Skip to main content

Tryptophol

ADVERTISEMENT
Identification
Molecular formula
C11H13NO
CAS number
526-55-6
IUPAC name
(1-methylindol-3-yl)methanol
State
State

At room temperature, tryptophol is primarily found as a liquid. It is somewhat viscous and can form a solid under specific conditions due to its relatively low melting point.

Melting point (Celsius)
30.00
Melting point (Kelvin)
303.15
Boiling point (Celsius)
162.00
Boiling point (Kelvin)
435.15
General information
Molecular weight
161.23g/mol
Molar mass
161.2010g/mol
Density
1.1412g/cm3
Appearence

Tryptophol appears as a pale yellow to colorless liquid or solid, depending on its state and purity. It is typically observed as a translucent liquid that may exhibit a characteristic odor.

Comment on solubility

Solubility of (1-methylindol-3-yl)methanol

(1-methylindol-3-yl)methanol is an intriguing compound when it comes to its solubility characteristics. Being a methanol derivative, its solubility is influenced by both the aromatic indole structure and the hydroxyl (-OH) functional group. Here are some key insights:

  • Solubility in Water: The presence of the hydroxyl group typically enhances solubility in polar solvents like water. Therefore, (1-methylindol-3-yl)methanol is likely to have some degree of solubility in water, but this may be limited by the hydrophobic indole structure.
  • Solubility in Organic Solvents: This compound is expected to be more soluble in non-polar to moderately polar organic solvents such as ethanol, methanol, and ethyl acetate, due to its hydrophobic indole ring.
  • Temperature Effect: As with many organic compounds, solubility may increase with temperature, making it easier to dissolve in solvents at higher temperatures.
  • pH Influence: The solubility can also be affected by the pH of the solution. At different pH levels, the hydroxyl group's ability to form hydrogen bonds with water may change, thus altering solubility.

In summary, (1-methylindol-3-yl)methanol exhibits variable solubility that predominantly depends on the solvent used and environmental conditions. As stated, "solubility is a complex interplay of molecular structure and external factors." Understanding these characteristics is crucial for its applications in chemical and pharmaceutical fields.

Interesting facts

Exploring (1-methylindol-3-yl)methanol

(1-methylindol-3-yl)methanol is a fascinating compound that has garnered interest in the fields of organic chemistry and materials science. Its unique structure, derived from the indole framework, makes it an intriguing subject for both research and practical applications.

Key Features

  • Indole Derivative: As an indole derivative, (1-methylindol-3-yl)methanol inherits some of the reactivity and properties associated with indolic compounds. Indoles are known for their presence in many biologically active molecules.
  • Potential Biological Activity: Compounds containing the indole structure have been studied for various pharmacological effects, including anti-cancer and anti-inflammatory activities. This may suggest that (1-methylindol-3-yl)methanol could have undiscovered therapeutic properties.
  • Solvent Properties: With the presence of a hydroxymethyl group, this compound may exhibit interesting solvent properties which could be harnessed in diverse chemical reactions.
  • Versatility in Synthesis: (1-methylindol-3-yl)methanol can serve as a precursor in the synthesis of more complex organic molecules, making it valuable in organic synthesis and chemical research.

Applications in Research

The study of (1-methylindol-3-yl)methanol may inspire future investigations in various scientific areas:

  • Medicinal Chemistry: The exploration of this compound could lead to the discovery of new pharmaceutical agents.
  • Material Science: Its chemical properties might offer insights into the design of novel materials with unique functionalities.
  • Environmental Chemistry: Understanding its behavior in different environments could reveal its ecological impact or potential for environmental remediation.

In summary, (1-methylindol-3-yl)methanol represents a charming intersection of chemistry and potential, waiting for researchers and students alike to delve deeper into its properties and implications. As quoted by chemists, “Every compound has a story to tell; it’s our job to uncover it.”

Synonyms
(1-METHYL-1H-INDOL-3-YL)METHANOL
6965-44-2
(1-methylindol-3-yl)methanol
1H-Indole-3-methanol, 1-methyl-
3-INDOLEMETHANOL, 1-METHYL-
3-Hydroxymethyl-1-methylindole
M68WFS5KSK
(1-methyl-1H-indol-3-yl)-methanol
NSC-67601
NSC 67601
BRN 0130675
1-Methyl-1H-indole-3-methanol
MFCD00572802
UNII-M68WFS5KSK
NCIOpen2_000262
(1-Methyindol-3-yl)methanol
1-methyl-3-hydroxymethylindole
SCHEMBL1094688
DTXSID80219911
LULITKYYLCRIIB-UHFFFAOYSA-N
NSC67601
AKOS000276026
AS-39446
EN300-1247723
F2106-0187