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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:
Recommended Products
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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)
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
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