Advanced Search



2,2,6,6-Tetramethylpiperidine

ALDRICH/115754 - ≥99%

Synonym: 2,2,6,6-tetramethylpiperidide; 2,2,6,6-tetramethylpiperidine; Norpempidine; TEMP; TMPH

CAS Number: 768-66-1
Empirical Formula (Hill Notation): C9H19N
Molecular Weight: 141.25
EC Number: 212-199-3
MDL Number: MFCD00005985
Linear Formula: C9H19N
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-115754-5G 5 g
 $46.10
1/EA		 Add To Favorites
45-115754-10G 10 g
 $86.60
1/EA		 Add To Favorites
45-115754-25G 25 g
 $151.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 115754-5G.
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 115754-10G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 115754-25G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 115754-5G

 

assay ≥99%
bp 152 °C (lit.)
density 0.837 g/mL at 25 °C (lit.)
InChI 1S/C9H19N/c1-8(2)6-5-7-9(3,4)10-8/h10H,5-7H2,1-4H3
InChI key RKMGAJGJIURJSJ-UHFFFAOYSA-N
Quality Level 200 
refractive index n20/D 1.445 (lit.)
SMILES string CC1(C)CCCC(C)(C)N1
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.
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.
Packaging: 5, 10, 25 g in glass bottle
Purity ≥99%
bp 152 °C (lit.)
Density 0.837 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.445 (lit.)
UNSPSC 12352005

The following items have been added to your cart:

Choose a favorite list for this item:
Catalog Number Description Price
$

Returns/Order support

Please fill out the form below if you want to request order support from Krackeler Scientific.


Quick Order

* Required


New Tariffs & Effects on Pricing

Tariff note: As we navigate the current environment of tariff surcharges and mid-year manufacturer price increases, we want to keep you informed. While we have avoided making specific decisions thus far, we anticipate that we will be forced to implement a cost adjustment policy to offset the fees we have already been absorbing. We are committed to transparency and moderation in this process.

800-334-7725
office@krackeler.com


Play Video

To Request a Quote

  1. Search or Browse for items and add to them to your Shopping Cart.
  2. Click the "Request Quote" button at the bottom of the Shopping Cart page.
  3. Fill out required fields.
  4. Optionally you can convert to standard checkout mode by choosing a payment type.
  5. Click "Request Quote" at the bottom of the page.

You will be contacted with a quote.

To Order From a Quote

  1. Register and login to the website.
  2. Receive a quote from your sales representative or customer service.
  3. Have your copy of the quote in hand.
  4. Visit our quote module to search for your quote.
Back to Top