The molecular weight of this product is not determined. However, historical data suggests that is it to be around 2 kDa.
426717
Poly(ethylene-co-acrylic acid)
acrylic acid 5 wt. %, beads
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250 G
CHF 61.20
About This Item
Linear Formula:
(CH2CH2)x[CH2CH(CO2H)]y
CAS Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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description
drop point 105 °C Mettler
Quality Level
form
beads
composition
acrylic acid, 5 wt. %
hardness
≤2.5 dmm (ASTM D 5, 25 °C)
viscosity
575 cP(145 °C, Brookfield)(lit.)
acid number
37‑44 mg KOH/g
transition temp
Tm 99-101 °C
density
0.93 g/mL at 25 °C
SMILES string
C=C.OC(=O)C=C
InChI
1S/C3H4O2.C2H4/c1-2-3(4)5;1-2/h2H,1H2,(H,4,5);1-2H2
InChI key
QHZOMAXECYYXGP-UHFFFAOYSA-N
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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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Ning Luo et al.
Colloids and surfaces. B, Biointerfaces, 50(2), 89-96 (2006-06-06)
Poly(ethylene-co-acrylic acid) (EAA) films were reacted with glycine, 12-aminododecanoic acid, aspartic acid, 5-aminoisophthalic acid, ethanolamine, diethylamine, dimethylamine, N-isopropylamine, and dimethylaminoethyleneamine to prepare EAA films with negatively charged, non-charged, hydrophilic, and hydrophobic functionalities. Attenuated total reflectance Fourier transform infrared spectroscopy, differential
Newton C Fawcett et al.
Langmuir : the ACS journal of surfaces and colloids, 20(16), 6651-6657 (2004-07-28)
Yoshimoto et al. [Anal. Chem. 2002, 74, 4306-4309] reported that a quartz crystal microbalance or QCM changed its response to sucrose solutions according to its angle of immersion. The effect was tentatively attributed to gravity-caused stress on the viscous interface
Christoph Meyer et al.
Analytical and bioanalytical chemistry, 382(3), 679-690 (2004-08-04)
Three poly(ethylene-co-acrylic) acid copolymers (-CH(2)CH(2)-)(x)[CH(2)CH(CO(2)H)-](y) with different chain lengths and mass fractions of acrylic acid were covalently immobilized as stationary phases on silica via two variants of spacer molecules (3-aminopropyltriethoxysilane and 3-glycidoxypropyltrimethoxysilane). Different mobilities of the alkyl chains in the
Siri Schauff et al.
Analytical chemistry, 79(21), 8323-8326 (2007-10-09)
The separation process in reversed-phase high-performance liquid chromatography employing C18 phases is mainly due to hydrophobic interactions. The separation of tocopherol isomers, exhibited by the C30 phases, however, is additionally driven by shape selectivity. This phenomenon is investigated by suspended-state
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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Any molecular weight information available of this coplolymer (426717: Poly(ethylene-co-acrylic acid), acrylic acid 5 wt. %, beads)?
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