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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

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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)
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)
Water soluble novel phthalocyanines containing dodeca-amino groups.
Sesalan B S, et al.
Dyes and Pigments, 79(3), 259-264 (2008)
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
L Kanerva et al.
International journal of dermatology, 35(12), 852-856 (1996-12-01)
Epoxy resin compounds (ERC) include a large number of sensitizing chemicals such as epoxy resins (ER), hardeners (curing agents), and reactive diluents. Allergic contact dermatitis (ACD) caused by ERCS is often occupational. We report a patient, sensitized to a hardener

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