Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged,Desiccated 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504754280 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754280 |
| Canonical Smiles | CCCCOC(=O)OCCCC |
| IUPAC Name | dibutyl carbonate |
| InChIKey | QLVWOKQMDLQXNN-UHFFFAOYSA-N |
| INCHI | 1S/C9H18O3/c1-3-5-7-11-9(10)12-8-6-4-2/h3-8H2,1-2H3 |
| Isomeric SMILES | CCCCOC(=O)OCCCC |
| Molecular Weight | 174.23 |
| Reaxy-Rn | 1759273 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1759273&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 | Organic acids and derivatives |
| Class | Organic carbonic acids and derivatives |
| Subclass | Carbonic acid diesters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Carbonic acid diesters |
| Alternative Parents | Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carbonic acid diester - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as carbonic acid diesters. These are compounds comprising the carbonic acid diester functional group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jan 12, 2026 | C303940 | |
| Certificate of Analysis | Jan 12, 2026 | C303940 | |
| Certificate of Analysis | Jan 12, 2026 | C303940 | |
| Certificate of Analysis | Apr 07, 2025 | C303940 | |
| Certificate of Analysis | Apr 07, 2025 | C303940 | |
| Certificate of Analysis | Apr 07, 2025 | C303940 | |
| Certificate of Analysis | Sep 02, 2024 | C303940 |
| Sensitivity | Moisture Sensitive |
|---|---|
| Refractive Index | 1.41 |
| Flash Point(°C) | 76°C |
| Boil Point(°C) | 207.2°C |
| Melt Point(°C) | < 25°C |
| Molecular Weight | 174.240 g/mol |
| XLogP3 | 3.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 8 |
| Exact Mass | 174.126 Da |
| Monoisotopic Mass | 174.126 Da |
| Topological Polar Surface Area | 35.500 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 100.000 |
| 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. Yi-Ying Zhuang, Xiao-Chao Chen, Kai-Chun Zhao, Guo-Sheng Zhang, Yu-Fen Xie, Yong Lu, Ye Liu. (2023) Pd-catalyzed anti-Markovnikov Hydrocarboxylation of Vinylarenes with Formic Acid Free of Auxiliary Additive. Asian Journal of Organic Chemistry, 12 (7): (e202300216). [PMID:] [10.1002/ajoc.202300216] |
| 2. 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] |
| 3. Xiangzhu Ye, Jiawei Ruan, Lifang Chen, Zhiwen Qi. (2024) Structure effects of imidazolium ionic liquids on integrated CO2 absorption and transformation to dimethyl carbonate. Journal of Environmental Chemical Engineering, [PMID:] [10.1016/j.jece.2024.112790] |
| 4. Xiang Hui, Jianhui Shi, Jiajun Zhang, Yan Cao, Huiquan Li, Peng He, Liguo Wang. (2025) Enhancing C-N bond formation in amine carbonylation through dual hydrogen bonding catalysis under mild reaction conditions. Green Energy & Environment, [PMID:] [10.1016/j.gee.2025.05.010] |