Direkt zum Inhalt
Merck

P3418

Sigma-Aldrich

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

mol wt 2,000-11,000

Synonym(e):

Aspartic acid homopolymer sodium salt

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

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

Form

powder

Qualitätsniveau

Mol-Gew.

2,000-11,000

Farbe

white to off-white

Lagertemp.

−20°C

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Anwendung


  • 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).

Angaben zur Herstellung

Prepared by thermal polycondensation.

Hinweis zur Analyse

Molecular weight based on viscosity.

Sonstige Hinweise

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

Besitzen Sie dieses Produkt bereits?

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

Die Dokumentenbibliothek aufrufen

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
Kovacs, J.
The Journal of Organic Chemistry, 26, 1084-1084 (1961)
Lin Gui et al.
Nanomedicine (London, England), 5(5), 703-714 (2010-07-29)
Applying nanoscale assembly to the design of a thrombolytic agent. poly-alpha,beta-DL-aspartyl-L-alanine (molecular weight: 15726 atomic mass units) from the thermal polycondensation of DL-aspartic acid and the amidation of polysuccimide with L-alanine. The correlation of concentration and pH with nanofeatures, the
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

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.