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3-Methyl-4-aminopyridine

3-Methyl-4-aminopyridine Suppliers list
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Products Intro: Product Name:3-Methyl-4-aminopyridine
CAS:1990-90-5
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Products Intro: Product Name:4-Amino-3-picoline
CAS:1990-90-5
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CAS:1990-90-5
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CAS:1990-90-5
Purity:98% Package:1kg;1USD
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Products Intro: CAS:1990-90-5
Purity:98% Package:1KG;10KG;50KG

3-Methyl-4-aminopyridine manufacturers

3-Methyl-4-aminopyridine Basic information
Product Name:3-Methyl-4-aminopyridine
Synonyms:3-METHYL-PYRIDIN-4-YLAMINE;4-Pyridinamine, 3-methyl-;3-METHYL-4-AMINOPYRIDINE;3-METHYL-4-PYRIDINYLAMINE;4-AMINO-3-PICOLINE;3-methyl-4-pyridinamin;4-amino-3-picolin;philips1908
CAS:1990-90-5
MF:C6H8N2
MW:108.14
EINECS:217-872-5
Product Categories:Pyridine Series;Boronic Acid;VARIOUSAMINE;Pyridine;Amines;Pyridines;Pyridines derivates
Mol File:1990-90-5.mol
3-Methyl-4-aminopyridine Structure
3-Methyl-4-aminopyridine Chemical Properties
Melting point 106-107
Boiling point 192.78°C (rough estimate)
density 0.9581 (rough estimate)
refractive index 1.5400 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form powder to crystal
pkapK1: 9.43(+1) (25°C)
color Crystals from C6H6/pet ether
InChIInChI=1S/C6H8N2/c1-5-4-8-3-2-6(5)7/h2-4H,1H3,(H2,7,8)
InChIKeyVGJLGPCXUGIXRQ-UHFFFAOYSA-N
SMILESC1=NC=CC(N)=C1C
CAS DataBase Reference1990-90-5(CAS DataBase Reference)
Safety Information
Hazard Codes C,Xi,Xn
Risk Statements 23/24/25-36/37/38-34-22-20/21/22
Safety Statements 22-36/37/39-45-36-27-26
RIDADR 2811
WGK Germany WGK 3
RTECS TJ5140000
Hazard Note Harmful
HS Code 29333999
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
ToxicityLD50 orl-rat: 446 mg/kg TXAPA9 21,315,72
MSDS Information
3-Methyl-4-aminopyridine Usage And Synthesis
Chemical PropertiesCrystals
Uses4-Amino-3-methylpyridine is a non depolarizing muscular relaxant with antagonist effect that functions on neuromuscular transmission and in central nervous systems in rats. A central cholinergic agent.
Safety ProfileModerately toxic by ingestion.When heated to decomposition it emits toxic fumes ofNOx.
Synthesis
3-Methyl-4-nitropyridine N-Oxide

1074-98-2

3-Methyl-4-aminopyridine

1990-90-5

Step 2: A mixed solution of 3-methyl-4-nitropyridine-N-oxide (30.0 g, 195 mmol) with 10% palladium-carbon catalyst (6.0 g) in ethanol (450 mL) was subjected to a hydrogen atmosphere (5 bar) and the reaction was stirred at room temperature for 36 hours. Upon completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad to remove the catalyst, followed by evaporation of the solvent under reduced pressure to afford the target product 3-methyl-4-aminopyridine (20.0 g, 95% yield).

References[1] Nucleosides, Nucleotides and Nucleic Acids, 2002, vol. 21, # 11-12, p. 737 - 751
[2] Patent: WO2015/22073, 2015, A1. Location in patent: Page/Page column 39
[3] Patent: WO2005/63744, 2005, A2. Location in patent: Page/Page column 232
[4] Journal of the American Chemical Society, 1954, vol. 76, p. 4184
[5] Pharmaceutical Bulletin, 1956, vol. 4, p. 174,177
3-Methyl-4-aminopyridine Preparation Products And Raw materials
Raw materials3-Methyl-4-nitropyridine N-Oxide-->Palladium-->Activated carbon-->Hydrogen-->Ethanol
Preparation Products5-Azaindole
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