4,4'-Dimethyl-2,2'-dipyridyl - Moligand™, ≥98% , CAS No.1134-35-6

CAS: 1134-35-6 Cat. No.: D102980 Molecular Weight: 184.24 Beilstein Registry Number: 128995 EC Number: 214-483-2

GRADE & PURITY Moligand™, ≥98%

Synonyms

HY-W002003 | AS-17512 | 4,4'-dimethyl 2,2'-bipyridine | 4,4'dimethyl 2,2'bipyridine | EN300-754538 | B0852 | EINECS 214-483-2 | SY011392 | AM84345 | DTXSID3061552 | FT-0609153 | 4,4'-Dimethyl-2,2'-dipyridyl, 99.5%, purified by sublimation | BBL104382 | 2,

Storage

Room temperature,Desiccated,Cool

Shipped In

Normal

Specifications

Synonyms

HY-W002003 | AS-17512 | 4, 4'-dimethyl 2, 2'-bipyridine | 4, 4'dimethyl 2, 2'bipyridine | EN300-754538 | B0852 | EINECS 214-483-2 | SY011392 | AM84345 | DTXSID3061552 | FT-0609153 | 4, 4'-Dimethyl-2, 2'-dipyridyl, 99.5%, purified by sublimation | BBL104382 | 2,

Specifications & Purity

Moligand™, ≥98%

Storage

Room temperature, Desiccated, Cool

Shipped In

Normal

Grade

Moligand™

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488181979
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181979
• Canonical Smiles: CC1=CC(=NC=C1)C2=NC=CC(=C2)C
• IUPAC Name: 4-methyl-2-(4-methylpyridin-2-yl)pyridine
• InChIKey: NBPGPQJFYXNFKN-UHFFFAOYSA-N
• INCHI: 1S/C12H12N2/c1-9-3-5-13-11(7-9)12-8-10(2)4-6-14-12/h3-8H,1-2H3
• Isomeric SMILES: CC1=CC(=NC=C1)C2=NC=CC(=C2)C
• WGK Germany: 3
• RTECS: DW1765000
• Molecular Weight: 184.24
• Beilstein: 128995
• Reaxy-Rn: 128995
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=128995&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Pyridines and derivatives
      • Subclass Bipyridines and oligopyridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Pyridines and derivatives
• Subclass: Bipyridines and oligopyridines
• Intermediate Tree Nodes: Not available
• Direct Parent: Bipyridines and oligopyridines
• Alternative Parents: Methylpyridines Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Bipyridine - Methylpyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as bipyridines and oligopyridines. These are organic compounds containing two pyridine rings linked to each other.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

CCR1 Tchem C-C chemokine receptor type 1 (1730 Activities)

Discover Target: CCR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CCR5 Tclin C-C chemokine receptor type 5 (5640 Activities)

Discover Target: CCR5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Histidine-rich protein (528 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mycobacterium tuberculosis (203094 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasmodium falciparum (966862 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Ferriprotoporphyrin IX (165 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in ethanol, acetic acid, benzene, toluene. Highly soluble in water at pH < 2.
• Melt Point(°C): 171-173°C
• Molecular Weight: 184.240 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 184.1 Da
• Monoisotopic Mass: 184.1 Da
• Topological Polar Surface Area: 25.800 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 161.000
• 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

References

1. Yu-Ling Yang, Gang Wang, Ping Zhu, Lei Tang, Zhi-Xiang Zeng, Li-Jing Zhu.  (2023)  In situ deposition of double Fe-based Fenton catalysts on the porous membrane for the development of multi-defense against various foulants toward highly efficient water purification.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.144498]

2. Yu-Ling Yang, Man-Man Li, Li-Jing Zhu, Gang Wang, Zhi-Xiang Zeng.  (2022)  Zwitterionic polyvinylidene fluoride membranes with strong underwater superoleophobicity and oil-fouling resistance for oily water purification.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2022.107593]

3. Song Yang, Jiang Lan Ying.  (2017)  Fabrication and characterization of dual-layer hollow-fiber ultrafiltration membranes.  JOURNAL OF POLYMER RESEARCH,  24  (8): (1-14).  [PMID:] [10.1007/s10965-017-1271-y]

4. Ziyu Zhou, Shuo Li, Xiuqian Ding, Kun Zhang, Jie Zhou, Xin Zhou.  (2025)  Aggregation-Induced Photosensitization of Long-Chain-Substituted Osmium Complexes for Lysosomes Targeting Photodynamic Therapy.  ACS Applied Bio Materials,      [PMID:40074675] [10.1021/acsabm.5c00224]

5. Yinchao Jin, Hongyu Chen, Gongpu Wen, Jie Zhou, Zhaohui Wang, Feng Zhang, Zhaoliang Cui.  (2024)  Fabrication of alkali-resistant PVDF membranes via atom transfer radical polymerization.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2024.112816]