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448672

Sigma-Aldrich

Poly(ethylene-co-acrylic acid)

acrylic acid 15 wt. %

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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:
24868425
NACRES:
NA.23

composition

acrylic acid, 15 wt. %

hardness

≤15 dmm (ASTM D 5, 25 °C)

viscosity

600 cP(140 °C, Brookfield)(lit.)

acid number

112‑130 mg KOH/g

transition temp

Tm (DSC) 87 °C (at peak)

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

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315

Hazard Classifications

Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>977.0 °F - closed cup

Flash Point(C)

> 525 °C - closed cup

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

448672-1KG:
448672-VAR:
448672-250G:
448672-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH2130
MKBD9362
MKBC8500
MKBC0303
04906BJ

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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
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
Xiaodi Su et al.
Journal of colloid and interface science, 287(1), 35-42 (2005-05-26)
In this study, we use the quartz crystal microbalance with dissipation monitoring (QCM-D) to study the immobilization of the enzyme horseradish peroxidase (HRP) on poly(ethylene-co-acrylic acid) (PEAA) films. The surface polarity of spin-coated PEAA films was varied by heat treatments
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
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