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2,5-Dimethylpyridine

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2,5-Dimethylpyridine Basic information

Product Name:
2,5-Dimethylpyridine
Synonyms:
  • 2,5-two Methyl pyridine
  • 2,5-Lutidine 95%
  • 2,5-dimethyl-pyridin
  • 5-methyl-2-methylpyridine
  • pyridine,2,5-dimethyl-
  • 25L
  • 2,5-LUTIDINE
  • 2,5-DIMETHYLPYRIDINE
CAS:
589-93-5
MF:
C7H9N
MW:
107.15
EINECS:
209-666-9
Product Categories:
  • Biochemistry
  • Reagents for Oligosaccharide Synthesis
Mol File:
589-93-5.mol
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2,5-Dimethylpyridine Chemical Properties

Melting point:
−15 °C(lit.)
Boiling point:
157 °C(lit.)
Density 
0.926 g/mL at 25 °C(lit.)
vapor pressure 
2.4 mm Hg ( 20 °C)
refractive index 
n20/D 1.499(lit.)
Flash point:
118 °F
pka
6.4(at 25℃)
form 
clear liquid
color 
Colorless to Light orange to Yellow
Water Solubility 
77g/L(23 ºC)
Sensitive 
Hygroscopic
LogP
1.708 (est)
CAS DataBase Reference
589-93-5(CAS DataBase Reference)
NIST Chemistry Reference
Pyridine, 2,5-dimethyl-(589-93-5)
EPA Substance Registry System
2,5-Dimethylpyridine (589-93-5)
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Safety Information

Hazard Codes 
Xn,F,Xi
Risk Statements 
10-20/21/22-36/37/38
Safety Statements 
16-26-36/37/39-45
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
RTECS 
OK9625000
HazardClass 
3.2
PackingGroup 
III
HS Code 
2933399990

MSDS

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2,5-Dimethylpyridine Usage And Synthesis

Uses

2,5-Lutidine was used to displace CO from the haem iron.

Synthesis Reference(s)

Tetrahedron Letters, 17, p. 383, 1976 DOI: 10.1016/S0040-4039(00)93738-9

General Description

The FT-IR and FT-Raman spectra of 2,5-lutidine was studied.

Purification Methods

Steam distil the lutidine from a solution containing 1-2 equivalents of 20% H2SO4 until about 10% of the base has been carried over with the non-basic impurities, then the acidic solution is made alkaline, and the base is separated, dried with NaOH and fractionally distilled twice. Dry the distillate with Na and fractionally distil it through a Todd column (p 11) packed with glass helices. The hydrochloride has m 219o(dec), and the picrate has m 170.5o (from EtOH or H2O). [Beilstein 20 H 244, 20 II 160, 20 III/IV 2774, 20/6 V 27.]

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