.)

densidade

0.786 g/mL at 25 °C (lit.)

Formato

neat

cadeia de caracteres SMILES

CC#N

InChI

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

chave InChI

WEVYAHXRMPXWCK-UHFFFAOYSA-N

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Aplicação


  • 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).

Outras notas

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.

Pictogramas

FlameExclamation mark

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

35.6 °F - closed cup

Ponto de fulgor (°C)

2.0 °C - closed cup


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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
Elke H J Krekels et al.
Clinical pharmacokinetics, 53(6), 553-563 (2014-02-06)
From a previously validated paediatric population pharmacokinetic model, it was derived that non-linear morphine maintenance doses of 5 μg/kg(1.5)/h, with a 50 % dose reduction in neonates with a postnatal age (PNA) <10 days, yield similar morphine and metabolite concentrations
N Sorvillo et al.
Journal of thrombosis and haemostasis : JTH, 12(5), 670-679 (2014-07-01)
Acquired deficiency of ADAMTS13 causes a rare and life-threatening disorder called thrombotic thrombocytopenic purpura (TTP). Several studies have shown that aberrant glycosylation can play an important role in the pathogenesis of autoimmune diseases.N-linked glycosylation and putative O-fucosylation sites have been
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
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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