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Butamben

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Identification
Molecular formula
C13H19NO3
CAS number
94-25-7
IUPAC name
butyl 3-[(dimethylamino)methyl]-4-hydroxy-benzoate
State
State

At room temperature, Butamben is a solid. It is often used in topical formulations due to its anesthetic properties.

Melting point (Celsius)
47.00
Melting point (Kelvin)
320.15
Boiling point (Celsius)
366.00
Boiling point (Kelvin)
639.15
General information
Molecular weight
237.30g/mol
Molar mass
237.3010g/mol
Density
1.0647g/cm3
Appearence

Butamben appears as a white, crystalline solid. It is commonly used in its pure form for applications requiring a local anesthetic. The crystalline nature makes it suitable for formulation in various pharmaceutical applications.

Comment on solubility

Solubility of Butyl 3-[(Dimethylamino)methyl]-4-hydroxy-benzoate

Butyl 3-[(dimethylamino)methyl]-4-hydroxy-benzoate, often referred to by its IUPAC name, exhibits interesting solubility characteristics due to its unique molecular structure. The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of polar functional groups, such as the hydroxyl group (-OH) and the dimethylamino group, enhances its interaction with polar solvents like water.
  • Hydrophobic Characteristics: The butyl group contributes hydrophobic properties, which can affect overall solubility in nonpolar solvents.
  • pH Dependency: The solubility may vary with pH levels, particularly as the dimethylamino group can be protonated in acidic conditions, potentially increasing solubility in aqueous environments.
  • Temperature Effects: Increased temperature typically enhances solubility for many compounds, and this may apply to butyl 3-[(dimethylamino)methyl]-4-hydroxy-benzoate as well.

In summary, while this compound may solubilize readily in polar solvents due to its functional groups, the influence of hydrophobic regions makes it less soluble in nonpolar environments. As always, specific solubility can depend on various external factors, including solvent choice and environmental conditions.

Interesting facts

Interesting Facts about Butyl 3-[(Dimethylamino)methyl]-4-hydroxy-benzoate

Butyl 3-[(dimethylamino)methyl]-4-hydroxy-benzoate is a fascinating compound widely studied for its chemical properties and applications in various fields. Here are some intriguing facts about this compound:

  • Structural Versatility: The presence of a hydroxy group (-OH) and a dimethylamino group (-N(CH3)2) in its structure contributes to the compound's reactivity and interaction with other substances.
  • Cosmetic Applications: This compound is often utilized in the formulation of cosmetic products due to its ability to act as an emollient, providing moisture and improving skin texture.
  • Antimicrobial Properties: Studies have indicated that compounds of this type can exhibit antimicrobial properties, making them valuable in personal care products and helping to preserve formulations against microbial contamination.
  • pH Stability: It remains stable over a range of pH levels, which is crucial for maintaining the efficacy of products in which it is used.
  • Research Potential: The unique characteristics of butyl 3-[(dimethylamino)methyl]-4-hydroxy-benzoate make it a compound of interest in ongoing research related to drug delivery systems and pharmacology.

In summary, butyl 3-[(dimethylamino)methyl]-4-hydroxy-benzoate exemplifies the intersection of chemistry and practical application, showcasing the incredible opportunities that exist in the study of chemical compounds. As scientists continue to explore its properties and potential uses, we may uncover even more exciting applications in the future.

Synonyms
6279-54-5
Butyl 3-((dimethylamino)methyl)-4-hydroxybenzoate
NSC 11380
BRN 2981871
EJ6Z67N2X1
NSC-11380
BENZOIC ACID, 3-((DIMETHYLAMINO)METHYL)-4-HYDROXY, BUTYL ESTER
UNII-EJ6Z67N2X1
DTXSID90211865
3-((Dimethylamino)methyl)-4-hydroxy butyl ester benzoic acid
4,3-CRESOTIC ACID, .ALPHA.-(DIMETHYLAMINO)-, BUTYL ESTER
DTXCID20134356
4,3-CRESOTIC ACID, ALPHA-(DIMETHYLAMINO)-, BUTYL ESTER
NSC11380