Basic information Safety Supplier Related

3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4

Basic information Safety Supplier Related

3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4 Basic information

Product Name:
3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4
Synonyms:
  • 3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4
  • 3-(2-Pyridinyl)propanoic acid
  • 2-PYRIDINEPROPANOIC ACID
  • 2-Pyridylpropanoic acid
  • 3-Pyridin-2-yl-propionic acid sulfate
  • 3-Pyridin-2-yl-propionic acid H2SO4 ,95%
  • 3-pyridin-2-ylpropanoic acid(SALTDATA: 0.02Na2SO4)
  • 3-Pyridin-2-yl-propionic acid sulfuric acid
CAS:
15197-75-8
MF:
C8H9NO2
MW:
151.16
Product Categories:
  • pharmacetical
Mol File:
15197-75-8.mol
More
Less

3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4 Chemical Properties

Melting point:
140-145°C
Boiling point:
287.4±15.0 °C(Predicted)
Density 
1.193±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
solid
pka
3.87±0.10(Predicted)
color 
Light brown
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
37/38-41
Safety Statements 
26-39
WGK Germany 
3
HS Code 
2933399990
More
Less

3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4 Usage And Synthesis

Synthesis

2859-68-9

15197-75-8

The general procedure for the synthesis of 3-pyridin-2-yl-propanoic acid from 3-(pyridin-2-yl)propan-1-ol was as follows: 3-(2-pyridinyl)-propanol (1 g, 7.6 mmol), water (13 mL), and concentrated sulfuric acid (0.59 mL, 5.1 mmol) were added to a 50 mL round-bottom flask equipped with a stirrer. Potassium permanganate (1.8 g, 11.3 mmol) was added to the stirring reaction mixture in batches over a period of 30 min while the reaction temperature was controlled at 50 °C. After the addition was completed, the reaction continued to be stirred at 50 °C until the color of the mixture changed to brown. Subsequently, the reaction mixture was warmed up to 80 °C and heated for 1 h. After completion of the reaction, it was filtered. The filtrate was concentrated to dryness under reduced pressure to afford the crude product 3-(2-pyridyl)-propionic acid (1.14 g), which could be used directly in the next step of the reaction without further purification. To obtain the pure product, the above crude product was dissolved in ethanol (10 mL), activated charcoal (0.1 g) was added, refluxed for 5 min and then hot filtered. The filtrate was cooled and crystallized to give pure 3-(2-pyridyl)-propionic acid (0.88 g, 78% yield).

References

[1] ACS Catalysis, 2018, vol. 8, # 7, p. 6738 - 6744
[2] Patent: US6162927, 2000, A
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 22, p. 9156 - 9169
[4] Journal of the American Chemical Society, 1951, vol. 73, p. 3156,3167
[5] Organic Process Research and Development, 2017, vol. 21, # 9, p. 1388 - 1393

3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4 Preparation Products And Raw materials

Raw materials

3-PYRIDIN-2-YL-PROPIONIC ACID H2SO4Supplier

SiChuang NanBu Honesty Technology Co., Ltd.
Tel
0838-5675166 15883665058
Email
nbcxkj@126.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
PharmaBlock Sciences (Nanjing),Inc.
Tel
025-86918202 4000255188
Email
sales@pharmablock.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com