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10095-14-4

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10095-14-4 Usage

Description

6-Hydroxyhexyl acrylate, with the molecular formula C9H16O3, is a clear, colorless liquid characterized by a distinctive odor. It is a chemical compound that plays a significant role in the production of polymers and resins, particularly in the formulation of UV-curable adhesives, coatings, and inks. Known for its low volatility, low skin irritation, and minimal toxicity, 6-hydroxyhexyl acrylate is recognized as a versatile and valuable component within the chemical industry.

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.

Check Digit Verification of cas no

The CAS Registry Mumber 10095-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,9 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10095-14:
(7*1)+(6*0)+(5*0)+(4*9)+(3*5)+(2*1)+(1*4)=64
64 % 10 = 4
So 10095-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O3/c1-2-9(11)12-8-6-4-3-5-7-10/h2,10H,1,3-8H2

10095-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxyhexyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names 6-hydroxyhexyl 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:10095-14-4 SDS

10095-14-4Relevant articles and documents

PROCESS FOR PREPARING 4-HYDROXYBUTYL ACRYLATE

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Paragraph 0524; 0525; 0526; 0527; 0528; 0529; 0530; 0531, (2015/04/22)

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.

Acrylic-based adhesive composition

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, (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.

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