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Dimethyltryptamine hydrochloride

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Identification
Molecular formula
C17H27Cl2N
CAS number
1513-23-9
IUPAC name
(4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

The compound is typically in a solid state at room temperature, often found as a crystalline powder or small crystals.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
228.00
Boiling point (Kelvin)
501.15
General information
Molecular weight
339.32g/mol
Molar mass
339.3200g/mol
Density
1.1000g/cm3
Appearence

This compound typically appears as a crystalline powder that is white or off-white in color. It may also appear as colorless crystals depending on purity.

Comment on solubility

Solubility of (4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride

The solubility of (4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride is an intriguing topic due to the presence of different structural components influencing its behavior in various solvents.

Factors Affecting Solubility

Several factors contribute to the solubility of this compound:

  • Polarity: The compound's ammonium group generally increases its polarity, suggesting a higher solubility in polar solvents like water.
  • Hydrogen Bonding: The presence of the chloride ion can also facilitate hydrogen bonding, further enhancing solubility in aqueous solutions.
  • Hydrophobic Interactions: The bulky norbornane structure may introduce hydrophobic characteristics, potentially limiting solubility in highly polar solvents.

General Solubility Characteristics

In general, ionic compounds like this ammonium chloride tend to be soluble in:

  • Water: The ionic nature often leads to good solubility in aqueous environments.
  • Polar Organic Solvents: Solvents like methanol and ethanol may also dissolve this compound effectively, given their polarity.

Conversely, solubility may decrease in:

  • Non-Polar Solvents: Compounds such as hexane or benzene are less likely to dissolve the compound due to mismatched polarities.

In conclusion, while the general expectation is for (4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride to be soluble in polar solvents, precise solubility details can vary and require empirical testing for confirmation.

Interesting facts

Interesting Facts about (4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride

The compound known as (4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride is a fascinating compound within the realm of organic chemistry, combining the intricacies of quaternary ammonium salts with unique structural components.

Chemical Structure and Properties

This compound boasts a complex structure that includes:

  • Quaternary Ammonium Salt: As a quaternary ammonium compound, it has a positively charged nitrogen atom, which contributes to its distinct chemical behavior and interaction properties.
  • Chlorophenyl Substitution: The presence of the 4-chlorophenyl group introduces noteworthy properties, impacting the compound's reactivity and solubility characteristics.
  • Norbornan Framework: The use of the 1,7,7-trimethylnorbornan structure provides steric hindrance that can affect the compound's biological activity, making it an intriguing subject for study.

Applications and Biological Significance

This compound is not just a structural curiosity; it has several potential applications:

  • Pharmaceutical Research: Compounds of this nature often show promise in drug design, as they can target specific biological pathways.
  • Antimicrobial Properties: Quaternary ammonium compounds are known for their antimicrobial activity, making this compound a candidate for disinfectants or antiseptics.
  • Industrial Uses: The stability and reactivity of ammonium salts allow for utilization in various industrial applications, including surfactants and corrosion inhibitors.

Future Research Directions

Scientists are continually exploring the potential of compounds like (4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride. Future research may focus on:

  • Investigating structure-activity relationships to optimize its biological efficacy.
  • Examining its interactions with various biological systems to unveil potential therapeutic effects.
  • Exploring novel synthesis techniques to enhance yield and purity for various applications.

In conclusion, the study of (4-chlorophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride opens up a world of possibilities in both academic research and practical applications, making it a compelling subject for chemists and students alike. The blend of its intricate structure and promising functionalities highlights the importance of ongoing investigations in the field of organic chemistry.

Synonyms
(+-)-endo-N-(p-Chlorobenzyl)-2-bornanamine hydrochloride
24652-88-8
2-BORNANAMINE, N-(p-CHLOROBENZYL)-, HYDROCHLORIDE, endo-(+-)-
RefChem:256679