2,6-Diaminopurine - ≥98% , CAS No.1904-98-9

CAS: 1904-98-9 Cat. No.: D103226 Peso molecular: 150.14 Número EC: 217-605-2
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
49P95BAU4Z | 2,6-Diaminopurine, 98% | 9H-Purine-2,6-diamine | 1H-Purine-2,6-diamine | 2,6-Diamino-purin-9-yl | SQ 21065 | 26-diaminopurine | 7H-purine-2,6-diamine | 2,6-Diaminopurine | NSC 743 | 2-Aminoadenine | 2,6-diamino-9h-purine | X 79
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
D103226-1g
8
9,90US$
5g
D103226-5g
8
10,90US$
25g
D103226-25g
3

30,90US$

46,90US$
Guardar 16,00 US$ (34.12%)
100g
D103226-100g
2

122,90US$

184,90US$
Guardar 62,00 US$ (33.53%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
49P95BAU4Z | 2, 6-Diaminopurine, 98% | 9H-Purine-2, 6-diamine | 1H-Purine-2, 6-diamine | 2, 6-Diamino-purin-9-yl | SQ 21065 | 26-diaminopurine | 7H-purine-2, 6-diamine | 2, 6-Diaminopurine | NSC 743 | 2-Aminoadenine | 2, 6-diamino-9h-purine | X 79
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488183122
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183122
Sonrisas canónicasC1=NC2=NC(=NC(=C2N1)N)N
IUPAC Name7H-purine-2,6-diamine
InChIKeyMSSXOMSJDRHRMC-UHFFFAOYSA-N
INCHI1S/C5H6N6/c6-3-2-4(9-1-8-2)11-5(7)10-3/h1H,(H5,6,7,8,9,10,11)
Isómeros SMILES C1=NC2=NC(=NC(=C2N1)N)N
WGK Alemania 3
RTECS UO7524000
Peso molecular 150.14
Reaxy-Rn 9624
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9624&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseImidazopyrimidines
SubclassPurines and purine derivatives
Intermediate Tree Nodes Not available
Direct Parent6-aminopurines
Alternative Parents Aminopyrimidines and derivatives  Imidolactams  Imidazoles  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 6-aminopurine - Aminopyrimidine - Imidolactam - Pyrimidine - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors primary amino compound - 2,6-diaminopurine
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
XDH Tclin Xanthine dehydrogenase (1038 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDPK1 Tchem 3-phosphoinositide dependent protein kinase-1 (3758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GDA Tbio Guanine deaminase (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK1 Tchem Cyclin-dependent kinase 1 (3927 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-3 (638 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HFF (3142 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Human alphaherpesvirus 2 (4932 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human gammaherpesvirus 4 (1538 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human alphaherpesvirus 3 (4092 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human betaherpesvirus 5 (5122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human alphaherpesvirus 1 (11089 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human gammaherpesvirus 8 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

22 results found

Lot NumberCertificate TypeFechaArticulo
B2626082Certificate of AnalysisJul 31, 2025 D103226
H2526808Certificate of AnalysisJul 31, 2025 D103226
H2513764Certificate of AnalysisJul 31, 2025 D103226
H2513576Certificate of AnalysisJul 31, 2025 D103226
H2513575Certificate of AnalysisJul 31, 2025 D103226
E2607011Certificate of AnalysisJul 31, 2025 D103226
B1828104Certificate of AnalysisJul 28, 2025 D103226
H2420310Certificate of AnalysisAug 01, 2024 D103226
H2420311Certificate of AnalysisAug 01, 2024 D103226
H2420312Certificate of AnalysisAug 01, 2024 D103226
J1431019Certificate of AnalysisJul 17, 2023 D103226
L2213403Certificate of AnalysisNov 25, 2022 D103226
L2213374Certificate of AnalysisNov 25, 2022 D103226
L2213341Certificate of AnalysisNov 25, 2022 D103226
L2213119Certificate of AnalysisNov 25, 2022 D103226
L2213115Certificate of AnalysisNov 25, 2022 D103226
C2331652Certificate of AnalysisNov 25, 2022 D103226
G2424047Certificate of AnalysisNov 25, 2022 D103226
K2228109Certificate of AnalysisSep 27, 2022 D103226
K2228108Certificate of AnalysisSep 27, 2022 D103226
C23311656Certificate of AnalysisJul 27, 2022 D103226
G2225025Certificate of AnalysisJul 27, 2022 D103226

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Propiedades químicas y físicas
Sensibilidadair sensitive
Punto de inflamación (°C)>110℃
Punto de fusión (°C)>300°C
Peso molecular150.140 g/mol
XLogP3-0.900
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass150.065 Da
Monoisotopic Mass150.065 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity150.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Yongyan Yang, Gangying Feng, Jingfei Wang, Ruiting Zhang, Shuangling Zhong, Jia Wang, Xuejun Cui.  (2022)  Injectable chitosan-based self-healing supramolecular hydrogels with temperature and pH dual-responsivenesses.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:36460241] [10.1016/j.ijbiomac.2022.11.279]
2. Bingran Guo, Jianing Guo, Wenlu Yang, Xiyao Tian, Xi Wang, Zhonghua Xiang, Mingxing Wu.  (2022)  Highly dispersed iron/nickel dual-sites in hierarchical porous carbon materials as high-performance bifunctional oxygen electrocatalysts for Zn-air batteries.  RENEWABLE ENERGY,      [PMID:] [10.1016/j.renene.2022.11.036]
3. Gangying Feng, Shitong Zhang, Shuangling Zhong, Miao Tan, Yongyan Yang, Yueming Dou, Xuejun Cui.  (2021)  Temperature and pH dual-responsive supramolecular hydrogels based on riboflavin sodium phosphate and 2,6-Diaminopurine with thixotropic and fluorescent properties.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2021.127548]
4. Jun Jing, Zhiyong Li, Yuanchao Pei, Huiyong Wang, Jianji Wang.  (2013)  Equilibrium partitioning of drug molecules between aqueous and amino acid ester-based ionic liquids.  JOURNAL OF CHEMICAL THERMODYNAMICS,      [PMID:] [10.1016/j.jct.2013.02.011]
5. Ji An-Lan, Ding Rui, Liang Xuan, Liu Xiao, Zhang Yu-Chen, Wang Yu-Han, Zhang Yu-Lin, Lei Ming-Di, Zhang Yi-Wen, Fu Jie, Wang Wei-Jie, Liu Jie.  (2025)  Unlocking superior corrosion inhibition in HCl: thiol-functionalized purine derivatives outperform amino analogues via synergistic electrochemical and quantum mechanisms.  Reaction Kinetics Mechanisms and Catalysis,      [PMID:] [10.1007/s11144-025-02814-2]
6. Qamar-un-Nisa Tariq, Maher-un-Nisa Tariq, Saira Manzoor, Qiyao Yu, Jian-Guo Zhang.  (2025)  Development of super-heat-resistant purine-based coordination polymers for applications in energetic materials.  DALTON TRANSACTIONS,      [PMID:40720132] [10.1039/D5DT01509J]
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