88194-15-4

Usage

Uses

Used in Plastics Industry:
1,3-Benzenedicarboxylic acid, 5-(2-propenyloxy)is used as a plasticizer to enhance the flexibility and durability of plastics. Its ability to increase the workability and longevity of plastic materials makes it a valuable component in this industry.
Used in Adhesives Production:
In the adhesives industry, 1,3-Benzenedicarboxylic acid, 5-(2-propenyloxy)is utilized to improve the adhesive properties of various formulations. Its incorporation into adhesives results in stronger bonds and better performance under different conditions.
Used in Cellulose Acetate Manufacturing:
1,3-Benzenedicarboxylic acid, 5-(2-propenyloxy)plays a crucial role in the manufacturing of cellulose acetate, a versatile material used in the production of films, fibers, and other products. Its presence contributes to the desirable properties of cellulose acetate.
Used in Lacquers Production:
This chemical is also used in the production of lacquers, which are coatings applied to various surfaces for protection and aesthetic purposes. The use of 1,3-Benzenedicarboxylic acid, 5-(2-propenyloxy)in lacquers improves their durability and resistance to wear.
Used in Food Packaging and Pharmaceuticals:
Due to its relatively low toxicity, 1,3-Benzenedicarboxylic acid, 5-(2-propenyloxy)has been approved for use in food packaging and pharmaceuticals. It contributes to the flexibility and stability of packaging materials and is utilized in the formulation of certain pharmaceutical products.
However, there are environmental concerns associated with the use of 1,3-Benzenedicarboxylic acid, 5-(2-propenyloxy)-, as it has the potential to leach out of plastics and accumulate in the environment. This may pose risks to both wildlife and human health, and as such, its use is subject to ongoing scrutiny and regulation.

Upstream product

• 21368-39-8 dimethyl 5-(prop-2-en-1-yloxy)benzene-1,3-dicarboxylate 
• 22326-31-4 5-sulfoisophthalic acid 
• 39630-68-7 diethyl 5-hydroxyisophthalate 
• 618-83-7 5-Hydroxyisophthalic acid 
• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 106-95-6 allyl bromide 

Downstream Products

• 169203-74-1 5-(allyloxy)isophthaloyl chloride 
• 362515-46-6 {3-[3-allyloxy-5-(3-tert-butoxycarbonylamino-propylcarbamoyl)-benzoylamino]-propyl}-carbamic acid tert-butyl ester 
• 362515-48-8 {5-[3-allyloxy-5-(5-tert-butoxycarbonylamino-pentylcarbamoyl)-benzoylamino]-pentyl}-carbamic acid tert-butyl ester 
• 362515-49-9 {3-[3-(3-tert-butoxycarbonylamino-propylcarbamoyl)-5-hydroxy-benzoylamino]-propyl}-carbamic acid tert-butyl ester 
• 362515-52-4 5-allyloxy-N,N'-bis-[3-(2-chloro-acetylamino)-propyl]-isophthalamide 
• 362515-53-5 5-allyloxy-N,N'-bis-[4-(2-chloro-acetylamino)-butyl]-isophthalamide 
• 362515-50-2 {4-[3-(4-tert-butoxycarbonylamino-butylcarbamoyl)-5-hydroxy-benzoylamino]-butyl}-carbamic acid tert-butyl ester 
• 362515-54-6 5-allyloxy-N,N'-bis-[5-(2-chloro-acetylamino)-pentyl]-isophthalamide 
• 362515-51-3 {5-[3-(5-tert-butoxycarbonylamino-pentylcarbamoyl)-5-hydroxy-benzoylamino]-pentyl}-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Linker functionalisation triggers an alternative 3D-topology for Zn-isophthalate-4,4′-bipyridine frameworks

A series of four Zn2+ metal-organic frameworks containing functionalised isophthalate linkers and 4,4′-bipyridine pillars have been prepared and characterised. Isophthalates which contain -OC3H2n+1 alkoxy side chains (with n = 1, 2 or 3) form frameworks with a 3D pillared-layer topology instead of the typical 2D layer topology of the renowned coordination polymers with an interdigitated structure (CIDs), which is found for shorter -OC2H5 side chains. The gas adsorption properties of the materials were analysed using N2, CO2 and O2 adsorption measurements at low temperatures.

Tuning the adsorption behaviors of water, methanol, and ethanol in a porous material by varying the flexibility of substituted groups

Exploring the adsorption and separation of water, methanol, and ethanol is important concerning the use of a sustainable energy source from biofuel. In this paper, the effects of the flexibility of substituted groups have been studied based on three iso-reticular metal-organic frameworks (MOFs), in which the pore surface is decorated with propargyl (-CH2-C≡CH), allyl (-CH2-CH=CH2), and propyl (-CH2-CH2-CH3) groups respectively. These substituted groups stretch into the channel, acting as gates, and the gate-opening for guests is controlled by the flexibility as well as host-guest interactions. Our study results indicate that (i) the adsorption capacity of water, methanol and ethanol enhances accordingly with the increase of the flexibility of substituted groups; (ii) the adsorptive discrimination of water, methanol, and ethanol on this porous sorbent could be tuned by varying the substituted groups.

Parallel combinatorial synthesis of glycodendrimers and their hydrogelation properties

A series of glycodendrons has been assembled using a parallel combinatorial approach, and it has been shown that subtle structural variations between dendrons give rise to significant differences in their hydrogelation behavior.

Synthesis of a Chiral Macrocyclic Dibenzodicyclohexanotetraamide-Containing Stationary Phase for Liquid Chromatography

Allyloxy-substituted macrocyclic dibenzodicyclohexanotetraamide 2 was prepared by the following sequence. Mono-Boc-protected chiral 1,2-cyclohexanediamine (3) was treated with isophthaloyl chloride followed by removal of the Boc group to form bisisophthal

THE INHIBITION OF GLUTAMATE DEHYDROGENASE BY DERIVATIVES OF ISOPHTHALIC ACID

A range of compounds, structurally related to glutamate, have been tested as inhibitors of pea leaf glutamate dehydrogenase assayed in either direction.Only 5-N-substituted derivatives of aminoisophthalic acid completely inhibited the enzyme when tested at concentrations equal to either those of 2-oxoglutarate or glutamate.A minimum of three carbon atoms attached linearly to the amino group was required for maximum inhibition, inhibition was removed if there was any substitution on the first carbon.The 5-N-substituted derivatives also inhibited yeast (to a greater extent) and bovine liver (to a lesser extent) glutamate dehydrogenases.Key Word Index - Pisum sativum; Leguminoseae; yeast; bovine; glutamate dehydrogenase inhibition; isophthalic acid derivatives.