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1 1 1 trifluoroacetone

Manufactured by Merck Group
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Sourced in Italy, United States

1,1,1-trifluoroacetone is a chemical compound used as a laboratory reagent. It has the molecular formula C₃H₃F₃O. The compound is a volatile, colorless liquid with a pungent odor.

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Lab products found in correlation

Trifluoromethanesulfonic acid, by Merck Group (1 mentions) Trimethylamine, by Merck Group (1 mentions) 1 4 dibromobutane, by Fluorochem (1 mentions) N butyllithium, by Merck Group (1 mentions) Methanol, by Merck Group (1 mentions) Dichloromethane, by Merck Group (1 mentions) Glutaraldehyde, by Merck Group (1 mentions) Tetrahydrofuran, by Merck Group (1 mentions) Polyvinyl alcohol (pva), by Merck Group (1 mentions) N methyl 2 pyrrolidone, by Merck Group (1 mentions) Polyvinylidene difluoride, by Merck Group (1 mentions) Magnesium sulfate, by Merck Group (1 mentions) Acetonitrile, by Merck Group (1 mentions) Sodium bicarbonate, by Merck Group (1 mentions) Sodium chloride (nacl), by Merck Group (1 mentions) Ethyl acetate, by Merck Group (1 mentions)

2 protocols using 1 1 1 trifluoroacetone

1

Synthesis of Brominated Organic Compounds

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2-Bromobiphenyl and 1,4-dibromobutane were reagent grade and purchased from Fluorochem (Hadfield, UK). n-Butyllithium (BuLi, 2.5 M in hexane), tetrahydrofuran (THF, anhydrous), dichloromethane (DCM), 1,1,1-trifluoroacetone, trifluoromethanesulfonic acid (TFSA), trimethylamine (TMA, 4.2 M in ethanol), poly(vinyl alcohol) (PVA, Mw = 89–98,000, 99% hydrolyzed), polyvinylidene difluoride (PVDF, Mw = 534,000), glutaraldehyde (GA) (50 wt% in water), N-methyl-2-pyrrolidone (NMP), and methanol (anhydrous) were reagent grade and purchased from Sigma-Aldrich (Milano, Italy). All the reagents were used as received.
Narducci R., Becerra-Arciniegas R.A., Pasquini L., Ercolani G., Knauth P, & Di Vona M.L. (2022). Anion-Conducting Polymer Electrolyte without Ether Linkages and with Ionic Groups Grafted on Long Side Chains: Poly(Alkylene Biphenyl Butyltrimethyl Ammonium) (ABBA). Membranes, 12(3), 337.
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2

Synthesis and Characterization of SCECGE

Cited 1 time
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Ethyl acetate (>99%), acetonitrile (99.9%), 1,1,1-trifluoroacetone (>98%), sodium chloride (99.9%), sodium bicarbonate (99.9%), magnesium sulfate (>99%) and Oxone® potassium monopersulfate compound (CAS no: 70693-62-8) were purchased from Sigma Aldrich, St. Louis, MO, USA. 4-4′-methylene biscyclohexaneamine PACM (99%) were obtained from Air Products, Allentown, PA, USA. SCECGE, was synthesized as previously reported [21 (link)]. All chemicals in this work were used as received.
Kinaci E., Can E., Scala J.J, & Palmese G.R. (2020). Epoxidation of Cardanol’s Terminal Double Bond. Polymers, 12(9), 2104.
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