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426717

Sigma-Aldrich

Poly(ethylene-co-acrylic acid)

acrylic acid 5 wt. %, beads

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About This Item

Linear Formula:
(CH2CH2)x[CH2CH(CO2H)]y
CAS Number:
9010-77-9
MDL number:
MFCD00133995
UNSPSC Code:
12162002
PubChem Substance ID:
24866722
NACRES:
NA.23

description

drop point 105 °C Mettler

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.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H335,H412

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

Certificates of Analysis (COA)

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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
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
J Wegmann et al.
Analytical chemistry, 73(8), 1814-1820 (2001-05-08)
A new approach for the synthesis of long alkyl chain length stationary phases for use in reversed-phase liquid chromatography is described. Poly(ethylene-co-acrylic acid) copolymers (i.e., (-CH2CH2-)x[CH2CH(CO2H)-]y) with different levels of acrylic acid were covalently bonded to silica via glycidoxypropyl or
Optician's occupational allergic contact dermatitis, paresthesia and paronychia caused by anaerobic acrylic sealants.
L Kanerva et al.
Contact dermatitis, 44(2), 117-119 (2001-02-24)
A P Martínez-Camacho et al.
Carbohydrate polymers, 91(2), 666-674 (2012-11-06)
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
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