Description

Cyanines are formally compounds with two nitrogen atoms linked by an odd number of methene units. 26 28 The nitrogen atoms are parts of the heterocyclic units (such as indole, benzoxazol, or benzothiazol) . The structures and optical properties of representative cyanine dyes used for in vivo imaging are presented[1]. Cyanines are characterized by long wavelength, tunable absorption and emission, very high extinction coefficient (up to 300,000 M 1 cm 1), good water solubility, and relatively straightforward synthesis[2].–20°C (Powder, protect from light)-Applications–Formula-C25H26N2O4-Citation–References-[1]Altman RB, et al. Cyanine fluorophore derivatives with enhanced photostability. Nat Methods. 2011 Nov 13;9(1):68-71.|[2]Shindy, H. A. (2017). Fundamentals in the chemistry of cyanine dyes: A review. Dyes and Pigments, 145, 505–513. doi:10.1016/j.dyepig.2017.06.029-CASNumber-260430-02-2-MolecularWeight-418.49-Compound Purity-98.0-SMILES-CC[N+]1=C(/C=C/C=C(N2CCCCCC([O-])=O)/OC3=C2C=CC=C3)OC4=CC=CC=C41-Research_Area-Others-Solubility-DMSO : ≥ 30 mg/mL-Target-Fluorescent Dye-Isoform–Pathway-Others-MCE Product type-Dye Reagents