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164127

Sigma-Aldrich

2,2′-(4-Methylphenylimino)diethanol

technical grade, 90%

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:
24850052
NACRES:
NA.22

grade

technical grade

Quality Level

100

Assay

90%

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(2,2′-(p-Tolylimino)diethanol) was used to evaluate the antimicrobial activity of root canal sealers against Enterococcus faecalis and Candida albicans by the agar diffusion test.

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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Prasanna Neelakantan et al.
The Journal of clinical pediatric dentistry, 33(2), 117-122 (2008-01-01)
Sealers with prolonged antimicrobial activity are needed by the fact that microorganisms are commonly recovered from teeth with failed endodontic therapy. The aim of this study was to evaluate the duration of antimicrobial activity of ten root canal sealers (Apexit
L Kanerva et al.
Acta dermato-venereologica, 73(2), 126-129 (1993-04-01)
Dental personnel are exposed to many sensitizing compounds at work and often develop multiple delayed allergies. Here we report on a dentist who got sensitized to several products that have not, or only seldom, caused sensitization earlier. These products were:
M Jontell et al.
Journal of dental research, 74(5), 1162-1167 (1995-05-01)
Monomeric resin components from dental composites are toxic to fibroblasts in culture and thus may interfere with the local immune system of the pulp, reducing its effective defense potential, either by cytotoxicity or by a more specific immune mechanism. Therefore
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
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
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