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Chlorophyll c1

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Identification
Molecular formula
C35H32N4O10
CAS number
11004-75-2
IUPAC name
3-[7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic acid
State
State

At room temperature, chlorophyll c1 is typically found as a solid, often as part of a complex mixture of similar compounds in phytoplankton. It is not usually found in pure form due to its involvement in the photosynthetic processes of marine organisms.

Melting point (Celsius)
356.00
Melting point (Kelvin)
629.15
Boiling point (Celsius)
954.00
Boiling point (Kelvin)
1 227.15
General information
Molecular weight
640.93g/mol
Molar mass
640.9290g/mol
Density
1.1000g/cm3
Appearence

Chlorophyll c1 is a natural pigment found in certain algae and cyanobacteria. It is usually found as a green solid due to its role in photosynthesis, where it absorbs light most efficiently. Chlorophyll c1 typically appears in a mixture with other pigments and its own isolated form is rarely observed.

Comment on solubility

Solubility of 3-[7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic acid (C35H32N4O10)

Understanding the solubility of complex compounds such as 3-[7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic acid is crucial for its potential applications. Given its intricate structure, the solubility characteristics can be summarized as follows:

  • Aqueous Solubility: This compound features multiple carboxylic acid groups (-COOH), which tend to enhance its solubility in water due to their ability to ionize and form hydrogen bonds with water molecules.
  • Organic Solubility: The presence of hydrophobic regions within the porphyrin structure may limit its solubility in non-polar solvents. It may be sparingly soluble or insoluble in organic solvents such as hexane or toluene.
  • pH Dependence: The solubility can vary significantly with changes in pH. In more acidic or basic conditions, the ionization of the carboxylic groups can influence its overall solubility.

In conclusion, while the presence of carboxylic acid groups suggests a degree of solubility in polar solvents, the overall behavior in solution can be complex and may require careful characterization. As noted, this compound's solubility profile is likely influenced by factors such as structural features, pH levels, and the nature of the solvent.

Interesting facts

Interesting Facts about 3-[7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic Acid

This compound, a highly intricate porphyrin derived structure, reveals a fascinating interplay of chemical architecture and biological significance. Porphyrins are known for their roles in essential biological functions, such as oxygen transport and photosynthesis, with hemoglobin and chlorophyll being prime examples.

Key Features

  • Complex Structure: The compound contains multiple carboxylic acid groups, which contribute to its solubility and reactivity in various environments.
  • Versatile Applications: Given its porphyrin framework, this compound could be explored for applications in fields such as photodynamic therapy, sensors, and catalysis.
  • Metal Coordination: Porphyrins often exhibit the ability to chelate metal ions, potentially allowing them to participate actively in electron transfer reactions.

The structure’s intricate design, specifically the presence of multiple carboxyethyl and carboxymethyl groups, enhances its potential to interact with biomolecules. This complex nature necessitates thorough research to unlock its possible therapeutic applications. As noted by prominent chemists, "The modification of porphyrins can lead to innovative solutions in drug design and delivery."

Overall, this compound stands as a testament to the creativity found within chemical synthesis and how intricate design can lead to exciting possibilities in both scientific research and practical applications.

Synonyms
Uroporphyrinogen III
1976-85-8
Urogen III
Uroporphyrinogens
uroporphyrinogen-III
uro'gen III
21H,23H-Porphine-2,7,12,18-tetrapropanoic acid, 3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro-
3-[7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic acid
CHEBI:15437
DTXSID40173444
3,3',3'',3'''-[3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,18-tetrayl]tetrapropanoic acid
3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro-21H,23H-porphine-2,7,12,18-tetrapropanoic acid
3,3',3'',3'''-(3,8,13,17-Tetrakis(carboxymethyl)-5H,10H,15H,20H,22H,24H-porphyrin-2,7,12,18-tetrayl)tetrapropionic acid
3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro-2,7,12,18-Porphinetetrapropionate
3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro-2,7,12,18-Porphinetetrapropionic acid
3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro-21H,23H-Porphine-2,7,12,18-tetrapropanoate
3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,18-tetrapropanoate
3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,18-tetrapropanoic acid
3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,18-tetrapropionic acid
3-[9,14,20-tris(2-carboxyethyl)-5,10,15,19-tetrakis(carboxymethyl)-21,22,23,24-tetraazapentacyclo[16.2.1.1^{3,6}.1^{8,11}.1^{13,16}]tetracosa-1(20),3,5,8,10,13,15,18-octaen-4-yl]propanoic acid
uroporphyrinogen
3,3',3'',3'''-(3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,18-tetrayl)tetrapropanoic acid
3-(7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl)propanoic acid
3-(9,14,20-tris(2-carboxyethyl)-5,10,15,19-tetrakis(carboxymethyl)-21,22,23,24-tetraazapentacyclo(16.2.1.1^(3,6).1^(8,11).1^(13,16))tetracosa-1(20),3,5,8,10,13,15,18-octaen-4-yl)propanoic acid
3-(9,14,20-tris(2-carboxyethyl)-5,10,15,19-tetrakis(carboxymethyl)-21,22,23,24-tetraazapentacyclo(16.2.1.13,6.18,11.113,16)tetracosa-1(20),3,5,8,10,13,15,18-octaen-4-yl)propanoic acid
3-[9,14,20-tris(2-carboxyethyl)-5,10,15,19-tetrakis(carboxymethyl)-21,22,23,24-tetraazapentacyclo[16.2.1.13,6.18,11.113,16]tetracosa-1(20),3,5,8,10,13,15,18-octaen-4-yl]propanoic acid
SCHEMBL80064
DTXCID3095935
Uroporphyrinogen III (6CI,7CI)
NS00122081
C01051
Q897727
2,7,12,18-Porphinetetrapropionic acid, 3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro-
2,7,12,18-Porphinetetrapropionic acid, 3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro- (8CI)
21H,23H-Porphine-2,7,12,18-tetrapropanoic acid, 3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydro- (9CI)
3,8,13,17-Tetrakis(carboxymethyl)-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,18-tetrapropionate
UP2