Description
2,6-Diaminopurine (CAS No. 1904-98-9) is a high-purity biochemical compound with the molecular formula C5H6N6, widely utilized in nucleic acid research and pharmaceutical development. This heterocyclic aromatic organic compound, also known by its IUPAC name 7H-purine-2,6-diamine, serves as a critical precursor in the synthesis of nucleoside analogs and modified DNA/RNA bases. Our product is rigorously tested for purity (≥98% by HPLC) and is supplied as a lyophilized powder, ensuring optimal stability and solubility for experimental use. Ideal for researchers studying mutagenesis, antiviral drug design, and enzymatic mechanisms involving purine metabolism. Each batch is accompanied by comprehensive analytical documentation, including 1H NMR and mass spectrometry data.
Properties
- CAS Number: 1904-98-9
- Complexity: 150
- IUPAC Name: 7H-purine-2,6-diamine
- InChI: InChI=1S/C5H6N6/c6-3-2-4(9-1-8-2)11-5(7)10-3/h1H,(H5,6,7,8,9,10,11)
- InChI Key: MSSXOMSJDRHRMC-UHFFFAOYSA-N
- Exact Mass: 150.06539422
- Molecular Formula: C5H6N6
- Molecular Weight: 150.14
- SMILES: C1=NC2=NC(=NC(=C2N1)N)N
- Topological: 107
- Monoisotopic Mass: 150.06539422
- Synonyms: 2,6-Diaminopurine, 1904-98-9, 7H-purine-2,6-diamine, 2-Aminoadenine, 9H-Purine-2,6-diamine, 1H-Purine-2,6-diamine, Purine, 2,6-diamino-, 2,6-diamino-9h-purine, Purine-2,6-diyldiamine, NSC 743, SQ 21065, CCRIS 923, Group4_Adenines, EINECS 217-605-2, 49P95BAU4Z, CHEBI:40235, AI3-25010, NSC-743, DIAMINOPURINE, 2,6-, NSC743, DTXSID0062052, 2,6-DIAMINOPURINE [MI], DTXCID6035998, diaminopurine, 26-diaminopurine, X 79, 2,6-Diamino-purin-9-yl, purine-2,6-diamine, 2,6-Diaminopurine, 98%, CHEMBL388596, 133762-79-5, 6AP, MFCD00213668, UNII-49P95BAU4Z, CCRIS 3903, 2-6-Diaminopurine, Purine,6-diamino-, MFCD00071537, Purine, 2, 6-diamino-, Oprea1_670021, SCHEMBL24052, SCHEMBL24053, SCHEMBL95407, 9H-Purine-2,6-diamine #, MLS001066366, SCHEMBL134492, SCHEMBL2316818, SCHEMBL2867588, SCHEMBL2953673, SCHEMBL6322394, SCHEMBL8009783, SCHEMBL16513167, (2-amino-7H-purin-6-yl)-amine, HMS2267N10, ALBB-023319, BCP30955, BDBM50208879, MFCD00047146, SBB000103, AKOS003368184, AKOS015896933, AKOS028109333, 9H-Purine-2,6-diamine0.5M H2SO4, AC-8693, CS-W014347, FD04050, GS-3048, HY-W013631, 9H-Purine-2,6-diamine;2-Aminoadenine, BP-13206, SMR000112503, ST012425, SY036886, TS-00060, DB-015922, D1625, NS00026227, C22439, EN300-101012, AC-907/34116038, Q4596802, Z1255486094
Application
2,6-Diaminopurine is primarily used as a building block for synthesizing modified nucleosides with potential antiviral and anticancer properties. In molecular biology, it serves as an adenine analog for studying DNA repair mechanisms and polymerase fidelity. The compound has shown promise in developing novel therapeutic agents targeting viral reverse transcriptases and cellular kinases.
Safety and Hazards
GHS Hazard Statements
- H302 (88.2%): Harmful if swallowed [Warning Acute toxicity, oral]
- H312 (88.2%): Harmful in contact with skin [Warning Acute toxicity, dermal]
- H315 (88.2%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (88.2%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H332 (88.2%): Harmful if inhaled [Warning Acute toxicity, inhalation]
- H335 (86.3%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
- H351 (90.2%): Suspected of causing cancer [Warning Carcinogenicity]
Precautionary Statements
- P203, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P318, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Acute Tox. 4 (88.2%)
- Acute Tox. 4 (88.2%)
- Skin Irrit. 2 (88.2%)
- Eye Irrit. 2 (88.2%)
- Acute Tox. 4 (88.2%)
- STOT SE 3 (86.3%)
- Carc. 2 (90.2%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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