N, N′-diisopropylcarbodiimide

<strong>N,N′-diisopropylcarbodiimide</strong>_x000D_ <strong>Catalog number:</strong> B2015871_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 5 mL_x000D_ <strong>Molecular Weight or Concentration:</strong> 51.3_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-30°C_x000D_ <strong>Keywords:</strong> N,N′-Diisopropylcarbodiimide_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: Budischowsky D, Sulaeva I, Hettegger H, Ludwig R, Rosenau T, Potthast A. Fluorescence labeling of C1-oxidized cellulose. Part 1: Method development Carbohydr Polym. 2022 Nov 1;295:119860._x000D_ 2: Kawashima H, Sohma Y, Nakanishi T, Kitamura H, Mukai H, Yamashita M, Akaji K, Kiso Y. A new class of aggregation inhibitor of amyloid-β peptide based on an O-acyl isopeptide Bioorg Med Chem. 2013 Nov 1;21(21):6323-7._x000D_ 3: Lüttenberg S, Sondermann F, Scherkenbeck J. Anthelmintic PF1022A: stepwise solid-phase synthesis of a cyclodepsipeptide containing N-methyl amino acids Tetrahedron. 2012 Feb 25;68(8):2068-2073._x000D_ 4: Surh I, Behl M, Elmore SA, Chhabra RS. Comparative dermal toxicity of dicyclohexylcarbodiimide and diisopropylcarbodiimide in rodents Cutan Ocul Toxicol. 2012 Sep;31(3):177-87._x000D_ 5: National Toxicology Program. Toxicology and carcinogenesis studies of diisopropylcarbodiimide (Cas No. 693-13-0) in F344/N rats and B6C3F1 mice (dermal studies) Natl Toxicol Program Tech Rep Ser. 2007 Feb;(523):1-286._x000D_ 6: Hayes BB, Gerber PC, Griffey SS, Meade BJ. Contact hypersensitivity to dicyclohexylcarbodiimide and diisopropylcarbodiimide in female B6C3F1 mice Drug Chem Toxicol. 1998 May;21(2):195-206._x000D_ 7: Baktır Z, Akkurt M, Kandinska MI, Bogdanov MG, Büyükgüngör O. (S)-Methyl 2-[(3R,4R)-2-benzyl-3-(2-fur-yl)-1-oxo-1,2,3,4-tetra-hydro-isoquinoline-4-carboxamido]-3-(1H-indol-3-yl)propanoate Acta Crystallogr Sect E Struct Rep Online. 2009 Jun 6;65(Pt 7):o1461-2._x000D_ 8: Witt KL, Tice RR, Shelby MD, Chhabra RS, Zeiger E. Induction of micronucleated erythrocytes in rodents by diisopropylcarbodiimide and dicyclohexylcarbodiimide: dependence on exposure protocol Environ Mol Mutagen. 1999;33(1):65-74._x000D_ 9: Hicks J, Mansikkamäki A, Vasko P, Goicoechea JM, Aldridge S. A nucleophilic gold complex Nat Chem. 2019 Mar;11(3):237-241._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/17893812">10: Liu B, Yang Y, Cui D, Tang T, Chen X, Jing X. C-H activation motivated by N,N'-diisopropylcarbodiimide within a lutetium complex stabilized by an amino-phosphine ligand Dalton Trans. 2007 Oct 10;(38):4252-4. </a>_x000D_ _x000D_ <strong>Products Related to N,N′-diisopropylcarbodiimide can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>