≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Argon charged Ships Ice chest + Ice pads 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.
6-N-Hydroxylaminopurine is a base analog and has mutagenic activity.
| Canonical Smiles | C1=NC2=C(N1)C(=NC=N2)NO |
|---|---|
| IUPAC Name | N-(7H-purin-6-yl)hydroxylamine |
| InChIKey | CBCQWVQNMGNYEO-UHFFFAOYSA-N |
| INCHI | 1S/C5H5N5O/c11-10-5-3-4(7-1-6-3)8-2-9-5/h1-2,11H,(H2,6,7,8,9,10) |
| Isomeric SMILES | C1=NC2=C(N1)C(=NC=N2)NO |
| Alternate CAS | 5667-20-9 |
| PubChem CID | 21876 |
| NSC Number | 516286 |
| MeSH Entry Terms | 6-N-hydroxylaminopurine;N(6)-hydroxyaminopurine;N(6)-hydroxylaminopurine;N-hydroxyadenine |
| Molecular Weight | 151.13 |
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 | Organoheterocyclic compounds |
| Class | Imidazopyrimidines |
| Subclass | Purines and purine derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Purines and purine derivatives |
| Alternative Parents | Arylhydroxamates Pyrimidines and pyrimidine derivatives Imidolactams Imidazoles Heteroaromatic compounds N-organohydroxylamines Azacyclic compounds Organopnictogen compounds Organic oxygen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Purine - Arylhydroxamate - Imidolactam - Pyrimidine - Heteroaromatic compound - Imidazole - Azole - Azacycle - N-organohydroxylamine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as purines and purine derivatives. These are aromatic heterocyclic compounds containing a purine moiety, which is formed a pyrimidine-ring ring fused to an imidazole ring. |
| External Descriptors | hydroxylamines - 6-aminopurines - nucleobase analogue |
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| Molecular Weight | 151.130 g/mol |
|---|---|
| XLogP3 | 0.100 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | 151.049 Da |
| Monoisotopic Mass | 151.049 Da |
| Topological Polar Surface Area | 86.700 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 143.000 |
| 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 |
