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Glycidyl Phenyl Ether - >99.0%(GC), high purity , CAS No.122-60-1

    Grade & Purity:
  • ≥99%(GC)
In stock
Item Number
G156841
Grouped product items
SKU Size
Availability
Price Qty
G156841-5g
5g
5
$9.90
G156841-25g
25g
3
$12.90
G156841-50g
50g
2
$16.90
G156841-100g
100g
2
$21.90
G156841-500g
500g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$52.90

Basic Description

Synonyms 2-(Phenoxymethyl)oxirane | Phenylglycidyl ether | Phenyl glycidyl ether | 1,2-Epoxy-3-phenoxypropane | 2,3-Epoxypropyl phenyl ether | Phenyl 2,3-epoxypropyl ether
Specifications & Purity ≥99%(GC)
Storage Temp Room temperature,Argon charged
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Phenol ethers
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Phenol ethers
Alternative Parents Phenoxy compounds  Alkyl aryl ethers  Oxacyclic compounds  Epoxides  Dialkyl ethers  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Oxacycle - Organoheterocyclic compound - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteromonocyclic compound
Description 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 aromatic ether

Associated Targets(Human)

Lymphoblastoid cell (5959 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHO (4503 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488183133
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488183133
IUPAC Name 2-(phenoxymethyl)oxirane
INCHI InChI=1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2
InChIKey FQYUMYWMJTYZTK-UHFFFAOYSA-N
Smiles C1C(O1)COC2=CC=CC=C2
Isomeric SMILES C1C(O1)COC2=CC=CC=C2
WGK Germany 3
UN Number 2810
Packing Group I
Molecular Weight 150.18
Beilstein 2744
Reaxy-Rn 2744
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2744&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

42 results found

Lot Number Certificate Type Date Item
D2527191 Certificate of Analysis Mar 29, 2025 G156841
D2527215 Certificate of Analysis Mar 29, 2025 G156841
D2527189 Certificate of Analysis Mar 29, 2025 G156841
D2527190 Certificate of Analysis Mar 29, 2025 G156841
A2521404 Certificate of Analysis Dec 26, 2024 G156841
A2521405 Certificate of Analysis Dec 26, 2024 G156841
A2522075 Certificate of Analysis Dec 26, 2024 G156841
A2522067 Certificate of Analysis Dec 26, 2024 G156841
A2510477 Certificate of Analysis Dec 16, 2024 G156841
F2411181 Certificate of Analysis May 30, 2024 G156841
F2411179 Certificate of Analysis May 30, 2024 G156841
F2411180 Certificate of Analysis May 30, 2024 G156841
D2423237 Certificate of Analysis Apr 10, 2024 G156841
D2423235 Certificate of Analysis Apr 10, 2024 G156841
D2423236 Certificate of Analysis Apr 10, 2024 G156841
C2401292 Certificate of Analysis Feb 22, 2024 G156841
L2318276 Certificate of Analysis Dec 11, 2023 G156841
L2318325 Certificate of Analysis Dec 11, 2023 G156841
L2318275 Certificate of Analysis Dec 11, 2023 G156841
I2312544 Certificate of Analysis Sep 02, 2023 G156841
I2312545 Certificate of Analysis Sep 02, 2023 G156841
I2312546 Certificate of Analysis Sep 02, 2023 G156841
G2326878 Certificate of Analysis Jul 03, 2023 G156841
G2326790 Certificate of Analysis Jul 03, 2023 G156841
G2326638 Certificate of Analysis Jul 03, 2023 G156841
G2326631 Certificate of Analysis Jul 03, 2023 G156841
G2326629 Certificate of Analysis Jul 03, 2023 G156841
G2326627 Certificate of Analysis Jul 03, 2023 G156841
G2326625 Certificate of Analysis Jul 03, 2023 G156841
D2320640 Certificate of Analysis Apr 14, 2023 G156841
D2320644 Certificate of Analysis Apr 14, 2023 G156841
D2320654 Certificate of Analysis Apr 14, 2023 G156841
D2320657 Certificate of Analysis Apr 14, 2023 G156841
D2320655 Certificate of Analysis Apr 14, 2023 G156841
D2320656 Certificate of Analysis Apr 14, 2023 G156841
D2320648 Certificate of Analysis Apr 14, 2023 G156841
D2320649 Certificate of Analysis Apr 14, 2023 G156841
D2320647 Certificate of Analysis Apr 14, 2023 G156841
H2213186 Certificate of Analysis Jun 23, 2022 G156841
H2213184 Certificate of Analysis Jun 20, 2022 G156841
H2213182 Certificate of Analysis Jun 20, 2022 G156841
H2215039 Certificate of Analysis Jun 20, 2022 G156841

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Chemical and Physical Properties

