Chemodex

1,1'-Dimethyl-3,3,3',3'-tetramethyl indocarbocyanine iodide

Product Code:
 
CDX-D1024
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
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Chemical Structure

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CDX-D1024-M05050 mg£116.00
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CDX-D1024-M100100 mg£191.00
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CDX-D1024-M250250 mg£371.00
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This product comes from: Switzerland.
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  • Further Information
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Further Information

Appearance:
Dark purple solid.
CAS:
25470-94-4
Description:
DiIC1(3) is a fluorescent carbocyanine dye used mainly for assessing membrane potential in mitochondria and plasma membranes, especially in flow cytometry and fluorescence microscopy. DiIC1(3) has short alkyl chains (methyl groups), so it diffuses more easily but is less stably anchored in membranes than longer-chain versions like DiIC12(3) or DiIC18(3). It is ideal for dynamic membrane potential assessments, not long-term labeling. The dye can be used as a non-reactive fluorophore, for control experiments and for calibration. Spectral Data: Excitation max: ~ 555nm, Emission max: ~570nm (accord. Lit).
EClass:
32160000
Form:
solid
GHS Symbol:
GHS07
Handling Advice:
Keep under inert gas. Protect from light and oxygen.
Hazards:
H315-H319-H335
InChi:
InChI=1S/C25H29N2.HI/c1-24(2)18-12-7-9-14-20(18)26(5)22(24)16-11-17-23-25(3,4)19-13-8-10-15-21(19)27(23)6;/h7-17H,1-6H3;1H/q+1;/p-1
InChiKey:
ZGBJQZCIUVDAHE-UHFFFAOYSA-M
MDL:
MFCD10001220
Molecular Formula:
C25H29N2 . I
Molecular Weight:
484.43
Package Type:
Vial
Precautions:
P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
CN1C=2C(C(C)(C)C1=CC=CC=3C(C)(C)C=4C([N+]3C)=CC=CC4)=CC=CC2.[I-]
Solubility Chemicals:
Soluble in DMSO.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

Documents

References

(1) P.M.W. French & J.R. Taylor; Opt. Lett. 11, 297 (1986) | (2) H. Sato, et al.; J. Raman Spectr. 19, 129 (1988) | (3) A.S. Tatikolov, et al.; Chem. Phys. Lett. 190, 291 (1992) | (4) Z.-H. Peng, et al.; J. Mater. Chem. 6, 559 (1996) | (5) A.L. Mikheikin, et al.; J. Biomol. Struct. Dyn. 18, 59 (2000) | (6) H.M. Shapiro; Cytometry 43, 223 (2001) | (7) M. Matsui, et al.; Tetrahedr. 71, 3528 (2015)