Basic information Safety Supplier Related

Isonipecotic acid

Basic information Safety Supplier Related

Isonipecotic acid Basic information

Product Name:
Isonipecotic acid
Synonyms:
  • Isonipecotic acid, 4-Carboxypiperidine
  • 4 - piperidine forMic acid
  • Isonipecotic aci
  • Isonipecotic acid, 99% 25GR
  • Piperidin-4-carboxylic acid
  • 4-PIPERIDINECARBOXYLIC ACID FOR SYNTHESI
  • Piperidine-4-carboxylic acid or isonipecotic acid
  • AKOS BBS-00003783
CAS:
498-94-2
MF:
C6H11NO2
MW:
129.16
EINECS:
207-872-3
Product Categories:
  • Acids and Derivatives
  • Amines and Anilines
  • Nitrogen cyclic compounds
  • blocks
  • Carboxes
  • Heterocycles
  • Carboxylic Acids
  • Pyrans, Piperidines &Piperazines
  • Piperidine
  • Organic acids
  • Terfenadine Fexofenadine Ketanserin
  • Carboxylic Acids
  • Pyrans, Piperidines & Piperazines
Mol File:
498-94-2.mol
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Isonipecotic acid Chemical Properties

Melting point:
>300 °C(lit.)
Boiling point:
239.22°C (rough estimate)
Density 
1.1426 (rough estimate)
refractive index 
1.4587 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Water
form 
Powder
pka
pK1:3.73(+1);pK2:10.72(0) (25°C)
color 
White to faint pink-beige
Water Solubility 
soluble
Merck 
14,5189
BRN 
112553
CAS DataBase Reference
498-94-2(CAS DataBase Reference)
EPA Substance Registry System
4-Piperidinecarboxylic acid (498-94-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
NS5150000
TSCA 
T
HazardClass 
IRRITANT
HS Code 
29333999

MSDS

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Isonipecotic acid Usage And Synthesis

Chemical Properties

white to faint pink-beige powder

Uses

A GABA-A receptor partial agonist

Synthesis Reference(s)

Synthesis, p. 623, 1984
Tetrahedron Letters, 35, p. 8783, 1994 DOI: 10.1016/S0040-4039(00)78497-8

Purification Methods

It crystallises from H2O or EtOH as needles. The hydrochloride recrystallises from H2O or aqueous HCl with m 293odec (also 298odec, 300odec). [Wibaut Recl Trav Chim Pays-Bas 63 141 1944, IR: Zacharius et al. J Am Chem Soc 76 2908 1954, Beilstein 22/1 V 244.]

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