2,4,6-Triaminopyrimidine - ≥98% , CAS No.1004-38-2

CAS: 1004-38-2 Cat. No.: T123280 Peso molecular: 125.13 Beilstein Registry Number: 118448 Número EC: 213-720-7 PubChem CID: 13863
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
W-108962 | D6ZP6F2ECK | 2,4,6-triaminopyrimidin-1-ium | 2,4,6-triamino pyrimidine | 2,4,6-Triaminopyrimidine | (4,6-diamino-pyrimidin-2-yl)-amine | 2,4,6-Pyrimidinetriamine; Pyrimidine, 2,4,6-triamino- (6CI,7CI,8CI); 2,4,6-Triaminopyrimidine; NSC 26493; P
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
T123280-5g
10
9,90US$
25g
T123280-25g
2
14,90US$
100g
T123280-100g
2
33,90US$
500g
T123280-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
142,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

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Storage & shipping

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

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Quality documents

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

📚

Literature proof

Cited in 18 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

2,4,6-Triaminopyrimidine is an organic cation used to block paracellular conductance pathways of several epithelia in the rat kidney, ultimately affecting sodium and potassium excretion.

Specifications

Sinónimos
W-108962 | D6ZP6F2ECK | 2, 4, 6-triaminopyrimidin-1-ium | 2, 4, 6-triamino pyrimidine | 2, 4, 6-Triaminopyrimidine | (4, 6-diamino-pyrimidin-2-yl)-amine | 2, 4, 6-Pyrimidinetriamine; Pyrimidine, 2, 4, 6-triamino- (6CI, 7CI, 8CI); 2, 4, 6-Triaminopyrimidine; NSC 26493; P
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488181911
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181911
Sonrisas canónicasC1=C(N=C(N=C1N)N)N
IUPAC Namepyrimidine-2,4,6-triamine
InChIKeyJTTIOYHBNXDJOD-UHFFFAOYSA-N
INCHI1S/C4H7N5/c5-2-1-3(6)9-4(7)8-2/h1H,(H6,5,6,7,8,9)
Isómeros SMILES C1=C(N=C(N=C1N)N)N
WGK Alemania 3
PubChem CID 13863
Peso molecular 125.13
Beilstein 118448

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
ClaseDiazines
SubclassPyrimidines and pyrimidine derivatives
Intermediate Tree Nodes Not available
Direct ParentAminopyrimidines and derivatives
Alternative Parents Imidolactams  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Aminopyrimidine - Imidolactam - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aminopyrimidines and derivatives. These are organic compounds containing an amino group attached to a pyrimidine ring. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
External Descriptors a small molecule
Estructura 3D
Modelo de Estructura Química Interactiva





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.

32 results found

Lot NumberCertificate TypeFechaArticulo
D2624328Certificate of AnalysisMar 30, 2026 T123280
D2624329Certificate of AnalysisMar 30, 2026 T123280
D2624330Certificate of AnalysisMar 30, 2026 T123280
L2522687Certificate of AnalysisNov 20, 2025 T123280
L2522685Certificate of AnalysisNov 20, 2025 T123280
L2509534Certificate of AnalysisNov 20, 2025 T123280
J2515497Certificate of AnalysisOct 09, 2025 T123280
J2515494Certificate of AnalysisOct 09, 2025 T123280
J2515492Certificate of AnalysisOct 09, 2025 T123280
J2515493Certificate of AnalysisOct 09, 2025 T123280
L2116173Certificate of AnalysisSep 17, 2025 T123280
L2109697Certificate of AnalysisSep 09, 2025 T123280
L2109695Certificate of AnalysisSep 09, 2025 T123280
I2518523Certificate of AnalysisSep 08, 2025 T123280
I2518521Certificate of AnalysisSep 08, 2025 T123280
I2518431Certificate of AnalysisSep 08, 2025 T123280
D2516594Certificate of AnalysisJan 21, 2025 T123280
D2516583Certificate of AnalysisJan 21, 2025 T123280
D2516582Certificate of AnalysisJan 21, 2025 T123280
C2429916Certificate of AnalysisMar 13, 2024 T123280
C2401551Certificate of AnalysisJan 25, 2024 T123280
C2401553Certificate of AnalysisJan 25, 2024 T123280
C2401552Certificate of AnalysisJan 25, 2024 T123280
C2401550Certificate of AnalysisJan 25, 2024 T123280
D23231183Certificate of AnalysisDec 07, 2022 T123280
D23231182Certificate of AnalysisDec 07, 2022 T123280
D23231152Certificate of AnalysisDec 07, 2022 T123280
D23231151Certificate of AnalysisDec 07, 2022 T123280
D23231141Certificate of AnalysisDec 07, 2022 T123280
I2212403Certificate of AnalysisJul 29, 2022 T123280
I2212402Certificate of AnalysisJul 29, 2022 T123280
L2109672Certificate of AnalysisNov 26, 2021 T123280

