Skip to Content
Merck
All Photos(1)

Key Documents

746991

Sigma-Aldrich

Polystyrene-block-poly(acrylic acid)

Synonym(s):

Poly(styrene)-block-poly(acrylic acid)

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H6N(C8H8)m(C3H4O2)nH
UNSPSC Code:
12352100
NACRES:
NA.23

form

solid

mol wt

Mn 27,000-31,000 (polystyrene)
Mn 31,000-37,000 (total)
Mn 4,000-6,000 (poly(acrylic acid))

mp

258-263 °C

PDI

≤1.3

Looking for similar products? Visit Product Comparison Guide

Application

Polystyrene-block-polyacrylic acid is a diblock copolymer used for making polymeric vesicles (polymersomes) and other encapsulation applications.1-9 This PS-block-PAA copolymer is 15 wt. % AA; and should form vesicles in water in the 100 nm range. The polystyrene degree of polymerization (DP) is 275 and the polyacrylic acid DP is 50.

Legal Information

Sold for research purposes only.  Not for use in humans.  Before opening or using this product, please read the following terms and conditions.  Use of this product shall constitute acknowledgement and acceptance of these terms and conditions: Use of this product may be covered by one or more of the following US patents and corresponding claims outside the US: 7,714,075; 7,250,479; 7,666,962; 6,642,318; 6,747,111, and pending applications (W2010/8356).  For details contact Aldrich Chemical Company, Inc.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Multiple Morphologies of PAA-b-PSt Assemblies throughout RAFT Dispersion Polymerization of Styrene with PAA Macro-CTA
Wei-Dong He,
Macromolecules, 44, 3358-3365 (2011)
Qiang Tian et al.
Langmuir : the ACS journal of surfaces and colloids, 36(17), 4820-4826 (2020-04-11)
The interactions between natural colloidal organic matter and actinides in solutions are complex and not fully understood. In this work, a crew-cut polystyrene-b-poly(acry1ic acid) (PS-b-PAA) micelle is proposed as a model particle for humic acid (HA) colloid with the aim
Amphiphilic core?shell nanospheres obtained by intramicellar shell crosslinking of polymer micelles with poly(ethylene oxide) linkers
Haiyong Huang,
Chemical Communications (Cambridge, England), 13, 1415-1415 (1998)
Effect of Poly(acrylic acid) Block Length Distribution on Polystyrene-b-Poly(acrylic acid) Aggregates in Solution. 1. Vesicles
Owen Terreau,
Langmuir, 19, 5601-5607 (2003)
Preparation of orthogonally-functionalized core Click cross-linked nanoparticles
Rachel K. O?Reilly,
New. J. Chem., 31, 718-724 (2007)

Articles

Reversible addition–fragmentation chain transfer (RAFT) polymerization is rapidly moving to the forefront in construction of drug and gene delivery vehicles.

The development of drugs that target specific locations within the human body remains one of the greatest challenges in biomedicine today.

Over the past two decades, the rapid advance of controlled living polymerization (CLP) techniques.

Professor Robert K. Prud’homme introduces flash nanoprecipitation (FNP) for nanoparticle fabrication, which is a scalable, rapid mixing process for nanoparticle formulations.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service