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Dobutamine

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Identification
Molecular formula
C18H23NO3
CAS number
34368-04-2
IUPAC name
4-[2-[[3-(3-hydroxyphenyl)-2-methyl-propyl]amino]ethyl]benzene-1,2-diol
State
State

At room temperature, dobutamine is a solid, but it is commonly used in solution form for clinical applications due to its pharmaceutical properties.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.20
Boiling point (Celsius)
461.70
Boiling point (Kelvin)
734.90
General information
Molecular weight
301.38g/mol
Molar mass
301.3710g/mol
Density
1.2600g/cm3
Appearence

Dobutamine typically appears as a white to off-white crystalline powder. It is often provided in a concentrated form for medical or laboratory use where it is reconstituted into a solution for administration.

Comment on solubility

Solubility of 4-[2-[[3-(3-hydroxyphenyl)-2-methyl-propyl]amino]ethyl]benzene-1,2-diol

The solubility of the compound 4-[2-[[3-(3-hydroxyphenyl)-2-methyl-propyl]amino]ethyl]benzene-1,2-diol (C18H23NO3) can be influenced by various factors due to its complex structure. This compound, also referred to as a substituted phenol, possesses functional groups that can interact favorably with solvents.

Key Points Regarding Solubility:

  • Polarity: The presence of hydroxyl (-OH) groups contributes to the compound's ability to engage in hydrogen bonding, potentially enhancing solubility in polar solvents such as water.
  • Structure: With a relatively large hydrophobic (non-polar) structure, solubility may decrease in highly polar environments but improve in non-polar solvents.
  • Temperature Effects: Increased temperature generally leads to higher solubility for many solid compounds; however, this may vary based on the balance between kinetic and thermodynamic factors.
  • pH Influence: As a weak base or acid, the solubility of this compound may also be pH-dependent, altering its ionization state and subsequently its solubility profile.

In summary, while the solubility is likely to be influenced by the interplay of its hydrophilic and hydrophobic characteristics, empirical testing is essential to determine its precise solubility parameters in various solvents. As with many organic compounds, the exploration of solubility is vital for applications in pharmaceuticals, analytical chemistry, and materials science.

Interesting facts

Interesting Facts about 4-[2-[[3-(3-hydroxyphenyl)-2-methyl-propyl]amino]ethyl]benzene-1,2-diol

This compound is a fascinating example of a *polyphenolic* structure, characterized by its complex arrangement which combines various functional groups. Here are some intriguing aspects:

  • Structural Diversity: The molecule features a unique combination of a *benzene ring*, *aliphatic chains*, and *hydroxyl groups*, showcasing the rich diversity of organic compounds.
  • Biological Significance: Compounds like this one often exhibit interesting biological activities. They may play roles in processes such as enzymatic inhibition or modulation of cell signaling pathways, making them valuable in pharmaceutical research.
  • Potential Applications: Due to its polyphenolic nature, this compound could be explored for its potential as an antioxidant or anti-inflammatory agent, contributing to the development of therapeutic agents.
  • Analogues in Nature: This structure has similarities to naturally occurring compounds found in various plants, hinting at *evolutionary biochemical connections* and the potential for mimicry in synthetic chemical design.
  • Synthetic Pathways: The synthesis of such compounds often involves multi-step reactions that can showcase a chemist's skills in *organic synthesis* and demonstrate the need for careful reaction condition management.

Researchers are encouraged to delve deeper into the properties and potential uses of such compounds, as they may hold the key to future scientific advancements in drug development and chemical engineering.

In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” Exploring derivatives and analogues of this compound could lead to *breakthroughs* in various fields!

Synonyms
NINDS_000435
Spectrum2_001535
Spectrum3_001568
Spectrum4_000164
Spectrum5_000649
BSPBio_003076
KBioGR_000647
DivK1c_000435
SPBio_001350
CHEMBL1620636
SCHEMBL13495715
KBio1_000435
KBio3_002576
IDI1_000435
NCGC00178313-01
BRD-A13912374-003-03-6