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412368

Sigma-Aldrich

PAMAM dendrimer

ethylenediamine core, generation 0.0 solution, 20 wt. % in methanol

Synonym(s):

Poly(amidoamine)

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About This Item

Linear Formula:
NH2(CH2)2NH2]:(G=0);dendri PAMAM(NH2)4
CAS Number:
Molecular Weight:
516.68
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

description

amino surface groups

Quality Level

form

liquid

mol wt

generation 0.0

feature

core type ethylenediamine core (2-carbon core)

concentration

20 wt. % in methanol

no. Surface Groups

4

refractive index

n20/D 1.364

bp

64.7 °C

density

0.854 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

NCCNC(=O)CCN(CCN(CCC(=O)NCCN)CCC(=O)NCCN)CCC(=O)NCCN

InChI

1S/C22H48N10O4/c23-5-9-27-19(33)1-13-31(14-2-20(34)28-10-6-24)17-18-32(15-3-21(35)29-11-7-25)16-4-22(36)30-12-8-26/h1-18,23-26H2,(H,27,33)(H,28,34)(H,29,35)(H,30,36)

InChI key

SENLDUJVTGGYIH-UHFFFAOYSA-N

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General description

PAMAM dendrimer is a poly(amidoamine) that is categorized under the class of dendritic polymers, which can be prepared by a two-step reaction that forms generations around the central ethylenediamine core. It consists of nitrogen and amide as functional groups that are structured in regular branched upon branched pattern. PAMAM is majorly used as a high capacity chelating agent.

Application

PAMAM dendrimer belongs to the family of dendrimers, which can be used in biomedical and drug delivery applications.

Physical form

Contains 4 surface primary amino groups

Legal Information

Manufactured by Dendritech®, Inc.
Dendritech is a registered trademark of Dendritech, Inc.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup


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PAMAM dendrimer-based multifunctional conjugate for cancer therapy: synthesis, characterization, and functionality
Majoros I, et al.
Biomacromolecules, 7(2), 572-579 (2006)
Poly (amidoamine)(PAMAM) dendrimers: from biomimicry to drug delivery and biomedical applications
Esfand R and Tomalia DA
Drug Discovery Today, 6(8), 427-436 (2001)
Poly (ethylene glycol)-conjugated PAMAM dendrimer for biocompatible, high-efficiency DNA delivery
Luo D, et al.
Macromolecules, 35(9), 3456-3462 (2002)
Dendritic chelating agents. 1. Cu (II) binding to ethylene diamine core poly (amidoamine) dendrimers in aqueous solutions
Diallo MS, et al.
Langmuir, 20(7), 2640-2651 (2004)
Dendrimer enhanced ultrafiltration. 1. Recovery of Cu (II) from aqueous solutions using PAMAM dendrimers with ethylene diamine core and terminal NH2 groups
Diallo MS, et al.
Environmental Science & Technology, 39(5), 1366-1377 (2005)

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