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Zinc 2-mercaptobenzothiazole

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Identification
Molecular formula
C14H8N2S4Zn
CAS number
155-04-4
IUPAC name
zinc;1,3-benzothiazole-2-thiolate
State
State

At room temperature, zinc 2-mercaptobenzothiazole is typically in a solid state, presenting as a powder.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.15
General information
Molecular weight
316.85g/mol
Molar mass
316.8500g/mol
Density
1.7000g/cm3
Appearence

Zinc 2-mercaptobenzothiazole typically appears as a pale yellow or white powder. It is often used in its solid form in industrial applications.

Comment on solubility

Solubility of Zinc 1,3-Benzothiazole-2-Thiolate

Zinc 1,3-benzothiazole-2-thiolate is a complex compound that exhibits interesting solubility properties influenced by its structural components. Generally, solubility can depend on several factors such as temperature, pH, and the presence of other ions in the solution.

Key Factors Affecting Solubility

  • Polar Nature: The polar characteristics of the benzothiazole ring can facilitate solubility in polar solvents, though the thiol groups may introduce some hydrophobic behavior.
  • pH Sensitivity: The solubility may vary significantly with changes in pH, as the ionization of thiol functions can either enhance or reduce solubility.
  • Temperature: Increasing temperature typically enhances solubility for many compounds; however, this behavior should be experimentally verified for this specific compound.
  • Complex Formation: Zinc may form complexes with certain ligands, affecting its overall solubility in various environments.

In summary, while zinc compounds are generally known for their high solubility in aqueous solutions, the unique structure of 1,3-benzothiazole-2-thiolate suggests a nuanced solubility profile. For practical applications, it is advisable to test solubility under different conditions to determine the best solvent system. As researchers often say, "Solubility is the key to reactivity," and understanding the solubility of zinc 1,3-benzothiazole-2-thiolate is crucial for its utilization in various chemical processes.

Interesting facts

Interesting Facts about Zinc 1,3-Benzothiazole-2-Thiolate

Zinc 1,3-benzothiazole-2-thiolate, often noted for its unique features, is fascinating for several reasons:

  • Coordination Chemistry: This compound exhibits interesting coordination chemistry due to the presence of both zinc and the benzothiazole moiety. It can form stable complexes that have applications in various fields.
  • Biological Significance: Benzothiazole derivatives are known for their biological activities, including antimicrobial and antifungal properties. This raises intriguing possibilities for applications in pharmaceuticals and crop protection.
  • Synthetic Versatility: The synthesis of zinc 1,3-benzothiazole-2-thiolate can be accomplished through various methods, showcasing the flexibility and diversity of techniques in organometallic chemistry.
  • Material Science: Due to its unique electronic properties, this compound can play a role in material science, particularly in the creation of conductive polymers or sensors.
  • Research Applications: Scientists are continually exploring the applications of this compound in catalysis, which could lead to the development of more efficient and environmentally friendly reactions.

In the words of a renowned chemist, “The beauty of chemistry lies not just in the compounds, but in their potential to transform our understanding of the world.”
Zinc 1,3-benzothiazole-2-thiolate exemplifies this idea, embodying a bridge between basic chemistry and practical applications in technology and medicine.

Synonyms
Zinc 2-mercaptobenzothiazole
155-04-4
Bantex
2-Mercaptobenzothiazole zinc salt
Zenite
Zetax
Zenite special
Vulkacit ZM
Hermat Zn-mbt
Pennac ZT
Tisperse MB-58
Zinc 2-benzothiazolethiolate
Caswell No. 917
2-MERCAPTOBENZOTHIAZOLEZINCSALT
ZINC MERCAPTOBENZOTHIAZOLE
Zinc benzothiazolethiolate
HMM5IX9Q3B
USAF GY-7
Zinc mercaptobenzothiazolate
OXAF
Zinc benzothiazolylmercaptide
Zinc 2-mercaptobenzothiazolate
Bis(2-benzothiazolylthio)zinc
Zinc benzothiazolyl mercaptide
Mercaptobenzothiazole zinc salt
Zinc mercaptobenzothiazole salt
2-Benzothiazolethiol zinc salt
Zinc benzothiazol-2-ylthiolate
Zinc benzothiazyl-2-mercaptide
Zinc bis(mercaptobenzothiazole)
Bis(mercaptobenzothiazolato)zinc
HSDB 5419
Bis(benzothiazole-2-thiolato)zinc
Zinc bis(2-mercaptobenzothiazole)
ZnMB
EINECS 205-840-3
ZMBT
EPA Pesticide Chemical Code 051705
2-Benzothiazolethiol, zinc salt (2:1)
zinc bis(1,3-benzothiazole-2-thiolate)
2-Mercaptobenzothiazole, zinc
Zinc, bis(2-benzothiazolethiolato)-
EC 205-840-3
NSC 285168
NSC-285168
ZINC MERCAPTOBENZOTHIAZOLE [HSDB]
2(3H)-Benzothiazolethione, zinc salt (2:1)
UNII-HMM5IX9Q3B
Hermat ZnMBT
Tisperse MB58
Zinc 2benzothiazolethiolate
Zinc 2mercaptobenzothiazole
Zinc benzothiazol2ylthiolate
Zinc benzothiazyl2mercaptide
Bis(2benzothiazolylthio)zinc
Zinc 2mercaptobenzothiazolate
2Benzothiazolethiol zinc salt
SCHEMBL410383
Bis(benzothiazole2thiolato)zinc
2Mercaptobenzothiazole zinc salt
DTXSID6020808
Zinc bis(2mercaptobenzothiazole)
PGNWIWKMXVDXHP-UHFFFAOYSA-L
Zinc, bis(2benzothiazolethiolato)
zinc;1,3-benzothiazole-2-thiolate
2(3H)Benzothiazolethione, zinc salt
Zinc(II) benzo[d]thiazole-2-thiolate
2Benzothiazolethiol, zinc salt (2:1)
FM41186
CS-0188512
NS00075634
Z0033
E77122
Q27094435
zinc(2+) bis(2-sulfanylidene-7aH-1,3-benzothiazol-7a-ide)