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5-Hydroxypentyl acrylate is a versatile chemical compound belonging to the class of acrylate monomers. It is known for its ability to polymerize and form strong, durable materials, as well as its good thermal and chemical resistance.

57198-94-4

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57198-94-4 Usage

Uses

Used in Polymer and Coating Production:
5-Hydroxypentyl acrylate is used as a monomer in the production of various polymers and coatings. Its polymerization ability contributes to the creation of strong and durable materials, making it suitable for a wide range of applications.
Used in Adhesive and Sealant Manufacturing:
In the adhesive and sealant industry, 5-hydroxypentyl acrylate is used as a key component to enhance the performance and properties of these products. Its strong bonding capabilities and resistance to harsh conditions make it an ideal choice for various industrial applications.
Used in Industrial Product Development:
5-Hydroxypentyl acrylate is utilized in the development of other industrial products due to its low volatility and low odor. These characteristics make it an attractive option for use in consumer products, where minimizing odor and maintaining a stable product performance are essential.
Overall, 5-hydroxypentyl acrylate is a valuable chemical compound that improves the performance and properties of a wide range of products across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 57198-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57198-94:
(7*5)+(6*7)+(5*1)+(4*9)+(3*8)+(2*9)+(1*4)=164
164 % 10 = 4
So 57198-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O3/c1-2-8(10)11-7-5-3-4-6-9/h2,9H,1,3-7H2

57198-94-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxypentyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names hydroxypentyl acrylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57198-94-4 SDS

57198-94-4Downstream Products

57198-94-4Relevant academic research and scientific papers

Polymerizable liquid crystal compound, and optical antisotropic compsn.

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Paragraph 0070, (2016/10/10)

The present description relates to a polymerizable liquid crystal compound, a polymerizable liquid crystal composition including the same, and an optically anisotropic body. The polymerizable liquid crystal compound includes a radical derived from the first liquid crystal molecule including a mesogen group having a non-aromatic ring; a radical derived from the second liquid crystal molecule including a mesogen group that has a structure different from said mesogen group having a non-aromatic ring and includes a ring containing a double bond; and a linker that has a specific structure and links the sp3-hybridized carbon in the non-aromatic ring of the radical derived from the first liquid crystal molecule and the sp2-hybridized carbon in the mesogen group of the radical derived from the second liquid crystal molecule, wherein at least one of the radicals derived from the first and the second liquid crystal molecules may include one or more polymerizable groups which are connected to the mesogen group directly or via spacer groups. Such polymerizable liquid crystal compound makes it possible to exhibit stable reverse wavelength dispersion solely or by being mixed with other liquid crystal materials.

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

Popescu, Dragos,Hoogenboom, Richard,Keul, Helmut,Moeller, Martin

experimental part, p. 80 - 89 (2010/08/20)

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

-

, (2008/06/13)

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

Kumakura, M.,Kojima, T.,Kaetsu, I.

, p. 65 - 72 (2007/10/02)

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.

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