Catalog Number: B2014666 (1 g)
2,2′-Dipyridyl Disulfide is a high quality 2,2′-Dipyridyl Disulfide for Peptide Synthesis. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.
Live enquiry about this product via Text/SMS: 1-858-900-3210.
Catalog number: B2014666
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 220.31
Supplied as: Solid
Applications: molecular tool for various biochemical applications
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.
1: Tian H, Ba W, Zhang X, Wang X, Dong Y, Li X, Ru S. mRNA-miRNA sequencing reveals mechanisms of 2,2′-dipyridyl disulfide-induced thyroid disruption in Japanese flounder (Paralichthys olivaceus) Aquat Toxicol. 2022 Jul;248:106191.
2: Katayama H, Nagata K. Application of 2,2′-dipyridyl disulfide-mediated thiazolidine ring-opening reaction to glycoprotein synthesis: Total chemical synthesis of evasin-3 J Pept Sci. 2021 Feb;27(2):e3290.
3: Malthouse JP, Brocklehurst K. A kinetic method for the study of solvent environments of thiol groups in proteins involving the use of a pair of isomeric reactivity probes and a differential solvent effect. Investigation of the active centre of ficin by using 2,2′- and 4,4′- dipyridyl disulphides as reactivity probes Biochem J. 1980 Jan 1;185(1):217-22.
4: Maruyama K, Nagasawa H, Suzuki A. 2,2′-Bispyridyl disulfide rapidly induces intramolecular disulfide bonds in peptides Peptides. 1999;20(7):881-4.
5: Kanishchev OS, Dolbier WR Jr. Synthesis and characterization of 2-pyridylsulfur pentafluorides Angew Chem Int Ed Engl. 2015 Jan 2;54(1):280-4.
6: Ismaylova SR, Matsulevich ZV, Borisova GN, Borisov AV, Khrustalev VN. Dichloridobis(pyridine-2-thiol-ato-κ²N,S)tin(IV): a new polymorph Acta Crystallogr Sect E Struct Rep Online. 2012 Jul 1;68(Pt 7):m875-6.
7: Santa T, Matsumura D, Huang C, Kitada C, Imai K. Design and synthesis of a hydrophilic fluorescent derivatization reagent for carboxylic acids, 4-N-(4-N-aminoethyl)piperazino-7-nitro-2,1,3-benzoxadiazole (NBD-PZ-NH2), and its application to capillary electrophoresis with laser-induced fluorescence detection Biomed Chromatogr. 2002 Dec;16(8):523-8.
8: Song J, Si Y, Guo W, Wang D, Fu Y. Organosulfide-Based Deep Eutectic Electrolyte for Lithium Batteries Angew Chem Int Ed Engl. 2021 Apr 26;60(18):9881-9885.
9: Salih E, Howard S, Chishti SB, Cohen SG, Liu WS, Cohen JB. Labeling of cysteine 231 in acetylcholinesterase from Torpedo nobiliana by the active-site directed reagent, 1-bromo-2-[14C] pinacolone. Effects of 2,2′-dipyridyl disulfide and other sulfhydryl reagents J Biol Chem. 1993 Jan 5;268(1):245-51.
10: Fan Q, Si Y, Guo W, Fu Y. Insight into Chemical Reduction and Charge Storage Mechanism of 2,2′-Dipyridyl Disulfide toward Stable Lithium-Organic Battery J Phys Chem Lett. 2021 Jan 21;12(2):900-906.
Products Related to 2,2′-Dipyridyl Disulfide can be found at Chemicals
|Dimensions||8 × 8 × 8 in|
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