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Butamben

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Identification
Molecular formula
C17H27N2O2
CAS number
94-25-7
IUPAC name
(1-methyl-4-piperidyl) 4-(butylamino)benzoate
State
State

Butamben is typically in a solid state at room temperature, appearing as a crystalline powder.

Melting point (Celsius)
63.00
Melting point (Kelvin)
336.20
Boiling point (Celsius)
440.50
Boiling point (Kelvin)
713.70
General information
Molecular weight
278.42g/mol
Molar mass
278.3970g/mol
Density
1.0863g/cm3
Appearence

Butamben is a white crystalline powder that is odorless. It can also appear in the form of colorless crystals.

Comment on solubility

Solubility of (1-methyl-4-piperidyl) 4-(butylamino)benzoate

The solubility of (1-methyl-4-piperidyl) 4-(butylamino)benzoate can be influenced by a variety of factors, leading to unique interactions with solvents. Typically, this compound showcases the following solubility characteristics:

  • Solvent Compatibility: This compound is generally more soluble in organic solvents, such as ethanol or methanol, due to its non-polar and polar functional groups.
  • Temperature Effects: Increased temperature can enhance the solubility, often making it more readily soluble when heated, as solubility typically increases with temperature for most organic compounds.
  • pH Dependence: The solubility may also vary with pH, as the ionization of amino groups can lead to increased solubility in acidic or basic conditions.

In summary, the solubility of (1-methyl-4-piperidyl) 4-(butylamino)benzoate is impacted by its molecular structure and the environment in which it is dissolved. It is essential to experiment with different solvents and conditions to determine the optimal solubility for specific applications.

Interesting facts

Interesting Facts about (1-methyl-4-piperidyl) 4-(butylamino)benzoate

(1-methyl-4-piperidyl) 4-(butylamino)benzoate is a fascinating compound that falls under the category of synthetic organic chemicals. Here are some intriguing aspects of this compound:

  • Pharmacological Interest: This compound has garnered attention in the pharmaceutical industry due to its potential therapeutic effects. It is often studied for its role in the development of new medications, particularly those targeting neurological disorders.
  • Structural Diversity: The compound showcases an interesting structure that combines a piperidine ring with a benzoate moiety. This structural diversity makes it a valuable scaffold for medicinal chemistry research.
  • Potential Interactions: Researchers are particularly interested in how this compound interacts with various neurotransmitter systems in the brain, which could lead to significant advancements in understanding mental health treatments.
  • Application in Synthesis: (1-methyl-4-piperidyl) 4-(butylamino)benzoate serves as a useful intermediate in organic synthesis, paving the way for the creation of other complex molecules.
  • Safety and Handling: Like many chemical compounds, proper safety protocols are essential when handling this substance. Appropriate personal protective equipment (PPE) should always be used in laboratory settings.

As a chemistry student or researcher, delving into the properties and applications of (1-methyl-4-piperidyl) 4-(butylamino)benzoate can provide valuable insights into the world of organic chemistry and its implications for medicine and pharmaceuticals. Exploring such compounds can inspire innovations that improve healthcare solutions.

Synonyms
Paridocaine
7162-37-0
Paridocaina
Paridocaine [INN]
Paridocainum
Paridocainum [INN-Latin]
Paridocaina [INN-Spanish]
BRN 1476858
UNII-795182TM5G
1-Methyl-4-piperidinol p-butylaminobenzoate
N-Methyl-4-piperidyl p-(butylamino)benzoate
795182TM5G
DTXSID50221864
BENZOIC ACID, p-(BUTYLAMINO)-, 1-METHYL-4-PIPERIDYL ESTER
Paridocainum (INN-Latin)
Paridocaina (INN-Spanish)
DTXCID80144355
(1-methylpiperidin-4-yl) 4-(butylamino)benzoate
SCHEMBL2110671
CHEMBL2104812
NS00010508
(1-Methylpiperidin-4-yl)4-(butylamino)benzoate
Q27266714