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13461-16-0

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13461-16-0 Usage

Description

N,N-dimethylethylenethiourea (DMTU) is a chemical compound that serves as a rubber vulcanization accelerator and antioxidant in the rubber industry, enhancing the durability and heat resistance of rubber materials. It also exhibits applications in the production of agrochemicals and metalworking fluids, and due to its strong inhibitory effect on nitric oxide synthase, it holds potential as a therapeutic agent for treating nitric oxide-related conditions.

Uses

Used in Rubber Industry:
NNDIMETHYLETHYLENETHIOUREA is used as a rubber vulcanization accelerator and antioxidant for improving the durability and heat resistance of natural and synthetic rubbers.
Used in Agrochemical Production:
NNDIMETHYLETHYLENETHIOUREA is used as an ingredient in the production of herbicides, fungicides, and pesticides, contributing to the effectiveness of these products in controlling plant diseases and pests.
Used in Metalworking Fluids:
NNDIMETHYLETHYLENETHIOUREA is used in the formulation of metalworking fluids to enhance their performance and protect metal surfaces during manufacturing processes.
Used in Pharmaceutical Applications:
NNDIMETHYLETHYLENETHIOUREA is used as a potential therapeutic agent for treating conditions related to nitric oxide imbalance, such as cardiovascular and neurological diseases, due to its strong inhibitory effect on nitric oxide synthase.
It is crucial to handle NNDIMETHYLETHYLENETHIOUREA with care due to its toxic and hazardous nature, ensuring safety in its applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13461-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,6 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13461-16:
(7*1)+(6*3)+(5*4)+(4*6)+(3*1)+(2*1)+(1*6)=80
80 % 10 = 0
So 13461-16-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2S/c1-6-3-4-7(2)5(6)8/h3-4H2,1-2H3

13461-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethylimidazolidine-2-thione

1.2 Other means of identification

Product number -
Other names 1,3-Dimethyl-2-imidazolidinethione

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:13461-16-0 SDS

13461-16-0Relevant articles and documents

Metal-Free C?H Borylation of N-Heteroarenes by Boron Trifluoride

Iashin, Vladimir,Berta, Dénes,Chernichenko, Konstantin,Nieger, Martin,Moslova, Karina,Pápai, Imre,Repo, Timo

supporting information, p. 13873 - 13879 (2020/10/02)

Organoboron compounds are essential reagents in modern C?C coupling reactions. Their synthesis via catalytic C?H borylation by main group elements is emerging as a powerful tool alternative to transition metal based catalysis. Herein, a straightforward metal-free synthesis of aryldifluoroboranes from BF3 and heteroarenes is reported. The reaction is assisted by sterically hindered amines and catalytic amounts of thioureas. According to computational studies the reaction proceeds via frustrated Lewis pair (FLP) mechanism. The obtained aryldifluoroboranes are further stabilized against destructive protodeborylation by converting them to the corresponding air stable tetramethylammonium organotrifluoroborates.

Precursor reaction kinetics control compositional grading and size of CdSe1-: XSx nanocrystal heterostructures

Hamachi, Leslie S.,Yang, Haoran,Jen-La Plante, Ilan,Saenz, Natalie,Qian, Kevin,Campos, Michael P.,Cleveland, Gregory T.,Rreza, Iva,Oza, Aisha,Walravens, Willem,Chan, Emory M.,Hens, Zeger,Crowther, Andrew C.,Owen, Jonathan S.

, p. 6539 - 6552 (2019/07/10)

We report a method to control the composition and microstructure of CdSe1-xSx nanocrystals by the simultaneous injection of sulfide and selenide precursors into a solution of cadmium oleate and oleic acid at 240 °C. Pairs of substituted thio- and selenoureas were selected from a library of compounds with conversion reaction reactivity exponents (kE) spanning 1.3 × 10-5 s-1 to 2.0 × 10-1 s-1. Depending on the relative reactivity (kSe/kS), core/shell and alloyed architectures were obtained. Growth of a thick outer CdS shell using a syringe pump method provides gram quantities of brightly photoluminescent quantum dots (PLQY = 67 to 90%) in a single reaction vessel. Kinetics simulations predict that relative precursor reactivity ratios of less than 10 result in alloyed compositions, while larger reactivity differences lead to abrupt interfaces. CdSe1-xSx alloys (kSe/kS = 2.4) display two longitudinal optical phonon modes with composition dependent frequencies characteristic of the alloy microstructure. When one precursor is more reactive than the other, its conversion reactivity and mole fraction control the number of nuclei, the final nanocrystal size at full conversion, and the elemental composition. The utility of controlled reactivity for adjusting alloy microstructure is discussed.

Synthesis, spectroscopic characterization and in vitro anticancer activity of new platinum(II) complexes with some thione ligands?in the presence of triethylphosphine

Jomaa, Mohammed Yagoub,Altaf, Muhammed,Ahmad, Saeed,Bhatia, Gaurav,Singh, Jatinder,Altuwaijri, Saleh,Isab, Anvarhusein A.

, p. 787 - 795 (2017/10/13)

Seven new platinum(II) complexes (1–7) of triethylphosphine (Et3P) and thiones (L) with general formula, cis-[Pt(Et3P)2(L)2]Cl2 were prepared and characterized by elemental analysis, FTIR and NMR (1H, 13C & 31P) measurements. The analytical and spectroscopic data suggested the formation of the desired complexes. The complexes were tested for in vitro cytotoxicity against four cell lines: Hela (human cervical adenocarcinoma), MCF-7 (human breast carcinoma), A549 (human lung carcinoma), and HTC15 (human colon carcinoma). The anticancer activity values of compounds 1–6 are much better than cisplatin and carboplatin as indicated by their IC50 values.

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