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173738

Sigma-Aldrich

3,3′-Diethylthiacarbocyaniniodid

Dye content 95 %

Synonym(e):

3-Ethyl-2-(3-[3-ethyl-2(3H)benzothiazolyliden]-1-propenyl)-benzothiazoliumiodid, DiSC2(3)

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About This Item

Empirische Formel (Hill-System):
C21H21IN2S2
CAS-Nummer:
905-97-5
Molekulargewicht:
492.44
Beilstein:
4117818
MDL-Nummer:
MFCD00011956
UNSPSC-Code:
12352103
PubChem Substanz-ID:
57647646
NACRES:
NA.23

Form

solid

Qualitätsniveau

100

Zusammensetzung

Dye content, 95%

mp (Schmelzpunkt)

268-270 °C (dec.) (lit.)

λmax

560 nm

SMILES String

[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

InChIKey

VZBILKJHDPEENF-UHFFFAOYSA-M

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Allgemeine Beschreibung

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.

Anwendung

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.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKBT8856V
02231TX
03005MO

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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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