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Key Documents

374032

Sigma-Aldrich

4-(Dimethylamino)phenylacetic acid

97%

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About This Item

Linear Formula:
(CH3)2NC6H4CH2CO2H
CAS Number:
Molecular Weight:
179.22
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:

Assay

97%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

105-108 °C (lit.)

application(s)

peptide synthesis

SMILES string

CN(C)c1ccc(CC(O)=O)cc1

InChI

1S/C10H13NO2/c1-11(2)9-5-3-8(4-6-9)7-10(12)13/h3-6H,7H2,1-2H3,(H,12,13)

InChI key

KQGHTOZUPICELS-UHFFFAOYSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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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J H Lee et al.
Journal of biomedical materials research, 40(2), 180-186 (1998-04-29)
Functional group gradients were prepared on low-density polyethylene (PE) sheets. The surface density of grafted functional groups was gradually changed along the sample length by way of corona discharge treatment with gradually increasing power following graft copolymerization of acrylic acid
D Shiino et al.
Journal of biomaterials science. Polymer edition, 7(8), 697-705 (1996-01-01)
A new "intelligent' polymer system was developed utilizing the binding and exchange of phenylboronic acid (PBA) with polyols and/or glucose. In this improved system, an amine component was incorporated into the polymer chain along with PBA, to enhance binding between
4-n,n-dialkylaminophenethanols, -alkanoic acids and esters: new accelerators for dental composites.
G M Brauer et al.
Journal of dental research, 60(7), 1343-1348 (1981-07-01)
M Reyes-Parada et al.
Life sciences, 54(25), 1955-1963 (1994-01-01)
4-Dimethylaminophenethylamine (DMAPEA) was characterized as an MAO substrate. This compound was unaffected by MAO-A, while its oxidation by MAO-B was linear as a function of both time and enzyme concentration, with Km = 5.8 microM and Vmax = 21.2 pmol/min/mg
J H Lee et al.
Biomaterials, 18(4), 351-358 (1997-02-01)
Functional group gradient surfaces where the surface density of grafted functional groups changes gradually along the sample length were prepared on low density polyethylene (PE) sheets by corona discharge treatment with gradually increasing power and graft copalymerization of acrylic acid

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