14236-13-6

Basic information

• Product Name: 4-tert-butylphthalic acid
• Synonyms: 4-tert-butylphthalic acid
• CAS NO: 14236-13-6
• Molecular Formula: C₁₂H₁₄O₄
• Molecular Weight: 222.23716
• Mol File: 14236-13-6.mol

Chemical Properties

• Melting Point: 160-161 °C
• Boiling Point: 375.7±42.0 °C(Predicted)
• Appearance: /
• Density: 1.226±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.35±0.10(Predicted)
• CAS DataBase Reference: 4-tert-butylphthalic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tert-butylphthalic acid(14236-13-6)
• EPA Substance Registry System: 4-tert-butylphthalic acid(14236-13-6)

Safety Data

• Hazardous Substances Data: 14236-13-6(Hazardous Substances Data)

Usage

Uses

Used in Plastics Industry:
4-tert-butylphthalic acid is used as a plasticizer to enhance the flexibility and resilience of plastics. Its incorporation into plastic materials allows for improved performance and durability in various applications.
Used in Coatings Industry:
As a component in coatings, 4-tert-butylphthalic acid contributes to the overall properties of the coating, such as adhesion, durability, and resistance to environmental factors. This makes it suitable for use in various types of coatings, including automotive, architectural, and industrial coatings.
Used in Adhesives Industry:
In the adhesives industry, 4-tert-butylphthalic acid is used to improve the adhesive properties of various formulations. Its addition can enhance the bonding strength, flexibility, and resistance to environmental stress, making it suitable for a wide range of adhesive applications.
Used in Other Industrial Products:
4-tert-butylphthalic acid is also utilized in the production of other industrial products, such as sealants, elastomers, and gaskets. Its versatility and properties make it a valuable component in these applications, contributing to their performance and longevity.

Upstream product

• 7397-06-0 4-t-butyl-o-xylene 
• 31592-22-0 2,6-di-tert-butyl-1,4-naphthoquinone 
• 7732-18-5 water 
• 91-20-3 naphthalene 
• 32703-79-0 4-tert-butylphthalic anhydride 
• 3905-64-4 2,6-di-tert-butylnaphthalene 
• 95-47-6 o-xylene 

Downstream Products

• 32703-79-0 4-tert-butylphthalic anhydride 
• 50727-07-6 4-tert-butylphthalimide 
• 52319-94-5 4-tert-butyl-phthalic acid diethyl ester 
• 32703-80-3 4-(t-butyl)phthalonitrile 

Relevant articles and documents

Preparation method of 4 -tert-butyl phthalonitrile (by machine translation)

The invention discloses a preparation method of 4 -tert-butylphthalonitrile, and belongs to the technical field of organic synthesis. To the technical scheme, o-xylene and chlorobutane are reacted under the action of catalyst iodine to obtain 4 -tert-butylphthalyl chloride; 4 -tert-butyl phthalic acid is reacted with ammonia solution to obtain 4 -tert-butylphthalamide; 4 -tert-butylphthalamide and dehydrating agent are subjected to dehydration reaction to obtain 4 - 4 - 4 -tert-butylphthalonitrile; and the tert-butylphthalonitrile is obtained through dehydration 4 - 4 . The method has the advantages of mild reaction conditions, high yield, low cost and suitability for industrial production, and is a synthetic method with industrial production value. (by machine translation)

Preparation method of 4-tertiary butyl o-phthalaldehyde

The invention discloses a preparation method of 4-tertiary butyl o-phthalaldehyde, and belongs to the field of organic synthesis. The technical scheme includes that the preparation method includes thesteps: taking the 4-tertiary butyl o-phthalaldehyde as

Metallo-β-lactamase inhibitory activity of phthalic acid derivatives

4-Butyl-3-methylphthalic acid was recognized as a metallo-β-lactamase inhibitor. The structure-activity relationship study of substituted phthalic acids afforded 3-phenylphthalic acid derivatives as potent IMP-1 inhibitors. On the other hand, 3-substituted with 4-hydroxyphenyl phthalic acid derivative displayed a potent combination effect with biapenem (BIPM) against Pseudomonas aeruginosa that produce IMP-1.

Synthesis of Tetrakis(4-tert-butylbenzo)porphin and its Metal Complexes

The condensation of 4-tert-butylphthalimide with sodium and zinc acetates leads to the zinc complex of tetrakis(4-tert-butylbenzo)porphin, which forms the free ligand under the influence of boiling trifluoroacetic acid.A series of metalloporphyrins were obtained from tetrakis(4-tert-butylbenzo)porphin and metal acetates.

Soluble trans-Di-1-alkynyl- and Poly-trans-ethynyl(tetraalkylphthalocyaninato)metal IVB Derivatives

The hitherto unknown peripheric substituted trans-dihalogeno(tetra-tert-butylphthalocyaninato)metal IVB derivatives 5a,b and 6a,b as well as trans-dichlorogermanium (6c) were converted into the monomeric, soluble trans-di-1-alkynyl(tetra-tert-butylphthalocyaninato)metal IVB compounds 10a - h and trans-di-1-alkynylgermanium compounds 10i - l, respectively, by the reaction with various 1-alkynyl Grignard derivatives 9a - e.The high solubility of all products in organic solvents and the strong ring-current effect of the macrocycle on the axial ligands are remarkable.The formally analogous reaction with the bidentate ethynediyldi-Grignard compound 9f leads to the soluble, acetylene-bridged polymers 12a - c.These are considered as model compounds for a new kind of one-dimensional conductors proposed by us.