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Merck
CN

I504

2-Imidazolidinethione

98%

Synonym(s):

2-Mercaptoimidazoline, 2-Thioxoimidazolidine, N,N′-Ethylenethiourea

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About This Item

Empirical Formula (Hill Notation):
C3H6N2S
CAS Number:
96-45-7
Molecular Weight:
102.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24895980
EC Number:
202-506-9
Beilstein/REAXYS Number:
106275
MDL number:
MFCD00005276

Key Documents

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Product Name

2-Imidazolidinethione, 98%

InChI key

PDQAZBWRQCGBEV-UHFFFAOYSA-N

InChI

1S/C3H6N2S/c6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)

SMILES string

S=C1NCCN1

assay

98%

mp

196-200 °C (lit.)

Quality Level

200

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Application

  • 2-Imidazolidinethione has been used as a source of nitrogen and sulfur in the preparation of heteroatom functionalized carbon dots with enhanced photoluminescence (PL) emissions.
  • It is a precursor for the synthesis of gel-polymer electrolyte based on cross-linked polyepichlorohydrin terpolymer (GECO), which can be used in lithium-sulfur batteries.
  • It is also used as a vulcanization accelerator in the preparation of styrene-butadiene rubber (SBR) and rubber composites.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Repr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN6545
BCCM6353
BCCL3262
BCCM1408
BCCL8788

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A method to improve the mechanical performance of styrene-butadiene rubber via vulcanization accelerator modified silica.
Zhong, Bangchao et al.
Composites Science and Technology, 117, 46-53 (2015)
A highly stretchable gel-polymer electrolyte for lithium-sulfur batteries.
Choudhury, Soumyadip et al.
Polymer, 112, 447-456 (2017)
Prominence of fusion temperature and engineering heteroatoms on multifarious emissive shifts in carbon dots.
Velusamy, Jayaramakrishnan et al.
Journal of Colloid and Interface Science, 528, 237-247 (2018)
Kate Jones et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 878(27), 2563-2566 (2009-11-17)
This study reports a sensitive analytical method suitable for the quantitative analysis of ethylenethiourea (ETU) in human urine and its application to samples from the general population. Sample preparation involved the use of diatomaceous earth extraction columns to remove matrix
F Ahmadi et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(1), 29-36 (2009-09-22)
The hydrogen-bonding interaction of 2-Imidazolidinethione with DNA and guanine has been investigated using UV/vis, circular dichroism, differential pulse voltammetry and ab initio chemical mechanic quantum procedures. The bonding constant of 2-Imidazolidinethione with DNA was measured by UV/vis spectroscopy and is
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