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Hplc grade acn

Manufactured by Carlo Erba
Sourced in France

HPLC-grade ACN is a high-purity acetonitrile (ACN) solvent specifically designed for use in high-performance liquid chromatography (HPLC) applications. It meets the stringent requirements for HPLC-grade solvents, ensuring consistent and reliable performance in analytical and preparative chromatographic techniques.

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2 protocols using hplc grade acn

1

Synthesis and Purification of Silibinin Derivatives

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Silibinin 1 was purchased from Sigma-Aldrich (Milano, Italy). HPLC-grade ACN and CH3OH were purchased from Carlo Erba Reagents and Sigma-Aldrich. Unless otherwise indicated, other chemicals were obtained from Sigma Aldrich. For the experimental synthesis procedures of tyrosol-based building blocks 68, see Romanucci et al. 2021 [37 (link)]. It must be noted that the experimental procedures for the synthesis of compounds 1012 and 1315 were described in detail only for the stereoisomer of silybin A (SilA, 1a): the same reaction conditions (temperature, stoichiometric ratios, and time of reaction) were used for silybin B (SilB, 1b) and silibinin (Sil, 1ab) as a natural mixture. Reactions were monitored by TLC (precoated silica gel plate F254, Merck, Upper Gwynedd, PA, USA) and column chromatography: Merck Kieselgel 60 (70–230 mesh). The analysis was performed with a Shimadzu (Tokyo, Japan) LC-8A HPLC system equipped with a Shimadzu SCL-10A VP System control and Shimadzu SPD-10A VP UV-VIS Detector. HPLC purifications were carried out on a Phenomenex Gemini RP18 column (10 μm particle size, 21.20 mm × 250 mm i.d.) using a linear gradient of ACN in 0.1 M NH4Ac in H2O, pH 7.0, from 20% to 100% over 30 min at a flow rate of 8 mL/min, with detection at 288 and 260 nm. MALDI spectral data were acquired on a MALDI TOFTOF AB Sciex 5800 mass spectrometer.
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2

Cocaine and Metabolite Analysis Protocol

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Stock solutions at 1 mg mL -1 of BZE in MeOH and cocaine base were provided by Sigma-Aldrich (Saint-Quentin-Fallavier, France). The working solutions at 1 µg mL -1 were obtained by dilution of the stock solution (1 mg mL -1 ) in HPLC-grade ACN (Carlo Erba, Val-de-Reuil, France). These solutions were stored at -20°C. MeOH, EtOH, and isooctane were purchased from Carlo Erba. Acetic acid and anhydrous ACN were provided by Sigma-Aldrich. 1 M NaOH and 0.1 M HCl were obtained using deionized water (Milli-Q purification system, Millipore, Molsheim, France) and Titrisol solutions from Merck (Darmstadt, Germany). MAA, TRIM, and 3-(trimethoxysilyl)propyl methacrylate (γ-MAPS) were purchased from Sigma-Aldrich. Azo-N,N'-diisobutyronitrile (AIBN) was purchased from Acros Organics (Noisy-le-Grand, France). MAA was distilled under vacuum in order to remove inhibitors and stored at -20°C. TRIM, AIBN, and γ-MAPS were of satisfactory purity so they were used without further purification. Fused-silica capillaries with a UV transparent fluorocarbon polymer coating (PTFE-coated silica capillaries, 100 µm i.d. x 375 µm outer diameter (o.d.)) were purchased from Polymicro Technologies (Photon Lines, Saint Germain-en-Laye, France).
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