≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application
Therapeutic use to:
Combat ammonia poisoning
Treat seasonal allergy rhinitis
Involved in studies on the effects of imidazole drugs on chronotropic and inotropic effects
Pharmacological activity for topical mydriatics and vasoconstrictors
Radioprotector for mice treated with ionizing radiation
| Sonrisas canónicas | C1CN=C(N1)CC2=CC=CC3=CC=CC=C32.[N+](=O)(O)[O-] |
|---|---|
| IUPAC Name | 2-(naphthalen-1-ylmethyl)-4,5-dihydro-1H-imidazole;nitric acid |
| InChIKey | ZAHXYMFVNNUHCP-UHFFFAOYSA-N |
| INCHI | 1S/C14H14N2.HNO3/c1-2-7-13-11(4-1)5-3-6-12(13)10-14-15-8-9-16-14;2-1(3)4/h1-7H,8-10H2,(H,15,16);(H,2,3,4) |
| Isómeros SMILES | C1CN=C(N1)CC2=CC=CC3=CC=CC=C32.[N+](=O)(O)[O-] |
| Peso molecular | 273.29 |
| Reaxy-Rn | 3779329 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3779329&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 |
| Clase | Naphthalenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenes |
| Alternative Parents | Imidolactams Organic nitrates Imidazolines Organic nitro compounds Organic nitric acids Propargyl-type 1,3-dipolar organic compounds Carboximidamides Carboxamidines Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Naphthalene - Imidolactam - 2-imidazoline - Organic nitrate - Organic nitric acid - Organic nitric acid or derivatives - Organic nitro compound - Amidine - Carboxylic acid amidine - Carboximidamide - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. |
| 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 |
|---|---|---|---|
 C23241231 | Certificate of Analysis | Jan 19, 2026 | N170703 |
| C23241244 | Certificate of Analysis | Jan 19, 2026 | N170703 |
| C23241246 | Certificate of Analysis | Jan 19, 2026 | N170703 |
| K1828068 | Certificate of Analysis | Jun 17, 2024 | N170703 |
| K1828069 | Certificate of Analysis | Jun 17, 2024 | N170703 |
| Punto de fusión (°C) | 167-170°C |
|---|---|
| Peso molecular | 273.290 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 273.111 Da |
| Monoisotopic Mass | 273.111 Da |
| Topological Polar Surface Area | 90.400 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 297.000 |
| 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 | 2 |
