Chemodex

1,1'-Dioctadecyl-3,3,3',3'-tetramethyl indotricarbocyanine iodide

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Product Details
Synonyms DiIC18(7); DiR; Cy7 DiC18
Product Type Chemical
Properties
Formula C63H101N2 . I
MW 1013.4
CAS 100068-60-8
Source/Host Chemicals Synthetic
Purity Chemicals ≥97% (HPLC)
Appearance Dark purple solid.
Solubility Soluble in DMSO or methanol.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturer's product datasheet.

InChi Key JLIOTPLALDYAEH-UHFFFAOYSA-M
Smiles CC1(C)C2=C(C=CC=C2)N(CCCCCCCCCCCCCCCCCC)C1=CC=CC=CC=CC3=[N+](CCCCCCCCCCCCCCCCCC)C4=C(C3(C)C)C=CC=C4.[I-]
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Keep under inert gas.
Protect from light and oxygen.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
DiIC18(7) [DiR] is a lipophilic, near-infrared fluorescent cyanine dye. The dye is useful for labeling cytoplasmic membranes and has been widely used for near-infrared in vivo imaging and for in vitro studies. The two long 18-carbon chains insert into the cell membrane, resulting in specific and stable cell staining with no or minimal dye transfer between cells. DiR diffuses laterally to stain the entire cell, allowing it to be used as an anterograde and retrograde tracer of neurons. In intact tissue, the dye does not transfer from labeled to unlabeled cells, but some transfer may occur when the membrane is disrupted, for example, after sectioning. Cell staining can be effected using the dye at 1-10 uM concentration and 10-20 min incubation time. The dye can be used for labeling nanoparticles and extracellular vescicles. The dye is weakly fluorescent until incorporated into membranes. Spectral Data: Excitation max: ~ 748nm, Emission max: ~780nm (MeOH).
Product References
(1) V. Kalchenko, et al.; J. Biomed. Opt. 11, 050507 (2006) | (2) M. Eisenblatter, et al.; J. Nucl. Med. 50, 1676 (2009) | (3) A. Wagh, et al.; ioconjug. Chem. 23, 981 (2012) | (4) H. Liu & D. Wu; Curr. Drug Deliv. 13, 40 (2016) | (5) M.T. Berninger, et al.; Eur. Radiol. 27, 1105 (2017) | (6) X. Zhang, et al.; ACS Appl. Mater. Interfaces 10, 30155 (2018) | (7) M. Riehl, et al.; Eur. J. Pharm. Sci. 132, 27 (2019) | (8) M. Bhogal, et al.; Sci. Rep. 12, 6338 (2022) | (9) J. Santelices, et al.; Bio. Protoc. 12, e4447 (2022)
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