32223-72-6

Usage

Uses

Used in the Production of Polyurethane Polymers:
4-(Octyloxy)phenyl isocyanate is used as a key component in the synthesis of polyurethane polymers, which are versatile materials known for their wide range of applications across various industries.
Used in Foam Industry:
In the foam industry, 4-(Octyloxy)phenyl isocyanate is used as a raw material for producing flexible and rigid foams, which are utilized in furniture, bedding, automotive seating, and insulation applications. Its hydrophobic nature contributes to the water resistance of these foams.
Used in Coatings Industry:
4-(Octyloxy)phenyl isocyanate is used as a binder in the formulation of coatings, providing durability, water resistance, and low surface energy, which are desirable properties in coatings for various surfaces including wood, metal, and plastic.
Used in Adhesives Industry:
As a component in adhesive formulations, 4-(Octyloxy)phenyl isocyanate is used to enhance the bonding strength and water resistance of adhesives, making them suitable for a variety of substrates and environments.
Used in Sealants Industry:
4-(Octyloxy)phenyl isocyanate is used in the production of sealants to provide excellent adhesion, flexibility, and resistance to water and environmental factors, which are crucial for sealing applications in construction and industrial settings.

InChI:InChI=1/C15H21NO2/c1-2-3-4-5-6-7-12-18-15-10-8-14(9-11-15)16-13-17/h8-11H,2-7,12H2,1H3

Upstream product

• 2493-84-7 p-octyloxybenzoic acid 
• 75-44-5 phosgene 
• 39905-45-8 4-octyloxyaniline 
• 32315-10-9 bis(trichloromethyl) carbonate 

Downstream Products

• 112923-05-4 (4-Octyloxy-phenyl)-carbamic acid 2-morpholin-4-yl-ethyl ester; hydrochloride 
• 1056029-94-7 N-(1-deoxy-D-glucitol-1-yl)-N'-(4-octyloxyphenyl)urea 
• 1056029-95-8 N-(1-deoxy-D-glucitol-1-yl)-N-methyl-N'-(4-octyloxyphenyl)urea 
• 1056029-96-9 N-[tris(hydroxymethyl)methyl]-N'-(4-octyloxyphenyl)urea 

Relevant academic research and scientific papers

Oxime Carbamate-Discovery of a series of novel FAAH inhibitors

A series of novel oxime carbamates have been identified as potent inhibitors of the key regulatory enzyme of the endocannabinoid signaling system, fatty acid amide hydrolase (FAAH). In this Letter, the rationale behind the discovery and the biological evaluations of this novel class of FAAH inhibitors are presented. Both in vitro and in vivo results of selected targets are discussed, along with inhibition kinetics and molecular modeling studies.1.

A family of hydrogels based on ureido-linked aminopolyol-derived amphiphiles and bolaamphiphiles: Synthesis, gelation under thermal and sonochemical stimuli, and mesomorphic characterization

This article describes the systematic preparation of a novel family of carbohydrate amphiphiles and bolaamphiphiles in which hydrophilic and hydrophobic units are connected via a ureido or bis(ureido) moiety. The sugar core is derived from aminopolyols such as D-glucamine (1), N-methyl-D-glucamine (2), or the sugar-like species tris(hydroxymethyl)aminomethane (3). The O-unprotected derivatives behave as self-organizing nonionic surfactants with good water gelation ability, which can be induced under thermal or ultra-sound-driven stimuli. In addition, some derivatives of 1 and 2, and rarely 3 also formed lyotropic liquid crystals with lamellar or hexagonal structures that exhibit low-temperature transitions.

Comparison of base-promoted and self-catalyzed conditions in the synthesis of isocyanates from amines using triphosgene

Comparison of base-promoted and self-catalyzed conditions for the synthesis of isocyanates from amines and triphosgene shows no advantage in using an amine base in the majority of cases. The workup and isolation of the product is simplified under base-free conditions. Yields of between 50 and 90% after distillation were common. Only acid-sensitive substrates need a base catalyst. Copyright Taylor & Francis Group, LLC.