Butyronitrile

Manufactured by Merck Group

Butyronitrile is a colorless, volatile organic compound. It is a four-carbon nitrile with the chemical formula CH3CH2CH2CN. Butyronitrile is used as a laboratory reagent and an intermediate in the production of other chemical compounds.

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Lab products found in correlation

O xylene, by Merck Group (1 mentions) P xylene, by Merck Group (1 mentions) M xylene, by Merck Group (1 mentions) Hexamethylphosphoramide, by Merck Group (1 mentions) Methanol, by Merck Group (1 mentions) Propionitrile, by Merck Group (1 mentions) Valeronitrile, by Merck Group (1 mentions)

2 protocols using butyronitrile

Synthesis of Benzothiadiazole Derivatives

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2,1,3-benzothiadiazole (>99.0%) and 1,4-dinitrobenzene (>99.0%) were purchased from TCI America. p-xylene, m-xylene, o-xylene, hexamethylphosphoramide and butyronitrile were purchased from Sigma Aldrich. Cyclohexanone was purchased from TCI America. Other solvents (>99.0% with extra dried condition) were purchased from Acros Organics and used without any pretreatment.

Noh J., Doan H.A., Job H., Robertson L.A., Zhang L., Assary R.S., Mueller K., Murugesan V, & Liang Y. (2024). An integrated high-throughput robotic platform and active learning approach for accelerated discovery of optimal electrolyte formulations. Nature Communications, 15, 2757.

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Purification of Nitrile Solvents

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General 1 and 2 were prepared as described elsewhere. 27, 28 Acetonitrile (MeCN), propionitrile (EtCN), butyronitrile (PrCN), valeronitrile (BuCN), caprylonitrile (HepCN), ethylene glycol (EG), methanol (MeOH) and ethanol (EtOH) solvents were purchased from Sigma Aldrich. MeCN was HPLC grade, MeOH and EtOH were spectroscopy grade and they were used without further purification. The other nitriles and the ethylene glycol were used after column chromatography purification using a mixed stationary phase (aluminium oxide 'Alumina B' and activated carbon) to remove the luminescent impurities.

Szakács Z., Rousseva S., Bojtár M., Hessz D., Bitter I., Kállay M., Hilbers M., Zhang H, & Kubinyi M. (2018). Experimental evidence of TICT state in 4-piperidinyl-1,8-naphthalimide - a kinetic and mechanistic study. Physical chemistry chemical physics : PCCP, 20(15).

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