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Merck
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주요 문서

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173738

Sigma-Aldrich

3,3′-Diethylthiacarbocyanine iodide

Dye content 95 %

동의어(들):

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

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C21H21IN2S2
CAS Number:
905-97-5
Molecular Weight:
492.44
Beilstein:
4117818
MDL number:
MFCD00011956
UNSPSC 코드:
12352103
PubChem Substance ID:
57647646
NACRES:
NA.23

양식

solid

구성

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

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.

애플리케이션

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.

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319,H335

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKBT8856V
03005MO
02231TX

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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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