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Merck

1.03725

Acetonitrilo

≥99.9% (GC), suitable for UHPLC, LiChrosolv®

Sinónimos:

ACN, Cianometano, Cianuro de metilo, Nitrilo de etilo

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About This Item

Fórmula lineal:
CH3CN
Número CAS:
75-05-8
Peso molecular:
41.05
NACRES:
NA.03
EC Index Number:
200-835-2
UNSPSC Code:
41116004
MDL number:
MFCD00001878
Beilstein/REAXYS Number:
741857
assay:
≥99.9% (GC)
technique(s):
HPLC: suitable
LC/MS: suitable
UHPLC: suitable
application(s):
PFAS testing
bp:
81-82 °C (lit.)
vapor pressure:
72.8 mmHg ( 20 °C)
97 hPa ( 20 °C)

Nombre del producto

Acetonitrilo, for UHPLC-MS LiChrosolv®

InChI

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

SMILES string

CC#N

InChI key

WEVYAHXRMPXWCK-UHFFFAOYSA-N

agency

suitable for ASTM® 7968
suitable for ASTM® 7979
suitable for DIN 38407-42
suitable for EPA 1633
suitable for EPA 8327
suitable for GB 31604.35-2016
suitable for GB 5009.253-2016
suitable for ISO 21675 2019

reg. compliance

suitable for FDA C-010.02

vapor density

1.41 (vs air)

vapor pressure

72.8 mmHg ( 20 °C)
97 hPa ( 20 °C)

product line

LiChrosolv®

assay

≥99.9% (GC)

form

liquid

autoignition temp.

524 °C
973 °F

expl. lim.

16 %

technique(s)

HPLC: suitable
LC/MS: suitable
UHPLC: suitable

refractive index

n20/D 1.344 (lit.)

bp

81-82 °C (lit.)

mp

−45 °C (lit.)

transition temp

flash point 2 °C

density

0.786 g/mL at 25 °C (lit.)

application(s)

PFAS testing

format

neat

storage temp.

2-30°C

Quality Level

200

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Legal Information

ASTM is a registered trademark of American Society for Testing and Materials
LICHROSOLV is a registered trademark of Merck KGaA, Darmstadt, Germany

Application

Intended for U/HPLC and LC-MS/MS applications.

Featured as a solvent in screening of benzofurans and ethylphenidate psychostimulants in serum, urine, and hair samples by UHPLC-MS/MS.
The product is an organic solvent, used as a mobile phase/extraction solvent in the ultra-high performance liquid chromatorgraphy - tandem mass spectrometry (UHPLC-MS/MS) analysis of pesticides in tobacco samples.

General description

LiChrosolv® solvents show high degree of UV transmittance, low particle count, low acidity and alkalinity and low evaporation residue level. This makes them suitable for reproducible separations.
Acetonitrile is a polar aprotic solvent, which is used as an intermediate in organic synthesis. It has a low viscosity, high elution strength and miscibility in water that make it viable in many chromatography systems. It can also be utilized in spectrophotometric and fluorimetric technques.

Other Notes

Explore various lab safety accessories and equipment for safe handling of solvents to increase your safety level from the first usage.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Gabrieli Bernardi et al.
Talanta, 161, 40-47 (2016-10-23)
An effective method has been developed and validated for the determination of residues of 55 pesticides in tobacco. The proposed sample preparation method is based on acetonitrile extraction, low-temperature precipitation (LTP) and dispersive solid phase extraction (d-SPE) clean-up. Gas chromatography
Acetonitrile, the polarity chameleon.
P K Zarzycki et al.
Analytical and bioanalytical chemistry, 397(3), 905-908 (2010-04-13)
Roberto Nisticò et al.
Nanomaterials (Basel, Switzerland), 9(8) (2019-08-02)
The photodegradation of an aqueous solution of diclofenac (DCF) has been attempted in the presence of hydrogen peroxide and organic/inorganic hybrid magnetic materials under simulated and real solar light. The hybrid magnetic materials have been prepared via coprecipitation synthesis starting
Intoxication caused by new psychostimulants: analytical methods to disclose acute and chronic use of benzofurans and ethylphenidate
Barcelo B, et al.
International Journal of Legal Medicine, 131(6), 1543-1553 (2017)
Duygu Eryavuz Onmaz et al.
Clinica chimica acta; international journal of clinical chemistry, 497, 120-124 (2019-07-28)
Imatinib has favorable pharmacokinetic properties, but primary and secondary resistance mechanisms may cause a decrease in clinical response over time. There is a positive correlation between serum imatinib concentrations and treatment response. Our aim was to develop a method for

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