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SARCOSINE-N-DITHIOCARBAMATE, also known as SDC, is a versatile chemical compound belonging to the dithiocarbamate family. It is recognized for its metal chelation capabilities and robust antioxidant properties. SDC demonstrates potential therapeutic benefits across a spectrum of diseases, including cancer, neurodegenerative disorders, and cardiovascular conditions. Its antifungal and antimicrobial attributes further enhance its value in the development of pharmaceuticals and agricultural products. SDC emerges as a multifunctional compound with a broad range of applications in medicine, biotechnology, and agriculture.

40520-03-4

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40520-03-4 Usage

Uses

Used in Pharmaceutical Development:
SARCOSINE-N-DITHIOCARBAMATE is used as a therapeutic agent for its potential benefits in treating various diseases such as cancer, neurodegenerative disorders, and cardiovascular diseases. Its metal chelation and antioxidant properties contribute to its efficacy in these applications.
Used in Antifungal and Antimicrobial Applications:
SARCOSINE-N-DITHIOCARBAMATE is used as an antifungal and antimicrobial agent due to its studied properties, which make it a valuable component in the development of new pharmaceuticals aimed at combating fungal and microbial infections.
Used in Agricultural Products:
SARCOSINE-N-DITHIOCARBAMATE is used as a component in agricultural products for its antifungal and antimicrobial properties, potentially enhancing crop protection and yield.
Used in Biotechnology Research:
SARCOSINE-N-DITHIOCARBAMATE is used as a research tool in biotechnology for its metal chelation and antioxidant capabilities, facilitating studies in various biological and medical fields.
Each application leverages the unique properties of SARCOSINE-N-DITHIOCARBAMATE, highlighting its multifaceted utility in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 40520-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,2 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40520-03:
(7*4)+(6*0)+(5*5)+(4*2)+(3*0)+(2*0)+(1*3)=64
64 % 10 = 4
So 40520-03-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO2S2/c1-5(4(8)9)2-3(6)7/h2H2,1H3,(H,6,7)(H,8,9)

40520-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name SARCOSINE-N-DITHIOCARBAMATE

1.2 Other means of identification

Product number -
Other names N-Dithiocarboxy-sarkosin

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:40520-03-4 SDS

40520-03-4Downstream Products

40520-03-4Relevant academic research and scientific papers

Nitric oxide switches on the photoluminescence of molecularly engineered quantum dots

Wang, Suhua,Han, Ming-Yong,Huang, Dejian

, p. 11692 - 11694 (2009)

(Figure Presented) The photoluminescence of nonfluorescent molecularly engineered quantum dots (QDs) with iron(III) dithiocarbamates was selectively switched on by nitric oxide. Such functional QDs consisted of CdSe-ZnS nanocrystals as fluorophores and surface bound tris(N-(dithiocarboxy) sarcosine)iron(III) as reactive centers for nitric oxide. The fluorescence of the QDs was quenched by energy transfer between the excited QD cores and the surface bound iron(III) dithiocarbamates due to their optical energy overlapping. Nitric oxide restored the fluorescence of the QDs through reduction of the surface bound iron(III) complexes to iron(I) -NO adducts and thus shutting down the energy transfer pathway. The fluorescence of the iron(III) complex engineered QDs was selectively and quantitatively restored by nitric oxide but not by other reactive oxygen species. Such a property of the functional QDs could be used for sensing nitric oxide based on the fluorescence "turn on" mechanism.

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