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Benzocaine

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Identification
Molecular formula
C9H11NO2
CAS number
94-09-7
IUPAC name
2-phenylethyl 2-aminobenzoate
State
State

At room temperature, Benzocaine is a solid.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
165.19g/mol
Molar mass
165.1890g/mol
Density
1.1700g/cm3
Appearence

Benzocaine appears as a white, odorless, crystalline powder. It is generally tasteless, but it can have a slightly bitter taste. This substance is known for its local anesthetic properties and is commonly used in various topical anesthetic products.

Comment on solubility

Solubility of 2-phenylethyl 2-aminobenzoate

2-phenylethyl 2-aminobenzoate, commonly utilized in various chemical applications, exhibits interesting solubility characteristics that depend on several factors.

Factors Influencing Solubility:

  • Polarity: The presence of both amine and ester functional groups contributes to the compound's overall polarity. This characteristic influences its solubility in different solvents.
  • Temperature: Typically, increased temperature enhances solubility, allowing for better dissolution in solvents. However, the exact influence may vary based on the specific environment.
  • pH Levels: The solubility can change with altering pH levels due to the ionizable nature of the amine group. It is more soluble in basic conditions where the amine can be protonated.

Generally, 2-phenylethyl 2-aminobenzoate is more soluble in organic solvents such as ethanol and acetone than in water. This solubility trend is due to its hydrophobic phenyl group, which reduces interaction with polar solvents. That said, the compound may show limited solubility in highly polar environments.

It is essential to consider these factors when working with 2-phenylethyl 2-aminobenzoate to achieve optimal results in various applications!

Interesting facts

Interesting Facts about 2-Phenylethyl 2-Aminobenzoate

2-Phenylethyl 2-aminobenzoate is an intriguing compound, notable for its fascinating molecular structure and potential applications. Here are some captivating insights about this compound:

  • Biological Significance: This compound has garnered attention for its possible biological activities. It is related to benzoate derivatives, which are significant in the realm of medicinal chemistry.
  • Applications in Pharmaceuticals: Research indicates that 2-phenylethyl 2-aminobenzoate may serve as a precursor in the synthesis of drugs, particularly in the development of anti-inflammatory and analgesic agents.
  • Family Ties: The compound includes a phenylethyl moiety, which is often found in various natural products and has been linked to the structure of several important neurotransmitters, including phenethylamine.
  • Synthetic Pathways: Chemists utilize various synthetic routes to access this compound. Techniques often involve typical organic reactions, showcasing the compound’s role as a building block in organic synthesis.
  • Potential in Aromatherapy: Its phenylethyl component might contribute to characteristic scents, hinting at potential uses in the fragrance industry—highlighting its versatility beyond pharmaceuticals.

In summary, 2-phenylethyl 2-aminobenzoate represents a synergy between structure and function, making it a subject of ongoing research and enthusiasm within the scientific community. Researchers continuously explore its properties and applications, emphasizing the continuously unfolding stories behind chemical compounds.

Synonyms
PHENETHYL ANTHRANILATE
2-Phenylethyl 2-aminobenzoate
133-18-6
Phenylethyl anthranilate
2-Phenylethyl anthranilate
Benzylcarbinyl anthranilate
Benzoic acid, 2-amino-, 2-phenylethyl ester
Anthranilic acid, phenethyl ester
2-Phenylethyl o-aminobenzoate
2-Phenylethyl-o-aminobenzoate
beta-Phenethyl-o-aminobenzoate
FEMA No. 2859
beta-Phenylethyl anthranilate
beta-Phenethyl o-aminobenzoate
NSC 66441
CCRIS 4695
EINECS 205-098-0
UNII-8HBK71OD81
8HBK71OD81
DTXSID5025861
.beta.-Phenethyl-o-aminobenzoate
AI3-36132
Anthranilic acid, phenylethyl ester
NSC-66441
MLS002693572
DTXCID305861
.beta.-Phenylethyl anthranilate
PHENETHYL ANTHRANILATE [FHFI]
PHENYLETHYL ANTHRANILATE [FCC]
CAS-133-18-6
SMR001307335
Benzyl carbinyl anthranilate
phenethyl 2-aminobenzoate
WLN: ZR BVO2R
beta -phenylethyl anthranilate
MLS002303059
SCHEMBL446803
BENZYLCARBINYL ANTRANILC
beta -phenethyl-O-aminobenzoate
CHEMBL1488668
.beta.-Phenethyl o-aminobenzoate
FEMA 2859
CHEBI:191913
HMS3039J07
NSC66441
Tox21_202175
Tox21_303500
AKOS010555379
ANTRANILIC ACID,PHENETHYL ESTER
Phenethyl anthranilate, >=98%, FCC
2-PHENETHYL-ORTHO-AMINOBENZOATE
BETA-PHENETHYL-ORTHO-AMINOBENZOATE
NCGC00091901-01
NCGC00091901-02
NCGC00257318-01
NCGC00259724-01
DS-000794
NS00013109
Q27270507
205-098-0