N, N-Diisopropylethylamine

<strong>N,N-Diisopropylethylamine</strong>_x000D_ <strong>Catalog number:</strong> B2014985_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 25 mL_x000D_ <strong>Molecular Weight or Concentration:</strong> 129.24_x000D_ <strong>Supplied as:</strong> Liquid_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> RT_x000D_ <strong>Keywords:</strong> N-Ethyldiisopropylamine, DIPEA, Ethyldiisopropylamine, ‘Hünig’s base’_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Zhou H, Fan R, Yang J, Sun X, Liu X, Wang XC. N,N-Diisopropylethylamine-Mediated Electrochemical Reduction of Azobenzenes in Dichloromethane J Org Chem. 2022 Nov 4;87(21):14536-14543._x000D_ 2: Wei WJ, Gao HQ, Luo XH, Tang YZ. Dielectric Relaxation and Dielectric Switching Behaviors in (N,N-Diisopropylethylamine) Tetrachloroantimonate(III) Chemistry. 2023 Jan 9;29(2):e202202916._x000D_ 3: Hong Z, Ruan J, Chen X, Qian C, Ge X, Zhou S. On the Origin of the Promoting Effect Exerted by Magnesium in the ZnCl(2)-Catalyzed Synthesis of N,N-Diisopropylethylamine ACS Omega. 2020 Nov 11;5(46):29903-29912._x000D_ 4: Hong Z, Ruan J, Chen X, Qian C, Ge X, Zhou S. Correction to "On the Origin of the Promoting Effect Exerted by Magnesium in the ZnCl(2)-Catalyzed Synthesis of N,N-Diisopropylethylamine" ACS Omega. 2021 Feb 10;6(7):5074._x000D_ 5: Huang JJ, Liao HC, Hsu CE, Liu YR, Chang YF, Chou SY. Synthesis of Spirocyclopropane-Containing 4H-Pyrazolo[1,5-a]indoles via Alkylative Dearomatization and Intramolecular N-Imination of an Indole-O-(Methylsulfonyl)oxime Molecules. 2023 Aug 31;28(17):6374._x000D_ 6: Nazareth A, Joppich M, Panthani A, Fisher D, Giese RW. Alkylation with dialkylsulfate and diisopropylethylamine J Chromatogr. 1985 Feb 20;319(3):382-6._x000D_ 7: Guo L, Worth AJ, Mesaros C, Snyder NW, Glickson JD, Blair IA. Diisopropylethylamine/hexafluoroisopropanol-mediated ion-pairing ultra-high-performance liquid chromatography/mass spectrometry for phosphate and carboxylate metabolite analysis: utility for studying cellular metabolism Rapid Commun Mass Spectrom. 2016 Aug 30;30(16):1835-45._x000D_ 8: Monteiro LS, Suárez AS. High yielding synthesis of N-ethyl dehydroamino acids Amino Acids. 2012 Oct;43(4):1643-52._x000D_ 9: Wichitnithad W, Nantaphol S, Noppakhunsomboon K, Rojsitthisak P. An update on the current status and prospects of nitrosation pathways and possible root causes of nitrosamine formation in various pharmaceuticals Saudi Pharm J. 2023 Feb;31(2):295-311._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/32977642">10: Marinović M, Perković I, Fontinha D, Prudêncio M, Held J, Pessanha de Carvalho L, Tandarić T, Vianello R, Zorc B, Rajić Z. Novel Harmicines with Improved Potency against Plasmodium Molecules. 2020 Sep 23;25(19):4376. </a>_x000D_ _x000D_ <strong>Products Related to N,N-Diisopropylethylamine can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>