Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 500-22-1
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Plastic bottles, Plastic buckets
Delivery Time: 7-15 days
Payment Terms: T/T, L/C, D/A, Western Union
Supply Ability: TON
CAS No:: |
500-22-1 |
Appearance:: |
Clear Brown - Yellow Liquid |
Molecular Formula:: |
C6H5NO |
Molecular Weight:: |
107.11 |
EINECS NO:: |
207-900-4 |
MDL NO:: |
MFCD00006382 |
CAS No:: |
500-22-1 |
Appearance:: |
Clear Brown - Yellow Liquid |
Molecular Formula:: |
C6H5NO |
Molecular Weight:: |
107.11 |
EINECS NO:: |
207-900-4 |
MDL NO:: |
MFCD00006382 |
Product Description:
Product Name:Pyridine-3-aldehyde CAS 500-22-1
Synonyms:
Pyridinecarboxaldehyde;
Nicotinaldehyde;
Chemical & Physical Properties
Appearance:Clear brown - yellow liquid
Assay: 99%+
Boiling point:78-81℃10 mmHg
Melting point:8℃
Flash point:140℃
Pka:3.43±0.10
PH:5.4 (111g/l, H2O, 20℃)
Density:1.141 g/mL at 20℃3
Application
3-pyridine-formaldehyde is an intermediate of pyrazinone.3-methylpyridine reacts with glacial acetic acid and hydrogen peroxide, the reaction temperature is 63℃, the reaction time is 17h, the molar ratio of 3-methylpyridine, glacial acetic acid and hydrogen peroxide is 1:4:3.5, and 3-pyridine nitrogen oxide is obtained; 3-pyridine nitride oxide reacts with acetic anhydride, the reaction temperature is 92℃, the reaction time is 4h, the molar ratio of 3-pyridine nitride oxide and acetic anhydride is 1:2.3, and acetic acid - 3-pyridine methyl ester is obtained; acetic acid-3-pyridine methyl ester reacts with potassium hydroxide solution, the reaction time is 5h, the molar ratio of the acetic acid-3-pyridine methyl ester and potassium hydroxide is 1:1.8, the reaction obtains 3-pyridine methanol; 3-pyridinolinol is cooled by ice water and PCC is added. The molar ratio of the 3-pyridinolinol and PCC is 1:2.5 and the temperature is 2℃. It then reacts at room temperature, at 23 degrees Celsius, and is monitored by thin layer chromatography until the reaction is complete.
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