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4,5-METHYLENEDITHIO-1,3-DITHIOLE-2-THIONE, also known as MDDT, is a chemical compound derived from dithiolethiones, which are known for their potential health benefits. It possesses antioxidant and anti-inflammatory properties, making it a promising candidate for the treatment of various diseases and conditions. MDDT has shown promise in protecting cells from oxidative stress and reducing inflammation. However, research on MDDT is ongoing, and further studies are needed to fully understand its potential uses and benefits.

70800-59-8

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70800-59-8 Usage

Uses

Used in Pharmaceutical Industry:
4,5-METHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as a potential therapeutic agent for various diseases and conditions due to its antioxidant and anti-inflammatory properties. It is being studied for its potential to protect cells from oxidative stress and reduce inflammation, which could be beneficial in the treatment of various health issues.
Used in Cosmetics Industry:
4,5-METHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as an ingredient in cosmetics for its potential antioxidant and anti-inflammatory properties. It may help protect the skin from oxidative stress and reduce inflammation, contributing to healthier and more youthful-looking skin.
Used in Food Industry:
4,5-METHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as a food additive for its potential antioxidant properties. It may help protect food products from oxidation, extending their shelf life and maintaining their quality.
Used in Research:
4,5-METHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as a research compound to study its potential health benefits and applications. Ongoing research aims to fully understand its potential uses and benefits, as well as its mechanisms of action in protecting cells from oxidative stress and reducing inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 70800-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,0 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70800-59:
(7*7)+(6*0)+(5*8)+(4*0)+(3*0)+(2*5)+(1*9)=108
108 % 10 = 8
So 70800-59-8 is a valid CAS Registry Number.

70800-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Methylenedithio-1,3-dithiole-2-thione

1.2 Other means of identification

Product number -
Other names [1,3]dithiolo[4,5-d][1,3]dithiole-5-thione

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:70800-59-8 SDS

70800-59-8Relevant academic research and scientific papers

TWO-DIMENSIONAL CHARACTER OF CRYSTAL STRUCTURE OF ORGANIC CONDUCTOR, (BMDT-TTF)3PF6(1,2-DICHLOROETHANE)

Kato, Reizo,Kobayashi, Akiko,Sasaki, Yukiyoshi,Kobayashi, Hayao

, p. 993 - 996 (1984)

In the crystal of (BMDT-TTf)3PF6(1,2-dichloroethane) (BMDT-TTF=bis(methylenedithio)-tetrathiafulvalene), there are two crystallographically independent BMDT-TTf molecules whose molecular planes are approximately perpendicular to each other.This new type of molecular arrangement achieves the two-dimensional S...S network.

Organic compound crystal and field-effect transistor

-

Page/Page column 12-14, (2008/12/08)

A field-effect transistor includes a channel-forming region composed of an organic compound crystal including π-electron conjugated molecules each containing chalcogen atoms as a constituent, wherein the distance between chalcogen atoms of adjacent π-elec

Synthesis, crystal structure and electrochemical properties of [NBu4][Ni(mdt)2]: A potential precursor for new materials (mdt = 1,3-dithiole-4,5-dithiolate)

Veldhuizen, Yvonne S. J.,Veldman, Nora,Spek, Anthony L.,Cassoux, Patrick,Carlier, Roger,Mulder, Martijn J. J.,Haasnoot, Jaap G.,Reedijk, Jan

, p. 2989 - 2993 (2007/10/03)

Reaction of methylenedithio-1,3-dithiol-2-one with sodium methanolate resulted in the anionic ligand mdt2- (mdt = 1,3-dithiole-4,5-dithiolate) which has been co-ordinated to nickel. The salt [NBu4][Ni(mdt)2] was successfully crystallised and its crystal structure showed that the Ni(mdt)2 unit is significantly distorted from planarity. Electrochemical studies showed that [NBu4][Ni(mdt)2] can be further oxidised in two steps via the neutral [Ni(mdt)2] complex to a partially oxidised positively charged complex. The neutral complex has also been successfully synthesized by oxidation with TCNQ. The redox potential of the oxidation from the neutral to the partially oxidised positive Ni(mdt)2 complex is relatively low, +0.60 V, making this compound a promising precursor for the preparation of conducting materials, based on derived cation radical salts.

