≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ethyl trichloroacetate undergoes atom-transfer radical addition reaction with styrene catalyzed by the Ru-pentamethylcyclopentadienyl complexes.
Ethyl trichloroacetate was used in the synthesis of dichlorocarbon precursor, phenyl(trichloromethyl)methyl.
| Pubchem Sid | 488181149 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181149 |
| Sourires canoniques | CCOC(=O)C(Cl)(Cl)Cl |
| IUPAC Name | ethyl 2,2,2-trichloroacetate |
| InChIKey | SJMLNDPIJZBEKY-UHFFFAOYSA-N |
| INCHI | 1S/C4H5Cl3O2/c1-2-9-3(8)4(5,6)7/h2H2,1H3 |
| Isomères SMILES | CCOC(=O)C(Cl)(Cl)Cl |
| WGK Allemagne | 1 |
| Poids moléculaire | 191.44 |
| Beilstein | 1761567 |
| Reaxy-Rn | 1761567 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1761567&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 |
| Classe | 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 Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl chlorides |
| 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 - Organochloride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound |
| Description | 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 | Date | Article |
|---|---|---|---|
 D2428209 | Certificate of Analysis | Feb 05, 2026 | E104083 |
| K2105062 | Certificate of Analysis | May 09, 2025 | E104083 |
| C2513431 | Certificate of Analysis | Nov 16, 2024 | E104083 |
| C2513432 | Certificate of Analysis | Nov 16, 2024 | E104083 |
| C2513483 | Certificate of Analysis | Nov 16, 2024 | E104083 |
| C2611043 | Certificate of Analysis | Nov 16, 2024 | E104083 |
| E2628026 | Certificate of Analysis | Nov 16, 2024 | E104083 |
| D2428207 | Certificate of Analysis | Apr 17, 2024 | E104083 |
| D2428208 | Certificate of Analysis | Apr 17, 2024 | E104083 |
| D2428210 | Certificate of Analysis | Apr 17, 2024 | E104083 |
| D2429209 | Certificate of Analysis | Apr 17, 2024 | E104083 |
| K2105059 | Certificate of Analysis | Aug 07, 2023 | E104083 |
| B2310624 | Certificate of Analysis | Oct 21, 2021 | E104083 |
| C2308365 | Certificate of Analysis | Oct 21, 2021 | E104083 |
| D2310297 | Certificate of Analysis | Oct 21, 2021 | E104083 |
| D2310337 | Certificate of Analysis | Oct 21, 2021 | E104083 |
| Solubilité | solubility alcohol: miscible(lit.) diethyl ether: miscible(lit.) water: insoluble(lit.) |
|---|---|
| Sensibilité | Air Sensitive |
| Indice de réfraction | 1.4507 |
| Point d'éclair (°F) | 163.4 °F |
| Point d'éclair (°C) | 65℃ |
| Point d'ébullition (°C) | 168°C |
| Poids moléculaire | 191.440 g/mol |
| XLogP3 | 2.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 189.936 Da |
| Monoisotopic Mass | 189.936 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 107.000 |
| 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. Ruiyao Wu, Zhen Niu, Zhu Xia, Jianyun He, Chenxi Bai. (2023) Synthesis and dynamic crosslinking of a hydroxyl-functionalized ethylene-propylene copolymer: Preparation of an elastomer with reprocessability and shape memory properties. POLYMER, [PMID:] [10.1016/j.polymer.2023.126396] |
| 2. Baozheng Tian, Xianwei Zhang, Hong Fan. (2019) Synthesis of polyethylene-g-polydimethylsiloxane graft copolymers by copolymerization of ethylene with polydimethylsiloxane macromonomer. EUROPEAN POLYMER JOURNAL, [PMID:] [10.1016/j.eurpolymj.2019.06.016] |
| 3. Xiufeng Hao, Chundi Zhang, Lin Li, Hexin Zhang, Yanming Hu, Daifeng Hao, Xuequan Zhang. (2017) Use of Vanadium Complexes Bearing Naphthalene-Bridged Nitrogen-Sulfonate Ligands as Catalysts for Copolymerization of Ethylene and Propylene. Polymers, 9 (8): (325). [PMID:30971000] [10.3390/polym9080325] |
| 4. Xiaoyu Qi, Zhenguo Liu, Wei Gao. (2025) One-Pot Synthesis of Thiophenoxyimino Vanadium Complexes and Highly Active Catalysis on Ethylene Polymerization. APPLIED ORGANOMETALLIC CHEMISTRY, 40 (1): (e70492). [PMID:] [10.1002/aoc.70492] |
