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Imidazole - 3M pH 6.0

<strong>Imidazole - 3M pH 6.0</strong>_x000D_ <strong>Catalog number:</strong> B2015668_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 10 mL_x000D_ <strong>Molecular Weight or Concentration:</strong> 68.08 g/mol_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> Imidazole - 3M Recrystallized Solution, pH 6.0_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: Ahad A, Shakeel F, Raish M, Ahmad A, Bin Jardan YA, Al-Jenoobi FI, Al-Mohizea AM. Thermodynamic Solubility Profile of Temozolomide in Different Commonly Used Pharmaceutical Solvents Molecules. 2022 Feb 21;27(4):1437._x000D_ 2: Tan C, Chen Y, Peng X, Chen Z, Cai S, Cross TA, Fu R. Revealing weak histidine (15)N homonuclear scalar couplings using Solid-State Magic-Angle-Spinning NMR spectroscopy J Magn Reson. 2020 Jul;316:106757._x000D_ 3: Miecznikowski JR, Jasinski JP, Kaur M, Bonitatibus SC, Almanza EM, Kharbouch RM, Zygmont SE, Landy KR. Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase J Vis Exp. 2020 Mar 19;(157)._x000D_ 4: Sheng J, Venkatesh GM, Duddu SP, Grant DJ. Dehydration behavior of eprosartan mesylate dihydrate J Pharm Sci. 1999 Oct;88(10):1021-9._x000D_ 5: Ueda K, Higashi K, Yamamoto K, Moribe K. Inhibitory effect of hydroxypropyl methylcellulose acetate succinate on drug recrystallization from a supersaturated solution assessed using nuclear magnetic resonance measurements Mol Pharm. 2013 Oct 7;10(10):3801-11._x000D_ 6: Ahn Y, Song Y, Kwak SY, Kim H. Highly ordered cellulose II crystalline regenerated from cellulose hydrolyzed by 1-butyl-3-methylimidazolium chloride Carbohydr Polym. 2016 Feb 10;137:321-327._x000D_ 7: Renault S, Bertrand S, Carreaux F, Bazureau JP. Parallel solution-phase synthesis of 2-alkylthio-5-arylidene-3,5-dihydro-4H-imidazol-4-one by one-pot three-component domino reaction J Comb Chem. 2007 Nov-Dec;9(6):935-42._x000D_ 8: Shang J, Rambo BM, Hao X, Xiang JF, Gong HY, Sessler JL. Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening Chem Sci. 2016 Jul 1;7(7):4148-4157._x000D_ 9: Adams CJ, Kurawa MA, Orpen AG. Coordination chemistry in the solid state: reactivity of manganese and cadmium chlorides with imidazole and pyrazole and their hydrochlorides Inorg Chem. 2010 Nov 15;49(22):10475-85._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/2394126">10: Jacobsen IA, Pegg DE, Starklint H, Barfort P, Diaper MP. Hypothermic preservation of rabbit kidneys for 48 hours using low ionic strength solutions Cryobiology. 1990 Aug;27(4):423-9. </a>_x000D_ _x000D_ <strong>Products Related to Imidazole - 3M pH 6.0 can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>

Product Specifications

Short Description

Catalog Number: B2015668 (10 mL)

Weight

0.8

Length

2

Width

0.9

Height

0.9

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