New Tetrathiafulvalene Donors with Extended Peripheral Substituents by Addition of Heterocycles: Synthesis, Properties, and Molecular Structures

Yamada, Jun-Ichi,Tanaka, Satoru,Segawa, Junko,Hamasaki, Miho,Hagiya, Kenji,Anzai, Hiroyuki,Nishikawa, Hiroyuki,Ikemoto, Isao,Kikuchi, Koichi

, p. 3952 - 3960 (2007/10/03)

Syntheses of the bis(heterocycle)-fused bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) derivatives 7 and 8, the heterocycle-fused BEDT-TTF, methylenedithio(ethylenedithio)tetrathiafulvalene (MET), and ethylenedithiotetrathiafulvalene derivatives 9-11, and the 1,3-dioxolane derivative of MET 12a and its analogues 12b-d are described. The heterocycle-fused ketones 17 and 19 with cis ring fusions could be prepared by the BF3-promoted reaction of tin dithiolate 13 with dihaloheterocycles 15 and 16 in good yields, respectively, and served as key intermediates for the (RO)3P- and/or Me3Al-promoted coupling syntheses of these new tetrathiafulvalene donors 7-12. Further, the electrochemical properties of new donors 8-12 by the use of cyclic voltammetry and the molecular structures of 9a, 10a, 11, and 12a by X-ray crystallographic analyses are also reported.

1,3-Dithiol-4,5-dithiolate and 5,6-Dihydro-1,4-diselenin-2,3-dithiolate Nickel Complexes

Abramov,Petrov

, p. 1635 - 1640 (2007/10/03)

With the goal of obtaining new ethylenedithiolate transition metals complexes, unstable tetrabutylammonium bis(1,3-dithiol-4,5-dithiolato)niccolate(III) and stable tetrabutylammonium bis(5,6-dihydro-1,4-diselenin-2,3-dithiolato)niccolate(III) were synthesized. The two complexes were characterized by elemental analysis and IR and electron absorption spectroscopy, and the second, also by voltammetry. A new convenient procedure was proposed for preparation of 1,3-dithiol-2-thione which is a key initial compound in the synthesis of the title complexes.

The Vinylogue of Bis-4,5-methylenedithiotetrathiafulvalene: A New Electron Donor

Hansen, Thomas Kruse,Lakshmikantham, M. V.,Cava, Michel P.,Becher, Jan

, p. 2873 - 2876 (2007/10/02)

A new electron donor vinylogue-BMDT-TTF 5 has been synthesized (overall yield from 8 16 percent).The compound represents a structural modification of the molecular frameword that has led to highly conducting, even superconducting, organic charge transfer (CT) complexes.Like other tetrathiafulvalene (TTF)-based donors 5 undergoes a reversible two-electron oxidation as shown by cyclic voltammetry.

TRANSITION-METAL 1,2-DIHETEROLENES AND POLYHETEROTETRAHETERAFULVALENES: PRECURSORS OF CONDUCTING SOLIDS

Papavassiliou, G. C.,Kakoussis, V. C.,Lagouvardos, D. J.,Mousdis, G. A.

, p. 171 - 184 (2007/10/02)

Methods for synthesis and properties of oxygen-, sulfur-, selenium-, and nitrogen-containing transition-metal 1,2-diheterolenes and polyheterotetraheterafulvalenes are described.Also, the preparation and properties of some conducting salts based on these compounds are briefly discussed.

NEW MOLECULAR CONDUCTORS: VARIATION ON THE BEDTTTF SKELETON

Laversanne, R.,Dupart, E.,Delhaes, P.

, p. 179 - 190 (2007/10/02)

New organic conductors obtained by modification of the BEDTTTF molecule are presented.The synthesis of these compounds is detailed and some physical properties are given.

THE STUDY OF CHARGE TRANSFER COMPLEXES OF BEDT-TTF DERIVATIVES

Saito, Gunzi,Hayashi, Hitoshi,Enoki, Toshiaki,Inokuchi, Hiroo

, p. 341 - 344 (2007/10/02)

We have synthesized BEDT-TTF derivatives, which include eight sulfur atoms per molecule, and prepared several charge transfer (CT) complexes with TCNQs, p-quinones, and TCNEs in order to clarify the steric effect of substituents, R.Some of the CT complexes revealed high conductivities.

Tetrathiafulvalenes. XIX. Synthesis and Properties of Electron Conducting Poly-Dithiolene Complexes with Ethylene Tetrathiolat and Tetrathiafulvalene Tetrathiolat as Bridge Ligands

Poleschner, H.,John, W.,Hoppe, F.,Fanghaenel, E.

, p. 957 - 975 (2007/10/02)

-Dithiolo-1,3-dithiol-2,5-dione 7 and 5-(5-oxo-dithiolo-1,3-dithiole-2-ylidene)-dithiolo-1,3-dithiol-2-one 8 were synthesized from 1,3-dithiole-2-thione-4,5-dithiolat.The ligands react with salts of iron, cobalt, nickel

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