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2-Amino-4,6-dimethylpyridine - 98%, high purity , CAS No.5407-87-4

    Grade & Purity:
  • ≥98%
In stock
Item Number
A123441
Grouped product items
SKU Size
Availability
Price Qty
A123441-1g
1g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$10.90
A123441-5g
5g
5
$38.90
A123441-10g
10g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$70.90
A123441-25g
25g
2
$128.90
A123441-100g
100g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$461.90

Basic Description

Synonyms 4,6-Dimethyl-2-aminopyridine | 7NVZ9DW9Q5 | STL557611 | W-105678 | 2-amino-4,6-dimethyl pyridine | 2-amino-4.6-dimethylpyridine | 2-Pyridinamine 4,6-dimethyl- | BRN 0002048 | AM20070146 | BBL103801 | Z1192367241 | AKOS005145684 | 2-Pyridinamine, 4,6-dimet
Specifications & Purity ≥98%
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Pyridines and derivatives
Subclass Aminopyridines and derivatives
Intermediate Tree Nodes Not available
Direct Parent Aminopyridines and derivatives
Alternative Parents Methylpyridines  Imidolactams  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Methylpyridine - Aminopyridine - Imidolactam - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as aminopyridines and derivatives. These are organic heterocyclic compounds containing an amino group attached to a pyridine ring.
External Descriptors Not available

Associated Targets(Human)

NOS2 Tchem Nitric oxide synthase, inducible (3 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
NOS1 Tchem Nitric oxide synthase, brain (2 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
NOS3 Tchem Nitric oxide synthase, endothelial (3 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
NOS1 Tchem Nitric-oxide synthase, brain (1786 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NOS3 Tchem Nitric-oxide synthase, endothelial (1452 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NOS1 Tchem Nitric oxide sythases; iNOS & nNOS (685 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PIK3R1 Tchem PI3-kinase p110-alpha/p85-alpha (2589 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

PIK3CA PI3-kinase p110-alpha subunit (51 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504753040
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504753040
IUPAC Name 4,6-dimethylpyridin-2-amine
INCHI InChI=1S/C7H10N2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3,(H2,8,9)
InChIKey BRBUBVKGJRPRRD-UHFFFAOYSA-N
Smiles CC1=CC(=NC(=C1)N)C
Isomeric SMILES CC1=CC(=NC(=C1)N)C
WGK Germany 3
RTECS US1818000
Molecular Weight 122.17
Reaxy-Rn 2048
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2048&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

4 results found

Lot Number Certificate Type Date Item
C2302457 Certificate of Analysis Mar 08, 2023 A123441
I2203214 Certificate of Analysis Sep 08, 2022 A123441
I1424056 Certificate of Analysis Jul 18, 2022 A123441
D1429056 Certificate of Analysis Feb 17, 2022 A123441

Chemical and Physical Properties

Boil Point(°C) 231°C
Melt Point(°C) 67°C
Molecular Weight 122.170 g/mol
XLogP3 1.300
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 122.084 Da
Monoisotopic Mass 122.084 Da
Topological Polar Surface Area 38.900 Ų
Heavy Atom Count 9
Formal Charge 0
Complexity 92.900
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

Citations of This Product

1. Li-Jing Zhu, Li-Ping Zhu, Pei-Bin Zhang, Bao-Ku Zhu, You-Yi Xu.  (2016)  Surface zwitterionicalization of poly(vinylidene fluoride) membranes from the entrapped reactive core–shell silica nanoparticles.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  468  (110). 
2. Li-Jing Zhu, Li-Ping Zhu, Yi-Fan Zhao, Bao-Ku Zhu, You-Yi Xu.  (2014)  Anti-fouling and anti-bacterial polyethersulfone membranes quaternized from the additive of poly(2-dimethylamino ethyl methacrylate) grafted SiO2 nanoparticles.  Journal of Materials Chemistry A,  (37): (15566-15574). 
3. Li-Jing Zhu, Li-Ping Zhu, Jin-Hong Jiang, Zhuan Yi, Yi-Fan Zhao, Bao-Ku Zhu, You-Yi Xu.  (2014)  Hydrophilic and anti-fouling polyethersulfone ultrafiltration membranes with poly(2-hydroxyethyl methacrylate) grafted silica nanoparticles as additive.  JOURNAL OF MEMBRANE SCIENCE,  451  (157). 
4. Zhuan Yi, Liping Zhu, Liang Cheng, Baoku Zhu, Youyi Xu.  (2012)  A readily modified polyethersulfone with amino-substituted groups: Its amphiphilic copolymer synthesis and membrane application.  POLYMER,  53  (350). 

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