3,5-Lutidine

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
3,5-Lutidine Structure
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.)
Fp 128 °F
storage temp. 2-8°C
solubility Sol
pka6.15(at 25℃)
form Liquid
color Clear yellow
Water Solubility 33 g/L (20 ºC)
Sensitive Hygroscopic
BRN 105682
InChIKeyHWWYDZCSSYKIAD-UHFFFAOYSA-N
LogP1.780
CAS DataBase Reference591-22-0(CAS DataBase Reference)
NIST Chemistry ReferencePyridine, 3,5-dimethyl-(591-22-0)
EPA Substance Registry System3,5-Dimethylpyridine (591-22-0)
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 Information
ProviderLanguage
3,5-Dimethylpyridine English
SigmaAldrich English
ACROS English
ALFA English
3,5-Lutidine Usage And Synthesis
Chemical PropertiesCLEAR YELLOW LIQUID
Uses3,5-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 ExplosibilityFlammable
Purification MethodsDry 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.]
2-HYDROXY-4,5,6-TRIMETHYLNICOTINONITRILE 2-MERCAPTO-4,5,6-TRIMETHYLNICOTINONITRILE 3,5-DIETHYL-2-N-PROPYLPYRIDINE 2-Chloro-3-cyanopyridine N,N-Dimethylformamide 2-CHLORO-3,5-BIS(TRIFLUOROMETHYL)PYRIDINE Poly(dimethylsiloxane) Dimethylpyridine, 2,4-: (2,4-Lutidine),2,4-DIMETHYLPYRIDINE(2,4-LUTIDINE),2,4-LUTIDINE 98+% DIMETHYL 4-(4-METHOXYPHENYL)-2,6-DIMETHYLPYRIDINE-3,5-DICARBOXYLATE 3,5-Lutidine 3-Aminopyridine 2,6-Lutidine 3,5-PYRIDINEDICARBOXYLIC ACID Dimethyl sulfoxide ETHYL 5-CYANO-6-(METHYLSULFANYL)-2-PHENYLNICOTINATE 2,3-LUTIDINE/2,3-DIMETHYL PYRIDINE,2,3-LUTIDINE,2,3-DIMETHYLPYRIDINE(2,3-LUTIDINE),2,3-LUTIDINE 98+%,2,3-Lutidine,99% PYRIDINITRIL 3,4-LUTIDINE 3,4-DIMETHYLPYRIDINE,3,4-Lutidine98%,3,4-LUTIDINE 98%

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