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Propiedades químicas y físicas
SolubilidadSlightly soluble in ethanol and ether
Sensibilidadair sensitive
Punto de fusión (°C)246°C-252°C
Peso molecular125.130 g/mol
XLogP3-0.800
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass125.07 Da
Monoisotopic Mass125.07 Da
Topological Polar Surface Area104.000 Ų
Heavy Atom Count9
Formal Charge0
Complexity85.000
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. Sizhao Zhang, Jing Wang, Zhao Wang, Guangyu Xu, Yonggang Jiang, Yunyun Xiao, Feng Ding.  (2023)  Reusable Nanoporous Al2O3-Containing Polyimide Aerogels for Thermal Insulation of Aircraft.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.3c02863]
2. Yu Li, Jiangnan Li, Deliang Zhu, Guangcun Qian, Hongyan Tang.  (2023)  Facile dual-functionalization of NF membranes with excellent chlorine resistance and good antifouling property by in-situ grafting of zwitterions.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.123660]
3. Mengling Chang, Zhiming Pan, Dandan Zheng, Sibo Wang, Guigang Zhang, Masakazu Anpo, Xinchen Wang.  (2023)  Salt-Melt Synthesis of Poly Heptazine Imides with Enhanced Optical Absorption for Photocatalytic Hydrogen Production.  ChemSusChem,  16  (13): (e202202255).  [PMID:36882386] [10.1002/cssc.202202255]
4. Yao Chen, Xin Xin, Dong Yang, Hanjie Ren, Yuchen Gao, Zhanfeng Zhao, Wenjing Wang, Ke An, Jiangdan Tan, Zhongyi Jiang.  (2021)  Pyrimidine-modified g-C3N4 nanosheets for enhanced photocatalytic H2 evolution.  MATERIALS RESEARCH BULLETIN,      [PMID:] [10.1016/j.materresbull.2021.111498]
5. Wenhua Tang, Ying Tian, BoWen Chen, Yayan Xu, Bingpeng Li, Xufeng Jing, Junjie Zhang, Shiqing Xu.  (2020)  Supramolecular Copolymerization Strategy for Realizing the Broadband White Light Luminescence Based on N-Deficient Porous Graphitic Carbon Nitride (g-C3N4).  ACS Applied Materials & Interfaces,      [PMID:31916432] [10.1021/acsami.9b19338]
6. Xingchen He, Yixu Gu, Shichao Ai, Manman Xie, Qian Lu, Yiqing Wang, Jianquan Wang.  (2018)  Electron-rich heterocycle induced tunable emitting fluorescence of graphitic carbon nitride quantum dots.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2018.08.091]
7. Xiuping He, Jiangtao Wang, Xiaoqi Mei.  (2017)  Dummy Fragment Template Molecularly Imprinted Polymers for the Selective Solid-phase Extraction of Gonyautoxins from Seawater.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2016.1256408]
8. Yan Ke, Mingzhu Yuan, Xinglong Li, Yuan Liu, Yangyang Li, Yuanxu Liu, Xiangang Lin, Qinghua Liu, Yupeng Yuan.  (2025)  An electron delocalization with n-π∗ transitions of graphitic carbon nitride photocatalyst for visible-light-driven water decontamination.  ENVIRONMENTAL RESEARCH,      [PMID:39947385] [10.1016/j.envres.2025.121093]
9. Weilin Li, Rui Ma, Zheyang Liu, Zhehao Liu, Min Zhou, Baker Rhimi, Qiang Ma, Zhifeng Jiang, Weidong Shi.  (2025)  Boosting CO2 photoreduction by creating electron mediator in carbon-enriched poly(heptazine imide).  AICHE JOURNAL,      [PMID:] [10.1002/aic.18782]
