(1'S,2'S)-NICOTINE 1'-OXIDE
(1'S,2'S)-NICOTINE 1'-OXIDE Basic information
- Product Name:
- (1'S,2'S)-NICOTINE 1'-OXIDE
- Synonyms:
-
- (1'S,2'S)-NICOTINE 1'-OXIDE
- (1'S,2'S)-NICOTINE 1'-OXIDE AND (1'R,2'S)-NICOTINE 1'-OXIDE
- (1'S,2'S)-TRANS-NICOTINE 1'-OXIDE
- (1S,2S)-syn-Nicotine N'-oxide
- (1'S,2'S)-trans-Nicotine-1'-N-oxide
- (1S-cis)-3-(1-Methyl-1-oxido-2-pyrrolidinyl)pyridine
- (1S-cis)-3-(1-Methyl-2-pyrrolidinyl)pyridine N-Oxide
- 3-[(1S,2S)-1-Methyl-1-oxido-2-pyrrolidinyl] pyridine
- CAS:
- 51095-86-4
- MF:
- C10H14N2O
- MW:
- 178.23
- Product Categories:
-
- Mutagenesis Research Chemicals
- Nitric Oxide Reagents
- Nicotine Derivatives
- Aromatics
- Chiral Reagents
- Heterocycles
- Mol File:
- Mol File
(1'S,2'S)-NICOTINE 1'-OXIDE Chemical Properties
- Melting point:
- 182-183°C
- storage temp.
- Hygroscopic, -20°C Freezer, Under Inert Atmosphere
- solubility
- DMF: 50 mg/ml; DMSO: 30 mg/ml; Ethanol: 50 mg/ml; PBS (pH 7.2): 1 mg/ml
- form
- A crystalline solid
- pka
- 4.63±0.40(Predicted)
- color
- White to off-white
- Stability:
- Hygroscopic
(1'S,2'S)-NICOTINE 1'-OXIDE Usage And Synthesis
Chemical Properties
Off-White to Yellow Solid
Uses
Nicotine-1’-N-oxide is a derivative of Nicotine (N412420) found in the leaves, stems, and roots of N. tabacum, N. affinis and N. sylvestris. Nicotine-1’-N-oxide has also been identified as a metabolite of nicotine in animals and in man. The metabolism of nicotine in man proceeds by alternative routes of oxidation of nitrogen to form nicotine-1’-N-oxide (both diastereomers) or cotinine. The ratio of these two products has been suggested as an indicator of bladder cancer in humans.
Uses
Nicotine-1’-N-oxide is a derivative of nicotine found in the leaves, stems, and roots of N. tabacum, N. affinis and N. sylvestris. Nicotine-1’-N-oxide has also been identified as a metabolite of nicotine in animals and in man. The metabolism of nicotine
Definition
ChEBI: Trans-(S)-nicotine N(1')-oxide is an (S)-nicotine N(1')-oxide in which the N(1')-methyl group is on the opposite side of the pyrrolidine ring to the pyridine substituent. The major species at pH 7.3.
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