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Basic Blue 7

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Identification
Molecular formula
C17H19ClN2S
CAS number
2390-60-5
IUPAC name
4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethyl-aniline
State
State

At room temperature, the compound is typically in a solid state.

Melting point (Celsius)
200.00
Melting point (Kelvin)
473.15
Boiling point (Celsius)
384.30
Boiling point (Kelvin)
657.45
General information
Molecular weight
350.49g/mol
Molar mass
350.4920g/mol
Density
1.1908g/cm3
Appearence

The compound typically appears as a dark blue powder. In its aqueous form, it imparts a vivid blue color.

Comment on solubility

Solubility of 4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethyl-aniline

The solubility of 4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethyl-aniline can be influenced by several factors, including its unique chemical structure and ionic properties. Here are some key insights regarding its solubility:

  • Polarity: The presence of the benzothiazolium moiety suggests some degree of ionic character, which often increases solubility in polar solvents such as water.
  • Solvent Interaction: The compound may be soluble in organic solvents like ethanol and acetone, due to the hydrophobic dimethyl-aniline portion of its structure.
  • pH Dependence: The solubility may vary significantly with pH, as protonation states can alter the compound's overall charge and, consequently, its solubility.
  • Temperature Effects: Increasing temperature generally enhances solubility for many compounds, and thus, this compound might exhibit similar behavior.

In summary, while predictions regarding solubility can be made based on structural analysis, empirical data is essential for precise determination. Thus, experiments to assess solubility in various solvents at different temperatures and pH levels are recommended for a complete understanding.

Interesting facts

Interesting Facts about 4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethyl-aniline

4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethyl-aniline, a complex aromatic compound, presents a fascinating combination of structural features that invite examination from various perspectives in chemical science.

Chemical Structure and Features

  • Structure: The compound comprises a benzothiazole moiety, highlighting its role in heterocyclic chemistry. This heterocyclic ring structure is known for its significant biological and pharmaceutical activities.
  • Substituents: The presence of dimethyl groups in both the benzothiazole and aniline components contributes to its unique chemical properties, influencing its reactivity and solubility.
  • Charge Distribution: The quaternized nitrogen in the benzothiazole adds a positive charge, making this compound particularly interesting for studies in ion transport and electrochemical applications.

Applications in Science

This compound serves numerous roles, including:

  • Dyes and Pigments: Due to its vibrant color potential, it may have applications in textiles and biological staining.
  • Fluorescence: Its fluorescent properties open up applications in imaging technologies and bioassays.
  • Research Tool: The unique structural features make it invaluable in material science, particularly in the development of organic semiconductors.

Biological Significance

The interactions of compounds containing benzothiazole structures with biological systems are often noteworthy:

  • Antimicrobial Activity: Many benzothiazole derivatives exhibit strong activity against various pathogens, leading to exploration in medicinal chemistry.
  • Cancer Research: Compounds with similar frameworks have been studied for their potential to inhibit tumor cell growth.

As a compound rich in diversity and utility, 4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethyl-aniline exemplifies how intricate molecular design can yield significant scientific advancements. So the next time you see a compound with such a name, remember the layers of complexity and potential that lie within!

Synonyms
2-[4-(dimethylamino)phenyl]-3,6-dimethyl-1,3-benzothiazol-3-ium
thioflavin T cation
Thioflavin T ion
8RD3NXV2ZV
CHEMBL57267
20096-11-1
CHEBI:76034
4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethylaniline
2-(4-(dimethylamino)phenyl)-3,6-dimethylbenzo[d]thiazol-3-ium
47070-20-2
Benzothiazolium, 2-(4-(dimethylamino)phenyl)-3,6-dimethyl-
Thioflavin T, 1
Tfx
thioflavin T(1+)
UNII-8RD3NXV2ZV
cid_16954
SCHEMBL1577265
DTXSID90862917
2-(4-Dimethylamino-phenyl)-3,6-dimethyl-benzothiazol-3-ium
BBL034001
BDBM50100134
STL058959
AKOS005711437
NCGC00165339-01
MLS-0327108.0001
Q27145690
[4-(3,6-dimethyl-benzothiazol-2-yl)-phenyl]-dimethyl-amine
2-(4-Dimethylamino-phenyl)-3,6-dimethyl-benzothiazol-3-ium(thioflavin T)