M8765
Myosmine
≥98%
Synonym(s):
3-(1-Pyrrolin-2-yl)pyridine
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About This Item
Empirical Formula (Hill Notation):
C9H10N2
CAS Number:
Molecular Weight:
146.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥98%
Form:
solid
InChI
1S/C9H10N2/c1-3-8(7-10-5-1)9-4-2-6-11-9/h1,3,5,7H,2,4,6H2
SMILES string
C1CN=C(C1)c2cccnc2
InChI key
DPNGWXJMIILTBS-UHFFFAOYSA-N
assay
≥98%
form
solid
storage temp.
2-8°C
Quality Level
Gene Information
rat ... Chrna4(25590)
Application
Myosmine can be used as a reactant in thesynthesis of nicotinoid derivatives through N-nitrosation.
Tobacco alkaloid
Reactant for:
Nitrosation reactions
Peroxidation reaction with hydrogen peroxide
Reactant for:
Nitrosation reactions
Peroxidation reaction with hydrogen peroxide
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
涉药品监管产品
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Sarah Vogt et al.
Toxicology, 222(1-2), 71-79 (2006-03-01)
The incidence of esophageal adenocarcinoma is rapidly rising in Western populations. Gastroesophageal reflux disease (GERD) is thought to be one of the most important risk factors. However, the mechanisms by which GERD enhances tumor formation at the gastroesophageal junction are
Zhao-Xiang Zhang et al.
Analytical and bioanalytical chemistry, 390(6), 1645-1652 (2008-01-30)
A novel on-column sequential preconcentration method based on the combination of field-amplified sample injection induced by acetonitrile and pseudo isotachophoresis (ITP)-acid stacking is developed for simply but efficiently concentrating alkaloid cations in a high-salt sample matrix in capillary electrophoresis. Acetonitrile
Wei Li et al.
Scientific reports, 7(1), 12126-12126 (2017-09-25)
Leaf senescence in plants is a coordinated process that involves remobilization of nutrients from senescing leaves to sink tissues. The molecular events associated with nutrient remobilization are however not well understood. In this study the tobacco system with a source-sink
Stefan Tyroller et al.
Journal of agricultural and food chemistry, 50(17), 4909-4915 (2002-08-09)
Myosmine has been regarded as a specific tobacco alkaloid until investigations pointed out that nuts and nut products constitute a significant source of myosmine. In the present study it is shown that the occurrence of myosmine is widespread throughout a
J Wilp et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 40(8), 1223-1228 (2002-06-18)
The tobacco alkaloid myosmine was detected in nut and nut products [J. Agric. Food Chem. 46 (1998) 2703]. Upon nitrosation, myosmine yields 4-hydroxy-1-(3-pyridyl)-1-butanone (HPB) and N-nitrosonornicotine (NNN) [J. Agric. Food Chem. 48 (2001) 392]. NNN is a strong oesophageal carcinogen
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