Tridecyl β-D-maltoside

<strong>Tridecyl β-D-maltoside</strong>_x000D_ <strong>Catalog number:</strong> B2013678_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 524.6 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> n-Tridecyl β-D-maltopyranoside_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: Zhang L, Di Y, Dan W. n-Tridecyl-amine chloride monohydrate Acta Crystallogr Sect E Struct Rep Online. 2011 Feb 26;67(Pt 3):o717._x000D_ 2: Sawatzki P, Mikeska T, Nieger M, Bolte M, Kolter T. (4S,5S)-4-[(1R)-1,2-Dihydroxyethyl]-5-tridecyl-1,3-oxazolidin-2-one Acta Crystallogr C. 2003 May;59(Pt 5):o225-7._x000D_ 3: Cosmetic Ingredient Review Expert Panel. Safety assessment of Salicylic Acid, Butyloctyl Salicylate, Calcium Salicylate, C12-15 Alkyl Salicylate, Capryloyl Salicylic Acid, Hexyldodecyl Salicylate, Isocetyl Salicylate, Isodecyl Salicylate, Magnesium Salicylate, MEA-Salicylate, Ethylhexyl Salicylate, Potassium Salicylate, Methyl Salicylate, Myristyl Salicylate, Sodium Salicylate, TEA-Salicylate, and Tridecyl Salicylate Int J Toxicol. 2003;22 Suppl 3:1-108._x000D_ 4: Kovalchuk VI, Aksenenko EV, Makievski AV, Fainerman VB, Miller R. Dilational interfacial rheology of tridecyl dimethyl phosphine oxide adsorption layers at the water/hexane interface J Colloid Interface Sci. 2019 Mar 15;539:30-37._x000D_ 5: Park B, Na SY, Bae IG. Uniform two-dimensional crystals of polystyrene nanospheres fabricated by a surfactant-assisted spin-coating method with polyoxyethylene tridecyl ether Sci Rep. 2019 Aug 7;9(1):11453._x000D_ 6: Jaras J, Navaruckiene A, Ostrauskaite J. Thermoresponsive Shape-Memory Biobased Photopolymers of Tetrahydrofurfuryl Acrylate and Tridecyl Methacrylate Materials (Basel). 2023 Mar 7;16(6):2156._x000D_ 7: Amin AY, Khassanov A, Reuter K, Meyer-Friedrichsen T, Halik M. Low-voltage organic field effect transistors with a 2-tridecyl1benzothieno[3,2-b]1benzothiophene semiconductor layer J Am Chem Soc. 2012 Oct 10;134(40):16548-50._x000D_ 8: Kuromitsu S, Fukunaga M, Lennard AC, Masuho Y, Nakada S. 3-(13-Hydroxytridecyl)-1-[13-(3-pyridyl)tridecyl]pyridinium chloride (YM-53792), a novel inhibitor of NF-AT activation Biochem Pharmacol. 1997 Nov 1;54(9):999-1005._x000D_ 9: Pisrik M, Pupk M, Luk M, Dev_nsky F, Hub_k L, Bukovsk_ M, Horvth B. The Synthesis, Self-Assembled Structures, and Microbicidal Activity of Cationic Gemini Surfactants with Branched Tridecyl Chains Molecules. 2019 Nov 30;24(23):4380._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/17999537">10: McErlean CS, Moody CJ. First synthesis of N-(3-carboxylpropyl)-5-amino-2-hydroxy-3- tridecyl-1,4-benzoquinone, an unusual quinone isolated from Embelia ribes J Org Chem. 2007 Dec 21;72(26):10298-301. </a>_x000D_ _x000D_ <strong>Products Related to Tridecyl β-D-maltoside can be found at</strong> <a href="https://moleculardepot.com/product-category/Carbohydrates/"> Carbohydrates</a>