Diethyl oxalate - AR, ≥99%, used for Diethyl oxalate was used in microemulsion synthesis of ZnO nanoparticles. It was also used in the synthesis of sym-1,4-diphenyl-1,4-dihydro-1,2,4,5-polytetrazine. various applications , CAS No.95-92-1

CAS: 95-92-1 Cat. No.: D110943 Formule: C6H10O4 Poids moléculaire: 146.14 Beilstein Registry Number: 606350 Numéro CE: 202-464-1
DISPONIBLE À COMMANDE
GRADE & PURITY AR ? Analytical Reagent grade — high-purity chemicals meeting strict assay limits for lab analysis. Use when accuracy matters and trace impurities could skew results. ≥99%
Synonyms
Diethyl ethanedioate
Storage
Room temperature,Argon charged
Shipped In
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Size
Allemagne (EU)
USA*
Price
Qty
100g
D110943-100g
—
1 En stock
12,06€
500g
D110943-500g
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3 En stock
18,14€
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Why this grade

AR, ≥99% AR for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Argon charged Ships FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Diethyl oxalate undergoes transesterification with phenol in the liquid phase over very efficient MoO3/TiO2 solid-acid sol-gel catalysts to form diphenyl oxalate. It undergoes Claisen condensation with active methylene group of ketosteroids to form glyoxalyl derivatives. It undergoes hydrogenation in the presence of high copper contented mesoporous Cu/SBA-15 catalysts to yield ethylene glycol.

Diethyl oxalate is used to prepare active pharmaceutical ingredients (API), plastics and dyestuff intermediates. It is also used as a solvent for cellulose esters, ethers, resins, perfumes and lacquers for electronics. It is involved in the transesterification reaction with phenol to get dipheny oxalate. It is also involved in the Claisen condensation ketosteroids to prepare glyoxalyl derivatives. Further, it is used to prepare sym-1,4-diphenyl-1,4-dihydro-1,2,4,5-polytetrazine. In addition to this, it is utilized in the microemulsion synthesis of zinc oxide nanoparticles.

Specifications

Synonymes
Diethyl ethanedioate
Spécifications et pureté
AR, ≥99%
Application
Diethyl oxalate was used in microemulsion synthesis of ZnO nanoparticles. It was also used in the synthesis of sym-1,4-diphenyl-1,4-dihydro-1,2,4,5-polytetrazine.
Conditions de stockage de stockage
Room temperature,Argon charged
Expédié en
FedEx DG Service
Grade
AR
Pureté
≥99%
Noms et identifiants
Pubchem Sid508816473
Sourires canoniquesCCOC(=O)C(=O)OCC
IUPAC Namediethyl oxalate
InChIKeyWYACBZDAHNBPPB-UHFFFAOYSA-N
INCHI1S/C6H10O4/c1-3-9-5(7)6(8)10-4-2/h3-4H2,1-2H3
Isomères SMILES CCOC(=O)C(=O)OCC
WGK Allemagne 1
RTECS RO2800000
Numéro ONU 2525
Groupe d'emballage III
Poids moléculaire 146.14
Beilstein 606350
Reaxy-Rn 606350
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=606350&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassDicarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentDicarboxylic acids and derivatives
Alternative Parents Carboxylic acid esters  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Dicarboxylic acid or derivatives - Carboxylic acid ester - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

15 results found

Lot NumberCertificate TypeDateArticle
I2607244Certificate of AnalysisAug 26, 2026 D110943
I2607245Certificate of AnalysisAug 26, 2026 D110943
E2622361Certificate of AnalysisMay 11, 2026 D110943
E2622363Certificate of AnalysisMay 11, 2026 D110943
E2622364Certificate of AnalysisMay 11, 2026 D110943
A2606046Certificate of AnalysisJun 06, 2024 D110943
F2419197Certificate of AnalysisJun 06, 2024 D110943
F2419221Certificate of AnalysisJun 06, 2024 D110943
F2419223Certificate of AnalysisJun 06, 2024 D110943
A2412079Certificate of AnalysisAug 08, 2022 D110943
C2331029Certificate of AnalysisAug 08, 2022 D110943
C2415145Certificate of AnalysisAug 08, 2022 D110943
H2217259Certificate of AnalysisAug 08, 2022 D110943
H2217260Certificate of AnalysisAug 08, 2022 D110943
H2217316Certificate of AnalysisAug 08, 2022 D110943

