≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships FedEx DG Service 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.
Description
1-Ethyl-2-nitrobenzene may be used as a solvent to compose the supported liquid membrane (SLM) for use in electromembrane extractions (EMEs).
| Pubchem Sid | 504754343 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754343 |
| Sorrisi canonici | CCC1=CC=CC=C1[N+](=O)[O-] |
| IUPAC Name | 1-ethyl-2-nitrobenzene |
| InChIKey | PXWYZLWEKCMTEZ-UHFFFAOYSA-N |
| INCHI | 1S/C8H9NO2/c1-2-7-5-3-4-6-8(7)9(10)11/h3-6H,2H2,1H3 |
| Isomeri SMILES | CCC1=CC=CC=C1[N+](=O)[O-] |
| WGK Germania | 3 |
| Peso molecolare | 151.16 |
| Beilstein | 1865655 |
| Reaxy-Rn | 1865655 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1865655&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 | Benzenoids |
| Classe | Benzene and substituted derivatives |
| Subclass | Nitrobenzenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Nitrobenzenes |
| Alternative Parents | Nitroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Nitrobenzene - Nitroaromatic compound - Organic nitro compound - C-nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic homomonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro 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 |
|---|---|---|---|
 H2621667 | Certificate of Analysis | Aug 08, 2026 | E468436 |
| H2621666 | Certificate of Analysis | Aug 08, 2026 | E468436 |
| H2621655 | Certificate of Analysis | Aug 08, 2026 | E468436 |
| H2621652 | Certificate of Analysis | Aug 08, 2026 | E468436 |
| L2530231 | Certificate of Analysis | Dec 22, 2025 | E468436 |
| L2530230 | Certificate of Analysis | Dec 22, 2025 | E468436 |
| L2530229 | Certificate of Analysis | Dec 22, 2025 | E468436 |
| K2510282 | Certificate of Analysis | Oct 30, 2025 | E468436 |
| K2510317 | Certificate of Analysis | Oct 30, 2025 | E468436 |
| K2510343 | Certificate of Analysis | Oct 30, 2025 | E468436 |
| G2507287 | Certificate of Analysis | Feb 11, 2025 | E468436 |
| G2507377 | Certificate of Analysis | Feb 11, 2025 | E468436 |
| G2507378 | Certificate of Analysis | Feb 11, 2025 | E468436 |
| B2507061 | Certificate of Analysis | Feb 21, 2024 | E468436 |
| B2428202 | Certificate of Analysis | Feb 21, 2024 | E468436 |
| B2428201 | Certificate of Analysis | Feb 21, 2024 | E468436 |
| B2428200 | Certificate of Analysis | Feb 21, 2024 | E468436 |
| B2428199 | Certificate of Analysis | Feb 21, 2024 | E468436 |
| B2428198 | Certificate of Analysis | Feb 21, 2024 | E468436 |
| B2428197 | Certificate of Analysis | Feb 21, 2024 | E468436 |
| Indice di rifrazione | 1.5354 |
|---|---|
| Punto di infiammabilità (°F) | 228.2 °F |
| Punto di infiammabilità (°C) | 109°C |
| Punto di ebollizione (°C) | 172-174 °C/18 mmHg |
| Punto di fusione (°C) | -13--10°C |
| Peso molecolare | 151.160 g/mol |
| XLogP3 | 2.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 151.063 Da |
| Monoisotopic Mass | 151.063 Da |
| Topological Polar Surface Area | 45.800 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 142.000 |
| 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. Tongfei Gao, Zhuangzhuang Dong, Jianhua Xiong, Hongxia Hao, Xiantao Shen, Wenge Tang, Zhen Tong, Chuixiu Huang. (2026) Liquid-Phase Microextraction Assisted Surface-Enhanced Raman Spectroscopy: On-site Quantification of Amphetamine-Type Stimulants in Complex Samples from Crime Scenes. ANALYTICA CHIMICA ACTA, [PMID:41997682] [10.1016/j.aca.2026.345427] |
