2-Amino-6-methylpyridine
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2-Amino-6-methylpyridine
structure -
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CAS No:
1824-81-3
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Formula:
C6H8N2
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Chemical Name:
2-Amino-6-methylpyridine
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Synonyms:
2-Pyridinamine,6-methyl-;2-Picoline,6-amino-;6-Methyl-2-pyridinamine;2-Amino-6-picoline;6-Amino-2-picoline;2-Amino-6-methylpyridine;6-Amino-2-methylpyridine;6-Methyl-2-pyridylamine;6-Methyl-2-aminopyridine;6-Methylpyridin-2-ylamine;NSC 1488;NSC 176163;NSC 6971;6-Methylpyridin-2-amine
- Categories:
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CAS No:
2-Amino-6-methylpyridine Basic Attributes
108.14
108.14
107048
217-360-1
35ANN6MRBM
6971|1488
DTXSID0044860
29333999
Characteristics
38.9
0.4
Yellow Crystalline Low Melting Solid
1.0275 (estimate)
41 °C
208.5 °C
218 °F
1.5560 (estimate)
very faint turbidity
Store below +30°C.
0.213mmHg at 25°C
Oral-rat LD50: 100 mg/kg; Subcutaneous-mouse LD50: 52 mg/kg
Flammable; burning produces toxic nitrogen oxide fumes
Safety Information
II
6.1
UN 2811 6.1/PG 3
3
25-36/37/38-24/25-23/24/25-24
26-36/37/39-45-37/39-28A
US1885000
T
Warehouse ventilated, low temperature and dry
Stable under normal temperatures and pressures.
P261-P280-P301 + P310-P302 + P350-P305 + P351 + P338-P310
H301-H310-H315-H319-H335
|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P261, P262, P264, P270, P271, P280, P301+P310, P302+P350, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 58 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
2-Amino-6-methylpyridine Use and Manufacturing
Derived from 2-methylpyridine amination. Pass liquid ammonia into the reaction tank, add high-speed nitrate iron, slowly add small pieces of metallic sodium in portions with stirring, and continue stirring for 3 hours after the addition. The ammonia is discharged naturally until the reaction solution is in the form of a thin slurry to obtain sodium ammonia solution. Anhydrous xylene was added to sodium amide, stirred and heated to remove residual ammonia gas. The temperature was raised to 120°C and 2-methylpyridine was added dropwise. After the addition was completed, the reaction was maintained at 124-129°C for 10 hours. Slowly add appropriate amount of water to hydrolyze at 90-100℃. After the hydrolysis is completed and stir for half an hour, the xylene layer is separated by standing, xylene is recovered by distillation, and then the 90-120℃ (1.33-2.67kPa) fraction is collected by vacuum distillation, which is 2 -Amino-6-picoline. The yield is 72%.
Intermediate.
2-Pyridinamine, 6-methyl-: ACTIVE
Computed Properties
Molecular Weight:108.14
XLogP3:0.4
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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