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1.59014

Supelco

Acetonitrile solution

suitable for LC/MS, LiChrosolv®, contains 0.1% (v/v) trifluoroacetic acid

Synonym(s):

Acetonitrile solution, ACN, ACN + TFA, Cyanomethane, Ethyl nitrile, Methyl cyanide

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About This Item

Linear Formula:
CH3CN
CAS Number:
Molecular Weight:
41.05
Beilstein:
4124158
MDL number:
UNSPSC Code:
41116004
NACRES:
NA.03

product name

Acetonitrile with 0.1% (v:v) trifluoroacetic acid, hypergrade for LC-MS LiChrosolv®

vapor pressure

97 hPa ( 20 °C)

Quality Level

product line

LiChrosolv®

form

liquid

concentration

0.095-0.105 % (v/v)

technique(s)

LC/MS: suitable

impurities

≤0.025 ppm K (Potassium)
≤0.05 ppm Al (Aluminium)
≤0.05 ppm Ca (Calcium)
≤0.05 ppm Fe (Iron)
≤0.05 ppm Mg (Magnesium)
≤0.25 ppm Na (Sodium)

color

APHA: ≤10

transition temp

flash point 2 °C

density

0.782 g/mL at 25 °C

format

mixture

storage temp.

2-30°C

SMILES string

CC#N

InChI

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

InChI key

WEVYAHXRMPXWCK-UHFFFAOYSA-N

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Application


  • Retention time prediction for post-translationally modified peptides: Ser, Thr, Tyr-phosphorylation.: This study presents a methodology for predicting retention times of phosphorylated peptides using high-performance liquid chromatography (HPLC) (Battellino et al., 2024).

  • Development and validation of a UPLC-PDA method for quantifying ceftazidime in dried blood spots.: This paper outlines a validated ultra-performance liquid chromatography photodiode array (UPLC-PDA) method for the quantification of ceftazidime, demonstrating its application and accuracy in analyzing dried blood samples (Lv et al., 2024).

  • A facile fabric phase sorptive extraction method for monitoring chloramphenicol residues in milk samples.: Describes a new method using fabric phase sorptive extraction for the efficient monitoring of chloramphenicol in milk, highlighting its simplicity and effectiveness (Ben Ayed et al., 2024).

  • Study of sample preparation influence on bacterial lipids profile in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.: This research investigates how different sample preparation methods affect the lipid profiles of bacteria analyzed by MALDI-TOF MS, providing insights into optimizing protocols for better accuracy (Arendowski et al., 2024).

  • Simple and robust LC-MS/MS method for quantification of colistin methanesulfonate and colistin in human plasma for therapeutic drug monitoring.: This article details a robust and straightforward liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the simultaneous determination of colistin methanesulfonate and colistin in human plasma, useful in clinical settings (Kim et al., 2023).

Preparation Note

Product filtered through a 0.2 μm filter

Analysis Note

Acid content: 0.095 - 0.105 % (v/v)
Identity: passes test
Color: ≤ 10 Hazen
Al (Aluminium): ≤ 0.05 ppm
Ca (Calcium): ≤ 0.05 ppm
Fe (Iron): ≤ 0.05 ppm
K (Potassium): ≤ 0.025 ppm
Mg (Magnesium): ≤ 0.05 ppm
Na (Sodium): ≤ 0.25 ppm
Gradient grade (at 210 nm): ≤ 1.0 mAU
Gradient grade (at 254 nm): ≤ 0.5 mAU
Suitable for LC-MS; Intensity of background mass peak based on reserpine(APCI/ESI positive): ≤ 2 ppb
Filtered by 0.2 µm filter.

Other Notes

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

Legal Information

LICHROSOLV is a registered trademark of Merck KGaA, Darmstadt, Germany

related product

Product No.
Description
Pricing

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - (Acetonitrile)

Flash Point(C)

2 °C - (Acetonitrile)


Certificates of Analysis (COA)

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Determination of plasma protein binding using a SupelTM C18 pin device based BioSPME method for efficient sample preparation, along with a comparison to the equilibrium dialysis method.

Determination of plasma protein binding using a SupelTM C18 pin device based BioSPME method for efficient sample preparation, along with a comparison to the equilibrium dialysis method.

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