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14889

Sigma-Aldrich

2,2′-(4-Methylphenylimino)diethanol

≥97.0% (NT)

Synonym(s):

2,2′-(p-Tolylimino)diethanol, N,N-Bis(2-hydroxyethyl)-p-toluidine, N-(p-Tolyl)diethanolamine

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About This Item

Linear Formula:
CH3C6H4N(CH2CH2OH)2
CAS Number:
3077-12-1
Molecular Weight:
195.26
Beilstein:
2099156
EC Number:
221-359-1
MDL number:
MFCD00020580
UNSPSC Code:
12352100
PubChem Substance ID:
57647227
NACRES:
NA.22

Assay

≥97.0% (NT)

form

solid

bp

338-340 °C (lit.)

mp

49-53 °C (lit.)

functional group

amine
hydroxyl

SMILES string

Cc1ccc(cc1)N(CCO)CCO

InChI

1S/C11H17NO2/c1-10-2-4-11(5-3-10)12(6-8-13)7-9-14/h2-5,13-14H,6-9H2,1H3

InChI key

JUVSRZCUMWZBFK-UHFFFAOYSA-N

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Application

2,2′-(4-Methylphenylimino)diethanol (p-tolyl diethanolamine) was used as an activating amine.

Caution

may discolor to brown on storage

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H317,H318,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5226
BCCM2033
BCCK0630
BCCL1432
BCCK4010

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M P Patel et al.
Biomaterials, 12(7), 649-652 (1991-09-01)
A number of useful room temperature polymerizing resins were formulated, based on poly(ethyl methacrylate) powder and a range of low shrinkage heterocyclic methacrylate monomers. N,N-dimethyl-p-toluidine or p-tolyl diethanolamine were used as activating amines, but the latter material is less active
S Fujisawa et al.
Journal of dental research, 62(7), 803-805 (1983-07-01)
The interaction between phospholipids and stabilizing lysosome agents such as acetylsalicylic acid (ASA), colchicine (CC), prednisolone (PD), etc., was studied using NMR spectroscopy. The peak intensity of protons arising from these compounds was reduced in liposomes containing lecithin and various
Ulrich Salz et al.
The journal of adhesive dentistry, 7(1), 7-17 (2005-05-17)
To investigate the influence of the acid-base reaction between acidic monomers and amines on the polymerization behavior of self-etching, self-curing adhesives, determine the effect of the application mode on the shear bond strength and morphology, and elucidate the adhesion performance
H H Xu et al.
Journal of biomedical materials research, 52(4), 812-818 (2000-10-18)
The strength and toughness of dental core buildup composites in large stress-bearing restorations need to be improved to reduce the incidence of fracture due to stresses from chewing and clenching. The aims of the present study were to develop novel
K Ikemura et al.
Dental materials journal, 15(2), 132-143 (1996-12-01)
To develop a self-etching primer for ground dentin, 4-acryloxyethyltrimellitic acid (4-AET) was newly synthesized, and the effect of concentrations varying from 0 (control) to 56.5 wt% 4-AET in the water/ HEMA primer on bonding to the dentin was investigated. Bond
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