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523925

Sigma-Aldrich

Poly(acrylic acid) solution

average Mw ~100,000, 35 wt. % in H2O

Synonyme(s) :

PAA

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About This Item

Formule linéaire :
(C3H4O2)n
Numéro CAS:
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Poids mol.

average Mw ~100,000

Concentration

35 wt. % in H2O

Densité

1.14 g/mL at 25 °C

Chaîne SMILES 

OC(=O)C=C

InChI

1S/C3H4O2.Na/c1-2-3(4)5;/h2H,1H2,(H,4,5);/q;+1/p-1

Clé InChI

NNMHYFLPFNGQFZ-UHFFFAOYSA-M

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Description générale

Poly (acrylic acid) (PAA) is hygroscopic, brittle and colorless in nature with Tg at nearly 106oC. At temperatures above 200, up to 250oC, it loses water and becomes an insoluble crosslinked polymer anhydride. Solubility of dried PAA in water increases with rise in temperature. Concentrated solutions of PAA in water are thixotropic in nature.

Application

PAA is used in the preparation of nano-hydroxyapatite polyacrylic acid (Hap/PAAc) biocomposites.†Other probable applications of PAA are: to study solute diffusion in Polyvinyl alcohol/PAA copolymer hydrogels†, synthesizing poly(N-isopropylacrylamide)-block-PAA copolymer which responds to both temperature and pH stimuli†, in preparing block copolymer of oligo (methyl methacrylate)/PAA for micellar delivery of hydrophobic drugs†, and as a thickening agent for adhesives.

Pictogrammes

CorrosionExclamation markEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

212.0 °F - closed cup

Point d'éclair (°C)

100 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Consulter la Bibliothèque de documents

T Inoue et al.
Journal of controlled release : official journal of the Controlled Release Society, 51(2-3), 221-229 (1998-08-01)
An AB block copolymer of oligo(methyl methacrylate) (oMMA) and poly(acrylic acid) (PAAc) has been synthesized. The block copolymer forms micelles in an aqueous medium, as confirmed by a fluorescence probe technique using pyrene. Doxorubicin hydrochloride was incorporated into the micelle
P L Zeeuwen et al.
The Journal of investigative dermatology, 116(5), 693-701 (2001-05-12)
Using serial analysis of gene expression on cultured human keratinocytes we found high expression levels of genes putatively involved in host protection and defense, such as proteinase inhibitors and antimicrobial proteins. One of these expressed genes was the recently discovered
Yanxia Wang et al.
International journal of pharmaceutics, 441(1-2), 170-180 (2012-12-15)
A novel galactose-decorated cross-linked micelles (cl-micelles) with ionic cores using cystamine (Cys) as a biodegradable cross-linker was prepared by using block ionomer complexes of poly(ethylene glycol)-b-poly(2-acryloxyethyl-galactose)-b-poly(acrylic acid) (PEG-b-PAEG-b-PAA) and Ca(2+) (PEG-b-PAEG-b-PAA cl-micelles/Cys). Doxorubicin (DOX) was successfully incorporated into the ionic
Daniel L Miller et al.
The Annals of thoracic surgery, 95(3), 1050-1056 (2013-01-22)
Skeletal chest wall reconstruction can be a challenge, depending on the indication, location, and health of the patient; various materials are available. Recently, biomaterials that are remodelable (bovine pericardium patch; Veritas, Synovis Life Technologies Inc, St Paul, MN) or absorbable
Lei Liu et al.
ACS nano, 7(2), 1368-1378 (2013-01-04)
Hierarchical FeOOH nanostructure array films constructed by different nanosized building blocks can be synthesized at the air-water interface via a bio-inspired gas-liquid diffusion method. In this approach, poly(acrylic acid) (PAA) as a crystal growth modifier plays a crucial role in

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