358916

Sigma-Aldrich

Vinylene trithiocarbonate

98%

Synonym(s):
1,3-Dithiole-2-thione
Empirical Formula (Hill Notation):
C3H2S3
CAS Number:
Molecular Weight:
134.24
Beilstein/REAXYS Number:
105686
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

mp

48-50 °C (lit.)

SMILES string

S=C1SC=CS1

InChI

1S/C3H2S3/c4-3-5-1-2-6-3/h1-2H

InChI key

WYKJWNVWJOKVQP-UHFFFAOYSA-N

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General description

Vinylene trithiocarbonate has been investigated as electrolyte additive for use in lithium ion batteries.

Application

Vinylene trithiocarbonate may be used in the synthesis of series of symmetrical 1,3-dithiole-2-thiones and -ones. It is suitable for use as substrate to investigate the omega class glutathione S-transferase enzymatic activity.

Packaging

1, 5 g in glass bottle

storage_class_code

13 - Non Combustible Solids

WGK Germany

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

Javier Girardini et al.
European journal of biochemistry, 269(22), 5512-5521 (2002-11-09)
Glutathione S-transferases (EC 2.5.1.18) (GSTs), are a family of multifunctional enzymes present in all living organisms whose main function is the detoxification of electrophilic compounds. GSTs are considered the most prominent detoxifying class II enzymes in helminths. We describe here...
A combined substituent and supramolecular approach for improving the electron donor properties of 1, 3-dithiole-2-thione derivatives.
Khan T, et al.
Journal of Materials Chemistry, 13(10), 2490-2498 (2003)
Vinylene carbonate and vinylene trithiocarbonate as electrolyte additives for lithium ion battery.
Chang C-C, et al.
Journal of Power Sources, 196(22), 9605-9611 (2011)

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