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About This Item
Empirical Formula (Hill Notation):
C3H6N2S
CAS Number:
Molecular Weight:
102.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-506-9
Beilstein/REAXYS Number:
106275
MDL number:
Assay:
98%
Quality Level
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
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.
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signalword
Danger
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
target_organs
Thyroid
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Repr. 1B - STOT RE 1
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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)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| I504-100G | 04061833857083 |
| I504-1KG | 04061826738832 |

