2,6-Lutidine

2,6-Lutidine

CAS Number108-48-5
Molecular FormulaC7H9N
Molecular Weight107.156
InChI KeyOISVCGZHLKNMSJ-UHFFFAOYSA-N
LogP1.7
Synonyms
  • 2,6-Dimethylpyridine
  • 2,6-LUTIDINE
  • 108-48-5
  • Lutidine
  • Pyridine, 2,6-dimethyl-
  • 2,6-Dimethypyridine
  • alpha,alpha'-Lutidine
  • alpha,alpha'-Dimethylpyridine
  • 2,6-dimethyl-pyridine
  • HSDB 79
  • NSC 2155
  • UNII-15FQ5D0T3P
  • 2,6-Lutidene
  • FEMA No. 3540
  • 2, 6- Lutidine
  • .alpha.,.alpha.'-Dimethylpyridine
  • EINECS 203-587-3
  • .alpha.,.alpha.'-Lutidine
  • AI3-24282
  • CHEBI:32548
  • OISVCGZHLKNMSJ-UHFFFAOYSA-N
  • MFCD00006345
  • 2,6-Lutidine-(dimethyl-d6)
  • LUT
  • alpha,alpha'-Lutidin
  • lutidin
  • 2,6Lutidine
  • 2,6 lutidine
  • 2-6-lutidine
  • 2.6-lutidine
  • 2,6-Lutdcine
  • 2,6 -lutidine
  • 2,6- lutidine
  • 2,6-dimethylpiridine
  • 2.6-dimethylpyridine
  • 2,6-dimethyl pyridin
  • 2,6-dimethyl pyridine
  • PubChem15897
  • ACMC-1BTAI
  • 2,6-Lutidine, 8CI

Applications:

Generic Screening Method for Complex Mixtures on Primesep 200

October 15, 2015

Condition

Column Primesep 200, 4.6*150 mm 5 µm, 100A
Mobile Phase MeCN/H2O
Buffer H2SO4
Flow Rate 1.0 ml/min
Detection UV, 215 nm

 

Description

Class of Compounds
Drug, Acid, Hydrophilic, Ionizable, Hormone
Analyzing Compounds Uracil, Epinephrine, DOPA, 2,6-Lutidine, Benzylamine, Hydroxytrypthophan, Homovanillic acid, Phenol, Tryptophan , 2,3-DHBA, Benzoic acid, Methylparaben, Ethylparaben, Toluene, Amitriptyline

 

Application Column

Primesep 200

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
2,3-Dihydroxybenzoic Acid
2,6-Lutidine
Amitriptyline
Benzoic Acid
Benzylamine
DOPA (3,4-dihydroxy-L-phenylalanine)
Epinephrine
Ethylparaben
Homovanillic Acid
Hydroxytryptophan
Methylparaben
Phenol
Toluene
Tryptophan
Uracil

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of Amino Acids, Bases, Acids, and Neutrals on Obelisc R

March 3, 2007


Separating basic, acidic and zwitterionic compounds in one run in reverse-phase HPLC can be very challenging. The methods might require the use of ion-pairing reagents and complex gradients that can make MS-compatibility difficult. Obelisc R column which has both positive and negative ion-pairs embedded in the stationary phase allows for fine tuning and separation of a wide range of compounds with different ionic properties. Acids, bases, amino acids and neutral compounds were separated isocratically in one run using a simple MS-compatible mobile phase of acetonitrile (ACN) and water with Ammonium Acetate (AmAc) buffer. Can also be UV detected at 250nm.

Condition

Column Obelisc R, 4.6×250 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 35/65%
Buffer AmAc 10 mM pH 4.0
Flow Rate 1.0 ml/min
Detection UV, 250 nm

 

Description

Class of Compounds
Drug, Acid, Bases, Neutral, Hydrophilic, Ionizable, Vitamin, Supplements, Amino acid
Analyzing Compounds Amino acids

 

Application Column

Obelisc R

SIELC has developed the Obelisc™ columns, which are mixed-mode and utilize Liquid Separation Cell technology (LiSC™). These cost-effective columns are the first of their kind to be commercially available and can replace multiple HPLC columns, including reversed-phase (RP), AQ-type reversed-phase, polar-embedded group RP columns, normal-phase, cation-exchange, anion-exchange, ion-exclusion, and HILIC (Hydrophilic Interaction Liquid Chromatography) columns. By controlling just three orthogonal method parameters - buffer concentration, buffer pH, and organic modifier concentration - users can adjust the column properties with pinpoint precision to separate complex mixtures.

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Application Analytes:
2,6-Lutidine
Benzoic Acid
Benzonitrile
Benzylamine
Phenol
Phenylalanine
Pyridine
Toluene
Tryptophan

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.