Solubility Soluble in water (2.4g/L);Soluble in benzene, ether, alcohol; Mixed in acetone, toluene
Sensitivity Air sensitive
Refractive Index 1.53
Flash Point(°F) 237.2°F
Flash Point(°C) 114.0°C
Boil Point(°C) 245 °C
Melt Point(°C) 3.5°C
Molecular Weight 150.170 g/mol
XLogP3 1.600
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 3
Exact Mass 150.068 Da
Monoisotopic Mass 150.068 Da
Topological Polar Surface Area 21.800 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 119.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 1
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Didi Dong, Xinyu Zhao, Chun Pu, Yao Yao, Bo Zhao, Ge Tian, Ganggang Chang, Xiaoyu Yang.  (2023)  Hierarchical Amino-Functionalized Ionic Liquids@MOF Composite Gel for Catalytic Conversion of CO2.  INORGANIC CHEMISTRY,  62  (49): (20528–20536). 
2. Lihua Zhu, Peiying Cheng, Zhiyin Xiao, Chunxin Lu, Bing Li, Xiujuan Jiang, Zhongquan Shen, Nianlong Qian, Wei Zhong, Yabing He.  (2024)  Incorporation of phenolic skeleton into imidazolium ionic polymers as recyclable catalysts for efficient fixation of CO2 into cyclic carbonates.  CHEMICAL ENGINEERING JOURNAL,  481  (148359). 
3. Xinlan Hu, Yanyun Li, Hongfeng Chen, Jue Cheng, Qingsong Lian.  (2024)  Self-assembly strengthening-toughening epoxy/Graphene composites through intermolecular π-π interactions with ultralow Graphene content.  POLYMER,  291  (126611). 
4. Hui Yang, Guoming Yuan, Enxiang Jiao, Kunxin Wang, WenJie Diao, Zhao Li, Kun Wu, Jun Shi.  (2023)  Low dielectric constant and high thermal stability of liquid crystal epoxy polymers based on functionalized poly(phenylene oxide).  EUROPEAN POLYMER JOURNAL,  198  (112378). 
5. Yang Feng, Hua Qiu, Panhong Deng, Zhuguang Nie, Jinqiu Chen, Kaijie Gong, Xiaodong Fan, Shuhua Qi.  (2023)  Tuning the static and dynamic properties of epoxy vitrimers through modulation of cross-link density.  EUROPEAN POLYMER JOURNAL,  196  (112308). 
6. Jinyi Liu, Haojie Yu, Li Wang, Sergey Z. Vatsadze, Dingning Chen, Xudong Wu, Xiaodan Gong, Yu Wang.  (2023)  One-step synthesis of ferrocenyl glycidyl ethers as combustion catalysts for the thermal decomposition of ammonium perchlorate.  POWDER TECHNOLOGY,  428  (118772). 
7. Ming Lei, Hua Huang, Junliang Liu, Feng Peng.  (2023)  A gemini ionic liquid and its low-temperature demulsification performance in water-in-crude oil emulsions.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  671  (131696). 
8. Wensheng Wei, Yuxin Wang, Zizhen Yan, Jiaxiang Hou, Guangwen Xu, Lei Shi.  (2023)  One-step DMC synthesis from CO2 under catalysis of ionic liquids prepared with 1,2-propylene glycol.  CATALYSIS TODAY,  418  (114052). 
9. Yupeng Chen, Chong Chen, Xue Li, Nengjie Feng, Lei Wang, Hui Wan, Guofeng Guan.  (2022)  Hydroxyl-ionic liquid functionalized metalloporphyrin as an efficient heterogeneous catalyst for cooperative cycloaddition of CO2 with epoxides.  Journal of CO2 Utilization,  62  (102107). 
10. Zhihang Ma, Xiao Wang, Junru Li, Xinlin Li, Chuanwei Zhang, Ruyi Zhang, Yan Gu, Pengfei Zhang.  (2022)  Isoconversional models toward the curing kinetics of self-healable epoxy resin TGDDM and acid anhydride.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (31): (e52718). 
11. Zizhao Qian, Yuanxiang Xiao, Xujun Zhang, Qing Li, Lujie Wang, Feiya Fu, Hongyan Diao, Xiangdong Liu.  (2022)  Bio-based epoxy resins derived from diphenolic acid via amidation showing enhanced performance and unexpected autocatalytic effect on curing.  CHEMICAL ENGINEERING JOURNAL,  435  (135022). 
12. Xiaofei Chen, Mingfeng Wei, Aibing Yang, Fengrui Jiang, Bao Li, Oxana A. Kholdeeva, Lixin Wu.  (2022)  Near-Infrared Photothermal Catalysis for Enhanced Conversion of Carbon Dioxide under Mild Conditions.  ACS Applied Materials & Interfaces,  14  (4): (5194–5202). 
13. Haolan Gou, Yingying Zhao, Yanglong Zhou, Wei Wei, Xiaoma Fei, Xiaojie Li, Xiaoya Liu.  (2021)  Effects of different imidazole accelerators on curing behavior and cross-linked network of epoxy resin/phenolic resin/benzoxazine ternary system.  POLYMERS FOR ADVANCED TECHNOLOGIES,  33  (2): (610-626). 
