Chemodex

1,1'-Dimethyl-3,3,3',3'-tetramethyl indotricarbocyanine perchlorate

Name: 1,1'-Dimethyl-3,3,3',3'-tetramethyl indotricarbocyanine perchlorate
Brand: Chemodex
SKU: CDX-D0884
Price: 161.00 CHF
Availability: InStock

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CDX-D0884-M05050 mgCHF 161.00

CDX-D0884-M100100 mgCHF 271.00

CDX-D0884-M250250 mgCHF 561.00

Specifications / Handling

More Information
Product Details
Synonyms	DiIC1(7); NK 2421; HITCP; HITC perchlorate; 1,1',3,3,3',3'-Hexamethyl-2,2'-indotricarbocyanine perchlorate
Product Type	Chemical
Properties
Formula	C₂₉H₃₃N₂ . ClO₄
MW	509.04
CAS	16595-48-5
Source/Host Chemicals	Synthetic
Purity Chemicals	≥98% (HPLC)
Appearance	Dark cooper crystals.
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	NHQOULZCPKJYMM-UHFFFAOYSA-M
Smiles	CC1(C)C=2C([N+](C)=C1C=CC=CC=CC=C3N(C)C=4C(C3(C)C)=CC=CC4)=CC=CC2.Cl(=O)(=O)(=O)[O-]
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

Scientific Background Information

Product Description

DiIC1(7) is a long-wavelength, membrane-potential sensitive, near-infrared NIR) fluorescent indocarbocyanine dye. Can be used for cellmembrane staining, cell tracking, in vivo imaging or lipid nanoparticle labeling. It is a slow-response potentiometric fluorophore and has also been used as a laser dye for infrared lasers. Spectral Data: Excitation max: ~ 740nm, Emission max: ~768nm (MeOH).

Product-specific References

(1) E.A. Nothnagel, et al.; Anal. Biochem. 163, 224 (1987) | (2) A.A. Ishchenko, et al.; Dyes Pigm. 10, 85 (1989) | (3) D. Andrews-Wilberforce & G. Patonay; Appl. Spectrosc. 43, 1450 (1989) | (4) M.A. Roberson, et al.; Anal. Lett. 23, 719 (1990) | (5) J. Hicks & G. Patonay; Anal. Chem. 62, 1543 (1990) | (6) L.M. Loura, et al.; Biophys. J. 71, 1823 (1996) | (7) P. Gaikwad, et al.; Opt. Mat. 31, 1559 (2009) | (8) M.P. Samtsov, et al.; J. Appl. Spectrosc. 80, 170 (2013) | (9) C. Banerjee, et al.; Phys. Chem. Chem. Phys. 16, 17272 (2014)

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