Direkt zum Inhalt
Merck

Fortfahren mit

P3418

Poly-(α,β)-DL-aspartic acid sodium salt

mol wt 2,000-11,000

Synonym(e):

Aspartic acid homopolymer sodium salt

Anmelden zur Ansicht der Organisations- und Vertragspreise.

Größe auswählen

Ansicht ändern
PackungsgrößeSKUVerfügbarkeitPreis
100 mg
Warenkorb auf Verfügbarkeit prüfen
€ 176,00
1 g
Warenkorb auf Verfügbarkeit prüfen
€ 842,00

Über diesen Artikel

CAS-Nummer:
UNSPSC Code:
12352209
NACRES:
NA.26
MDL number:

€ 176,00


Warenkorb auf Verfügbarkeit prüfen

Großbestellung anfragen
Technischer Dienst
Benötigen Sie Hilfe? Unser Team von erfahrenen Wissenschaftlern ist für Sie da.
Unterstützung erhalten


form

powder

Quality Level

mol wt

2,000-11,000

color

white to off-white

storage temp.

−20°C

Application


  • Improving the effectiveness of (-)-epigallocatechin gallate (EGCG) against rabbit atherosclerosis by EGCG-loaded nanoparticles prepared from chitosan and polyaspartic acid.: This research highlights the development of nanoparticles using polyaspartic acid to enhance the bioavailability and therapeutic effect of EGCG in treating atherosclerosis (Hong et al., 2014).

  • Polyaspartate, a biodegradable chelant that improves the phytoremediation potential of poplar in a highly metal-contaminated agricultural soil.: The study evaluates the use of polyaspartate in enhancing the phytoremediation capabilities of poplar trees, showcasing its environmental application for soil decontamination (Lingua et al., 2014).

  • Modulation of calcium oxalate dihydrate growth by selective crystal-face binding of phosphorylated osteopontin and polyaspartate peptide showing occlusion by sectoral (compositional) zoning.: This research investigates the role of polyaspartate in modulating the growth of calcium oxalate crystals, with implications for understanding kidney stone formation (Chien et al., 2009).

Preparation Note

Prepared by thermal polycondensation.

Analysis Note

Molecular weight based on viscosity.

Other Notes

For additional technical information on polyamino acids please visit the Polyamino acid FAQ resource.

Ähnliche Artikel vergleichen

Vollständigen Vergleich anzeigen

Unterschiede anzeigen

1 of 1

Dieser Artikel
P1818P4761P4636
form

powder

form

powder

form

powder

form

powder

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

color

white to off-white

color

white to light yellow

color

white to off-white

color

white to off-white

mol wt

2,000-11,000

mol wt

1,500-5,500 by MALLS

mol wt

15,000-50,000

mol wt

3,000-15,000


Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen


Artikel

Humankind has utilized protein materials throughout its existence, starting with the use of materials such as wool and silk for warmth and protection from the elements and continuing with the use of recombinant DNA techniques to synthesize proteins with unique and useful properties.


Kovacs, J.
The Journal of Organic Chemistry, 26, 1084-1084 (1961)
Fabio Nudelman et al.
Nanoscale, 2(11), 2436-2439 (2010-09-14)
Amorphous calcium carbonate (ACC) nanoparticles of different size are prepared using a flow system. Post-synthesis stabilization with a layer of poly[(α,β)-dl-aspartic acid] leads to stabilization of the ACC, but only for particles <100 nm. Larger and uncoated particles readily convert
Yangzhi Guping et al.
Drug delivery, 12(2), 89-96 (2005-04-15)
A new class of biodegradable poly-amino acid, alpha,beta-poly[(N-hydroxypropyl/aminoethyl)-DL-Aspartamide-co-L-Lysine] (PHAAL), was synthesized by ring-opening of poly[succinimide-co-lysine](PSL) with n-propanolamine and ethylene diamine after thermal copolycondensation of DL-Aspartic acid and L-lysine under reduced pressure. Different ratio feeds of PSL were obtained and characterized



Global Trade Item Number

SKUGTIN
P3418-100MG04061834367918
P3418-1G04061826686140

Questions

Reviews

No rating value

Active Filters