14. Wei Hui, Xiang Wang, Xiao-Ning Li, Hai-Jun Wang, Xue-Mei He, Xin-Yi Xu.  (2021)  Protic ionic liquids tailored by different cationic structures for efficient chemical fixation of diluted and waste CO2 into cyclic carbonates.  NEW JOURNAL OF CHEMISTRY,  45  (24): (10741-10748). 
15. Bo-Yun Liu, Min-Jie Chen, Liang Yang, Bo Zhao, Tao Xia, Gang-Gang Chang.  (2021)  Hollow MOF capsule encapsulated amino-functionalized ionic liquid for excellent CO2 catalytic conversion.  CHINESE JOURNAL OF CHEMICAL ENGINEERING,  40  (124). 
16. Yingchun Guo, Lei Feng, Changcheng Wu, Xiaomei Wang, Xu Zhang.  (2020)  Confined pyrolysis transformation of ZIF-8 to hierarchically ordered porous Zn-N-C nanoreactor for efficient CO2 photoconversion under mild conditions.  JOURNAL OF CATALYSIS,  390  (213). 
17. Wang Zhanwen, Li Shizhuo, Wang Jianhua, Han Enlin, Tian Guofeng, Wu Dezhen.  (2020)  Dielectric and mechanical properties of polyimide fiber reinforced cyanate ester resin composites with varying resin contents.  JOURNAL OF POLYMER RESEARCH,  27  (6): (1-5). 
18. Emmanuelia Akimana, Jichao Wang, Natalya V. Likhanova, Somboon Chaemchuen, Francis Verpoort.  (2020)  MIL-101(Cr) for CO2 Conversion into Cyclic Carbonates, Under Solvent and Co-Catalyst Free Mild Reaction Conditions.  Catalysts,  10  (4): (453). 
19. Yong Yang, Peng Yan, Dan Wang, Fang Xie, Dengmeng Song, Ning Wang, Jun Li.  (2024)  A2B2-zinc(II)porphyrin/divinylbenzene Copolymer as Efficiently Bifunctional Catalyst for Cycloaddition of CO2 with Epoxides.  EUROPEAN JOURNAL OF INORGANIC CHEMISTRY,    (e202400589). 
20. Zhengyu Yang, Jianmin Li, Yubin Wang, Mengyao Shi, Jide Wang, Changyan Guo.  (2025)  CO2 fixation for the synthesis of cyclic carbonates using Br-ZIF-L with enriched defects.  FUEL,  390  (134701). 
21. Wensheng Wei, Yuxin Wang, Guangwen Xu, Jinggang Zhao, Lei Shi.  (2025)  Construction of multifunctionally integrated catalyst via a self-assembly strategy for efficient CO2 cycloaddition.  FUEL,  388  (134499). 
22. Wen-Li Bao, Jie Kuai, Hai-Yang Gao, Meng-Qi Zheng, Zhong-Hua Sun, Ming-Yang He, Qun Chen, Zhi-Hui Zhang.  (2024)  Ionic liquid post-modified carboxylate-rich MOFs for efficient catalytic CO2 cycloaddition under solvent-free conditions.  DALTON TRANSACTIONS,     
23. Yunchang Fan, Huijie Shan, Yuanfeng Wu, Haibao Zhu.  (2025)  Ionic liquids-based ionic metal-organic frameworks (MOFs): A single catalyst with dual active centers for the cycloaddition of carbon dioxide.  APPLIED CATALYSIS A-GENERAL,  698  (120237). 
24. Lihua Zhu, Ziying Huang, Tianhao Ge, Chaoqi Jiang, Wei Zhong, Palanisamy Kannan.  (2024)  Ionic Polymers with Phenolic Hydroxyl Groups as Hydrogen Bond Donors Toward Enhanced Catalytic Performance for CO2 Conversion.  ChemistrySelect,  (30): (e202402251). 
25. Jinfa Yu, Xiangying Sun.  (2024)  Nitrogen-doped carbon dots as acid–base bifunctional and efficient catalysts for the cycloaddition of CO2 with epoxides.  NEW JOURNAL OF CHEMISTRY,  48  (10): (4245-4252). 
26. Wei Rong, Meili Ding, Yang Wang, Suyu Kong, Jianfeng Yao.  (2025)  Porous biochar with a tubular structure for photothermal CO2 cycloaddition: One-step doping versus two-step doping.  SEPARATION AND PURIFICATION TECHNOLOGY,  353  (128427). 
27. Yongbing Yuan, Xinyu Tang, Honghong Sun, Junkang Shi, Congshan Zhou, Derek O Northwood, Kristian E Waters, Hao Ma.  (2024)  Surface Modification of Calcined Kaolinite for Enhanced Solvent Dispersion and Mechanical Properties in Polybutylene Adipate/Terephthalate Composites.  MOLECULES,  29  (16): (3897). 
28. Yongjian Wei, Ying Li, Yunfei Xu, Yuze Zu, Yinghui Sun, Tong Xu, Haiou Liang, Jie Bai.  (2025)  Synergy of oxygen vacancies and surface Zn in tuned ZnO crystal facets for enhanced CO2 cycloaddition to epoxides.  APPLIED CATALYSIS B-ENVIRONMENTAL,  365  (124878). 

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