Nornicotine
Names
IUPAC name
3-[(2S )-2-Pyrrolidinyl]pyridine
Other names
Demethylnicotine
Identifiers
ChemSpider
ECHA InfoCard
100.165.066
UNII
InChI=1S/C9H12N2/c1-3-8(7-10-5-1)9-4-2-6-11-9/h1,3,5,7,9,11H,2,4,6H2/t9-/m0/s1
Key: MYKUKUCHPMASKF-VIFPVBQESA-N
InChI=1/C9H12N2/c1-3-8(7-10-5-1)9-4-2-6-11-9/h1,3,5,7,9,11H,2,4,6H2/t9-/m0/s1
Key: MYKUKUCHPMASKF-VIFPVBQEBM
Properties
C 9 H 12 N 2
Molar mass
148.209 g·mol−1
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Nornicotine is an alkaloid found in various plants including Nicotiana , the tobacco plant.[ 1] It is chemically similar to nicotine , but does not contain a methyl group .
It is a precursor to the carcinogen N -nitrosonornicotine that is produced during the curing and processing of tobacco.[ 2] Nornicotine can react in human saliva to form N-nitrosonornicotine ,[ 3] a known type 1 carcinogen.[ 4]
^ Laszlo C, Kaminski K, Guan H, Fatarova M, Wei J, Bergounioux A, Schlage WK, Schorderet-Weber S, Guy PA, Ivanov NV, Lamottke K, Hoeng J (November 2022). "Fractionation and Extraction Optimization of Potentially Valuable Compounds and Their Profiling in Six Varieties of Two Nicotiana Species" . Molecules . 27 (22): 8105. doi :10.3390/molecules27228105 . PMC 9694777 . PMID 36432206 .
^ Siminszky, B. (2005). "Conversion of nicotine to nornicotine in Nicotiana tabacum is mediated by CYP82E4, a cytochrome P450 monooxygenase" . Proceedings of the National Academy of Sciences . 102 (41): 14919–24. doi :10.1073/pnas.0506581102 . PMC 1253577 . PMID 16192354 .
^ Knezevich A, Muzic J, Hatsukami DK, Hecht SS, Stepanov I (February 2013). "Nornicotine nitrosation in saliva and its relation to endogenous synthesis of N'-nitrosonornicotine in humans" . Nicotine & Tobacco Research . 15 (2): 591–5. doi :10.1093/ntr/nts172 . PMC 3611998 . PMID 22923602 .
^ "List of Classifications – IARC Monographs on the Identification of Carcinogenic Hazards to Humans" . monographs.iarc.fr . Retrieved 2020-07-22 .