N,2,6-trimethylpyridin-4-amine

Base Information

Chemical Name:N,2,6-trimethylpyridin-4-amine
CAS No.:193690-76-5
Molecular Formula:C₈H₁₂N₂
Molecular Weight:136.197
Hs Code.:2933399090
DSSTox Substance ID:DTXSID30440955
Mol file:193690-76-5.mol

Synonyms:N,2,6-trimethylpyridin-4-amine;193690-76-5;4-Pyridinamine,N,2,6-trimethyl-(9CI);SCHEMBL883719;DTXSID30440955;AKOS006377211;SB54316

Suppliers and Price of N,2,6-trimethylpyridin-4-amine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
N,2,6-Trimethyl-4-pyridinamine
100mg
$ 155.00

TRC
N,2,6-Trimethyl-4-pyridinamine
10mg
$ 45.00

Crysdot
N,2,6-Trimethylpyridin-4-amine 95+%
1g
$ 353.00

Chemenu
N,2,6-trimethylpyridin-4-amine 95%
1g
$ 333.00

American Custom Chemicals Corporation
N,2,6-TRIMETHYLPYRIDIN-4-AMINE 95.00%
5MG
$ 496.44

Alichem
N,2,6-Trimethylpyridin-4-amine
1g
$ 474.21

Total 8 raw suppliers

Chemical Property of N,2,6-trimethylpyridin-4-amine

Chemical Property:

PSA：28.15000
LogP:1.16200
Storage Temp.:2-8°C(protect from light)
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:136.100048391
Heavy Atom Count:10
Complexity:93.4

Purity/Quality:

97% ^*data from raw suppliers

N,2,6-Trimethyl-4-pyridinamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC(=N1)C)NC

Technology Process of N,2,6-trimethylpyridin-4-amine

There total 5 articles about N,2,6-trimethylpyridin-4-amine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

: 193690-75-4
2,6-dimethyl-4-methoxycarbonylaminopyridine

: 193690-76-5
2,6-dimethyl-4-methylaminopyridine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 0.5h; Heating;
DOI:10.1002/jhet.5570340303

Reference yield:

: 1073-23-0
2,6-lutidine N-oxide

: 193690-76-5
2,6-dimethyl-4-methylaminopyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / H₂SO₄, HNO₃ / 3 h / 125 - 130 °C

2: 97 percent / H₂, gl. AcOH / 10percent Pd/C / 19 h / 50 °C / 2327.2 Torr

3: 100 percent / K₂CO₃ / acetone / 5 h / Ambient temperature

4: 98 percent / lithium aluminum hydride / tetrahydrofuran / 0.5 h / Heating

With lithium aluminium tetrahydride; sulfuric acid; hydrogen; nitric acid; potassium carbonate; acetic acid; palladium on activated charcoal; In tetrahydrofuran; acetone;
DOI:10.1002/jhet.5570340303

Reference yield:

: 4808-64-4
4-nitro-2,6-lutidine-1-oxide

: 193690-76-5
2,6-dimethyl-4-methylaminopyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / H₂, gl. AcOH / 10percent Pd/C / 19 h / 50 °C / 2327.2 Torr

2: 100 percent / K₂CO₃ / acetone / 5 h / Ambient temperature

3: 98 percent / lithium aluminum hydride / tetrahydrofuran / 0.5 h / Heating

With lithium aluminium tetrahydride; hydrogen; potassium carbonate; acetic acid; palladium on activated charcoal; In tetrahydrofuran; acetone;
DOI:10.1002/jhet.5570340303