2,6-Di-tert-butylpyridine, 97+%
2,6-Di-tert-butylpyridine, 97+%
2,6-Di-tert-butylpyridine, 97+%
Thermo Scientific Chemicals

2,6-Di-tert-butylpyridine, 97+%

CAS: 585-48-8 | C13H21N | 191.318 g/mol
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Catalog number H55761.03
also known as H55761-03
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Price (USD)
45.65
Special offer
Online exclusive
Ends: 30-Jun-2026
53.20
Save 7.55 (14%)
Each
Chemical Identifiers
CAS585-48-8
IUPAC Name2,6-di-tert-butylpyridine
Molecular FormulaC13H21N
InChI KeyUWKQJZCTQGMHKD-UHFFFAOYSA-N
SMILESCC(C)(C)C1=CC=CC(=N1)C(C)(C)C
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Colorless to light yellow
Assay (HPLC)>97.0%
FormLiquid
2,6-Di-tert-butylpyridine is used in the preparation of 2, 6-di-tert-butylpyridine hydrotriflate. It is used as a proton scavenger to check the progress of the living polymerization of isobutylene. It is associated with cerric ammonium nitrate and used in the alfa-enolation of aldehydes. It is involved in the preparation of vinyl triflate using polymer-bound 2,6-di-tert-butylpyridine.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2,6-Di-tert-butylpyridine is used in the preparation of 2, 6-di-tert-butylpyridine hydrotriflate. It is used as a proton scavenger to check the progress of the living polymerization of isobutylene. It is associated with cerric ammonium nitrate and used in the alfa-enolation of aldehydes. It is involved in the preparation of vinyl triflate using polymer-bound 2,6-di-tert-butylpyridine.

Solubility
Miscible with alcohol, acetone, and hexane. Immiscible with water.

Notes
Store in a cool place. Incompatible with strong acids and strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Laakia, J.; Kauppila, T. J.; Adamov, A.; Sysoev, A. A.; Kotiaho, T. Separation of isomeric amines with ion mobility spectrometry. Talanta. 2015, 132, 889-893.
  2. Chen, J.; Lu, F.; Xu, J. Formation of uniform hollow nanocages with heteroatom-doped MCM-41 structures. RSC Adv. 2015, 5 (7), 5068-5071.