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Bismuththiol
[CAS# 1072-71-5]

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Complete supplier list of Bismuththiol
Identification
Classification API >> Antibiotics >> Other antibiotics
Name Bismuththiol
Synonyms 1,3,4-Thiadiazole-2,5-dithiol; 2,5-Dimercapto-1,3,4-thiadiazole; DMTD
Molecular Structure CAS # 1072-71-5, Bismuththiol, 1,3,4-Thiadiazole-2,5-dithiol, 2,5-Dimercapto-1,3,4-thiadiazole, DMTD
Molecular Formula C2H2N2S3
Molecular Weight 150.23
CAS Registry Number 1072-71-5
EC Number 214-014-1
SMILES C1(=S)NNC(=S)S1
Properties
Water solubility 20 g/L (20 ºC)
Density 1.7±0.1 g/cm3, Calc.*
Melting point 162 ºC (Expl.)
Index of Refraction 1.757, Calc.*
Boiling Point 259.6±23.0 ºC (760 mmHg), Calc.*
Flash Point 110.8±22.6 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol   GHS05;GHS07 Danger    Details
Hazard Statements H302-H318-H319-H412    Details
Precautionary Statements P264-P264+P265-P270-P273-P280-P301+P317-P305+P351+P338-P305+P354+P338-P317-P330-P337+P317-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Serious eye damageEye Dam.1H318
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Specific target organ toxicity - single exposureSTOT SE3H335
SDS Available
up Discovory and Applicatios
Bismuththiol compounds represent a class of coordination complexes where bismuth is bound to thiol (sulfhydryl) groups. The discovery of these complexes can be traced back to early studies in coordination chemistry and medicinal chemistry. Bismuth compounds have historically been used for their antimicrobial properties, and the introduction of thiol ligands was a significant step in enhancing these properties and understanding the coordination behavior of bismuth with sulfur-containing ligands. The unique bonding between bismuth and sulfur in these complexes gives rise to distinctive chemical and biological properties.

The synthesis of bismuththiol complexes generally involves the reaction of bismuth salts, such as bismuth nitrate or bismuth chloride, with thiol-containing ligands. Common thiols used include cysteine, mercaptoacetic acid, and other organosulfur compounds. These reactions typically occur in aqueous or organic solvents under mild conditions, yielding stable complexes. The resulting bismuththiol complexes exhibit various coordination geometries, which can be characterized using spectroscopic methods such as infrared (IR) spectroscopy, nuclear magnetic resonance (NMR), and X-ray crystallography.

Bismuththiol complexes have found applications in both medicinal and materials chemistry. In medicine, these compounds are investigated for their antimicrobial, antiparasitic, and anti-ulcer properties. For example, bismuththiol compounds show activity against Helicobacter pylori, the bacteria responsible for gastric ulcers. The thiol ligands help improve the solubility and bioavailability of bismuth, enhancing its therapeutic effects. Additionally, these complexes exhibit low toxicity compared to other heavy metal-based drugs, making them suitable for medical applications.

In materials science, bismuththiol complexes are used to produce thin films and nanoparticles for electronic and optical applications. The sulfur atoms provide a means to form strong bonds with metal surfaces, making these complexes useful as stabilizers or linkers in nanotechnology. Researchers are exploring their potential in developing new catalysts and semiconductors due to the unique electronic properties imparted by the bismuth-sulfur interaction. The versatility of bismuththiol compounds continues to drive research into new applications and synthesis methods.
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