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523925

Sigma-Aldrich

Poly(acrylic acid) solution

average Mw ~100,000, 35 wt. % in H2O

Sinônimo(s):

PAA

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About This Item

Fórmula linear:
(C3H4O2)n
Número CAS:
9003-01-4
Número MDL:
MFCD00084394
Código UNSPSC:
12162002
ID de substância PubChem:
24874380
NACRES:
NA.23

peso molecular

average Mw ~100,000

concentração

35 wt. % in H2O

densidade

1.14 g/mL at 25 °C

cadeia de caracteres SMILES

OC(=O)C=C

InChI

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

chave InChI

NNMHYFLPFNGQFZ-UHFFFAOYSA-M

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Descrição geral

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.

Aplicação

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.

Palavra indicadora

Danger

Frases de perigo

H318,H335,H410

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

212.0 °F - closed cup

Ponto de fulgor (°C)

100 °C - closed cup

Equipamento de proteção individual

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

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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
Kang Zhong et al.
Carbohydrate polymers, 92(2), 1367-1376 (2013-02-13)
Phosphate rock (PHR), a traditional fertilizer, is abundant, but is hard to be utilized by plants. To improve the utilization of PHR, and to integrate water-retaining and controlled-release fertilizers, an agricultural superabsorbent polymer based on sulfonated corn starch/poly (acrylic acid)
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