Skip to main content

Procaine

ADVERTISEMENT
Identification
Molecular formula
C13H20N2O2
CAS number
51-05-8
IUPAC name
2,3-dihydroxypropyl 4-aminobenzoate
State
State

At room temperature, Procaine is commonly found as a solid. It is stable under normal conditions of temperature and pressure.

Melting point (Celsius)
61.00
Melting point (Kelvin)
334.15
Boiling point (Celsius)
318.00
Boiling point (Kelvin)
591.15
General information
Molecular weight
236.28g/mol
Molar mass
236.2810g/mol
Density
1.3200g/cm3
Appearence

Procaine is typically a white crystalline powder. It may also appear as crystals or a crystalline powder with a faintly bitter taste.

Comment on solubility

Solubility of 2,3-dihydroxypropyl 4-aminobenzoate

2,3-dihydroxypropyl 4-aminobenzoate, commonly known as a chemical compound that features both hydroxyl and amino functional groups, demonstrates interesting solubility characteristics.

In general, the solubility of this compound can be influenced by several factors:

  • Polarity: Due to the presence of hydroxyl (-OH) groups, 2,3-dihydroxypropyl 4-aminobenzoate is likely to exhibit good solubility in polar solvents such as water.
  • Hydrogen bonding: The ability of this compound to form hydrogen bonds with solvent molecules enhances its solubility.
  • Temperature: As with many organic compounds, increased temperature may improve the solubility of 2,3-dihydroxypropyl 4-aminobenzoate in aqueous solutions.

It is often noted that:

  • "Like dissolves like" - meaning that polar compounds tend to dissolve well in polar solvents.

Furthermore, the structural features of 2,3-dihydroxypropyl 4-aminobenzoate suggest that it should perform well in biological systems, making it potentially useful in pharmacological applications. However, comprehensive solubility data in various solvents may be required for a more detailed understanding.

In conclusion, the solubility of 2,3-dihydroxypropyl 4-aminobenzoate is influenced by its functional groups and environmental conditions, making it an intriguing study for chemists and researchers alike.

Interesting facts

Interesting Facts about 2,3-dihydroxypropyl 4-aminobenzoate

2,3-dihydroxypropyl 4-aminobenzoate, also known as a derivative of para-aminobenzoic acid (PABA), is a fascinating compound in the realm of biochemistry and pharmaceuticals. This compound boasts a variety of applications and interesting characteristics:

  • Biochemical Role: As a PABA derivative, it plays a significant role in the synthesis of folate, a crucial vitamin that aids in DNA synthesis and repair.
  • Cosmetic Uses: It is often incorporated into sunscreens due to its UV-absorbing properties, offering protection against harmful solar radiation.
  • Pharmaceutical Applications: Researchers are studying its potential use in therapeutic agents, particularly for its anti-inflammatory and analgesic properties.
  • Research Potential: The compound serves as a vital point of interest for scientists exploring the mechanisms of skin protection and cellular repair.
  • Histochemical Relevance: Its ability to react with certain tissues makes it valuable in histological studies, helping researchers visualize biological samples.

Furthermore, the structural features of 2,3-dihydroxypropyl 4-aminobenzoate enhance its reactivity, leading to various possible modifications that could expand its applications in medicinal chemistry. It's essential for aspiring chemists to appreciate the versatility of such compounds, as they exemplify the intersection of organic chemistry and biological function.

In summary, the exploration of this compound not only enriches our understanding of chemistry but also opens new avenues for innovation in health and cosmetic industries.

Synonyms
Lisadimate
136-44-7
Glyceryl paba
2,3-dihydroxypropyl 4-aminobenzoate
Glyceryl p-aminobenzoate
Lisadimato
Glycerol 1-(p-aminobenzoate)
1,2,3-Propanetriol, 1-(4-aminobenzoate)
p-Aminobenzoic acid monoglyceryl ester
(+/-)-Glycerol 1-(p-aminobenzoate)
A886B5N5IM
DTXSID8042002
Lisadimate (>85%)
Escalol 106
Lisadimatum
Lisadimate [USAN:INN]
Lisadimatum [INN-Latin]
Glyceryl para-aminobenzoate
Lisadimato [INN-Spanish]
Monoglycerol p-aminobenzoate
Glycerol 1-(4-aminobenzoate)
Glyceryl paraaminobenzoate
EINECS 205-244-3
(+-)-Glycerol 1-(p-aminobenzoate)
BRN 2727968
UNII-A886B5N5IM
1,2,3-Propanetriol 1-(4-aminobenzoate)
AI3-25249
1,2,3-Propanetriol, p-aminobenzoate
GLYCEROL MONO PARA AMINO BENZOATE
starbld0002197
1-(4-Aminobenzoate)-1,2,3-propanetriol
LISADIMATE [INN]
Lisadimate (USAN/INN)
LISADIMATE [USAN]
LISADIMATE [MART.]
Oprea1_234344
SCHEMBL62520
4-14-00-01136 (Beilstein Handbook Reference)
1,2,3-Propanetriol, 1-(4-aminobenzoate), (+-)-
CHEMBL2106668
DTXCID6022002
Tox21_113940
GLYCERYL P-AMINOBENZOATE [MI]
AKOS015913811
NCGC00262947-01
CAS-136-44-7
NS00024425
D04746
SR-01000944885
SR-01000944885-1
BRD-A76533773-001-01-9
Q27273763
1,2,3-PROPANETRIOL, 1-(4-AMINOBENZOATE), (+/-)-