2-Ethylpyridine

2-Ethylpyridine Basic information
Product Name:2-Ethylpyridine
Synonyms:2-ethvlpvridine;2-ethyl-pyridin;ALPHA-ETHYLPYRIDINE;2-ETHYLPYRIDINE;2-ETHYLPYRIDINE 98+%;2-Ethylpyridine,~99%;Pyridine, 2-ethyl-;2-ETHYL PYRIDINE FEMA NO.--------
CAS:100-71-0
MF:C7H9N
MW:107.15
EINECS:202-881-9
Product Categories:C7 and C8;Heterocyclic Building Blocks;Pyridines
Mol File:100-71-0.mol
2-Ethylpyridine Structure
2-Ethylpyridine Chemical Properties
Melting point -63°C
Boiling point 149 °C (lit.)
density 0.937 g/mL at 25 °C (lit.)
refractive index n20/D 1.496(lit.)
Fp 85 °F
storage temp. Flammables area
solubility 42g/l
pka5.89(at 25℃)
form clear liquid
color Colorless to Almost colorless
Odorat 0.01 % in propylene glycol. green grassy
Odor Typegreen
Water Solubility ca 45 g/L (20 ºC)
BRN 106480
LogP1.690
CAS DataBase Reference100-71-0(CAS DataBase Reference)
NIST Chemistry ReferencePyridine, 2-ethyl-(100-71-0)
EPA Substance Registry System2-Ethylpyridine (100-71-0)
Safety Information
Hazard Codes Xi
Risk Statements 10-36/37/38
Safety Statements 26-36
RIDADR UN 1993 3/PG 3
WGK Germany 3
8
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29333999
MSDS Information
ProviderLanguage
2-Ethylpyridine English
SigmaAldrich English
ACROS English
ALFA English
2-Ethylpyridine Usage And Synthesis
Chemical Propertiesclear colorless to yellowish liquid
Uses2-Ethylpyridine is used to study its effect on the proliferation and survival of human umbilical vein endothelial cells (HUVECs), HMVECs from lung, and NIH 3T3 cells. 2-Ethylpyridine linked with silica is a popular stationary phase for chiral and achiral separations in supercritical fluid chromatography.
Synthesis Reference(s)Tetrahedron Letters, 30, p. 1229, 1989 DOI: 10.1016/S0040-4039(00)72722-5
General Description2-Ethylpyridine, a nitrogen aromatic compound, is grouped under the class of azaarenes. It is generally found as a component of fuels and combustion products.
Purification MethodsPurify it further by conversion to the picrate, recrystallisation of the picrate and regeneration of the free base followed by distillation. [Beilstein 20/6 V 3.]
Sulfasalazine METHYL 2-PYRIDYLACETATE 2,6-Di-tert-butyl-4-methylpyridine DI-2-PYRIDYL KETOXIME DIPHENYL-2-PYRIDYLMETHANE 2,6-Diacetylpyridine Ethyl cellulose Hydroxyethyl Cellulose Hydroxyethyl starch 5-Ethylpyridine,3-ETHYLPYRIDINE,3-ETHYLPYRIDINE 98+% Chromium picolinate Ethyl maltol 2,6-Lutidine 2-Hydroxypyridine 4-ETHYLPYRIDINE,ETHYLPYRIDINE,GAMMA-ETHYLPYRIDINE 2-Pyridylacetonitrile 2-Benzoylpyridine 2-Ethylpyridine

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