≥99%, Containing polymerization inhibitor MEHQ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Main Applications
Ink, Coating, Photo resist, Adhesives, Stereo lithography
Basic Information
VEEA™: 2- (2-Vinyloxyethoxy)ethyl acrylate
VEEM™: 2- (2-Vinyloxyethoxy)ethyl methacrylate
(1) Radical polymerizable (meth)acryloyl group
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Polymerization is not inhibited by water and bases
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Has many co-polymerizable monomers
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Has no dark reaction
(2) Cationic polymerizable vinyl ether group
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Polymerization is not inhibited by oxygen
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Good dilutability
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Good adhesion
Features and Properties
1.VEEA™ and VEEM™ are monomers with unique structures having different types of polymerizable functional groups in one molecule: radical polymerizable
2.(meth)acryloyl groups and cationic polymerizable vinyl ether groups.
By selecting the polymerization method, unique polymers with (meth)acryloyl or vinyl ether groups as pendant groups can be obtained.
3.VEEA™ and VEEM™ have excellent UV curability as monomers.
Polymerization Method
Details of Functions
Reactive diluent
VEEA™ and VEEM™ can be used as a reactive diluent for heat, UV and EB curable inks.
VEEA™ and VEEM™ are less sensitive to curing inhibition by oxygen in the air, and even thin films (several microns)
UV Curing Properties of VEEA™
UV curing performance (1): UV irradiation equipment: PM25C-100 (USHIO Inc.) 250 W ultra-high pressure mercury vapor lamp (main wavelength = 365 nm), thickness: 300 μm, surface tackiness: judged by finger touch (++ = tack-free, — = uncured) (++ = tack-free, — = not cured)
UV curing performance (2): UV irradiation device: UB031-5BM (EyEGRAPHICS), 80 W high pressure mercury vapor lamp, thickness: 30 μm, line speed: 14 m/min, distance from light source: 10 cm, irradiation energy per pass: 125 mJ/cm2, Irradiation energy per pass: 125 mJ/cm2, Surface tackiness: Tack-free to the touch (++ = tack-free, — = not cured)
UV curing properties of VEEA™ and VEEM™ as reactive diluents
UV curing performance: UV irradiation device: UB031-5BM (EYEGRAPHICS Co., Ltd.) with 80 W high-pressure mercury lamp;
Thickness: 30 μm, Line speed: 14 m/min, Distance from light source: 10 cm, Irradiation energy per pass: 125 mJ/cm2, Surface tackiness: determined by finger touch (++ = tack free, — = uncured) Pencil hardness: measured after 10 passes curing. Acetone rubbing: measured after 10 passes curing
Polymer with a pendant Vinyl Ether Group
Thermal, UV, and EB curable polymers are obtained by radical or anionic polymerization.
Polymer with a pendant (Meth)Acryloyl Group
Thermal, UV, and EB curable polymers are obtained by cation polymerization.
Derivatives
Various acetals can be synthesized by addition reaction to vinyl ether groups.
Examples of Applications
Coatings: Wood coatings, Film coatings, Hard coatings, Optical disk coatings, Optical fiber coatings, etc.
Ink: Inkjet inks, Screen inks, Offset inks, Gravure inks, etc.
Photo Resists: Dry film resist, Semiconductor resist, Photosensitive resin plate, etc.
Adhesives
Stereo-lithography etc.
Utilities
| 정식 스마일 | C=CC(=O)OCCOCCOC=C |
|---|---|
| IUPAC Name | 2-(2-ethenoxyethoxy)ethyl prop-2-enoate |
| InChIKey | URQQDYIVGXOEDA-UHFFFAOYSA-N |
| INCHI | 1S/C9H14O4/c1-3-9(10)13-8-7-12-6-5-11-4-2/h3-4H,1-2,5-8H2 |
| 분자량 | 186.20 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| 분류 | Carboxylic acids and derivatives |
| Subclass | Acrylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acrylic acid esters |
| Alternative Parents | Enoate esters Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acrylic acid ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| 설명 | This compound belongs to the class of organic compounds known as acrylic acid esters. These are organic compounds containing and ester acrylic acid (CH2=CHC(=O)OH). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | 날짜 | 항목 |
|---|---|---|---|
 D2509360 | Certificate of Analysis | Apr 03, 2025 | V758200 |
| D2509585 | Certificate of Analysis | Apr 03, 2025 | V758200 |
| D2509586 | Certificate of Analysis | Apr 03, 2025 | V758200 |
| D2509587 | Certificate of Analysis | Apr 03, 2025 | V758200 |
| D2509599 | Certificate of Analysis | Apr 03, 2025 | V758200 |
| 용해성 | H2O：18g/L(30℃) Organic solvent: Dissolve arbitrarily |
|---|---|
| 끓는점(°C) | 115-116℃/13.3hPa |
