NORNICOTINE, DL-(RG)

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Company Name: J & K SCIENTIFIC LTD.  
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NORNICOTINE, DL-(RG) manufacturers

  • NORNICOTINE, DL-(RG)
  • NORNICOTINE, DL-(RG) pictures
  • $30.00
  • 2026-08-07
  • CAS:494-97-3
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 200000KG
  • NORNICOTINE, DL-(RG)
  • NORNICOTINE, DL-(RG) pictures
  • $8.00
  • 2020-02-18
  • CAS:494-97-3
  • Min. Order: 1KG
  • Purity: ＞98% HPLC
  • Supply Ability: 20 tons
NORNICOTINE, DL-(RG) Basic information
Product Name:NORNICOTINE, DL-(RG)
Synonyms:Nicotine EP Impurity F (nornicotine );NORNICOTINE, DL-(RG);(S)-2-(3-Pyridyl)pyrrolidine;(s)-nicotin;dl-Norcitine;l-Nor-nicotine;Nicotine, 1'-demethyl-, (S)-;Nornicotin
CAS:494-97-3
MF:C9H12N2
MW:148.21
EINECS:
Product Categories:Heterocycles;Metabolites & Impurities;Nicotine Derivatives;pharmacetical
Mol File:494-97-3.mol
NORNICOTINE, DL-(RG) Structure
NORNICOTINE, DL-(RG) Chemical Properties
alpha D22 -89° (c = 100)
Boiling point bp 270°; bp11 131°; bp3 105-107°
density d420 1.0737
refractive index nD20 1.5378
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Acetonitrile (Slightly), Chloroform (Slightly), Methanol (Sparingly)
form Oil
pka9.09±0.10(Predicted)
color visc liquid
Odorslt amine odor
Henry's Law Constant7.2×103 mol/(m3Pa) at 25℃, HSDB (2015)
Stability:Light Sensitive
EPA Substance Registry SystemPyridine, 3-(2S)-2-pyrrolidinyl- (494-97-3)
Safety Information
Hazardous Substances Data494-97-3(Hazardous Substances Data)
ToxicityLDLo ipr-rat: 23,500 mg/kg MEIEDD 10,963,83
MSDS Information
NORNICOTINE, DL-(RG) Usage And Synthesis
Chemical PropertiesPale Yellow to Reddish Brown Oil
Uses(S)-Nornicotine is a metabolite of Nicotine (N412420). Can catalyze aqueous aldol reactions.
UsesAgricultural or horticultural insecticide.
DefinitionChEBI: A pyridine alkaloid that is nicotine lacking the methyl group on the pyrrolidine nitrogen.
Production MethodsCommercial production of nornicotine, particularly the high-purity (S)-enantiomer, has evolved from traditional tobacco extraction to sophisticated synthetic and chemoenzymatic methods. One advanced approach begins with myosmine, a compound derived from nicotinic acid, which is then converted into (S)-nornicotine using highly selective biocatalysts such as imine reductases. Enzyme-driven processes that enable efficient, scalable production while minimizing impurities like tobacco-specific nitrosamines have been developed. Another method involves converting racemic (R,S)-nornicotine into high-purity (S)-nornicotine through a combination of immobilized enzymes and reducing agents
Mechanism of actionBroad-spectrum and fast acting. Mainly respiratory action but some contact and stomach activity
Safety ProfilePoison by intraperitoneal andintravenous routes. About 1/3 the toxicity of nicotine.Causes faintness, prostration, muscular weakness, severenausea, vomiting, diarrhea, and collapse withoutconvulsions. An insecticide. When heated todecomposition it em
IC 50Human Endogenous Metabolite
Pesticide TypeInsecticide; Metabolite
Tag:NORNICOTINE, DL-(RG)(494-97-3) Related Product Information
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