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Propriétés chimiques et physiques
SolubilitéMiscible with alcohols, ether and other common organic solvents.
SensibilitéMoisture sensitive.
Indice de réfraction1.4101
Point d'éclair (°F)168.8℉
Point d'éclair (°C)76°C
Point d'ébullition (°C)185°C
Point de fusion (°C)-41°C
Poids moléculaire146.140 g/mol
XLogP30.600
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass146.058 Da
Monoisotopic Mass146.058 Da
Topological Polar Surface Area52.600 Ų
Heavy Atom Count10
Formal Charge0
Complexity114.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Références
1. Zhao Yanna, Hou Wentong, Huang Yuqing, Zhang Ting, Zhang Yingying, Wang Yuqi, Bai Xiaowei.  (2023)  A Green Recyclable Vanillin-Based Polymer (Amide–Imide) Vitrimer.  JOURNAL OF POLYMERS AND THE ENVIRONMENT,      [PMID:] [10.1007/s10924-023-03048-w]
2. Xiaolong Yu, Juan Zhang, Yan Zheng.  (2020)  Perchlorate adsorption onto epichlorohydrin crosslinked chitosan hydrogel beads.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:33187716] [10.1016/j.scitotenv.2020.143236]
3. Dang Xiaofei, Li Qian, Li Huayi, Yang Yuan, Zhang Liaoyun, Hu Youliang.  (2014)  Ziegler-Natta catalysts with novel internal electron donors for propylene polymerization.  JOURNAL OF POLYMER RESEARCH,  21  (12): (1-8).  [PMID:] [10.1007/s10965-014-0619-9]
4. Hui Li, Changmiao Huang, Zixuan Teng, Yushu Luo, Chaocan Zhang, Lili Wu, Wenchao Huang, Tingting Zhao, Lijie Dong, Wanyu Chen.  (2024)  An Ionic Liquid Supramolecular Gel Electrolyte with Unique Wide Operating Temperature Range Properties for Zinc-Ion Batteries.  Polymers,  16  (12): (1680).  [PMID:38932030] [10.3390/polym16121680]
5. Shuang Liang, Hengkun Zhao, Xiangyuan Li, Yu Feng, Jingbo Zhao.  (2024)  Efficient Strategy to Enhance the Properties of Fully Biobased Linear Dimeric Acid Polyamides.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c01460]
6. Menghan Guo, Jie Ding, Guojing Ji, Tian Xie, Huiwen Pang, Xiang Li, Qin Zhong.  (2024)  Highly dispersed Ag/SiO2 catalyst with weak metal-support interaction for diethyl oxalate hydrogenation to ethyl glycolate.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.113898]
7. Tao Peng, Ji Lan, Peng Lu, Cong Deng, Ze-Yong Zhao, Yu-Zhong Wang.  (2024)  High-Performance Biobased Elastomers with Both High Strength and High Toughness.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c00290]
8. Xiaomeng Deng, Wensheng Wei, Zizhen Yan, Zhanguo Zhang, Yuxin Wang, Guangwen Xu, Jianjun Guo, Jinggang Zhao, Lei Shi.  (2024)  Product as additive for facilitating CO2 conversion into cyclic carbonate.  Journal of CO2 Utilization,      [PMID:] [10.1016/j.jcou.2024.102850]
9. Rongchi Zhang, Xuanbao Xiang, Donghai Sheng, Lin Zhang, Wanmeng Ren, Guoxin Xie, Shutao Wei, Huilian Dai.  (2025)  A Mechanically Robust Polyurethane Elastomer with Excellent Crack Tolerance, recyclability and Weathering Resistance via Microphase Dynamic Ordering.  Journal of Materials Chemistry A,      [PMID:] [10.1039/D5TA07448G]
10. Zhongzheng Zhu, Qitan Zheng, Junyi Yao, Siyu Liu, Hezhou Liu, Hua Li.  (2025)  Stress-free Two-way Shape Memory Polyurethane with High Reversible Strain and Excellent Mechanical Properties for Intelligent Actuators.  Advanced Industrial and Engineering Polymer Research,      [PMID:] [10.1016/j.aiepr.2025.11.004]
11. Xin Jing, Xiaoyun Li, Yuhua Zhao, Junwei Wang, Chunxia Niu.  (2026)  Mechanical Properties at High Temperatures and Thermal Properties of Polyurethane Elastomers With Different Amide Segments.  POLYMER ENGINEERING AND SCIENCE,      [PMID:] [10.1002/pen.70704]
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