≥95% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504751702 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751702 |
| Canonical Smiles | C1=CC=C(C=C1)N=NC2=CC=C(C3=CC=CC=C32)N |
| IUPAC Name | 4-phenyldiazenylnaphthalen-1-amine |
| InChIKey | IICHURGZQPGTRD-UHFFFAOYSA-N |
| INCHI | 1S/C16H13N3/c17-15-10-11-16(14-9-5-4-8-13(14)15)19-18-12-6-2-1-3-7-12/h1-11H,17H2 |
| Isomeric SMILES | C1=CC=C(C=C1)N=NC2=CC=C(C3=CC=CC=C32)N |
| RTECS | QJ0360000 |
| PubChem CID | 8562 |
| Molecular Weight | 247.3 |
| Reaxy-Rn | 747436 |
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 | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenes |
| Alternative Parents | Primary aromatic amines Benzene and substituted derivatives Azo compounds Propargyl-type 1,3-dipolar organic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthalene - Primary aromatic amine - Monocyclic benzene moiety - Azo compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homopolycyclic compound |
| Description | 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 | Date | Item |
|---|---|---|---|
 H2303716 | Certificate of Analysis | Jul 18, 2023 | P160468 |
| H2303717 | Certificate of Analysis | Jul 18, 2023 | P160468 |
| H2303720 | Certificate of Analysis | Jul 18, 2023 | P160468 |
| H2303721 | Certificate of Analysis | Jul 18, 2023 | P160468 |
| H2303728 | Certificate of Analysis | Jul 18, 2023 | P160468 |
| H2303805 | Certificate of Analysis | Jul 18, 2023 | P160468 |
| Molecular Weight | 247.290 g/mol |
|---|---|
| XLogP3 | 4.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 247.111 Da |
| Monoisotopic Mass | 247.111 Da |
| Topological Polar Surface Area | 50.700 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 309.000 |
| 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. Qikai Si, Yang Yu, Wenjie Xu, Zhenglong Yang, Hongwu Zhang, Ting Su, Christophe Len, Deyang Zhao. (2025) Efficient Alcoholysis Reaction from Furfural Alcohol to Ethyl Levulinate by Sulfonic Acid-Functionalized Furfural Residue. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.4c09398] |
