Ethylene glycol phenyl ether acrylate - ≥90%, contains stabilizer , CAS No.48145-04-6

CAS: 48145-04-6 Cat. No.: E102004 Summenformel: C₁₁H₁₂O₃ Molekulargewicht: 192.21 EG-Nummer: 256-360-6

GRADE & PURITY ≥90%, contains stabilizer

Synonyms

EINECS 256-360-6 | FT-0613283 | Ethylene glycol phenyl ether acrylate, 90%, contains 100ppm hydroquinone as inhibitor | 2-Phenoxyethanol acrylate | DTXSID4040715 | 2-Phenoxyethyl Acrylate (stabilized with MEHQ) | ETHYLENE GLYCOL MONOPHENYL ETHER MONOACRYL

Storage

Protected from light,Room temperature

Shipped In

Normal

Specifications

Synonyme

EINECS 256-360-6 | FT-0613283 | Ethylene glycol phenyl ether acrylate, 90%, contains 100ppm hydroquinone as inhibitor | 2-Phenoxyethanol acrylate | DTXSID4040715 | 2-Phenoxyethyl Acrylate (stabilized with MEHQ) | ETHYLENE GLYCOL MONOPHENYL ETHER MONOACRYL

Spezifikationen & Reinheit

≥90%, contains stabilizer

Storage

Protected from light,Room temperature

Verschickt in

Normal

Reinheit

≥90%

Namen und Kennungen

• Pubchem Sid: 504753589
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753589
• Kanonisches Lächeln: C=CC(=O)OCCOC1=CC=CC=C1
• IUPAC Name: 2-phenoxyethyl prop-2-enoate
• InChIKey: RZVINYQDSSQUKO-UHFFFAOYSA-N
• INCHI: 1S/C11H12O3/c1-2-11(12)14-9-8-13-10-6-4-3-5-7-10/h2-7H,1,8-9H2
• Isomere SMILES: C=CC(=O)OCCOC1=CC=CC=C1
• Molekulargewicht: 192.21
• Reaxy-Rn: 2102773
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2102773&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Phenol ethers

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Phenol ethers
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenol ethers
• Alternative Parents: Phenoxy compounds Alkyl aryl ethers Acrylic acid esters Enoate esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Phenol ether - Alkyl aryl ether - Acrylic acid ester - Monocyclic benzene moiety - Acrylic acid or derivatives - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Carboxylic acid derivative - Ether - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - Organooxygen compound - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

Discover Target: THRB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Solubility in water: Practically insoluble; Very soluble in Ethanol,Ether
• Empfindlichkeit: Light Sensitive
• Brechungsindex: 1.518
• Flammpunkt (°C): 113°C
• Siedepunkt (°C): 84°C
• Molekulargewicht: 192.210 g/mol
• XLogP3: 2.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 192.079 Da
• Monoisotopic Mass: 192.079 Da
• Topological Polar Surface Area: 35.500 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 183.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referenzen

1. Enke Feng, Xiaoqin Li, Zhongquan Yu, Zhiming Yang, Zhiqiang Wu, Mengzhen Zhang, Qin Wang, Xinxian Ma.  (2023)  Self-adaptive high-temperature gels with long-lasting underwater stability for environmentally tolerant flexible sensors and water-writing papers.  Journal of Materials Chemistry C,  12  (5): (1897-1908).  [PMID:] [10.1039/D3TC03889K]

2. Lin Li, Zhenpeng Zhang, Minhui Wang, Yanan Zhang, Xun Lu.  (2023)  UV-curable epoxy acrylate composite coatings with high flexibility, super-hydrophobicity, wear-resistance and self-healing property.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2023.107649]

3. Bin Guo, Mingxuan Wang, Diqin Zhang, Minyuan Sun, Yong Bi, Yuxia Zhao.  (2023)  High Refractive Index Monomers for Improving the Holographic Recording Performance of Two-Stage Photopolymers.  ACS Applied Materials & Interfaces,      [PMID:37167544] [10.1021/acsami.3c01446]

4. Yuewei Li, Shuqiang Peng, Ranjith Kumar Kankala, Lixin Wu, Ai-Zheng Chen, Shi-Bin Wang.  (2022)  3D printing of mechanically robust MXene-encapsulated polyurethane elastomer.  COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING,      [PMID:] [10.1016/j.compositesa.2022.107182]

5. Ke Li, Xingjie Zan, Chen Tang, Zhuangzhuang Liu, Jianghuan Fan, Gang Qin, Jia Yang, Wei Cui, Lin Zhu, Qiang Chen.  (2022)  Tough, Instant, and Repeatable Adhesion of Self-Healable Elastomers to Diverse Soft and Hard Surfaces.  Advanced Science,  9  (12): (2105742).  [PMID:35187853] [10.1002/advs.202105742]

6. Diqin Zhang, Yu Zhao, Zhen Zhang, Bin Guo, Jianhua Zhu, Yan Ye, Yuxia Zhao.  (2022)  Improving performance of two-stage photopolymers for volume holographic recording by fluorinated epoxy-amine cross-linked matrices.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (20): (52161).  [PMID:] [10.1002/app.52161]

7. Qiming Yan, Meng Zhou, Heqing Fu.  (2020)  Study on mussel-inspired tough TA/PANI@CNCs nanocomposite hydrogels with superior self-healing and self-adhesive properties for strain sensors.  COMPOSITES PART B-ENGINEERING,      [PMID:] [10.1016/j.compositesb.2020.108356]

8. Peng Shan, Bai Ligai, Shi Xiaoqian, Li Mingxue, Wang Laisen, Sun Fanrong, Liu Haiyan.  (2019)  A rapid method for on-line solid-phase extraction and determination of dioscin in human plasma using a homemade monolithic sorbent combined with high-performance liquid chromatography.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  412  (2): (473-480).  [PMID:31792597] [10.1007/s00216-019-02256-5]

9. Shenxin Pan, Chao Chang, Gang Wu, Zidong He, Chongyin Zhang, Shuqiang Xiong, Gangsheng Tong, Xinyuan Zhu.  (2025)  Bioinspired Antiswelling Hydrogel Sensors with High Strength and Rapid Self-Recovery for Underwater Information Transmission.  ACS Applied Materials & Interfaces,      [PMID:39878567] [10.1021/acsami.4c17863]

10. Azhu Wang, Xianwei Zhao, Zhiwei Shi, Chunyu Lv, Pei Li, Jun Yu, Han Rao, Haining Chen, Huicong Liu, Weiping Li, Xiaoyu Jiang.  (2024)  Developing high-efficiency photoinitiation systems by Leveraging highly Matched Interplays between photosensitizer and photoinitiator for enhanced energy transfer.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2024.113669]

11. Xiaobo Wang, Luxin Cao, Sen Liu, Daye Guo, Kaiyuan Liu, Shuyan Yu, Yongpeng Ma, Xiaojing Zhang, Kaiqi Fan.  (2025)  Hydrophobic Eutectogels for High-Humidity Environment Sensing.  JOURNAL OF APPLIED POLYMER SCIENCE,      [PMID:] [10.1002/app.58010]

12. Yanan Guo, Xuming Liu, Qin Zhang, Xin Liu.  (2026)  Closed-loop recyclable and ultra-low temperature resistant underwater adhesive.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.179712]

13. Qianyu Wei, Weicheng Gao, Tianze Zhang, Lixia Long, Jin Zhao, Lizhi Pan, Xubo Yuan.  (2026)  Printable environmentally robust hydrophobic eutectogel sensors with high strength and strong adhesion for human–machine interaction.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.179566]