3,6-Di(2-pyridyl)-1,2,4,5-tetrazine - ≥98%(HPLC) , CAS No.1671-87-0

CAS: 1671-87-0 Cat. No.: D155574 Peso molecular: 236.24 Beilstein Registry Number: 26(5)19,377 Número EC: 626-669-4
Disponible para pedir
GRADE & PURITY ≥98%(HPLC)
Synonyms
3,6-Di(2-pyridyl)-1,2,4,5-tetrazine | TIBOLONE [WHO-DD] | 3,6-Bis(2-pyridinyl)-1,2,4,5-tetrazine | 3,6-di(pyridin-2-yl)-1,2,4,5-tetrazine | 3,6-Di-2-pyridinyl-1,2,4,5-tetrazine | NSC238155 | NSC-238155 | DTXSID30311116 | C12H8N6 | 3,6-Di-2-pyridyl-1,2,4,5
Storage
Room temperature,Desiccated,Cool
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
D155574-1g
10
9,90US$
5g
D155574-5g
5
19,90US$
10g
D155574-10g
2
29,90US$
25g
D155574-25g
3
47,90US$
100g
D155574-100g
2

86,90US$

149,90US$
Guardar 63,00 US$ (42.03%)
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Why this grade

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

🌡

Storage & shipping

Room temperature,Desiccated,Cool 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

3,6-Di-2-pyridyl-1,2,4,5-tetrazine (DPTZ) undergoes solvothermal reaction with CuSO4.6H2O and Cu(Ac)2.H2O to afford copper containing coordination polymers. It reacts with enamine derivative of morpholine and 5-,6-,7- and 8-membered cyclic ketones to afford pyridazine derivatives. 3,6-Di-2-pyridyl-1,2,4,5-tetrazine undergoes solid-state reaction with fullerene C60 by high-speed vibration milling technique. It acts as electron-deficient diene in the inverse electron demand Diels Alder reaction.
3,6-Di-2-pyridyl-1,2,4,5-tetrazine may be used in the following studies: . Preparation of mononuclear, cyclic tetranuclear, and 1-D helical-chain Cu(II) complexes, via metal-assisted hydrolysis. . Synthesis of novel cyclic tetranuclear ZnII complex. . Synthesis of substituted 3,6-di(2-pyridyl)pyridazines, via inverse electron demand Diels Alder reaction with alkenes or alkynes.

Specifications

Sinónimos
3, 6-Di(2-pyridyl)-1, 2, 4, 5-tetrazine | TIBOLONE [WHO-DD] | 3, 6-Bis(2-pyridinyl)-1, 2, 4, 5-tetrazine | 3, 6-di(pyridin-2-yl)-1, 2, 4, 5-tetrazine | 3, 6-Di-2-pyridinyl-1, 2, 4, 5-tetrazine | NSC238155 | NSC-238155 | DTXSID30311116 | C12H8N6 | 3, 6-Di-2-pyridyl-1, 2, 4, 5
Especificaciones y pureza
≥98%(HPLC)
Condiciones de almacenamiento de almacenamiento
Room temperature, Desiccated, Cool
Enviado en
Normal
Pureza
≥98%(HPLC)
Nombres e identificadores
Pubchem Sid488189453
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488189453
Sonrisas canónicasC1=CC=NC(=C1)C2=NN=C(N=N2)C3=CC=CC=N3
IUPAC Name3,6-dipyridin-2-yl-1,2,4,5-tetrazine
InChIKeyJFBIRMIEJBPDTQ-UHFFFAOYSA-N
INCHI1S/C12H8N6/c1-3-7-13-9(5-1)11-15-17-12(18-16-11)10-6-2-4-8-14-10/h1-8H
Isómeros SMILES C1=CC=NC(=C1)C2=NN=C(N=N2)C3=CC=CC=N3
WGK Alemania 3
Peso molecular 236.24
Beilstein 26(5)19,377
Reaxy-Rn 405091
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=405091&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
ClaseTetrazines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentTetrazines
Alternative Parents Pyridines and derivatives  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Tetrazine - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as tetrazines. These are organic compounds containing a tetrazine ring, which is a six-membered aromatic heterocycle made up of four nitrogen atoms and a two carbon atoms.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLH Tchem DNA polymerase eta (21678 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Luciferin 4-monooxygenase (66902 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
NS1 Nonstructural protein 1 (33327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pos-1 Cytoplasmic zinc-finger protein (1690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mex-5 Zinc finger protein mex-5 (1676 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.

16 results found

Lot NumberCertificate TypeFechaArticulo
B2624094Certificate of AnalysisJan 27, 2026 D155574
B2624095Certificate of AnalysisJan 27, 2026 D155574
B2624096Certificate of AnalysisJan 27, 2026 D155574
L2114272Certificate of AnalysisSep 17, 2025 D155574
L2114273Certificate of AnalysisSep 17, 2025 D155574
L2114274Certificate of AnalysisSep 17, 2025 D155574
L2115119Certificate of AnalysisSep 17, 2025 D155574
H1714056Certificate of AnalysisMar 04, 2025 D155574
I2009136Certificate of AnalysisJul 16, 2024 D155574
I2009138Certificate of AnalysisJul 16, 2024 D155574
H2402220Certificate of AnalysisJun 11, 2024 D155574
G2429090Certificate of AnalysisJun 11, 2024 D155574
H2401395Certificate of AnalysisJun 11, 2024 D155574
H2401396Certificate of AnalysisJun 11, 2024 D155574
C2514053Certificate of AnalysisNov 30, 2021 D155574
F2512042Certificate of AnalysisNov 30, 2021 D155574

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Propiedades químicas y físicas
SolubilidadSlightly soluble in water.
Punto de fusión (°C)225°C
Peso molecular236.230 g/mol
XLogP3-0.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass236.081 Da
Monoisotopic Mass236.081 Da
Topological Polar Surface Area77.300 Ų
Heavy Atom Count18
Formal Charge0
Complexity227.000
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. Li Qiuying, Li Xifei, Liu Dekun, Xu Ruiyang, Wei Shaohua.  (2023)  The effect of strain rate on the tensile properties of nitrile butadiene rubber with dual crosslinked networks.  POLYMER BULLETIN,      [PMID:] [10.1007/s00289-023-04976-2]
2. Qiang Wang, Yi Shi, Qiuying Li, Chifei Wu.  (2021)  Toughening, recyclable and healable nitrile rubber based on multi-coordination crosslink networks after “tetrazine click” reaction.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2021.110415]
3. Qingtao Wang, Xun Wei, Yanxia Wu, Guofu Ma, Ziqiang Lei, Shufang Ren.  (2024)  Bimetallic iron complex constructed clusters and single atoms neighboring structure to enhance oxygen reduction reaction performance.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:38493654] [10.1016/j.jcis.2024.03.097]
4. Yarui Li, Huangjie Lu, Yingzhe Du, Jie Qiu, Peng Lin, Jian Lin.  (2025)  Highly efficient separation of high-valent actinide ions from lanthanides via fractional crystallization.  CHINESE JOURNAL OF STRUCTURAL CHEMISTRY,      [PMID:] [10.1016/j.cjsc.2025.100562]
5. Yarui Li, Guangtao Zhang, Xiaoyuan Zhou, Qing Zou, Jiarui Chen, Yunyi Cui, Peng Lin, Jian Lin.  (2025)  Highly selective crystallization of uranium complexes for actinide partitioning in nuclear waste streams.  Journal of Environmental Chemical Engineering,  13  (6): (120317).  [PMID:] [10.1016/j.jece.2025.120317]
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