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3,3'-DIETHYL-9-METHYLTHIACARBOCYANINE IODIDE, also known as a thiacarbocyanine iodide, is a synthetic dye with a brown powder appearance. It is a type of fluorescent stain that is commonly used in research and scientific applications due to its unique chemical properties.

3065-79-0

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3065-79-0 Usage

Uses

Used in Research Applications:
3,3'-DIETHYL-9-METHYLTHIACARBOCYANINE IODIDE is used as a staining agent for research purposes. It is particularly useful in various microscopy techniques, such as fluorescence microscopy, where its fluorescent properties allow for the visualization and differentiation of cellular structures and components.
Used in Biomedical Research:
In the field of biomedical research, 3,3'-DIETHYL-9-METHYLTHIACARBOCYANINE IODIDE is used as a vital staining agent for live cell imaging. Its ability to stain cellular components without causing significant phototoxicity or cell damage makes it a valuable tool for studying cell morphology, dynamics, and interactions in real-time.
Used in Diagnostic Applications:
3,3'-DIETHYL-9-METHYLTHIACARBOCYANINE IODIDE is also employed in diagnostic applications, where its staining properties can help in the identification and differentiation of various cell types and structures. This can be particularly useful in the diagnosis of certain diseases and conditions, as well as in the assessment of treatment efficacy.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,3'-DIETHYL-9-METHYLTHIACARBOCYANINE IODIDE is used as a component in the development of new drugs and therapies. Its unique chemical properties and staining capabilities can aid in the identification and targeting of specific cellular structures, potentially leading to the development of more effective and targeted treatments for various diseases and conditions.
Used in Environmental Science:
3,3'-DIETHYL-9-METHYLTHIACARBOCYANINE IODIDE is also utilized in environmental science applications, where it can be employed as a tracer or marker to study the behavior and distribution of pollutants, nutrients, or other substances in various ecosystems. This can help in understanding the impact of human activities on the environment and in developing strategies for environmental protection and remediation.

Check Digit Verification of cas no

The CAS Registry Mumber 3065-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3065-79:
(6*3)+(5*0)+(4*6)+(3*5)+(2*7)+(1*9)=80
80 % 10 = 0
So 3065-79-0 is a valid CAS Registry Number.

3065-79-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H55144)  3,3'-Diethyl-9-methylthiacarbocyanine iodide, 98%   

  • 3065-79-0

  • 250mg

  • 750.0CNY

  • Detail
  • Alfa Aesar

  • (H55144)  3,3'-Diethyl-9-methylthiacarbocyanine iodide, 98%   

  • 3065-79-0

  • 1g

  • 2402.0CNY

  • Detail

3065-79-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z)-3-ethyl-2-[(E)-3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methylprop-2-enylidene]-1,3-benzothiazole,iodide

1.2 Other means of identification

Product number -
Other names Benzothiazolium,3-ethyl-2-(3-(3-ethyl-2-benzothiazolinylidene)-2-methyl-1-propenyl)-,iodide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3065-79-0 SDS

3065-79-0Relevant academic research and scientific papers

CONDENSATION OF VILSMEIER COMPLEXES WITH HETEROCYCLIC COMPOUNDS. SYNTHESIS OF CARBOCYANINES

Makin, S. M.,Pomogaev, A. I.

, p. 1916 - 1918 (2007/10/02)

Carbocyanine dyes are formed in the reaction of the quaternary salts of heterocyclic bases containing an active methyl group with the complexes of carboxamides and phosphorus oxychloride.A series of carbocyanines were synthesized, including those containing various substituents at the meso position of the trimethine chain.

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