≥98% 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504752011 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752011 |
| Kanonisches Lächeln | C1=CC=C(C=C1)NC(=O)NN |
| IUPAC Name | 1-amino-3-phenylurea |
| InChIKey | MOCKWYUCPREFCZ-UHFFFAOYSA-N |
| INCHI | 1S/C7H9N3O/c8-10-7(11)9-6-4-2-1-3-5-6/h1-5H,8H2,(H2,9,10,11) |
| Isomere SMILES | C1=CC=C(C=C1)NC(=O)NN |
| PubChem CID | 10837 |
| Molekulargewicht | 151.17 |
| Beilstein | 12378 |
| Reaxy-Rn | 511107 |
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 |
| Klasse | Benzene and substituted derivatives |
| Subclass | N-phenylureas |
| Intermediate Tree Nodes | Not available |
| Direct Parent | N-phenylureas |
| Alternative Parents | Semicarbazides Organic carbonic acids and derivatives Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | N-phenylurea - Semicarbazide - Carbonic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as n-phenylureas. These are compounds containing a N-phenylurea moiety, which is structurally characterized by a phenyl group linked to one nitrogen atom of a urea 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 | Datum | Artikel |
|---|---|---|---|
 L2103085 | Certificate of Analysis | Sep 09, 2025 | P160543 |
| L2103087 | Certificate of Analysis | Sep 09, 2025 | P160543 |
| D2026093 | Certificate of Analysis | Feb 23, 2024 | P160543 |
| A2609030 | Certificate of Analysis | Dec 04, 2023 | P160543 |
| K2329301 | Certificate of Analysis | Dec 04, 2023 | P160543 |
| D2426101 | Certificate of Analysis | Dec 09, 2021 | P160543 |
| Schmelzpunkt (°C) | 123-125°C |
|---|---|
| Molekulargewicht | 151.170 g/mol |
| XLogP3 | 0.400 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 151.075 Da |
| Monoisotopic Mass | 151.075 Da |
| Topological Polar Surface Area | 67.200 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 132.000 |
| 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 |
