4-Aminopyridine/Fampridine

4-Aminopyridine/Fampridine structural formula

CAS Number 504-24-5
Molecular Formula C5H6N2
Molecular Weight 94.117 g/mol
InChI Key NUKYPUAOHBNCPY-UHFFFAOYSA-N
LogP 0.32
Synonyms
  • 4-Aminopyridine
  • Pyridin-4-amine
  • 4-Pyridinamine
  • 504-24-5
  • 5-22-09-00106
  • 4-Pyridinamine
  • 4-AMINOPYRIDIN
  • 4-Amino-Pyridine
  • 4-piridilamina
  • 4-Pyridinylamine
  • 4-Pyridylamin
  • 4-Pyridylamine
  • Avitrol
  • Fampridine
  • Neurelan
  • NSC 15041
  • p-Aminopyridine
  • Phillips 1861
  • PYRIDINE, 4-AMINO-
  • Pyridine-4-ylamine
  • γ-Aminopyridine
  • Amino-4 pyridine
  • Avitrol 200
  • BRN 0105782
  • Caswell No. 038
  • Compound 1861
  • EINECS 207-987-9
  • EPA Pesticide Chemical Code 069201
  • UNII-BH3B64OKL9
  • 4-AP
  • Dalfampridine
  • N07XX07
  • gamma-Aminopyridine

Applications:


HPLC Separation of Vitamin C, Vitamin Group B, and Related Impurities
Vitamin C (ascorbic acid) and Vitamins Group B are separated on Obelisc N mixed-mode column. Method can be used in quantitation and determination of polar vitamins in various formulations and dietary supplements. HPLC method can be based on UV, Evaporative Light Scattering Detection (ESLD), RI or MS detection. Effect of sample matrix can be eliminated by changing mobile phase conditions. Buffer concentration, buffer pH and amount of ACN will affect every vitamin differently due to difference in polar and ionic properties.

Condition

Column Obelisc N , 4.6x150 mm, 5 µm, 100A
Mobile Phase MeCN/H2O
Buffer AmAc pH 5.0
Flow Rate 1.0 ml/min
Detection UV, 250 nm
 

Description

Class of Compounds Drug, Vitamin B₆, Hydrophobic, Ionizable
Analyzing Compounds Pyridoxine, Ascorbic acid, Niacinamide, Pantothenic acid, Caffeine, Riboflavin, Barbituric Acid,  3- Aminopyrine


Application Analytes:

3-Aminopyridine
4-Aminopyridine/Fampridine
Ascorbic Acid
Barbituric Acid
Isonicotinic Acid
Nicotinic Acid
Pyridoxine
Vitamin B2 (Riboflavin)
Vitamin B6 (Pyridoxine)