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115754 Aldrich

2,2,6,6-Tetramethylpiperidine

≥99%

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Properties

Related Categories Acids & Bases, Bases, Building Blocks, C9, Chemical Synthesis,
assay   ≥99%
refractive index   n20/D 1.445(lit.)
bp   152 °C(lit.)
density   0.837 g/mL at 25 °C(lit.)

Description

Application

The lithium amide has been used to efficiently ortho deprotonate pyridine-3-carboxamides.1

Packaging

5, 10, 25 g in glass bottle

Price and Availability

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Precautionary statements 
Hazard Codes (Europe) 
Xn
Risk Statements (Europe) 
Safety Statements (Europe) 
26
RIDADR 
UN 1992 6.1(3) / PGIII
WGK Germany 
2
RTECS 
TN4220000
Flash Point(F) 
75.2 °F
Flash Point(C) 
24 °C

Protocols & Articles

Articles

COMU—Safer and More Efficient Peptide Coupling Reagent

Proteins and peptides are ubiquitous in all living systems. The chemical synthesis of peptidic structures for scientific research or drug discovery relies heavily on efficient coupling reagents. This...
Dr. Matthias Junkers
Aldrich Chemfiles, 2010 Volume 10 Article 1
Keywords: Calorimetry, Coupling reactions, Drug discovery, Epimerizations, Methods, Microwave synthesis, Peptide synthesis, Protocols, Racemizations, Reductions, Search, Sequences, Solid phase peptide synthesis, Solvents

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The molarity calculator tool provides lab-ready directions describing how to prepare an acid or base solution of specified Molarity (M) or Normality (N) from a concentrated acid or base solution.  To...

Peer-Reviewed Papers

References

Set your institution to view full text papers.

1. One-pot synthesis of 2,3-dihydro-pyrrolopyridinones using in situ generated formimines. Org. Lett. 8, 5889, (2006)

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Beil. 20,V,4,237

Aldrich MSDS 1, 1684:C / Corp MSDS 1 (2), 3299:D / FT-IR 2 (1), 564:D / FT-IR 1 (1), 361:A / FT-NMR 1 (1), 569:A / IR-Spectra (2), 191:B / IR-Spectra (3), 212:E / NMR-Reference 2 (1), 316:D / RegBook 1 (1), 383:M / Sax 6, 2547 / Sigma FT-IR 1 (1), 750:B / Structure Index 1, 54:B:9 / Vapor Phase 3, 452:C

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