Determine the necessary mass, volume, or concentration for preparing a solution.
≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504754039 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754039 |
| Sorrisi canonici | C=CCOC(=O)C1=CC=C(C=C1)C(=O)OCC=C |
| IUPAC Name | bis(prop-2-enyl) benzene-1,4-dicarboxylate |
| InChIKey | ZDNFTNPFYCKVTB-UHFFFAOYSA-N |
| INCHI | 1S/C14H14O4/c1-3-9-17-13(15)11-5-7-12(8-6-11)14(16)18-10-4-2/h3-8H,1-2,9-10H2 |
| Isomeri SMILES | C=CCOC(=O)C1=CC=C(C=C1)C(=O)OCC=C |
| Peso molecolare | 246.26 |
| Beilstein | 9(4)3307 |
| Reaxy-Rn | 2216839 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2216839&ln= |
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 | Benzenoids |
| Classe | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Phthalic acid and derivatives - Phthalate esters |
| Direct Parent | p-Phthalate esters |
| Alternative Parents | P-phthalic acid and derivatives Benzoic acid esters Benzoyl derivatives Dicarboxylic acids and derivatives Carboxylic acid esters Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Para-phthalic acid ester - Para_phthalic_acid - Benzoate ester - Benzoyl - Dicarboxylic acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as p-phthalate esters. These are ester derivatives of p-phthalic acids, which are based on a benzene 1,4-dicarboxylic acid skeleton. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Mar 18, 2026 | D155470 | |
| Certificate of Analysis | Mar 18, 2026 | D155470 | |
| Certificate of Analysis | Aug 23, 2025 | D155470 | |
| Certificate of Analysis | Aug 23, 2025 | D155470 | |
| Certificate of Analysis | May 10, 2023 | D155470 | |
| Certificate of Analysis | May 31, 2022 | D155470 | |
| Certificate of Analysis | May 31, 2022 | D155470 |
| Sensibilità | heat sensitive & light sensitive |
|---|---|
| Indice di rifrazione | 1.53 |
| Punto di infiammabilità (°F) | 158°C |
| Punto di infiammabilità (°C) | 158°C |
| Punto di ebollizione (°C) | 172°C/5mmHg |
| Peso molecolare | 246.260 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 8 |
| Exact Mass | 246.089 Da |
| Monoisotopic Mass | 246.089 Da |
| Topological Polar Surface Area | 52.600 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 282.000 |
| 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 |
| 1. Yifu Chen, Siwu Wu, Jianguo Mi, Ming Tian, Mingying Liang, Jialiang Chen, Zhenghai Tang, Wenjie Wu, Baochun Guo, Liqun Zhang. (2023) Spatial Structure Design toward Dielectric Elastomers by Separating Charge Centers in Chain Segments. MACROMOLECULES, [PMID:] [10.1021/acs.macromol.3c01683] |
| 2. Xinlong Dong, Binghe Zheng, Guoqing Zhang, Changren Xiao, Xiaoqing Yang. (2021) Preparation of Quasi-Thermoplastic Phase Change Polymer with Intrinsic Antileakage Performance for Battery Thermal Management. Advanced Materials Interfaces, 8 (18): (2100807). [PMID:] [10.1002/admi.202100807] |
| 3. Changren Xiao, Guoqing Zhang, Zhenghui Li, Xiaoqing Yang. (2020) Custom design of solid–solid phase change material with ultra-high thermal stability for battery thermal management. Journal of Materials Chemistry A, 8 (29): (14624-14633). [PMID:] [10.1039/D0TA05247G] |
| 4. Shuangping Xu, Juncheng Ma, Hongge Jia, Mingyu Zhang, Yanqing Qu, Chengbao Geng, Xiaozhou Zhao, Min Shao, Jingyu Xu, Xing Wang. (2025) Preparation of porous carbon derived from a lignin-based polymer through ZnCl2 activation for effective capture of iodine. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:39756754] [10.1016/j.ijbiomac.2024.139412] |
| 5. Yifu Chen, Siwu Wu, Baochun Guo, Binjie Jin, Haixin Yang, Jialiang Chen, Wenjie Wu, Liqun Zhang. (2024) Separating Charge Centers of Chain Segments in Dielectric Elastomer through Steric Hindrance Engineering. MACROMOLECULAR RAPID COMMUNICATIONS, [PMID:38771981] [10.1002/marc.202400295] |