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Merck

D188700

N,N′-Dimethylthiourea

99%

Sinónimos:

1,3-Dimethyl-2-thiourea, 1,3-Dimethylisothiourea, Dimethylthiocarbamide

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Acerca de este artículo

Fórmula lineal:
CH3NHCSNHCH3
Número CAS:
Peso molecular:
104.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-588-2
Beilstein/REAXYS Number:
605454
MDL number:
Assay:
99%
Form:
crystals
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InChI

1S/C3H8N2S/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6)

InChI key

VLCDUOXHFNUCKK-UHFFFAOYSA-N

SMILES string

CNC(=S)NC

assay

99%

form

crystals

Quality Level

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General description

N,N′-Dimethylthiourea, also known as 1,3-Dimethylisothiourea, is commonly used in organic reactions to synthesize N-containing compounds such as N-acyl-substituted 1,1-diaminoethylenes, amidines, ureas, and thioureas. It also acts as a nucleophilic catalyst in the bromination of alcohols using N-bromosuccinimide (NBS), during the conversion to the corresponding bromides.

Application

  • Pharmaceutical Analysis: Mao et al. developed an itaconic acid-based organic-polymer monolithic column for hydrophilic capillary electrochromatography, which was used in pharmaceutical analysis. N,N′-Dimethylthiourea could be utilized to improve the column′s performance by acting as a potential organic modifier to enhance the separation processes (Mao et al., 2024).
  • Agricultural Research: Li et al. examined the effect of the reactive oxygen scavenger N,N′-Dimethylthiourea on seed germination and radicle elongation of maize. This research could help in understanding how this chemical can be used to influence plant growth under stress conditions, potentially improving agricultural productivity (Li et al., 2023).

pictograms

Exclamation mark

signalword

Warning

hcodes

pcodes

Hazard Classifications

Skin Sens. 1

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Crystal structure of the 1: 2 adduct of bis (piperidinium) sulfate and 1, 3-dimethylthiourea
Cindy D, et al.
Acta Crystallographica Section E: Crystallographic Communications, 73, 651-653 (2017)
Thiourea-mediated halogenation of alcohols
Amar M R, et al.
The Journal of Organic Chemistry, 85, 12901-12911 (2020)
Synthesis, Characterization, and Reactivity of N-Acyl Chloroformamidines: Useful Building Blocks for the Construction of N-Acyl-Substituted 1, 1-Diaminoethylenes, Amidines, Ureas, and Thioureas
Yang W, et al.
Synthesis, 45, 347-354 (2013)
Watcharaporn Hoisang et al.
Nanomaterials (Basel, Switzerland), 9(12) (2019-12-15)
Highly luminescent silver indium sulfide (AgInS2) nanoparticles were synthesized by dropwise injection of a sulfur precursor solution into a cationic metal precursor solution. The two-step reaction including the formation of silver sulfide (Ag2S) nanoparticles as an intermediate and their conversion
Emily E Chea et al.
Biophysical journal, 118(1), 128-137 (2019-12-08)
Cytochrome c (cyt c) is known for its role in the electron transport chain but transitions to a peroxidase-active state upon exposure to oxidative species. The peroxidase activity ultimately results in the release of cyt c into the cytosol for

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