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Merck
CN

173738

3,3′-Diethylthiacarbocyanine iodide

Dye content 95 %

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C21H21IN2S2
CAS Number:
Molecular Weight:
492.44
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4117818
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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

SMILES string

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

InChI key

VZBILKJHDPEENF-UHFFFAOYSA-M

form

solid

composition

Dye content, 95%

mp

268-270 °C (dec.) (lit.)

λmax

560 nm

Quality Level

General description

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.

Application

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.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Phosphorescent sensitized fluorescent solid-state near-infrared light-emitting electrochemical cells.
Ho C, et al.
Physical Chemistry Chemical Physics, 13(39), 17729-17736 (2011)
Reconfigurable solid-state dye-doped polymer ring resonator lasers.
Chandrahalim H and Fan X
Scientific reports, 5(13), 18310-18310 (2015)
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
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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