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Penicillin G

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Identification
Molecular formula
C16H18N2O6S
CAS number
69-57-8
IUPAC name
2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid
State
State

At room temperature, 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid is typically found in a solid crystalline state.

Melting point (Celsius)
209.00
Melting point (Kelvin)
482.15
Boiling point (Celsius)
274.00
Boiling point (Kelvin)
547.15
General information
Molecular weight
333.36g/mol
Molar mass
333.3560g/mol
Density
1.6680g/cm3
Appearence

2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid is a crystalline solid. It may vary in color from white to pale yellow.

Comment on solubility

Solubility of 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid

The solubility of the compound C16H18N2O6S, known as 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid, is characterized by various factors, making it an intriguing subject for study. Here are some key points regarding its solubility:

  • Nature of Functional Groups: The presence of multiple polar functional groups, such as carboxyl (-COOH) and amino (-NH2), enhances its ability to interact with water, thus increasing solubility.
  • Salt Formation: This compound contains sulfonic acid groups, which can lead to the formation of water-soluble salts, further promoting solubility in aqueous solutions.
  • pH Dependence: The solubility can be highly dependent on the pH of the solution due to the ionization of carboxylic and amino groups. For instance, in acidic conditions, the protonation of amino groups can affect solubility differently than in basic conditions.
  • Concentration Effects: Like many compounds, at higher concentrations, the solubility may reach a limit where the solution becomes saturated.

In conclusion, the solubility of this compound is influenced by its structural characteristics and environmental conditions. It can be summarized that:

  1. High solubility in polar solvents, especially water.
  2. Increased solubility in acidic or neutral pH environments.
  3. Potential precipitation at certain concentrations or pH extremes.

Understanding the solubility behavior of this compound is essential for its applications in various chemical and pharmaceutical fields.

Interesting facts

Interesting Facts about 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic Acid

This fascinating compound is a member of the amino acid derivatives, showcasing a unique structure that makes it noteworthy in the field of biochemistry. Here are some compelling aspects:

  • Complex Structure: The compound features multiple functional groups, including carboxymethyl, amino, and sulfonyl moieties, contributing to its structural complexity and potential biological activity.
  • Potential Biological Role: Its structure suggests it could play a role in metabolic pathways, possibly acting as a precursor or derivative in synthesis processes related to amino acids and proteins.
  • Research Applications: Compounds like this one are often studied in relation to therapeutic applications, particularly in the fields of drug development and biochemical research. The presence of the sulfosulfanylmethyl group may indicate applications in pharmaceuticals or agricultural chemistry.
  • Noteworthy Mechanism: Research surrounding similar compounds reveals they may exhibit enzyme-inhibitory properties, which could be of great interest in the design of inhibitors for specific metabolic pathways.
  • Potential Environmental Significance: Given its structure, it might also show properties related to environmental sustainability, especially in bioremediation or as a biodegradable alternative in various applications.

As we delve deeper into the chemical properties and implications of 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid, it becomes clear that its intricate design underlines the remarkable complexity of biochemical interactions and the potential for innovative research avenues.

Synonyms
SCHEMBL9188225
N5-(1-((Carboxymethyl)amino)-1-oxo-3-(sulfothio)propan-2-yl)-DL-glutamine