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(2'S)-Nicotine 1-Oxide

Product Name
(2'S)-Nicotine 1-Oxide
CAS No.
2820-55-5
Chemical Name
(2'S)-Nicotine 1-Oxide
Synonyms
Acrylamide Impurity 17;(2'S)-Nicotine 1-Oxide;(S)-nicotine 1-N-oxide;(S)-3-(1-Methyl-2-pyrrolidinyl)pyridine 1-Oxide;3-(1-methylpyrrolidin-2-yl)-1-oxidopyridin-1-ium;3-(1-methylpyrrolidin-2-yl)-1-oxido-pyridin-1-ium;3-[(2S)-1-Methyl-2α-pyrrolidinyl]pyridine 1-oxide;Pyridine, 3-[(2S)-1-methyl-2-pyrrolidinyl]-, 1-oxide;3-(1-methylpyrrolidin-2-yl)-1-oxidanidyl-pyridin-1-ium
CBNumber
CB11175320
Molecular Formula
C10H14N2O
Formula Weight
178.23
MOL File
2820-55-5.mol
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(2'S)-Nicotine 1-Oxide Property

Boiling point:
347.9±30.0 °C(Predicted)
Density 
1.15±0.1 g/cm3(Predicted)
storage temp. 
Refrigerator, 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
8.79±0.40(Predicted)
Stability:
Very Hygroscopic
CAS DataBase Reference
2820-55-5
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Safety

HS Code 
2933399990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P321Specific treatment (see … on this label).

P330Rinse mouth.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Cayman Chemical
Product number
22153
Product name
(2'S)-Nicotine-1-oxide
Purity
≥98%
Packaging
1mg
Price
$37
Updated
2024/03/01
Cayman Chemical
Product number
22153
Product name
(2'S)-Nicotine-1-oxide
Purity
≥98%
Packaging
5mg
Price
$161
Updated
2024/03/01
Cayman Chemical
Product number
22153
Product name
(2'S)-Nicotine-1-oxide
Purity
≥98%
Packaging
10mg
Price
$283
Updated
2024/03/01
Cayman Chemical
Product number
22153
Product name
(2'S)-Nicotine-1-oxide
Purity
≥98%
Packaging
25mg
Price
$618
Updated
2024/03/01
TRC
Product number
N428000
Product name
(2''S)-Nicotine1-Oxide
Packaging
50mg
Price
$185
Updated
2021/12/16
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(2'S)-Nicotine 1-Oxide Chemical Properties,Usage,Production

Description

(2''S)-Nicotine-1-oxide is a metabolite of nicotine . It is formed when nicotine is metabolized in the liver by cytochrome P450 (CYP) isoform CYP2A6. (2''S)-Nicotine-1-oxide has been detected in human sperm and semen.

Chemical Properties

Light Yellow Crystals

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 metabolites of nicotine in animals and in man. The metabolism of nicotine i

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 metabolites 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.

Definition

ChEBI: A member of the class of pyridine N-oxides obtained by oxidation of the pyridine nitrogen of (S)-nicotine.

(2'S)-Nicotine 1-Oxide Preparation Products And Raw materials

Raw materials

Preparation Products

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(2'S)-Nicotine 1-Oxide Suppliers

Toronto Research Chemicals
Tel
--
Fax
--
Email
info@trc-canada.com
Country
Canada
ProdList
6038
Advantage
71

2820-55-5, (2'S)-Nicotine 1-OxideRelated Search:


  • 3-[(2S)-1-Methyl-2α-pyrrolidinyl]pyridine 1-oxide
  • 3-(1-methylpyrrolidin-2-yl)-1-oxidanidyl-pyridin-1-ium
  • 3-(1-methylpyrrolidin-2-yl)-1-oxido-pyridin-1-ium
  • 3-(1-methylpyrrolidin-2-yl)-1-oxidopyridin-1-ium
  • (S)-3-(1-Methyl-2-pyrrolidinyl)pyridine 1-Oxide
  • (S)-nicotine 1-N-oxide
  • Pyridine, 3-[(2S)-1-methyl-2-pyrrolidinyl]-, 1-oxide
  • (2'S)-Nicotine 1-Oxide
  • Acrylamide Impurity 17
  • 2820-55-5
  • Nicotine Derivatives
  • Aromatics
  • Chiral Reagents
  • Heterocycles
  • Mutagenesis Research Chemicals
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