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Chlorophyllin

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Identification
Molecular formula
C34H31N4O6
CAS number
11006-34-1
IUPAC name
3-[5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-3-yl]propanoic acid
State
State
Chlorophyllin is typically a solid at room temperature, existing in crystalline or powdered form.
Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
730.53g/mol
Molar mass
724.0000g/mol
Density
1.7000g/cm3
Appearence
Chlorophyllin appears as a dark green or blue-green powder. It is soluble in water, and its solutions are typically of a vibrant green hue.
Comment on solubility

Solubility of 3-[5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-3-yl]propanoic acid (C34H31N4O6)

The solubility of this complex compound can be attributed to its functional groups and molecular structure. Compounds like this typically exhibit the following behavior in solvents:

  • Polar Solvents: Given the presence of multiple carboxylic acid groups, this compound is likely to be highly soluble in polar solvents such as water. The hydrophilic nature of the carboxyl groups allows for favorable interactions with water molecules.

  • Non-Polar Solvents: In contrast, the solubility in non-polar solvents is expected to be low. The predominant non-polar interactions may hinder solvation, thereby reducing solubility.

  • Temperature Effects: The solubility of this compound may increase with temperature, as greater kinetic energy can help overcome intermolecular forces.

  • pH Influence: The solubility may also be pH-dependent due to the ionization of the carboxylic acid groups. In a higher pH environment, the carboxyl groups can deprotonate, enhancing solubility further.

In summary, the solubility characteristics of this compound are significantly influenced by its structure, particularly the presence of polar functional groups that favor solvation, making it more soluble in polar solvents while remaining poorly soluble in non-polar environments.

Interesting facts

Interesting Facts about 3-[5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-3-yl]propanoic acid

This fascinating compound, known for its complex structure, belongs to a class of compounds often investigated for their potential therapeutic applications. The compound features multiple carboxyethyl and carboxymethyl groups, which contribute to its reactivity and ability to form stable interactions with other molecules.

Key Characteristics

  • Multifunctional nature: The presence of several functional groups, particularly the pyrrole derivatives, enhances the compound's interaction with biological systems.
  • Research applications: This compound is often a subject of study in medicinal chemistry, particularly for its potential effects in drug development.
  • Synthetic challenges: The synthesis of such complex molecules can be quite challenging, often requiring multiple synthetic steps and careful control of reaction conditions.

As researchers explore the compound's properties, they often utilize advanced techniques such as NMR and mass spectrometry to decipher its structure and confirm the purity of synthesized samples. With increasing interest in compounds that exhibit both biological activity and structural complexity, this specific compound represents the exciting intersection of chemistry, biology, and pharmaceutical sciences.

In conclusion, 3-[5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-3-yl]propanoic acid is not just another compound. Instead, it is a gateway to deeper understanding and exploration in the realms of chemical science.

Synonyms
hydroxymethylbilane
Preuroporphyrinogen
71861-60-4
(Hydroxymethyl)bilane
CHEBI:16645
3,8,13,18-tetrakis(carboxymethyl)-5,10,15,22,23,24-hexahydro-19-(hydroxymethyl)-21H-biline-2,7,12,17-tetrapropanoic acid
3-[5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-1H-pyrrol-3-yl]propanoic acid
3,8,13,18-tetrakis(carboxymethyl)-19-(hydroxymethyl)bilane-2,7,12,17-tetrapropanoate
3,8,13,18-tetrakis(carboxymethyl)-19-(hydroxymethyl)bilane-2,7,12,17-tetrapropanoic acid
3,8,13,18-tetrakis(carboxymethyl)-5,10,15,22,23,24-hexahydro-19-(hydroxymethyl)-21H-Biline-2,7,12,17-tetrapropanoate
3-(5-{[3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl]methyl}-2-{[4-(2-carboxyethyl)-5-{[4-(2-carboxyethyl)-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl}-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl}-4-(carboxymethyl)-1H-pyrrol-3-yl)propanoic acid
3-[2-[[4-(2-carboxyethyl)-5-[[4-(2-carboxyethyl)-5-[[4-(2-carboxyethyl)-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-3-yl]propanoate
3-[2-[[4-(2-carboxyethyl)-5-[[4-(2-carboxyethyl)-5-[[4-(2-carboxyethyl)-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl]-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-3-yl]propanoic acid
3-(2-((4-(2-Carboxyethyl)-5-((4-(2-carboxyethyl)-5-((4-(2-carboxyethyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-3-yl)propanoate
3-(2-((4-(2-Carboxyethyl)-5-((4-(2-carboxyethyl)-5-((4-(2-carboxyethyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-3-yl)propanoic acid
3-(2-{[4-(2-carboxyethyl)-5-{[4-(2-carboxyethyl)-5-{[4-(2-carboxyethyl)-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl}-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl}-3-(carboxymethyl)-1H-pyrrol-2-yl]methyl}-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-3-yl)propanoic acid
3-(5-((3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl)methyl)-2-((4-(2-carboxyethyl)-5-((4-(2-carboxyethyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-3-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-4-(carboxymethyl)-1H-pyrrol-3-yl)propanoic acid
3-(5-((3-(2-carboxyethyl)-5-((3-(2-carboxyethyl)-5-((3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl)methyl)-4-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-4-(carboxymethyl)-1H-pyrrol-2-yl)methyl)-4-(carboxymethyl)-1H-pyrrol-3-yl)propanoic acid
Hydroxymethylbilane(HMB)
C01024
CHEMBL273676
SCHEMBL18547975
DTXSID001105025
NS00126252
Q2639442
3,8,13,18-Tetrakis(carboxymethyl)-5,10,15,22,23,24-hexahydro-19-(hydroxymethyl)-21H-biline-2,7,12,17-tetrapropionic acid