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I504

Sigma-Aldrich

2-Imidazolidinethione

98%

Synonym(s):

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

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100 G
$98.80
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$165.00

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100 G
$98.80
1 KG
$165.00

About This Item

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

$98.80

Available to ship onMay 01, 2025Details

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Quality Level

200

assay

98%

mp

196-200 °C (lit.)

SMILES string

S=C1NCCN1

InChI

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

InChI key

PDQAZBWRQCGBEV-UHFFFAOYSA-N

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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.[1]
  • 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.[2]
  • It is also used as a vulcanization accelerator in the preparation of styrene-butadiene rubber (SBR) and rubber composites.[3]

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Health hazardExclamation mark
GHS08,GHS07

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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_germany

WGK 3

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM6353
BCCL3262
BCCM1408
BCCL8788
BCCJ8091

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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)
A highly stretchable gel-polymer electrolyte for lithium-sulfur batteries.
Choudhury, Soumyadip et al.
Polymer, 112, 447-456 (2017)
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)
Eva Ekman et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 934, 53-59 (2013-07-31)
Ethylenethiourea (ETU) is of major toxicological concern, since in experimental animal studies, ETU has shown a large spectrum of adverse effects. High occupational exposure can be found among agricultural workers or during manufacturing of ethylenbisdithiocarbamates (EBDC). For the general public
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
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