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Merck
CN

283223

Poly(allylamine hydrochloride)

Mw 40,000-150,000

Synonym(s):

PAA HCl, PAH

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About This Item

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

Key Documents

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mol wt

Mw 40,000-150,000

InChI key

VVJKKWFAADXIJK-UHFFFAOYSA-N

InChI

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

SMILES string

Cl.NCC=C

form

solid

Quality Level

100

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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

signalword

Warning

hcodes

H302,H317

Hazard Classifications

Acute Tox. 4 Oral - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 1

ppe

dust mask type N95 (US), Eyeshields, Faceshields, 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)
Bing Wang et al.
Macromolecular bioscience, 12(11), 1534-1545 (2012-09-26)
The mechanism of the cellular uptake of polyelectrolyte microcapsules and its influences on the functions and toxicity of human SMCs are explored. The covalently assembled poly(allylamine hydrochloride)/glutaraldehyde microcapsules are easily ingested by SMCs mainly through macropinosis and caveolae-mediated endocytosis pathways.
Ankit Agarwal et al.
Biomaterials, 33(28), 6783-6792 (2012-07-13)
Biologic wound dressings contain animal-derived components and are susceptible to high infection rates. To address this issue, we report an approach that permits incorporation of non-toxic levels of the small molecule antiseptic 'chlorhexidine' into biologic dressings. The approach relies on
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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Recently, layer-by-layer (LbL) assembly has emerged as a versatile, gentle and, simple method for immobilization of functional molecules in an easily controllable thin film morphology.1,2 In this short review, we introduce recent advances in functional systems fabricated by using the mild, yet adaptable LbL technique.

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