10095-14-4

Basic information

• Product Name: 6-hydroxyhexyl acrylate
• Synonyms: 6-hydroxyhexyl acrylate;Acrylic acid 6-hydroxyhexyl ester;Einecs 233-227-0;2-Propenoic acid, 6-hydroxyhexyl ester
• CAS NO: 10095-14-4
• Molecular Formula: C₉H₁₆O₃
• Molecular Weight: 172.22154
• EINECS: 233-227-0
• Mol File: 10095-14-4.mol

Chemical Properties

• Boiling Point: 255.3 °C at 760 mmHg
• Flash Point: 100.6 °C
• Appearance: /
• Density: 0.994 g/cm³
• Vapor Pressure: 0.0025mmHg at 25°C
• Refractive Index: 1.452
• PKA: 15.16±0.10(Predicted)
• CAS DataBase Reference: 6-hydroxyhexyl acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: 6-hydroxyhexyl acrylate(10095-14-4)
• EPA Substance Registry System: 6-hydroxyhexyl acrylate(10095-14-4)

Safety Data

• Hazardous Substances Data: 10095-14-4(Hazardous Substances Data)

Usage

Uses

Used in Adhesives Industry:
6-Hydroxyhexyl acrylate is used as a reactive diluent for enhancing the performance of UV-curable adhesives. Its incorporation improves the curing process and the final adhesive's properties, such as adhesion strength and flexibility.
Used in Coatings Industry:
In the coatings industry, 6-Hydroxyhexyl acrylate serves as a reactive diluent in the formulation of UV-curable coatings. It contributes to faster curing times and improved coating characteristics, including durability, scratch resistance, and weather resistance.
Used in Inks Industry:
6-Hydroxyhexyl acrylate is utilized as a reactive diluent in the production of UV-curable inks. Its use results in inks with quick drying times, high gloss, and excellent color stability.
Used in Specialty Chemicals Production:
6-Hydroxyhexyl acrylate is used as a building block in the synthesis of other specialty chemicals. Its unique properties make it a valuable intermediate in the creation of various chemical compounds for diverse applications.
Used in Chemical Research and Development:
Due to its versatility and unique properties, 6-hydroxyhexyl acrylate is employed in research and development for exploring new applications and improving existing formulations in various chemical and material science fields.

InChI:InChI=1/C9H16O3/c1-2-9(11)12-8-6-4-3-5-7-10/h2,10H,1,3-8H2

Upstream product

• 629-11-8 1,6-hexanediol 
• 79-10-7 acrylic acid 
• 292638-85-8 acrylic acid methyl ester 

Downstream Products

• 130977-39-8 2-(Hydroxy-phenyl-methyl)-acrylic acid 6-hydroxy-hexyl ester 

Relevant articles and documents

PROCESS FOR PREPARING 4-HYDROXYBUTYL ACRYLATE

A process for preparing 4-hydroxybutyl acrylate by transesterifying an alkyl acrylate with 1,4-butanediol in the presence of a dialkyltin oxide such that each of the alkyl groups has 4 to 8 carbon atoms, characterized in that the amount of the dialkyltin oxide is adjusted to 0.00001 to 0.01 moles per one mole of the alkyl acrylate.

Hydroxy functional acrylate and methacrylate monomers prepared via lipase-catalyzed transacylation reactions

Candida antarctica lipase B (CAL-B, Novozyme 435) catalyzes the transacylation of methyl acrylate and methyl methacrylate with diols and triols in 2-methyl-2-butanol at 50 °C. Under the experimental conditions, up to 70 mol% of the acyl donor methyl acrylate was converted. Methyl methacrylate is the less efficient acyl donor (up to 60 mol%) due to the higher sterical hindrance in the enzymatic transacylation. Under the reaction conditions high yields of the mono-acylated products are obtained, which contain minor amounts of bis(meth)acrylates. In addition it was observed that Novozyme 435 catalyzes regioselectively the acylation of the primary hydroxyl groups. In comparison with the chemical catalyzed route no selectivity was observed for unsubstituted diols. For substituted diols more mono-acylated product was formed in the lipase-catalyzed reaction than in the chemical catalyzed reaction.

Acrylic-based adhesive composition

An Adhesive composition for us in surgery, especially ophthalmic surgery, comprises a mixture of a cyanoacrylate of general formula (I) and an acrylate compound of formula (II) where R4 is an alkylene group and Y is a cycloalkyl group or Y═OR where R═H or acryloyl. It is found that compositions of this type have a number of advantages over simple cyanoacrylate adhesives, including: (a) a longer cure time, allowing easier handling of the joint; (b) a more flexible cured product; (c) a tendency for the cured to come away from the tissue after a month or so thus facilitating healing; and (d) a substantially non-exothermic curing reaction, thereby avoiding thermal damage to the tissue.

FIBROUS POLYMERIC COMPOSITES IMMOBILIZING GLUCOSE OXIDASE

Fibrous polymeric composites immobilizing glucose oxidase have been prepared by the radiation polymerization of various glass-forming monomers at low temperatures.The radiation polymerization of the monomer solution containing the enzymes and fibrous material was studied as a function of the irradiation temperature, at which the polymerization rate and enzyme activity had optimum values.The nature of the monomer, monomer concentration and the thickness of the polymer matrix on the fibrous material was shown to affect the enzyme activity of the composites.