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3,5-Lutidine

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3,5-Lutidine Basic information

Product Name:
3,5-Lutidine
Synonyms:
  • pyridine,3,5-dimethyl-
  • Lutidine,98%
  • 3 5-LUTIDINE STANDARD FOR GC
  • 3,5-LUTIDINE, 98+%
  • 3,5-DIMETHYLPYRIDINE 98+%
  • 3,5-Dimetylpyridine
  • 3,5-Lutidine,99%
  • 3,5-dimethyl-pyridin
CAS:
591-22-0
MF:
C7H9N
MW:
107.15
EINECS:
209-708-6
Product Categories:
  • Biochemistry
  • Reagents for Oligosaccharide Synthesis
  • Pyridines derivates
  • Heterocyclic Compounds
  • K00001
Mol File:
591-22-0.mol
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3,5-Lutidine Chemical Properties

Melting point:
-9 °C (lit.)
Boiling point:
169-170 °C (lit.)
Density 
0.939 g/mL at 25 °C (lit.)
vapor pressure 
1.5 mm Hg ( 20 °C)
refractive index 
n20/D 1.504(lit.)
Flash point:
128 °F
storage temp. 
2-8°C
pka
6.15(at 25℃)
form 
Liquid
color 
Clear yellow
Water Solubility 
33 g/L (20 ºC)
Sensitive 
Hygroscopic
BRN 
105682
InChIKey
HWWYDZCSSYKIAD-UHFFFAOYSA-N
LogP
1.780
CAS DataBase Reference
591-22-0(CAS DataBase Reference)
NIST Chemistry Reference
Pyridine, 3,5-dimethyl-(591-22-0)
EPA Substance Registry System
3,5-Dimethylpyridine (591-22-0)
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Safety Information

Hazard Codes 
Xn,F,Xi,T
Risk Statements 
10-20/21/22-36/37/38-41-34-23/25-21
Safety Statements 
16-26-36-36/37-45-36/37/39
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
8
Hazard Note 
Irritant/Flammable
TSCA 
Yes
HazardClass 
3
PackingGroup 
III
HS Code 
29333999

MSDS

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3,5-Lutidine Usage And Synthesis

Chemical Properties

CLEAR YELLOW LIQUID

Uses

3,5-Lutidine is a reactant used in the synthesis of phthalazine and pyrazine compounds, as well as other pharmaceuticals.

Synthesis Reference(s)

Synthesis, p. 573, 1994 DOI: 10.1055/s-1994-25526

Flammability and Explosibility

Flammable

Purification Methods

Dry 3,5-lutidine with sodium and fractionally distil it through a Todd column (p 11) packed with glass helices. Dissolve (100mL) in dilute HCl (1:4) and steam distil this until 1L of distillate is collected. Excess conc NaOH is added to the residue which is again steam distilled. The base is extracted from the distillate, using diethyl ether. The extract is dried over K2CO3, and distilled. It is then fractionally crystallised by partial freezing. The hydrochloride has m 229o(sublimes at 190-231o), and the picrate has m 242-243o(dec, from H2O), 249-250o(dec, from AcOH). [Beilstein 20 II 161, 20 III/IV 2788, 20/6 V 60.]

3,5-Lutidine Preparation Products And Raw materials

Preparation Products

3,5-Lutidine Supplier

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