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Dipea

Manufactured by GL Biochem
Sourced in China

DIPEA is a commonly used organic compound in organic synthesis and biochemical applications. It functions as a mild and versatile base that can facilitate various chemical reactions. The core function of DIPEA is to promote deprotonation and acid-base reactions, making it a useful reagent in a wide range of laboratory settings.

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3 protocols using dipea

1

Solid-Phase Synthesis of C16 Peptide

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The synthesis of C16 was accomplished using a solid‐phase methodology on Fmoc Rink Amide‐MBHA resin (GL biochem, Shanghai, China) by a microwave synthesizer (CEM, NC, USA). Fmoc‐protected amino acids (GL Biochem, Shanghai, China) were used. After the quantified resin was swelled, deprotected, and washed, a mixed solution of Fmoc‐protected amino acid and activator (HBTU, HOBT, and DIPEA, all purchased from GL biochem, Shanghai, China) was added. Then the mixture was bubbled with nitrogen under microwave irradiation and washed with DMF (Samsung fine chemicals, Korea). The procedures of deprotection and coupling were repeated with the relevant Fmoc‐protected amino acids to create the peptide‐resin complex. Then resin was washed successively with DMF three times. The final peptide was cleaved using TFA/TIS/H2O (95:2.5:2.5, v/v/v) for 4 h at room temperature and precipitated with cold ethyl ether. Then ethyl ether was removed through centrifugation. All peptides were purified by preparative reversed‐phase high‐performance liquid chromatography (RP‐HPLC; Shimadzu LC‐10) on a C18 column (5 µm, 340 × 28 mm). The purity of C16 was demonstrated above 95%.
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2

Multifunctional Elastomeric Nanocomposites

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Poly(dimethylsiloxane) (PDMS) elastomer was obtained from Dow Corning (Sylgard 184). Ag nanowires dispersed in ethanol (CST-NW-S50) were ordered from Suzhou ColdStones Technology Co., Ltd. Silicone liquid (CAF-3) was purchased from Bluestar Silicones France Co., Ltd. Ethanol (purity 99.7%) was obtained from Sinapharm Chemical Reagent Co., Ltd. Fmoc–Tyr(tBu)–2-chlorotrityl resin, Fmoc–Gly–OH, Fmoc–Ala–OH, HOBT, TBTU and DIPEA were obtained from GL Biochem Co., Ltd. (Shanghai, China). 10,12-Pentacosadiynoic acid was purchased from Alfa-Aesar Co., Ltd. All other regents, compounds, and chemicals were obtained from commercial suppliers and used without further purification.
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3

Peptide Synthesis and Purification Protocol

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Peptide synthesis vessels were self-made. DIPEA, HOBt, HCTU, DIC, and 2-chlorotritylchloride resin were purchased from GL Biochem (Shanghai) Ltd. The crude peptides were dissolved with CH3CN/H2O and analysed or purified by analytical or semi-preparative RP-HPLC, respectively. A Vydac C4 or C18 column (5 μm, 4.6 mm × 250 mm) with a 1 mL min−1 flow rate was used for analytical RP-HPLC, and a Vydac C4 column (10 μm, 10 mm × 250 mm or 22 mm × 150 mm) with a 3–6 mL min−1 flow rate was used for semi-preparative RP-HPLC. The solvents systems were buffer A (0.1% TFA in water), buffer B (0.1% TFA in CH3CN). Data were recorded and analysed using the software system LC Solution.
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