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139432

Sigma-Aldrich

1,3,4-Thiadiazole-2,5-dithiol dipotassium salt

98%

Synonym(s):

Bismuthiol I dipotassium salt, 2,5-Dimercapto-1,3,4-thiadiazole dipotassium salt, Bismuththiol I dipotassium salt

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About This Item

Empirical Formula (Hill Notation):
C2K2N2S3
CAS Number:
4628-94-8
Molecular Weight:
226.43
Beilstein:
4917786
EC Number:
225-043-4
MDL number:
MFCD00003104
UNSPSC Code:
12352100
PubChem Substance ID:
24848411
NACRES:
NA.22

Assay

98%

mp

274-276 °C (dec.) (lit.)

SMILES string

[K]Sc1nnc(S[K])s1

InChI

1S/C2H2N2S3.2K/c5-1-3-4-2(6)7-1;;/h(H,3,5)(H,4,6);;/q;2*+1/p-2

InChI key

GPWLFGDMYSVEGN-UHFFFAOYSA-L

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General description

1,3,4-thiadiazole-2,5-dithiol undergoes copolymerization with 1+, 2+ and 3+ valent metals to form coordination polymers. It forms polymers with metals and can be useful in treatment of metal-polluted water.

Application

1,3,4-thiadiazole-2,5-dithiol (Bismuthiol I) was used in determination of tellurium in indium phosphide doped with cadmium telluride by electrothermal atomic absorption spectrometry.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Coordination polymers from 1, 3, 4-thiadiazole-2, 5-dithiol and metal ions.
Ortega P, etal.
Macromolecular Chemistry and Physics, 198(9), 2949-2956 (1997)
Determination of tellurium in indium phosphide by electrothermal atomic absorption spectrometry and ultraviolet-visible spectrophotometry.
Taddia M, et al.
Journal of Analytical Atomic Spectrometry, 10(6), 433-437 (1995)
Synthesis of metallic azoderivatives of 2-amino-5-mercapto-1, 3, 4-thiadiazole.
Ortega-Luoni P, et al.
Journal of the Chilean Chemical Society, 52(1), 1120-1122 (2007)
Yingchun Fu et al.
The journal of physical chemistry. B, 113(5), 1332-1340 (2009-01-14)
A novel and high-performance biosensing platform was prepared on the basis of one-pot biochemical preoxidation and electropolymerization of monomer (BPEM) for high-load and high-activity immobilization of enzymes. As representative materials here, 2,5-dimercapto-1,3,4-thiadiazole (DMcT) was used as the monomer, glucose oxidase
Yingchun Fu et al.
Analytical chemistry, 83(17), 6511-6517 (2011-07-26)
We report on the exploitation of metal-organic coordination polymers (MOCPs) as new and efficient matrixes to immobilize enzymes for amperometric biosensing of glucose or phenols. A ligand, 2,5-dimercapto-1,3,4-thiadiazole (DMcT), two metallic salts, NaAuCl(4) and Na(2)PtCl(6), and two enzymes, glucose oxidase
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