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Key Documents

T58203

Sigma-Aldrich

2,4,6-Tris(dimethylaminomethyl)phenol

95%

Synonym(s):

DMP-30

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About This Item

Linear Formula:
[(CH3)2NCH2]3C6H2OH
CAS Number:
Molecular Weight:
265.39
Beilstein:
795751
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

>1 (vs air)

Quality Level

vapor pressure

<0.01 mmHg ( 21 °C)

Assay

95%

refractive index

n20/D 1.516 (lit.)

bp

130-135 °C/1 mmHg (lit.)

density

0.969 g/mL at 25 °C (lit.)

SMILES string

CN(C)Cc1cc(CN(C)C)c(O)c(CN(C)C)c1

InChI

1S/C15H27N3O/c1-16(2)9-12-7-13(10-17(3)4)15(19)14(8-12)11-18(5)6/h7-8,19H,9-11H2,1-6H3

InChI key

AHDSRXYHVZECER-UHFFFAOYSA-N

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Application

2,4,6-Tris(dimethylaminomethyl)phenol can be used:
  • In the synthesis of water-soluble metal phthalocyanines bearing twelve dimethylamino groups.
  • To prepare phenolate anion-based branched/cross-linked anion exchange membranes (AEMs).
  • As a curing agent in the production of epoxy membranes.

Legal Information

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

300.2 °F - closed cup

Flash Point(C)

149 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Permeability and transport model of epoxy membranes with various surface morphologies.
Luo Y S, et al.
Journal of Applied Polymer Science, 130(4), 2938-2946 (2013)
Phenolate anion-based branched/cross-linked poly (arylene ether sulfone) hydroxide exchange membranes.
Zhou J, et al.
International Journal of Hydrogen Energy, 41(13), 5765-5775 (2016)
Water soluble novel phthalocyanines containing dodeca-amino groups.
Sesalan B S, et al.
Dyes and Pigments, 79(3), 259-264 (2008)
S H Brorson
Micron (Oxford, England : 1993), 29(2-3), 89-95 (1998-07-31)
The purpose of this study was to examine how antigen retrieval affected the yield of immunogold labeling on epoxy sections based on embedding with different amounts of accelerator. The concentration of accelerator DMP-30 (tri(dimethyl amino methyl) phenol) was varied in
A Schaper et al.
FEBS letters, 355(1), 91-95 (1994-11-21)
We present recent advances in DNA specimen preparation technique for scanning force microscopy (SFM) based on spreading on mica in the presence of cationic and non-ionic detergents. Reproducible DNA imaging in air and in n-propanol has been achieved in the

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