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Monoperoxyphthalic acid

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Identification
Molecular formula
C9H6O6
CAS number
113871-47-3
IUPAC name
4-(3-carboxypropanoylperoxy)-4-oxo-butanoic acid
State
State

At room temperature, Monoperoxyphthalic acid typically exists as a solid. It requires careful handling due to its potential as an oxidizer, and it should be kept in a controlled environment to maintain its stability.

Melting point (Celsius)
85.60
Melting point (Kelvin)
358.75
Boiling point (Celsius)
243.80
Boiling point (Kelvin)
516.95
General information
Molecular weight
174.13g/mol
Molar mass
174.1280g/mol
Density
1.8480g/cm3
Appearence

Monoperoxyphthalic acid is a white crystalline powder. It is sensitive to shock, heat, and friction, which can lead to explosive decomposition. It must be handled with care and stored in a cool, dry place away from direct sunlight and sources of ignition to prevent decomposition.

Comment on solubility

Solubility of 4-(3-carboxypropanoylperoxy)-4-oxo-butanoic acid

The solubility of 4-(3-carboxypropanoylperoxy)-4-oxo-butanoic acid can be influenced by several factors, making it a topic of interest in the field of chemical compounds. Here are some key points to consider:

  • Polarity: The presence of multiple functional groups in this compound impacts its polarity. The carboxylic acid group enhances solubility in polar solvents such as water.
  • Hydrogen bonding: The ability to form hydrogen bonds with water molecules can significantly increase solubility. The –COOH group is capable of engaging in such interactions.
  • pH sensitivity: The solubility may change with varying pH levels due to the ionization of the carboxylic acid. At higher pH, the carboxylic acid can deprotonate, increasing solubility in water.
  • Temperature effects: Generally, an increase in temperature can lead to enhanced solubility of organic compounds, possibly making it more soluble at elevated temperatures.

It's noteworthy to highlight that the solubility of 4-(3-carboxypropanoylperoxy)-4-oxo-butanoic acid can vary widely depending on the aforementioned factors, and understanding these helps in predicting its behavior in different environments. Always remember: "Solubility is not static, it is dynamic!"

Interesting facts

1,1,1-Tris(hydroxymethyl)propane

4-(3-carboxypropanoylperoxy)-4-oxo-butanoic acid is a fascinating compound for various reasons, particularly its potential role in organic synthesis and its applications in biochemical processes. Here are some captivating facts about this compound:

  • Peroxy Group: This compound features a peroxy group, which is known to impart unique reactivity compared to other functional groups. Peroxy compounds can readily decompose to release reactive radicals, making them interesting for initiating certain chemical reactions.
  • Biological Activity: Many peroxy acids, including this one, exhibit interesting biological activities. However, the specifics can vary based on the structure; understanding these nuances can lead to discoveries in medicinal chemistry.
  • Synthesis Pathways: The synthesis of this compound may involve various methodologies, including the formation of carboxylic acids and the careful manipulation of peroxide chemistry. Chemical students often find the methods for synthesizing such compounds an exciting part of their learning.
  • Versatile Applications: The unique structure of 4-(3-carboxypropanoylperoxy)-4-oxo-butanoic acid may allow it to be leveraged as a building block in the synthesis of more complex molecules. This can be particularly valuable in pharmaceuticals and agrochemicals.
  • Environmental Implications: Understanding the breakdown and reactivity of compounds like this could play an important role in fields like environmental chemistry, where the stability and degradation pathways of different chemicals are crucial for safety assessments.

In summary, 4-(3-carboxypropanoylperoxy)-4-oxo-butanoic acid is more than just a name; it represents a nexus of organic chemistry, potential applications in biological sciences, and intriguing synthetic methodologies. As with many compounds, further research could unveil even more secrets, making it a subject of ongoing interest in the field of chemistry.

Synonyms
Succinic acid peroxide
Alphozone
Succinic peroxide
Succinyl peroxide
Alfozono
Disuccinic acid peroxide
Disuccinoyl peroxide
123-23-9
Peroxydisuccinic acid
SUCCINOYL PEROXIDE
Peroyl SA
Succinic monoperoxyanhydride
Bis(3-carboxypropionyl) peroxide
Peroxide, bis(3-carboxypropionyl)
4,4'-Dioxybis(4-oxobutanoic acid)
HSDB 793
4,4'-Dioxo-4,4'-dioxydibutyric acid
Butanoic acid, 4,4'-dioxybis(4-oxo-
NSC 676
EINECS 204-611-5
45D0BBN3YW
Butanoic acid, 4,4'-dioxybis[4-oxo-
BRN 1799375
NSC-676
DISUCCINYL PEROXIDE
DTXSID3059555
4,4'-DIOXYBIS(4-OXOBUTANOIC ACID) [HSDB]
RefChem:889422
Bis(3carboxypropionyl) peroxide
DTXCID1033791
Peroxide, bis(3carboxypropionyl)
4,4'Dioxybis(4oxobutanoic acid)
Butanoic acid, 4,4'dioxybis(4oxo
Peroxide, bis(3-carboxypropionyl) (8CI)
4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid
UNII-45D0BBN3YW
Succinic acid, peroxide
Disuccinic acid, peroxide
WLN: QV2VOOV2VQ
WLN: QV1YVQOOYVQ1VQ
SCHEMBL42150
NSC676
Butanoic acid,4'-dioxybis[4-oxo-
NS00024011
A805032
4-(3-carboxy-1-oxopropyl)dioxy-4-oxobutanoic acid
Q27258831
4-oxidanylidene-4-(4-oxidanyl-4-oxidanylidene-butanoyl)peroxy-butanoic acid