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Procaine

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Identification
Molecular formula
C13H20N2O2S
CAS number
59-46-1
IUPAC name
S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate
State
State

At room temperature, Procaine is in a solid state. It is typically provided as a hydrochloride salt to enhance its stability and solubility which is commonly used for medical applications.

Melting point (Celsius)
141.00
Melting point (Kelvin)
414.20
Boiling point (Celsius)
378.30
Boiling point (Kelvin)
651.50
General information
Molecular weight
236.31g/mol
Molar mass
236.3070g/mol
Density
1.1750g/cm3
Appearence

Procaine is typically a white crystalline powder. However, it can also appear as a white, odorless crystalline substance. As a pure compound, it doesn't possess any color, and it's important to ensure its purity for medical applications.

Comment on solubility

Solubility of S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate

S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate, a compound featuring diverse functional groups, exhibits intriguing solubility characteristics. Understanding its solubility is crucial as it influences its application in various chemical processes.

Factors Affecting Solubility

The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of both a diethylamino group and a carbothioate group indicates moderate polarity, which can enhance solubility in polar solvents.
  • Hydrogen Bonding: The amino group might facilitate hydrogen bonding with solvents, further affecting solubility.
  • Temperature: Typically, an increase in temperature can improve the solubility of organic compounds.

General Solubility Behavior

In general, we can expect:

  • Good solubility in organic solvents such as ethanol and methanol.
  • Limited solubility in non-polar solvents due to its polar functional groups.
  • Possibly low solubility in water, although the presence of the amino group may grant some degree of solvation in water.

In summary, the solubility of S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate is a complex interplay of its functional groups, polarity, and environmental conditions. A thorough understanding of these solubility patterns is essential for effective utilization in research and industry.

Interesting facts

Interesting Facts about S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate

S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate, a complex organic compound, holds significance in various fields of chemistry and biotechnology. This compound showcases the intricate relationship between chemical structure and biological activity, making it a compelling subject of study for researchers. Here are some notable aspects:

  • Biological Activity: Several derivatives of carbothioate compounds exhibit biological activity, including antimicrobial and antiviral properties. Understanding S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate could lead to additional discoveries in medicinal chemistry.
  • Structure-Activity Relationship: The unique structural features of this compound, including the presence of a diethylamino group, may influence its interaction with biological targets. This allows for an exploration of the structure-activity relationship (SAR) which is crucial in drug design.
  • Synthesis Methods: The synthesis of this compound can involve various synthetic approaches, showcasing the versatility of organic chemistry. Exploring such methods can enhance understanding of reaction mechanisms and generative techniques.
  • Applications in Research: Compounds of this nature are often used as intermediates in the development of pharmaceuticals, as well as in chemical research to probe interactions within biological systems.

Researchers might be drawn to this compound not only for its potential applications but also for the insights it can provide into the behavior of thiocarbonyl compounds in biological systems. Overall, S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate serves as a prime example of the intersection between organic chemistry and biochemistry.

Synonyms
Thiocaine
Thicaine
Thiocain
120-49-0
USAF A-9870
beta-Diethylaminoethyl p-aminothiobenzoate
NSC 30308
BRN 2114277
p-Aminothiobenzoic acid, S-(2-(diethylamino)ethyl) ester
DTXSID50152644
3-14-00-01169 (Beilstein Handbook Reference)
S-[2-(diethylamino)ethyl] 4-aminobenzenecarbothioate
Benzenecarbothioic acid, 4-amino-, S-(2-(diethylamino)ethyl) ester
BENZOIC ACID, p-AMINOTHIO-, S-(2-(DIETHYLAMINO)ETHYL) ESTER
p-Aminothiobenzoic acid, S-[2-(diethylamino)ethyl] ester
DTXCID7075135
SCHEMBL13439968
WLN: ZR DVS2N2 & 2
NSC30308
NSC-30308
.beta.-Diethylaminoethyl p-aminothiobenzoate
Benzoic acid, S-[2-(diethylamino)ethyl] ester
Benzenecarbothioic acid, S-[2-(diethylamino)ethyl] ester
Benzenecarbothioic acid, 4-amino-, S-(2-(diethylamino)ethyl) ester (9CI)