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2-METHOXY-5-PICOLINE

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Products Intro: Product Name:2-METHOXY-5-PICOLINE
CAS:13472-56-5
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CAS:13472-56-5
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Products Intro: Product Name:2-Methoxy-5-methylpyridine
CAS:13472-56-5
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Company Name: Neostar United (Changzhou) Industrial Co., Ltd.
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Products Intro: Product Name:2-Methoxy-5-picoline
CAS:13472-56-5
Purity:0.99 Remarks:1KG,5KG,25KG,200KG

2-METHOXY-5-PICOLINE manufacturers

  • 2-methoxy-5-picoline
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  • $0.00 / 100gm
  • 2026-01-30
  • CAS:13472-56-5
  • Min. Order: 100gm
  • Purity: 99%min
  • Supply Ability: 100kgs
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  • 2025-12-01
  • CAS:13472-56-5
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  • Purity: 98.0%
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  • 2-METHOXY-5-PICOLINE
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  • $1.10 / 1g
  • 2025-11-18
  • CAS:13472-56-5
  • Min. Order: 1g
  • Purity: 99.00%
  • Supply Ability: 100 Tons min
2-METHOXY-5-PICOLINE Basic information
Product Name:2-METHOXY-5-PICOLINE
Synonyms:2-METHOXY-5-PICOLINE;2-Methoxy-5-methylpyridine;Pyridine,2-Methoxy-5-Methyl-;6-Methoxy-3-picoline;2-METHOXY-5-PICOLINE ISO 9001:2015 REACH
CAS:13472-56-5
MF:C7H9NO
MW:123.15
EINECS:
Product Categories:Pyridine
Mol File:13472-56-5.mol
2-METHOXY-5-PICOLINE Structure
2-METHOXY-5-PICOLINE Chemical Properties
Boiling point 165°C(lit.)
density 1.001±0.06 g/cm3(Predicted)
refractive index 1.5000 to 1.5040
storage temp. Sealed in dry,Room Temperature
form clear liquid
pka3.69±0.10(Predicted)
color Colorless to Light yellow
λmax279nm(CH3CN)(lit.)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36
HS Code 2933399990
MSDS Information
2-METHOXY-5-PICOLINE Usage And Synthesis
Chemical Propertiescolorless liquid
Synthesis
2-Bromo-5-methylpyridine

3510-66-5

Sodium Methoxide

124-41-4

2-METHOXY-5-PICOLINE

13472-56-5

Example 5: General procedure for the preparation of 2-methoxy-5-methylpyridine from 2-bromo-5-methylpyridine 1. 250 g (1.45 mol) of 2-bromo-5-methylpyridine, 2.1 g (1 mol%) of copper(I) bromide (CuBr), 14.5 g (2 mol%) of poly(ethylene glycol) dimethyl ether 500, and 457 g of 30% sodium methanol solution (precursor concentration of 14.5%) were added to a reactor. 2. the reaction mixture was heated to 90 °C and the progress of the reaction was monitored by GC until the conversion was >98.5% (reaction time totaled 17 hours). 3. upon completion of the reaction, the reaction mixture was quenched by slowly adding 750 g of water. 4. The pH of the mixture was adjusted to 9 by dropwise addition of hydrochloric acid, followed by filtration through decalite to remove insoluble material. 5. The aqueous phase was extracted twice with methyl tert-butyl ether (MTBE) (350 g each). 6. The organic phases were combined and subjected to vacuum fractionation to afford 162.8 g (1.32 mol, 91% yield) of 2-methoxy-5-methylpyridine with a GC purity of >98% (a/a).

References[1] Patent: US2008/71084, 2008, A1. Location in patent: Page/Page column 4
2-METHOXY-5-PICOLINE Preparation Products And Raw materials
Raw materials2-Bromo-5-methylpyridine-->Sodium Methoxide
Tag:2-METHOXY-5-PICOLINE(13472-56-5) Related Product Information
3-BROMO-6-METHOXY-2-PICOLINE 2-METHOXY-4-PICOLINE (2-METHOXY-4-METHYLPYRIDINE),2-METHOXY-4-PICOLINE 6-METHOXY-2-PICOLINE,2-METHOXY-6-PICOLINE 2-Methoxy-5-(trifluoromethyl)pyridine 4-CHLORO-2-METHOXY-PYRIDINE 2-METHOXY-5-NITRO-6-PICOLINE 5-Chloro-2-methoxypyridine 5-Bromo-2-methoxypyridine 2-Methoxy-5-nitropyridine 4-Amino-2-methoxypyridine 2-Methoxy-5-methyl-N,N-bis(1-methylethyl)-3-phenylbenzenepropanamine fumarate 2-METHOXY-5-PICOLINE 2,6-Dimethoxypyridine-3-carboxylic acid 2-METHOXYPYRIDINE-5-CARBONITRILE 3,5-Dibromo-2,6-dimethoxypyridine, 99% 2-METHOXY-6-PICOLINE,6-METHOXY-2-PICOLINE 5-BROMO-2-METHOXY-4-PICOLINE 3-Methoxy-2-Picoline

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