2-Amino-3-methylpyridine
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2-Amino-3-methylpyridine
structure -
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CAS No:
1603-40-3
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Formula:
C6H8N2
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Chemical Name:
2-Amino-3-methylpyridine
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Synonyms:
2-Pyridinamine,3-methyl-;3-Picoline,2-amino-;3-Methyl-2-pyridinamine;2-Amino-3-picoline;2-Amino-3-methylpyridine;2-Amino-β-picoline;3-Methyl-2-aminopyridine;3-Methylpyridin-2-ylamine;NSC 176169;NSC 450
- Categories:
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CAS No:
2-Amino-3-methylpyridine Basic Attributes
108.14
108.14
107892
216-501-4
Y2WWD85QY6
450
DTXSID3051759
29333999
Characteristics
38.9
0.9
Clear yellow Liquid After Melting
1.073 g/mL at 25 °C(lit.)
33.5 °C
222 °C
233 °F
n 20/D 1.5823(lit.)
H2O: soluble
Store below +30°C.
0.11mmHg at 25°C
Oral-rat LD50: 100 mg/kg; Subcutaneous-mouse LD50: 36 mg/kg
Flammable; burning produces toxic nitrogen oxide fumes
Safety Information
II
6.1
UN 2811 6.1/PG 3
3
23/24/25-33-36/37/38-25
36/37/39-45-37/39-28A-26
US1850000
T
Warehouse ventilated, low temperature and dry
Stable under normal temperatures and pressures.
P261-P280-P301 + P310-P311
H301-H311-H331-H373
|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P260, P261, P262, P264, P270, P271, P280, P301+P310, P302+P350, P302+P352, P304+P340, P305+P351+P338, P310, P311, P312, P314, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 47 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
2-Amino-3-methylpyridine Use and Manufacturing
1) Add 9021g of toluene, 538g of sodium metal, 70g of ethanolamine and 1900g of 3-picoline to the autoclave. After tightening the autoclave, open the autoclave inlet and the addition port of the dropping tank, and open the dropping tank And the kettle body valve, the hose through the feeding port into the bottom of the tank, with nitrogen replacement air for 1min, closed the lid of the feeding port, warmed to 60 , dropping liquid ammonia, control the pressure in the autoclave 3MPa, the final Liquid ammonia added amount of 600g. Fully respond.
2) The temperature was raised to 170 ° C, nitrogen was filled to a pressure of 5 MPa, and the reaction was sufficiently completed. When the pressure in the autoclave increased to 5.5 MPa, Pressure relief to 5MPa, repeat this operation until the pressure inside the reactor does not rise as the end of the reaction, down to room temperature.
3) The ammoniated liquid was taken out and slowly added dropwise to water (9 kg). The mixture was stirred and hydrolyzed and extracted, and the mixture was allowed to stand still. After the aqueous phase was extracted again with 3 L of toluene, the oil phases were combined and the oil phase was quantified by gas chromatography.Among them, 1928g of 2-amino-5-methylpyridine and 144g of 2-amino-3-methylpyridine.
2-Amino-3-methylpyridine is used in the synthesis of ketones from aldehydes.
2-Pyridinamine, 3-methyl-: ACTIVE
Computed Properties
Molecular Weight:108.14
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Exact Mass:108.068748264
Monoisotopic Mass:108.068748264
Topological Polar Surface Area:38.9
Heavy Atom Count:8
Complexity:72.9
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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