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115754

Sigma-Aldrich

2,2,6,6-Tetramethylpiperidine

≥99%

Synonym(s):

2,2,6,6-tetramethylpiperidide, 2,2,6,6-tetramethylpiperidine, Norpempidine, TEMP, TMPH

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About This Item

Empirical Formula (Hill Notation):
C9H19N
CAS Number:
Molecular Weight:
141.25
Beilstein:
103296
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Assay

≥99%

refractive index

n20/D 1.445 (lit.)

bp

152 °C (lit.)

density

0.837 g/mL at 25 °C (lit.)

SMILES string

CC1(C)CCCC(C)(C)N1

InChI

1S/C9H19N/c1-8(2)6-5-7-9(3,4)10-8/h10H,5-7H2,1-4H3

InChI key

RKMGAJGJIURJSJ-UHFFFAOYSA-N

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General description

2,2,6,6-Tetramethylpiperidineis a hindered secondary amine that is used to prepare metallo-amide bases and selective generation of silylketene acetals.

Application

2,2,6,6-Tetramethylpiperidine can be used as a reactant to synthesize:
  • Allylated tertiary amines via allylic amination of allylic chlorides.
  • Hydroxylamines via oxidation in the presence of oxone as an oxidant.
  • Sulfenamide compounds by reacting with heterocyclic thiols in the presence of iodine as an oxidant.
  • N-methylated amines via N-methylation by reacting with CO2 and phenylsilane.
  • Propargylamines via three-component Mannich coupling reaction with aldehydes and alkynes.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1A - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

98.6 °F - closed cup

Flash Point(C)

37 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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S Doruk Cezan et al.
Nature communications, 10(1), 276-276 (2019-01-19)
Triboelectric charging of insulators, also known as contact charging in which electrical charges develop on surfaces upon contact, is a significant problem that is especially critical for various industries such as polymers, pharmaceuticals, electronics, and space. Several methods of tribocharge
Kasper Wigh Lipsø et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 274, 65-72 (2016-11-28)
We demonstrate a method for the preparation of hyperpolarized water by dissolution Dynamic Nuclear Polarization at high magnetic field. Protons were polarized at 6.7T and 1.1K to >70% with frequency modulated microwave irradiation at 188GHz. 97.2±0.7% of the radical was
Gaku Akimoto et al.
The Journal of organic chemistry, 83(21), 13498-13506 (2018-10-23)
The reaction pathways of lithium 2,2,6,6-tetramethylpiperidide (LiTMP)-mediated deprotonative metalation of methoxy-substituted arenes were investigated. Importantly, it was experimentally observed that, whereas TMEDA has no effect on the course of the reactions, the presence of more than the stoichiometric amount of
Alex Basu et al.
Nanomaterials (Basel, Switzerland), 8(7) (2018-07-25)
A Ca2+-crosslinked wood-based nanofibrillated cellulose (NFC) hydrogel was investigated to build knowledge toward the use of nanocellulose for topical drug delivery applications in a chronic wound healing context. Proteins of varying size and isoelectric point were loaded into the hydrogel
Karima Ben Hamou et al.
Carbohydrate polymers, 181, 1061-1070 (2017-12-20)
Nanocomposites of polyvinyl acetate (PVAc) reinforced with two different TEMPO-oxidized cellulose nanofibrils (CNF) were prepared by casting/evaporation method. These two sets of CNF, designed as CNF-O-5min (5min of oxidation) and CNF-O-120min (120min of oxidation), are different by their surface charge

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