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Tmah 25 methanol solution

Manufactured by ABCR
Sourced in Poland, Germany

TMAH) 25% methanol solution is a chemical compound used as a solvent and developer in various industrial and laboratory applications. It is a clear, colorless liquid with a characteristic odor. The solution contains 25% tetramethylammonium hydroxide (TMAH) and 75% methanol. The core function of this product is to serve as a processing agent for specific materials and applications, where its chemical properties are utilized.

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2 protocols using tmah 25 methanol solution

1

Synthesis of PLA-Siloxane Hybrid Materials

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Polylactide (PLA) type Ingeo 2003D was purchased from NatureWorks (Minnetonka, MN, USA). The chemicals were purchased from the following sources: Tetraethoxysilane (TEOS) from Unisil (Poland), chlorodimethylsilane, tetramethylammonium hydroxide (TMAH) 25% methanol solution from ABCR, (R)-(+)-limonene, toluene, chloroform-d, Karstedt’s catalyst xylene solution from Aldrich, P2O5 from Avantor Performance Materials Poland S.A. toluene was degassed and dried by distilling it from P2O5 under argon atmosphere.
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2

Synthesis and Characterization of Siloxane-Methacrylate Composites

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The chemicals were purchased from the following sources: Tetraethoxysilane (TEOS), chlorodimethylsilane, tetramethylammonium hydroxide (TMAH) 25% methanol solution from ABCR (Karlsruhe, Germany), allyl methacrylate, methacryloxypropyltrimethoxysilane, toluene, chloroform-d, Karstedt’s catalyst xylene solution and isopropanol from Aldrich (St. Louis, MO, USA), P2O5 from Avantor Performance Materials Poland S.A. (Gliwice, Poland). Toluene was degassed and dried by distilling it from P2O5 under argon atmosphere. To test the connection strength of the joint, the composite materials Harmonize color Enamel XXL and Harmonize color A3.5, and a bond system Optibond Solo were obtained from Kerr Dental, Orange, CA, USA. The material was polymerized with a diode lamp emitting light in the 420 nm range (DemiUltra, Kerr Dental, Orange, CA, USA). Digital Light Microscope Keyence VHX 7000 with 100× to 1000× VH-Z100T lens and a VHX 7020 camera (Osaka, Japan). SEM-EDS analyses were recorded on a Quanta FEG 250 (FEI) instrument at 30 kV. 1H and COSY Nuclear Magnetic Resonance (NMR) spectra were recorded at 25 °C on a Bruker Ultra Shield 300 spectrometer using CDCl3 as a solvent. Chemical shifts are reported in ppm with reference to the residual solvent (CHCl3) peak.
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