10. Xiwei Guo, Ronan Brown, Yue Dong, Haoyu Feng, Yang Xiang, Dongxu Wang, Qi Zhang, He Zhu, Shiping Zhu.  (2025)  High-Performance Elastomer with Excellent Resistance to Low Temperature, Aging and Solvent.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202501171]
11. Dechao Wang, Hang Zhao, Jianglin Tu, Xun Zhu, Dingding Ye, Yang Yang, Hong Wang, Rong Chen, Qiang Liao.  (2024)  Photo–thermo-catalytic hydrogen production by an interfacial reactor with potassium-doped polymeric carbon nitride/titanium nitride.  Sustainable Energy & Fuels,  (14): (3092-3103).  [PMID:] [10.1039/D4SE00313F]
12. Yangjie Fu, Jiurui Chi, Yanling Wu, Jun Li, Meng Tan, Chunjuan Li, Hao Du, Derek Hao, Huayue Zhu, Qi Wang, Qiang Li.  (2025)  Synergistic electric fields induced by unilateral doping modulation for enhanced organic pollutant degradation and sterilization.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2025.162711]
13. Hongbo Xiao, Xin Huang, Wanyu Huang, Yufei Peng.  (2025)  Synthesis of Phosphorus-Nitrogen Synergistic Flame Retardant Containing Pyrimidine Ring/Vanillin for Improving Flame Retardancy, Smoke Suppressing, and Mechanical Properties of Epoxy Resin.  JOURNAL OF APPLIED POLYMER SCIENCE,      [PMID:] [10.1002/app.56678]
14. Xiaosha Guo, Xixi Di, Tian Tang, Yixuan Shi, Dong Liu, Wei Wang, Zhifeng Liu, Xiaohui Ji, Xianzhao Shao.  (2023)  Amine-functionalized Schiff base covalent organic frameworks supported PdAuIr nanoparticles as high-performance catalysts for formic acid dehydrogenation and hexavalent chromium reduction.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:38113545] [10.1016/j.jcis.2023.12.085]
15. Guoqiang Zhang, Wei Huang, Yangsen Xu, Yongliang Li, Chuanxin He, Xiangzhong Ren, Peixin Zhang, Hongwei Mi.  (2023)  Suppressing Defects-Induced Non-Radiative Recombination for Activating the Near-Infrared Photoactivity of Red Polymeric Carbon Nitride.  ADVANCED FUNCTIONAL MATERIALS,  33  (52): (2305935).  [PMID:] [10.1002/adfm.202305935]
16. Cunhuai Yu, Wanling Xiao, Ji Huang, Chao Hao, Pei Kang Shen, Zhi Qun Tian.  (2025)  Single yttrium atom coordinated by nitrogen and oxygen with an asymmetric 4d orbit as efficient oxygen reduction electrocatalyst.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:40154164] [10.1016/j.jcis.2025.137425]
17. Yue Li, Ping Liu, Zhongshan Guo, Wenqian Li, Haiyan Jiang, Yongchao Ma.  (2025)  π-Conjugation-Regulated Vesicular Carbon Nitride Z-Type Homojunctions: Toward Integration of Pollutant Degradation and Detection.  LANGMUIR,      [PMID:41428775] [10.1021/acs.langmuir.5c05500]
18. Qingye Liu, Xiaohui Wang, Wenbo Xu, Xuan Ning, Yu Yang, Peng Li, Yanling Hu, Xiaojun Li, Qingqing Li.  (2026)  An anisotropic multi-amine-mediated dynamic network for strong, tough, and self-strengthening conductive hydrogel.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.172956]
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