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About This Item
Linear Formula:
(CH2CH2)x[CH2CH(CO2H)]y
CAS Number:
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
InChI
1S/C3H4O2.C2H4/c1-2-3(4)5;1-2/h2H,1H2,(H,4,5);1-2H2
SMILES string
C=C.OC(=O)C=C
InChI key
QHZOMAXECYYXGP-UHFFFAOYSA-N
form
beads
composition
acrylic acid, 20 wt. %
density
0.96 g/mL at 25 °C
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Application
Processing and performance additive. Promotes crystallization of PET. Assists dispersion of additives in plastics.
Features and Benefits
Forms reversible ionic clusters (crosslinks). Promotes adhesion to various substrates, tougher, more chemically resistant and more transparent than parent acid copolymer.
signalword
Warning
hcodes
Hazard Classifications
Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>527.0 °F
flash_point_c
> 275 °C
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Catherine A Rimmer et al.
Analytical and bioanalytical chemistry, 382(3), 698-707 (2004-12-04)
A series of commercial monomeric and polymeric C(18), C(27), and C(30) stationary phases were compared with immobilized poly(ethylene-co-acrylic acid) stationary phases synthesized in-house. The columns were characterized on the basis of methylene selectivity, silanol activity, metal activity, pore size, shape
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The obtaining of chitosan extruded films was possible by using low density polyethylene (LDPE) as a matrix polymer and ethylene-acrylic acid copolymer as an adhesive, in order to ensure adhesion in the interphase of the immiscible polymers. The obtained blend
Optician's occupational allergic contact dermatitis, paresthesia and paronychia caused by anaerobic acrylic sealants.
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Journal of chromatography. A, 1156(1-2), 80-86 (2006-12-01)
The increased demand for chromatographic materials that are able to achieve a fast separation of large quantities of structure analogues is a great challenge. It is known that polymer based chromatographic materials have a higher loadability, compared to silica based
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