Chemodex

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

Product Code:
 
CDX-D0884
Product Group:
 
Dyes, Stains, and Probes
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
Short term: +4°C. Long term: -20°C
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Chemical Structure

Chemical Structure

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CDX-D0884-M05050 mg£156.00
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CDX-D0884-M100100 mg£255.00
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CDX-D0884-M250250 mg£516.00
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This product comes from: Switzerland.
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  • Further Information
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Further Information

Appearance:
Dark cooper crystals.
CAS:
16595-48-5
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).
EClass:
32160000
Form:
solid
GHS Symbol:
GHS03, GHS05
Handling Advice:
Keep under inert gas. Protect from light and oxygen.
Hazards:
H335-H333-H319-H318-H315-H314-H303-H272
InChi:
InChI=1S/C29H33N2.ClHO4/c1-28(2)22-16-12-14-18-24(22)30(5)26(28)20-10-8-7-9-11-21-27-29(3,4)23-17-13-15-19-25(23)31(27)6;2-1(3,4)5/h7-21H,1-6H3;(H,2,3,4,5)/q+1;/p-1
InChiKey:
NHQOULZCPKJYMM-UHFFFAOYSA-M
MDL:
MFCD00067693
Molecular Formula:
C29H33N2 . ClO4
Molecular Weight:
509.04
Package Type:
Vial
Precautions:
P210-P220-P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P370+P378-P403+P233
Purity:
>98% (HPLC)
Signal word:
Warning
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-]
Solubility Chemicals:
Soluble in DMSO or methanol.
Source / Host:
Synthetic
Transportation:
Excepted Quantity
UN Nummer:
UN1479
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

Documents

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)