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173738

Sigma-Aldrich

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:
905-97-5
Molecular Weight:
492.44
Beilstein/REAXYS Number:
4117818
MDL number:
MFCD00011956
UNSPSC Code:
12352103
PubChem Substance ID:
57647646
NACRES:
NA.23

form

solid

Quality Level

100

composition

Dye content, 95%

mp

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

InChI key

VZBILKJHDPEENF-UHFFFAOYSA-M

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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
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBT8856V
03005MO
02231TX

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