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173738

Sigma-Aldrich

3,3′-Diethylthiacarbocyanine iodide

Dye content 95 %

Sinonimo/i:

3-Ethyl-2-(3-[3-ethyl-2(3H)benzothiazolylidene]-1-propenyl)benzothiazolium iodide, DiSC2(3)

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About This Item

Formula empirica (notazione di Hill):
C21H21IN2S2
Numero CAS:
905-97-5
Peso molecolare:
492.44
Beilstein:
4117818
Numero MDL:
MFCD00011956
Codice UNSPSC:
12352103
ID PubChem:
57647646
NACRES:
NA.23

Stato

solid

Composizione

Dye content, 95%

Punto di fusione

268-270 °C (dec.) (lit.)

λmax

560 nm

Stringa SMILE

[I-].CCN1\C(Sc2ccccc12)=C\C=C\c3sc4ccccc4[n+]3CC

InChI

1S/C21H21N2S2.HI/c1-3-22-16-10-5-7-12-18(16)24-20(22)14-9-15-21-23(4-2)17-11-6-8-13-19(17)25-21;/h5-15H,3-4H2,1-2H3;1H/q+1;/p-1
VZBILKJHDPEENF-UHFFFAOYSA-M

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Descrizione generale

3,3′-Diethylthiacarbocyanine iodide (DTCI) is a cyanine dye, which acts as a donor in the electrochemical system. It can be used in the development of electrochemical cells.

Applicazioni

DTCI may be incorporated as a layer on gold nanorods, which can be used in surface enhanced resonance Raman spectroscopy (SERRS). It may be coated on a fused silica wafer, which can potentially be used in the development of solid state dye doped polymeric laser.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKBT8856V
03005MO
02231TX

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Controlled side-by-side assembly of gold nanorods and dye molecules into polymer-wrapped SERRS-active clusters.
McLintock A, et al.
Chemical Communications (Cambridge, England), 47(13), 3757-3759 (2011)
Alexander J Thompson et al.
The journal of physical chemistry. B, 119(32), 10170-10179 (2015-07-21)
Changes in microscopic viscosity represent an important characteristic of structural transitions in soft matter systems. Here we demonstrate the use of molecular rotors to explore the changes in microrheology accompanying the transition of proteins from their soluble states into a
Complex formation between 3; 3'-diethylthiacarbocyanine iodide and DNA and its investigation in aqueous solution
Anikovsky, M. Y., Tatikolov, A. S., & Kuzmin, V. A.
International Journal of Photoenergy, 1(1), 35-39 (1999)
M Giovanna Leonardi et al.
The Journal of membrane biology, 214(3), 157-164 (2007-06-15)
The pore-forming activity of Cry1Ab, Cry1Fa and Cry1Ca toxins and their interaction with leucine transport mediated by the K(+)/leucine cotransporter were studied in brush border membrane vesicles (BBMVs) isolated from the midgut of Ostrinia nubilalis and Sesamia nonagrioides. In both
Kristen C Hannah et al.
Biochemistry, 44(48), 15924-15929 (2005-11-30)
A symmetrical cyanine dye was previously shown to bind as a cofacial dimer to alternating A-T sequences of duplex DNA. Indirect evidence suggested that dimerization of the dye occurred in the minor groove. 1H NMR experiments reported here verify this
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