Skip to Content
Merck
All Photos(3)

Documents

301248

Sigma-Aldrich

Tris[2-(2-methoxyethoxy)ethyl]amine

95%

Synonym(s):

TDA-1, Tris(3,6-dioxaheptyl)amine

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
(CH3OCH2CH2OCH2CH2)3N
CAS Number:
70384-51-9
Molecular Weight:
323.43
Beilstein:
2369296
EC Number:
274-590-5
MDL number:
MFCD00010748
UNSPSC Code:
12352100
PubChem Substance ID:
24858174
NACRES:
NA.22

Assay

95%

form

liquid

refractive index

n20/D 1.4486 (lit.)

density

1.011 g/mL at 25 °C (lit.)

SMILES string

COCCOCCN(CCOCCOC)CCOCCOC

InChI

1S/C15H33NO6/c1-17-10-13-20-7-4-16(5-8-21-14-11-18-2)6-9-22-15-12-19-3/h4-15H2,1-3H3

InChI key

XGLVDUUYFKXKPL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Tris[2-(2-methoxyethoxy)ethyl]amine was used:
  • in oxidation of arylmethanols under phase-transfer conditions
  • as cryptand during phase-transfer glycosylation of 2-amino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine
  • as phase-transfer catalyst in synthesis of 1,3-dideaza-2′-deoxyadenosine and related benzimidazole 2′-deoxyribonucleosides

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

323.6 °F - closed cup

Flash Point(C)

162 °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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Liquid-liquid and solid-liquid phase-transfer glycosylation of pyrrolo [2, 3-d] pyrimidines: stereospecific synthesis of 2-deoxy-?-D-ribofuranosides related to 2'-deoxy-7-carbaguanosine.
Seela F, et al.
Journal of the Chemical Society. Perkin Transactions 1, 3, 697-702 (1998)
Stereoselective glycosylation of nitrobenzimidazole anions: synthesis of 1, 3-dideaza-2'-deoxyadenosine and related 2'-deoxyribofuranosides.
Seela F and Bourgeois W.
Synthesis, 12, 912-918 (1989)
Phase-Transfer Catalysed Permanganate Oxidations Using Tris [2-(2-Methoxyethoxy) Ethyl] Amine (Tda-1).
Mckillop A and Mills LS.
Synthetic Communications, 17(6), 647-655 (1987)
Falk Kunkel et al.
Molecules (Basel, Switzerland), 20(11), 20805-20822 (2015-11-28)
DNA methyltransferases (MTases) catalyze the transfer of the activated methyl group of the cofactor S-adenosyl-l-methionine (AdoMet or SAM) to the exocyclic amino groups of adenine or cytosine or the C5 ring atom of cytosine within specific DNA sequences. The DNA

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service