Accéder au contenu
Merck
Toutes les photos(1)

Documents

34442

Sigma-Aldrich

Acétonitrile

≥99.9% (GC), suitable for cDNA synthesis, DNA synthesis

Synonyme(s) :

ACN, Cyanométhane, Cyanure de méthyle, Éthylnitrile

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(1)

About This Item

Formule linéaire :
CH3CN
Numéro CAS:
75-05-8
Poids moléculaire :
41.05
Numéro Beilstein :
741857
Numéro CE :
200-835-2
Numéro MDL:
MFCD00001878
Code UNSPSC :
12191502
eCl@ss :
39031501
ID de substance PubChem :
329754743
Nomenclature NACRES :
NA.03

product name

Acétonitrile, suitable for DNA synthesis, ≥99.9% (GC)

Densité de vapeur

1.41 (vs air)

Niveau de qualité

100

Pression de vapeur

72.8 mmHg ( 20 °C)

Pureté

≥99.9% (GC)

Forme

liquid

Température d'inflammation spontanée

973 °F

Limite d'explosivité

16 %

Technique(s)

DNA synthesis: suitable
cDNA synthesis: suitable

Impuretés

≤0.0001% free alkali (as NH3)
≤0.001% free acid (as CH3COOH)
≤0.001% water (Karl Fischer)

Indice de réfraction

n20/D 1.344 (lit.)

Point d'ébullition

81-82 °C (lit.)

Pf

−45 °C (lit.)

Densité

0.786 g/mL at 25 °C (lit.)

Format

neat

Chaîne SMILES 

CC#N

InChI

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

Clé InChI

WEVYAHXRMPXWCK-UHFFFAOYSA-N

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

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).

Autres remarques

The article number 34442-4X2.5L will be discontinued. Please order the single bottle 34442-2.5L which is physically identical with the same exact specifications.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Danger

Classification des risques

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

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

35.6 °F - closed cup

Point d'éclair (°C)

2.0 °C - closed cup

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Les clients ont également consulté

Slide 1 of 4

1 of 4

Acétonitrile suitable for HPLC, gradient grade, ≥99.9%

Sigma-Aldrich

34851

Acétonitrile

Acétonitrile for gas chromatography ECD and FID SupraSolv®

Supelco

1.00017

Acétonitrile

Acétonitrile suitable for HPLC, gradient grade, ≥99.9%

Sigma-Aldrich

439134

Acétonitrile

Acétonitrile HPLC Plus, ≥99.9%

Sigma-Aldrich

34998

Acétonitrile

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
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
K Kishii et al.
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 20(5), 424-430 (2013-10-16)
The clinical relevance of Acinetobacter species, other than A. baumannii, as human pathogens has not been sufficiently assessed owing to the insufficiency of simple phenotypic clinical diagnostic laboratory tests. Infections caused by these organisms have different impacts on clinical outcome
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
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique