NICOTINE DITARTRATE DIHYDRATE

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Names

[ CAS No. ]:
6019-06-3

[ Name ]:
NICOTINE DITARTRATE DIHYDRATE

[Synonym ]:
nicotine ditartrate dihydrate

Chemical & Physical Properties

[ Density]:
1.38g/cm3

[ Boiling Point ]:
469.8ºC at 760 mmHg

[ Melting Point ]:
97-100ºC

[ Molecular Formula ]:
C18H30N2O14

[ Molecular Weight ]:
498.43600

[ Flash Point ]:
238ºC

[ Exact Mass ]:
498.17000

[ PSA ]:
264.71000

[ Index of Refraction ]:
1.646

MSDS

Safety Information

[ Hazard Codes ]:
T+:Very toxic; N:Dangerous for the environment;

[ Risk Phrases ]:
R26/27/28;R51/53

[ Safety Phrases ]:
S13-S28-S45-S61

[ RIDADR ]:
UN 1659 6.1 / PGII

Articles

The effect of varenicline on the development and expression of nicotine-induced behavioral sensitization and cross-sensitization in rats.

Addict. Biol. 20(2) , 248-58, (2015)

The present study focused on the evaluation of behavioral sensitization and cross-sensitization induced by nicotine and varenicline in rats. Furthermore, it examined the influence of varenicline, a pa...

Nicotinic receptor subtype-selective circuit patterns in the subthalamic nucleus.

J. Neurosci. 35(9) , 3734-46, (2015)

The glutamatergic subthalamic nucleus (STN) exerts control over motor output through nuclei of the basal ganglia. High-frequency electrical stimuli in the STN effectively alleviate motor symptoms in m...

Nicotine exploits a COPI-mediated process for chaperone-mediated up-regulation of its receptors.

J. Gen. Physiol. 143(1) , 51-66, (2014)

Chronic exposure to nicotine up-regulates high sensitivity nicotinic acetylcholine receptors (nAChRs) in the brain. This up-regulation partially underlies addiction and may also contribute to protecti...


More Articles


Related Compounds

  • Nicotine ditartrate
  • (2S,3S)-2,3-dihydroxybutanedioic acid,[2,5-dimethyl-1-(3-morpholin-4-ylpropyl)-4-phenylpiperidin-4-yl] propanoate
  • (-)-NICOTINE MONO TARTRATE
  • nicotine bi-l-(+)-tartrate
  • nicotine sulphate
  • Nicotine N-D-Glucoside
  • (2-methylimidazo[1,2-a]pyridin-3-yl)(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)methanone
  • benzo[d]thiazol-2-yl(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)methanone
  • methyl 4-(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidine-1-carbonyl)benzoate
  • benzo[c][1,2,5]thiadiazol-5-yl(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)methanone
  • 2-(4-chlorophenoxy)-1-(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)ethanone
  • (5-chloro-2-methoxyphenyl)(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)methanone
  • (3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)(3-(trifluoromethyl)phenyl)methanone
  • (7-methoxybenzofuran-2-yl)(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)methanone
  • (1-(methylsulfonyl)piperidin-4-yl)(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)methanone
  • 2-((2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)oxy)-1-(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)ethanone
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