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Salsolinol hydrochloride

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Identification
Molecular formula
C10H13NO2Cl
CAS number
4385-03-7
IUPAC name
1-methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol;chloride
State
State

At room temperature, Salsolinol hydrochloride is in a solid state. It is a hygroscopic compound, which means it can readily absorb moisture from the environment if not stored properly.

Melting point (Celsius)
248.00
Melting point (Kelvin)
521.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
229.67g/mol
Molar mass
229.7000g/mol
Density
1.3000g/cm3
Appearence

Salsolinol hydrochloride typically appears as a white to off-white crystalline solid. It is often supplied in a powdered form, making it easily measurable for laboratory and research purposes.

Comment on solubility

Solubility of 1-methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol;chloride

The solubility of 1-methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol;chloride can be influenced by its unique molecular structure and the presence of the chloride ion. Here are some key points to consider:

  • Water Solubility: Due to the ionic nature of the chloride salt, this compound is expected to exhibit a moderate to high solubility in water.
  • Polar Organic Solvents: It may also be soluble in polar organic solvents, which further enhances its utility in various chemical processes.
  • Temperature Dependence: Solubility is typically temperature-dependent, thus increasing the temperature could lead to higher solubility rates.
  • pH Influence: The solubility may vary with changes in pH, as protonation states of the compound can affect its overall solubility.

In conclusion, the solubility of 1-methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol;chloride is likely to be favorable in aqueous solutions and select organic solvents, making it a versatile compound in the realm of chemical reactions and formulations.

Interesting facts

Interesting Facts about 1-Methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol; Chloride

1-Methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol; chloride is a fascinating compound that has captured the attention of scientists due to its unique structure and potential applications. Here are some notable points that highlight its intriguing characteristics:

  • Structural Complexity: The compound features a heterocyclic ring system, specifically the isoquinoline, which contributes to its biological activity.
  • Physiological Relevance: Compounds similar to this one have been studied for their roles in neurotransmission and may exhibit therapeutic effects in neurological disorders.
  • Synthesis Exploration: The synthetic pathways to create this compound involve various methods, including multi-step synthesis and catalytic reactions, which are essential for creating complex organic molecules.
  • Research Insights: According to studies, derivatives of isoquinoline can influence several biological targets, making this compound a candidate for further pharmacological investigation.

The versatility of 1-methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol; chloride showcases the importance of heterocycles in medicinal chemistry. As stated in literature, “innovation in compound design leads to novel therapeutic strategies” - a principle that holds true for this compound, indicating that ongoing research could reveal new and important applications.

In summary, the study of 1-methyl-3,4-dihydroisoquinolin-2-ium-6,7-diol; chloride not only enriches our understanding of isoquinolines but also opens doors to advancements in drug development and therapeutic options.

Synonyms
3,4-Dihydro-1-methyl-6,7-isoquinolinediol hydrochloride
4722-05-8
6,7-ISOQUINOLINEDIOL, 3,4-DIHYDRO-1-METHYL-, HYDROCHLORIDE