≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
It was employed as substrate for use in an amperometric 3-electrode system for the determination of alkaline phosphatase,it also used in electrochemical immunoassays， the preparation of di-(2-nitro-1-naphthyl) hydrogen phosphate and 1-(2′-methyl-3′-indenyl)-2-naphthylamine and -2-naphthol (axially chiral ligands)
| Canonical Smiles | C1=CC=C2C(=C1)C=CC(=C2O)[N+](=O)[O-] |
|---|---|
| IUPAC Name | 2-nitronaphthalen-1-ol |
| InChIKey | MUCCHGOWMZTLHK-UHFFFAOYSA-N |
| INCHI | 1S/C10H7NO3/c12-10-8-4-2-1-3-7(8)5-6-9(10)11(13)14/h1-6,12H |
| Isomeric SMILES | C1=CC=C2C(=C1)C=CC(=C2O)[N+](=O)[O-] |
| WGK Germany | 3 |
| Molecular Weight | 189.17 |
| Reaxy-Rn | 2050016 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2050016&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 |
| Class | Naphthalenes |
| Subclass | Nitronaphthalenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Nitronaphthalenes |
| Alternative Parents | Naphthols and derivatives Nitroaromatic compounds 1-hydroxy-4-unsubstituted benzenoids Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | 2-nitronaphthalene - 1-naphthol - Nitroaromatic compound - 1-hydroxy-4-unsubstituted benzenoid - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as nitronaphthalenes. These are polycyclic aromatic compounds containing a naphthalene moiety substituted by one or more nitro groups. |
| 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 |
|---|---|---|---|
 K2528452 | Certificate of Analysis | Sep 22, 2025 | N139066 |
| L2510632 | Certificate of Analysis | Sep 22, 2025 | N139066 |
| L2510639 | Certificate of Analysis | Sep 22, 2025 | N139066 |
| L2510641 | Certificate of Analysis | Sep 22, 2025 | N139066 |
| Molecular Weight | 189.170 g/mol |
|---|---|
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 189.043 Da |
| Monoisotopic Mass | 189.043 Da |
| Topological Polar Surface Area | 66.100 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 226.000 |
| 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. Jiayue Dong, Peizeng Yang, Deyang Kong, Yiqiang Song, Junhe Lu. (2024) Formation of nitrated naphthalene in the sulfate radical oxidation process in the presence of nitrite. WATER RESEARCH, [PMID:38574612] [10.1016/j.watres.2024.121546] |
