Determine the necessary mass, volume, or concentration for preparing a solution.
≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Room temperature Ships Normal 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 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504755338 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504755338 |
| Sonrisas canónicas | CCOC(=O)C(C)Br |
| IUPAC Name | ethyl 2-bromopropanoate |
| InChIKey | ARFLASKVLJTEJD-UHFFFAOYSA-N |
| INCHI | 1S/C5H9BrO2/c1-3-8-5(7)4(2)6/h4H,3H2,1-2H3 |
| Isómeros SMILES | CCOC(=O)C(C)Br |
| WGK Alemania | 3 |
| RTECS | UA2451730 |
| Número ONU | 2920 |
| Grupo de embalaje | II |
| Peso molecular | 181.03 |
| Beilstein | 773920 |
| Reaxy-Rn | 773920 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773920&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 |
| Clase | Carboxylic acids and derivatives |
| Subclass | Alpha-halocarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Alpha-halocarboxylic acid derivatives |
| Alternative Parents | Carboxylic acid esters Monocarboxylic acids and derivatives Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alpha-halocarboxylic acid derivative - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as alpha-halocarboxylic acid derivatives. These are carboxylic acid derivatives containing a halogen atom bonded to the alpha carbon atom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Feb 05, 2026 | E400066 | |
| Certificate of Analysis | Dec 10, 2025 | E400066 | |
| Certificate of Analysis | Sep 15, 2025 | E400066 | |
| Certificate of Analysis | Sep 15, 2025 | E400066 | |
| Certificate of Analysis | Sep 15, 2025 | E400066 | |
| Certificate of Analysis | Sep 15, 2025 | E400066 | |
| Certificate of Analysis | May 07, 2025 | E400066 | |
| Certificate of Analysis | May 07, 2025 | E400066 | |
| Certificate of Analysis | May 07, 2025 | E400066 | |
| Certificate of Analysis | May 07, 2025 | E400066 | |
| Certificate of Analysis | May 07, 2025 | E400066 | |
| Certificate of Analysis | May 07, 2025 | E400066 | |
| Certificate of Analysis | Jan 15, 2025 | E400066 | |
| Certificate of Analysis | Jan 07, 2025 | E400066 | |
| Certificate of Analysis | Apr 12, 2024 | E400066 | |
| Certificate of Analysis | Apr 12, 2024 | E400066 | |
| Certificate of Analysis | Apr 12, 2024 | E400066 | |
| Certificate of Analysis | Feb 21, 2024 | E400066 | |
| Certificate of Analysis | Jul 07, 2023 | E400066 | |
| Certificate of Analysis | Mar 02, 2022 | E400066 | |
| Certificate of Analysis | Mar 02, 2022 | E400066 |
| Solubilidad | Immiscible in water. Soluble in alcohol and ether. |
|---|---|
| Sensibilidad | light sensitive |
| Índice de refracción | 1.449 |
| Punto de inflamación (°F) | 123.8 °F |
| Punto de inflamación (°C) | 51℃ |
| Punto de ebullición (°C) | 156-160°C |
| Peso molecular | 181.030 g/mol |
| XLogP3 | 1.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 179.979 Da |
| Monoisotopic Mass | 179.979 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 82.500 |
| 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 |
| 1. Man Zhang, Rubo Tian, Siyang Tang, Kejing Wu, Binshen Wang, Yingying Liu, Yingming Zhu, Houfang Lu, Bin Liang. (2023) The structure and properties of lignin isolated from various lignocellulosic biomass by different treatment processes. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:37285885] [10.1016/j.ijbiomac.2023.125219] |
| 2. Xue Tao, Wei Yan, Yu Caili, Zhou Zhongqun, Zhang Faai. (2023) RAFT polymerization of MMA in channels of different mesoporous materials. CHEMICAL PAPERS, 77 (7): (3713-3726). [PMID:] [10.1007/s11696-023-02734-2] |
| 3. Tian Wang, Boya Hao, Shilin Xu, Jie Meng, Tao Wen, Jian Liu, Haiyan Xu. (2022) Effective RNAi in leukemia cells is enhanced by spermine-modified pullulan combined with desloratadine. CARBOHYDRATE POLYMERS, [PMID:35725203] [10.1016/j.carbpol.2022.119646] |
| 4. Xu Xiang, Zeng Yanning, Yu Caili, Zhang Faai. (2019) Controlled RAFT polymerization of MMA in confined space of various pore sizes of SBA-15. JOURNAL OF POROUS MATERIALS, 27 (1): (95-105). [PMID:] [10.1007/s10934-019-00797-9] |
| 5. Yuan Wang, Yan-Ling Luo, Feng Xu, Ya-Shao Chen, Wei Tang. (2016) Redox-responsive PAEFc-b-PDMAEMA amphiphilic block copolymer self-assembly micelles: Physicochemical properties and anticancer drug controlled release. JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, [PMID:] [10.1016/j.jiec.2016.12.021] |
| 6. Deng Jun, Wu Sai, Yao Mengyun, Gao Changyou. (2016) Surface-anchored poly(acryloyl-L(D)-valine) with enhanced chirality-selective effect on cellular uptake of gold nanoparticles. Scientific Reports, 6 (1): (1-12). [PMID:27531648] [10.1038/srep31595] |
| 7. Jian Guan, Xiaodi Yu, Minghui He, Wenfeng Han, Ying Li, Zongjian Liu, Panpan Zhang, Haodong Tang. (2024) Synthesis of Ultrahigh Molecular Weight Poly (Trifluoroethyl Methacrylate) Initiated by the Combination of Palladium Nanoparticles with Organic Halides. Polymers, 16 (19): (2764). [PMID:39408474] [10.3390/polym16192764] |
| 8. Zongzheng Zuo, Shuxue Zhou. (2025) Comparative study on random and block fluorinated polyacrylates for fabrication of hydrophobic 2K polyurethane clearcoats. POLYMER, [PMID:] [10.1016/j.polymer.2025.128836] |
| 9. Sai Chen, Yue Yu, Ruirui Cao, Haihui Liu, Xingxiang Zhang. (2019) Fabrication and Characterization of Novel Shape-Stabilized Phase Change Materials Based on P(TDA-co-HDA)/GO Composites. Polymers, 11 (7): (1113). [PMID:31266181] [10.3390/polym11071113] |
| 10. Wenjie Mao, Jiajia Li, Xiaofeng Pan, Joji Tanaka, Wei You, Jian Zhu. (2025) RAFT Step-Growth Polymerization via ‘Grafting Through’. ACS Polymers Au, [PMID:41657391] [10.1021/acspolymersau.5c00084] |
| 11. Yuan Ming, Han Xiaofang, Zhang Zekai, Wang Ruijia, Guo Shengrong. (2025) Synthesis of ultra-high molecular weight poly(methyl methacrylate) initiated by the combination of copper nanopowder with organic halides. BMC Chemistry, 19 (1): (223). [PMID:40713622] [10.1186/s13065-025-01597-w] |