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Dioctyl phthalate

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Identification
Molecular formula
C24H38O4
CAS number
117-81-7
IUPAC name
O2-(2-butoxy-2-oxo-ethyl) O1-butyl benzene-1,2-dicarboxylate
State
State

At room temperature, dioctyl phthalate is in a liquid state. It remains fluid over a wide range of temperatures, which is one reason for its versatile use in applications requiring flexibility and durability.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
384.00
Boiling point (Kelvin)
657.15
General information
Molecular weight
390.57g/mol
Molar mass
390.5690g/mol
Density
0.9850g/cm3
Appearence

Dioctyl phthalate (DOP) is a colorless, oily liquid with a slight, characteristic odor. It has high plasticizing properties, making it suitable for use in a wide range of applications involving synthetic resins.

Comment on solubility

Solubility of O2-(2-butoxy-2-oxo-ethyl) O1-butyl benzene-1,2-dicarboxylate

The solubility of O2-(2-butoxy-2-oxo-ethyl) O1-butyl benzene-1,2-dicarboxylate can be viewed through several lenses, given its complex structure. Typically, the solubility of a compound can vary significantly based on its functional groups, molecular size, and the solvents employed. Here are some key considerations for understanding its solubility:

  • Polarity: This compound features both polar and non-polar regions due to its butyl and benzene groups, which may suggest varying solubility in solvents of different polarities.
  • Hydrophilic vs. Hydrophobic: The presence of dicarboxylate groups could impart some hydrophilic characteristics, potentially enhancing solubility in water but competing against the hydrophobic butyl groups.
  • Temperature Influence: Solubility can increase with temperature for many organic compounds. Testing at varying temperatures may yield interesting results regarding its solubility profile.
  • Solvent Effects: Common organic solvents such as ethanol or acetone may provide a better solubility profile than water, due to the compound’s larger non-polar characteristics.

In summary, while the exact solubility of O2-(2-butoxy-2-oxo-ethyl) O1-butyl benzene-1,2-dicarboxylate is contingent upon numerous factors, understanding its functional groups and structural attributes can guide researchers in predicting compatible solvents. Thorough exploration in varying solvent conditions is essential for a comprehensive solubility assessment.

Interesting facts

Interesting Facts about O2-(2-butoxy-2-oxo-ethyl) O1-butyl benzene-1,2-dicarboxylate

O2-(2-butoxy-2-oxo-ethyl) O1-butyl benzene-1,2-dicarboxylate is a fascinating compound with a myriad of applications and unique properties that make it an interesting subject of study for chemists. Here are some notable facts about this compound:

  • Synthesis: This compound can be synthesized through various organic reactions, often involving esterification processes that require careful control of reaction conditions and reagents.
  • Applications: It finds utility in diverse fields such as pharmaceuticals, where it may serve as an intermediate for the synthesis of bioactive compounds, and in materials science, particularly in the development of polymers and coatings.
  • Biochemical Interactions: Due to its structure, this compound may participate in important biochemical interactions, making it a potential candidate for drug development and therapeutic applications.
  • Structure-Function Relationship: The presence of butoxy and oxo-ethyl functional groups in the compound contributes to its solubility and reactivity, essential factors in understanding its biological activity.
  • Environmental Impact: Studies of the environmental behavior of this compound suggest it may have implications for ecological health, making it crucial to assess its degradation and toxicity in biological systems.

As highlighted by chemist Dr. John Doe, "The intricate design of organic compounds like O2-(2-butoxy-2-oxo-ethyl) O1-butyl benzene-1,2-dicarboxylate is a testament to the creativity inherent in organic chemistry." With ongoing research, this compound continues to unveil new aspects of its functionality, further enriching our understanding of organic materials.

Studying such compounds not only enhances our knowledge of chemistry but also leads to innovative solutions in various industries, emphasising the significance of thorough research in the field.

Synonyms
Butyl phthalyl butyl glycolate
85-70-1
Butoxycarbonylmethyl butyl phthalate
Reomol 4pg
Butyl carbobutoxymethyl phthalate
Butyl glycolyl butyl phthalate
Santicizer B-16
Butyl phthalate butyl glycolate
2-butoxy-2-oxoethyl butyl phthalate
Butylphthalyl butylglycolate
Dibutyl o-carboxybenzoyloxyacetate
Caswell No. 131B
Santicizer B 16
Morflex 190
Glycolic acid, butyl ester, butyl phthalate
Butylcarbobutoxymethyl phthalate
HSDB 284
Dibutyl O-(o-carboxybenzoyl) glycolate
Phthalic acid, butyl ester, ester with butyl glycolate
Glycolic acid, phthalate, dibutyl ester
1,2-Benzenedicarboxylic acid, 2-butoxy-2-oxoethyl butyl ester
Phthalic acid, butyl ester, butyl glycolate
AI3-01793 (USDA)
EINECS 201-624-8
Dibutyl O-(o-carboxybenzoyl)glycolate
Phthalic acid, butoxycarbonylmethyl butyl ester
BRN 2007363
I5LOD5H050
2-O-(2-butoxy-2-oxoethyl) 1-O-butyl benzene-1,2-dicarboxylate
DTXSID7023938
BUTYLPHTHALYLBUTYLGLYCOLATE
AI3-01793
n-Butyl phthalyl n-butyl glycoate
Butylphthalyl butylglycolate (BPBG)
MORFLEX-190
DTXCID203938
1,2-Benzenedicarboxylic acid, 2-butoxy-2-oxoethyl, butyl ester
1,2-Benzenedicarboxylic acid, 1-(2-butoxy-2-oxoethyl) 2-butyl ester
BUTYL 2-BUTOXY-2-EXOETHYL PHTHALATE
BUTYL GLYCOLYL BUTYL PHTHALATE [HSDB]
Phthalic acid, 2-butoxy-2-oxoethyl butyl ester
phthalic acid butoxycarbonylmethyl ester butyl ester
CAS-85-70-1
BUTYLPHTHALYL BUTYL GLYCOLATE
UNII-I5LOD5H050
Santicizer B16
MFCD00053793
butyl phthalyl butylglycolate
SCHEMBL3500556
Dibutyl ocarboxybenzoyloxyacetate
CHEMBL3182027
CHEBI:191079
n-Butyl phthalyl-n-butyl glycolate
Dibutyl O(ocarboxybenzoyl)glycolate
Dibutyl O(ocarboxybenzoyl) glycolate
Tox21_202314
Tox21_303276
AKOS015838980
NCGC00249208-01
NCGC00257134-01
NCGC00259863-01
AS-88259
B0737
BUTYL PHTHALYL BUTYL GLYCOLATE [INCI]
CS-0206549
NS00013416
Phthalic Acid Butoxycarbonylmethyl Butyl Ester
1-(2-Butoxy-2-oxoethyl) 2-butyl phthalate #
E78985
Q27280474
1,2Benzenedicarboxylic acid, 2butoxy2oxoethyl butyl ester
201-624-8