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283223

Sigma-Aldrich

Poly(allylamine hydrochloride)

average Mw 50,000

Synonym(s):

PAA HCl, PAH

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About This Item

Linear Formula:
[CH2CH(CH2NH2 · HCl)]n
CAS Number:
71550-12-4
EC Number:
415-050-2
MDL number:
MFCD00084396
UNSPSC Code:
12162002
PubChem Substance ID:
24857094
NACRES:
NA.23

form

solid

Quality Level

100

mol wt

average Mw 50,000

SMILES string

Cl.NCC=C

InChI

1S/C3H7N/c1-2-3-4/h2H,1,3-4H2

InChI key

VVJKKWFAADXIJK-UHFFFAOYSA-N

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Application

Used to make redox hydrogel-modified electrodes for measuring enzyme responses.

Packaging

The polyelectrolyte poly(allylamine hydrochloride) has been used in the preparation of an antireflective coating consisting of alternating layers of poly (allyamine hydrochloride) and silica nanoparticles

Other Notes

May contain up to ≤10% residual monomer.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H317

Hazard Classifications

Acute Tox. 4 Oral - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV4818
MKCS5814
MKCQ6709
MKCR7068
MKCQ3334

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Yancey, S.E. et al
Journal of Applied Physics, 99, 034313-034313 (2006)
Analytical Chemistry, 68, 4186-4186 (1990)
Zhi-Lu Yang et al.
Journal of biomedical materials research. Part A, 100(11), 3124-3133 (2012-07-21)
A simple method is developed to construct anticoagulant surfaces via passive adsorption of heparin onto the protonated plasma-polymerized allylamine (PPAam) films from phosphate-buffered saline (PBS). These protonated PPAam surfaces are found to have high affinity to heparin. Importantly, the heparin-functionalized
Magdalena Oćwieja et al.
Langmuir : the ACS journal of surfaces and colloids, 29(11), 3546-3555 (2013-01-17)
Systematic studies of silver particle deposition kinetics under diffusion transport on poly(allylamine hydrochloride) (PAH) modified mica were carried out. Monolayer coverage, quantitatively determined by AFM and SEM, was regulated within broad limits by adjusting the deposition time and the ionic
Ya Wang et al.
Macromolecular bioscience, 12(10), 1321-1325 (2012-09-12)
Fluorescent-magnetic-biotargeting multifunctional microcapsules (FMBMMs) are designed and fabricated via layer-by-layer assembly. It is found that the arginine-glycine-aspartate-modified FMBMMs were capable of sensitively detecting and efficiently isolating approximately 80% target cancer cells within 20 min. More importantly, FMBMMs present a general
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