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Adrenalone

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Identification
Molecular formula
C8H11NO3
CAS number
54-58-6
IUPAC name
5-(2-aminoethyl)benzene-1,2,4-triol
State
State

At room temperature, adrenalone is typically found in a solid state as crystalline powder.

Melting point (Celsius)
207.00
Melting point (Kelvin)
480.20
Boiling point (Celsius)
550.20
Boiling point (Kelvin)
823.40
General information
Molecular weight
167.18g/mol
Molar mass
167.1770g/mol
Density
1.3780g/cm3
Appearence

Adrenalone typically appears as a crystalline solid, which is often colorless to pale yellow. It is odorless and can absorb moisture from the air.

Comment on solubility

Solubility of 5-(2-aminoethyl)benzene-1,2,4-triol

The solubility of 5-(2-aminoethyl)benzene-1,2,4-triol (C8H11NO3), a compound with a complex structure, is influenced by several factors such as polarity, hydrogen bonding capacity, and molecular interactions. Here are some key points to consider:

  • Polarity: The presence of hydroxyl (-OH) groups contributes significantly to the compound's polarity, allowing it to interact favorably with polar solvents like water.
  • Hydrogen Bonding: The triol nature of the compound facilitates extensive hydrogen bonding, enhancing its solubility in aqueous environments. It can form hydrogen bonds with water molecules due to its multiple -OH groups.
  • Solvent Interaction: While this compound is likely soluble in polar solvents, its solubility in organic solvents might be limited due to the inability of nonpolar solvents to stabilize the polar functional groups.
  • Concentration Factors: The solubility may vary with concentration; higher concentrations could lead to saturation limits impacting the compound's ability to dissolve further.

In summary, the solubility of 5-(2-aminoethyl)benzene-1,2,4-triol in water is expected to be appreciable, attributed largely to its polar characteristics and the capacity to form hydrogen bonds. However, when exploring solubility possibilities in different solvents, it’s essential to consider the above factors to understand its behavior better.

Interesting facts

Interesting Facts about 5-(2-aminoethyl)benzene-1,2,4-triol

5-(2-aminoethyl)benzene-1,2,4-triol, often referred to in academic circles for its intriguing structural features and biological significance, is a fascinating compound with a myriad of applications and properties. Here are some noteworthy facts:

  • Structural Significance: The presence of an amino group and multiple hydroxyl groups in its structure makes this compound a key player in various chemical reactions, particularly in biosynthesis and organic synthesis.
  • Biological Relevance: This compound is related to many biologically active molecules, acting as a precursor or derivative of neurotransmitters, which can influence mood and cognitive functions.
  • Pharmaceutical Potential: Research indicates that compounds fitting this structural framework may have potential applications in drug development, particularly for neurological disorders.
  • Hydroxyl Groups: The three hydroxyl (OH) groups enable strong hydrogen bonding, enhancing solubility in biological systems and contributing to its reactivity.
  • Research Applications: Due to its unique properties, this compound is often utilized in laboratories for studies related to medicinal chemistry, biochemistry, and material science.

As a chemist delving into this compound, one cannot help but appreciate its complex structure and the role it plays in connecting chemical theory with practical applications. The investigation of its properties continues to open doors to innovative approaches in both scientific research and therapeutic interventions.

In the words of a noted chemist, "Every compound carries a story waiting to be uncovered, often revealing paths to unexpected discoveries."

Synonyms
oxidopamine
6-HYDROXYDOPAMINE
1199-18-4
5-(2-aminoethyl)benzene-1,2,4-triol
Oxidopamina
6-OHDA
2,4,5-Trihydroxyphenethylamine
Oxidopaminum
Topamine
Hydroxydopamine
1,2,4-Benzenetriol, 5-(2-aminoethyl)-
Oxidopamine [USAN:INN]
Oxidopaminum [INN-Latin]
5-(2-Aminoethyl)-1,2,4-benzenetriol
Oxidopamina [INN-Spanish]
CCRIS 4342
EINECS 214-842-3
BRN 2211011
8HW4YBZ748
CHEBI:78741
OXIDOPAMINE [INN]
OXIDOPAMINE [USAN]
CHEMBL337702
DTXSID0036768
4-13-00-02916 (Beilstein Handbook Reference)
Oxidopaminum (INN-Latin)
Oxidopamina (INN-Spanish)
MLS002207128
6 Hydroxydopamine
6-HD
NSC233898
SMR001306725
UNII-8HW4YBZ748
5-(2-aminoethyl)benzene-1,2,4-triol;hydrobromide
6-hydroxy-dopamine
Spectrum_000309
Spectrum2_001018
Spectrum3_001753
Spectrum4_000462
Oxidopamine (USAN/INN)
SCHEMBL37507
BSPBio_003486
KBioGR_000904
KBioSS_000789
DivK1c_000362
DOPAMINE, 6-HYDROXY-
SPBio_001175
cid_176170
DTXCID8016768
BDBM81264
KBio1_000362
KBio2_000789
KBio2_003357
KBio2_005925
KBio3_002706
NINDS_000362
KUC106765N
AKOS006230272
IDI1_000362
NCGC00167769-01
NCGC00167769-02
KSC-11-228-9
NCI60_001890
SBI-0051469.P003
NS00023890
D05294
AB00053512_09
Q780181
5-(2-azanylethyl)benzene-1,2,4-triol;hydrobromide
BRD-K41809988-003-09-3
214-842-3