≥97%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2′-Chloroacetophenone undergoes stereoselective reduction to (R)-2′-chloro-1-phenyl-ethanol by Saccharomyces cerevisiae B5. It is commonly used as lacrimator.
2′-Chloroacetophenone was employed as model substrate to investigate the enzymatic performance of Aspergillus terreus and Rhizopus oryzae in enantioselective bioreductions using glycerol as a co-solvent.
| Pubchem Sid | 488184725 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184725 |
| Sorrisi canonici | CC(=O)C1=CC=CC=C1Cl |
| IUPAC Name | 1-(2-chlorophenyl)ethanone |
| InChIKey | ZDOYHCIRUPHUHN-UHFFFAOYSA-N |
| INCHI | 1S/C8H7ClO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,1H3 |
| Isomeri SMILES | CC(=O)C1=CC=CC=C1Cl |
| WGK Germania | 3 |
| RTECS | AM6310000 |
| Numero UN | 3416 |
| Peso molecolare | 154.59 |
| Beilstein | 1858916 |
| Reaxy-Rn | 1858916 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1858916&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 oxygen compounds |
| Classe | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones - Aryl ketones - Phenylketones |
| Direct Parent | Alkyl-phenylketones |
| Alternative Parents | Acetophenones Benzoyl derivatives Aryl alkyl ketones Chlorobenzenes Aryl chlorides Vinylogous halides Organochlorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Alkyl-phenylketone - Acetophenone - Aryl alkyl ketone - Benzoyl - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Benzenoid - Monocyclic benzene moiety - Vinylogous halide - Organochloride - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Aromatic homomonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl 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 | Data | Oggetto |
|---|---|---|---|
 E2223038 | Certificate of Analysis | Mar 11, 2026 | C104178 |
| E2223041 | Certificate of Analysis | Mar 11, 2026 | C104178 |
| E2223042 | Certificate of Analysis | Mar 11, 2026 | C104178 |
| F1822133 | Certificate of Analysis | Dec 12, 2025 | C104178 |
| K2125789 | Certificate of Analysis | Sep 08, 2025 | C104178 |
| K2125809 | Certificate of Analysis | Sep 08, 2025 | C104178 |
| K2125853 | Certificate of Analysis | Sep 08, 2025 | C104178 |
| F2421144 | Certificate of Analysis | Mar 27, 2024 | C104178 |
| D2418604 | Certificate of Analysis | Mar 22, 2024 | C104178 |
| D2417219 | Certificate of Analysis | Mar 21, 2024 | C104178 |
| D2417220 | Certificate of Analysis | Mar 21, 2024 | C104178 |
| D2417221 | Certificate of Analysis | Mar 21, 2024 | C104178 |
| D2410234 | Certificate of Analysis | Mar 21, 2024 | C104178 |
| B2317251 | Certificate of Analysis | Mar 01, 2023 | C104178 |
| F23051043 | Certificate of Analysis | Mar 08, 2022 | C104178 |
| H2527067 | Certificate of Analysis | Mar 08, 2022 | C104178 |
| Sensibilità | Lachrymatory |
|---|---|
| Indice di rifrazione | 1.5438 |
| Punto di infiammabilità (°F) | 197.6 °F |
| Punto di infiammabilità (°C) | 92 °C |
| Punto di ebollizione (°C) | 229°C |
| Peso molecolare | 154.590 g/mol |
| XLogP3 | 2.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 154.019 Da |
| Monoisotopic Mass | 154.019 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 133.000 |
| 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. Guo-Chao Xu, Yue Wang, Ming-Hui Tang, Jie-Yu Zhou, Jing Zhao, Rui-Zhi Han, Ye Ni. (2018) Hydroclassified Combinatorial Saturation Mutagenesis: Reshaping Substrate Binding Pockets of KpADH for Enantioselective Reduction of Bulky–Bulky Ketones. ACS Catalysis, [PMID:] [10.1021/acscatal.8b02286] |
