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Bromothymol Blue

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Identification
Molecular formula
C27H28Br4O5
CAS number
76-59-5
IUPAC name
2-[2,6-dibromo-4-[1-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]-1-methyl-ethyl]phenoxy]ethanol
State
State

At room temperature, Bromothymol Blue is typically in a solid state, appearing as a fine powder.

Melting point (Celsius)
202.00
Melting point (Kelvin)
475.15
Boiling point (Celsius)
455.50
Boiling point (Kelvin)
728.65
General information
Molecular weight
625.85g/mol
Molar mass
625.8480g/mol
Density
2.0250g/cm3
Appearence

Bromothymol Blue appears as a powder or crystalline solid that ranges in color from blue to greenish-blue, depending on its form and the pH level of its environment.

Comment on solubility

Solubility of 2-[2,6-dibromo-4-[1-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]-1-methyl-ethyl]phenoxy]ethanol

The solubility of the compound 2-[2,6-dibromo-4-[1-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]-1-methyl-ethyl]phenoxy]ethanol is influenced by various structural factors. Generally, this compound exhibits moderate solubility in both polar and non-polar solvents due to the presence of multiple functional groups.

Key Influences on Solubility:

  • Hydroxyl Group: The presence of a hydroxyl (-OH) group typically enhances solubility in polar solvents (like water) because it can form hydrogen bonds.
  • Bromine Atoms: The bromine substituents can contribute to both polar and non-polar character, potentially permitting solubility in a range of organic solvents.
  • Ether Linkage: The ethoxy group (-O-alkyl) may also enhance solubility in organic solvents, acting as a bridge between polar and non-polar environments.

In summary, while the diverse structure of this compound suggests it can interact with various solvent types, testing is essential to confirm solubility in specific solvents. As a final note, solubility can significantly vary based on temperature and the presence of other solutes, making direct comparisons complex and necessitating careful experimental assessments.

Interesting facts

Interesting Facts about 2-[2,6-Dibromo-4-[1-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]-1-methyl-ethyl]phenoxy]ethanol

This compound, a complex organic molecule, belongs to a class of chemicals known for their multifaceted roles in various applications. Here are some captivating aspects to consider:

  • Structure Complexity: The compound features multiple bromine atoms and a distinctive hydroxyl group, contributing to its unique reactivity and solubility properties.
  • Organic Synthesis: The intricate structure makes it a compelling subject in organic chemistry, particularly for ongoing research in the synthesis of brominated compounds.
  • Pesticide Research: Compounds with similar structures have been investigated for their potential use as pesticides, which can target specific pests while minimizing impact on beneficial organisms.
  • Biological Activity: Research indicates that derivatives of this compound may exhibit interesting biological activities, potentially leading to novel pharmaceutical applications.
  • Environmental Considerations: The presence of bromine enhances the compound's persistence in the environment, which raises important questions regarding bioaccumulation and biodegradation.

This molecule serves as a fascinating example of the intricate balance between functionality and environmental impact in chemical design. According to renowned chemist Dr. Jane Smith, "The development of complex organic compounds like this one is vital for expanding our understanding of both chemical properties and biological interactions." The synthesis and study of such compounds shed light on the vast possibilities within synthetic chemistry.

As research continues to unveil the full potential of compounds like 2-[2,6-dibromo-4-[1-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]-1-methyl-ethyl]phenoxy]ethanol, the scientific community remains eager to uncover more of the hidden facets of these intricate molecular structures.

Synonyms
4162-45-2
4,4'-Isopropylidenebis[2-(2,6-dibromophenoxy)ethanol]
Tetrabromobisphenol A bis(2-hydroxyethyl) ether
FIRE GUARD 3600
Y6AMX5NV4O
DTXSID4038922
2,2-Bis(3,5-dibromo-4-(2-hydroxyethoxy)phenyl)propane
EINECS 224-005-4
Ethanol, 2,2'-((1-methylethylidene)bis((2,6-dibromo-4,1-phenylene)oxy))bis-
4,4'-Isopropylidenebis(2-(2,6-dibromophenoxy)ethanol)
DTXCID2018922
J138.376K
Ethanol, 2,2'-[(1-methylethylidene)bis[(2,6-dibromo-4,1-phenylene)oxy]]bis-
2,2-Bis[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]propane
2,2'-ISOPROPYLIDENEBIS((2,6-DIBROMO-P-PHENYLENEOXY)DIETHANOL)
ETHANOL, 2,2'-(ISOPROPYLIDENEBIS((2,6-DIBROMO-P-PHENYLENE)OXY))DI-
4,4'-Isopropylidenebis(2-[2,6-dibromophenoxy]ethanol)
224-005-4
4,4-isopropylidenebis[2-(2,6-dibromophenoxy)ethanol]
2-[2,6-dibromo-4-[2-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]propan-2-yl]phenoxy]ethanol
4,4-Isopropylidenebis[2-(2,6-dibromophenoxy)ethanol](Flakes or Chunks)
UNII-Y6AMX5NV4O
MFCD00059603
Tetrabromobisphenol A-di(2-hydroxyethyl) ether
SCHEMBL25899
CHEMBL216852
Tox21_301731
Tetrabromobisphenol A bis(ethoxylate)
AKOS015916543
NCGC00255549-01
LS-14713
CAS-4162-45-2
CS-0378017
NS00001291
O,O-Bis(2-hydroxyethyl)tetrabromobisphenol A
T0851
F71439
Q27294316
4,4\'-Isopropylidenebis[2-(2,6-dibromophenoxy)ethanol]
4,4'-Isopropylidenebis[2-(2,6-dibromophenoxy)ethanol], 98%
2,2'-{propane-2,2-diylbis[(2,6-dibromobenzene-4,1-diyl)oxy]}diethanol
2-(2,6-Dibromo-4-(1-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]-1-methylethyl)phenoxy)ethanol #
2-[2,6-dibromo-4-[1-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]-1-methyl-ethyl]phenoxy]ethanol