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4-Chlorophthalic acid

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Identification
Molecular formula
C8H5ClO4
CAS number
89-01-0
IUPAC name
4-chlorophthalic acid
State
State

At room temperature, 4-Chlorophthalic acid is found as a solid.

Melting point (Celsius)
179.00
Melting point (Kelvin)
452.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
186.57g/mol
Molar mass
186.5660g/mol
Density
1.6425g/cm3
Appearence

4-Chlorophthalic acid is a white crystalline solid. It is typically encountered in the form of fine crystals or powder. The compound is generally perceived as having minimal odor, typical of many aromatic carboxylic acids.

Comment on solubility

Solubility of 4-chlorophthalic acid

4-chlorophthalic acid, with the chemical formula C8H5ClO3, exhibits specific solubility characteristics that are important to understand in both laboratory and industrial applications.

When considering the solubility of 4-chlorophthalic acid, several key points emerge:

  • Solvent Behavior: It is known to have limited solubility in water, which is typical for many aromatic carboxylic acids.
  • Organic Solvents: It is more soluble in organic solvents such as ethanol, acetone, and ethyl acetate.
  • Temperature Dependency: The solubility also increases with temperature, making hot solvents more effective in dissolving this compound.

In conclusion, while 4-chlorophthalic acid may not dissolve readily in water, it demonstrates a greater affinity for organic solvents, and understanding these solubility parameters is crucial for practical applications. As a general guideline, think of it as “more welcoming towards organic friends” while remaining somewhat reserved in aqueous environments.

Interesting facts

Interesting Facts about 4-Chlorophthalic Acid

4-Chlorophthalic acid is a fascinating organic compound with unique properties and various applications in the field of chemistry. Here are some engaging facts to consider:

  • Structure and Derivation: This compound belongs to the phthalic acid family, which is characterized by the presence of two carboxylic acid groups attached to a benzene ring. The chlorine substituent at the 4-position distinguishes it from other isomers.
  • Applications: 4-Chlorophthalic acid is used primarily in the synthesis of various chemical compounds, such as dyes and pigments. Its derivatives can also be found in several industrial applications.
  • Reactivity: As a carboxylic acid, it can undergo typical acid reactions, including esterification. It can react with bases to form salts and can be involved in condensation reactions to create larger molecular structures.
  • Environmental Impact: The compound can be a subject of study regarding its environmental impact, especially in terms of its stability and potential bioaccumulation in ecosystems.
  • Research and Development: Ongoing research into 4-chlorophthalic acid includes its use in developing materials with specific properties, showcasing its versatility in modern chemistry.

In summary, 4-chlorophthalic acid is more than just a simple compound; it is a gateway to understanding carboxylic acids and their derivatives while offering insights into sustainability and innovation in chemical applications. As you explore the world of organic compounds, consider the intricate roles that such compounds play in our daily lives and the larger ecosystem.

Synonyms
4-CHLOROPHTHALIC ACID
89-20-3
1,2-Benzenedicarboxylic acid, 4-chloro-
Phthalic acid, 4-chloro-
4-Chloro-phthalic acid
4-chlorobenzene-1,2-dicarboxylic acid
UNII-F7T40O3AM6
F7T40O3AM6
EINECS 201-886-3
MFCD00044755
NSC 57755
NSC-57755
DTXSID2045022
4-CHLORO-1,2-BENZENEDICARBOXYLIC ACID
J95.379B
4-Chlorophthalicacid
4 -chlorophthalic acid
Maybridge1_002266
SCHEMBL1000440
DTXCID0025022
HMS547O22
Phthalic acid, 4-chloro-(8CI)
NSC57755
BBL035506
STL426764
AKOS015961629
CCG-233831
SB39651
4-chloro-1,2-benzenedicarboxylic acid;
AC-14544
AS-14281
SY083787
DB-057118
CS-0101178
NS00039312
C50120
Q27277785
201-886-3