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Merck

S3381

Sodium stearate

≥99%

Synonyme(s) :

Octadecanoic acid sodium salt, Stearic acid sodium salt

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About This Item

Formule linéaire :
CH3(CH2)16COONa
Numéro CAS:
822-16-2
Poids moléculaire :
306.46
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
24899554
EC Number:
212-490-5
Beilstein/REAXYS Number:
3576813
MDL number:
MFCD00036404

Nom du produit

Sodium stearate, ≥99%

InChI key

RYYKJJJTJZKILX-UHFFFAOYSA-M

InChI

1S/C18H36O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h2-17H2,1H3,(H,19,20);/q;+1/p-1

SMILES string

[Na+].CCCCCCCCCCCCCCCCCC([O-])=O

biological source

plant (vegetable)

assay

≥99%

form

powder

functional group

ester

lipid type

saturated FAs

shipped in

ambient

storage temp.

2-8°C

Quality Level

200

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Catégories apparentées

Application


  • Stability test of novel combined formulated dry powder inhalation system containing antibiotic: physical characterization and in vitro-in silico lung deposition results.: This study investigates a novel dry powder inhalation system formulated with an antibiotic and sodium stearate. It explores the physical characterization and lung deposition efficiency, demonstrating the potential for enhanced drug delivery to the lungs (Benke et al., 2019).

  • Protective effect of sodium stearate on the moisture-induced deterioration of hygroscopic spray-dried powders.: This research highlights the role of sodium stearate in protecting hygroscopic spray-dried powders from moisture-induced degradation, which is crucial for maintaining the stability and efficacy of pharmaceutical products (Yu et al., 2018).

  • Dissolution of a poorly water-soluble drug dry coated with magnesium and sodium stearate.: This study examines the use of sodium stearate in enhancing the dissolution rates of poorly water-soluble drugs, which is critical for improving drug bioavailability (Tay et al., 2012).

Classe de stockage

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
0000503797
0000503797
0000494449
0000494449
0000467433

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Andrea Dichlberger et al.
Journal of lipid research, 52(12), 2198-2208 (2011-10-06)
Lipid droplets, also called lipid bodies (LB) in inflammatory cells, are important cytoplasmic organelles. However, little is known about the molecular characteristics and functions of LBs in human mast cells (MC). Here, we have analyzed the genesis and components of
Natasha Fillmore et al.
PloS one, 10(3), e0120257-e0120257 (2015-03-15)
Successful stem cell therapy requires the optimal proliferation, engraftment, and differentiation of stem cells into the desired cell lineage of tissues. However, stem cell therapy clinical trials to date have had limited success, suggesting that a better understanding of stem
Mihye Lim et al.
Nanoscale, 11(21), 10463-10471 (2019-05-22)
In this study, we designed and synthesized far-red- and near-infrared-emitting Cu-doped InP-based quantum dots (QDs), and we also demonstrated their highly specific and sensitive biological imaging ability. Cu-doped InP/ZnS (core/shell) QDs were prepared using the hot colloidal synthesis method in
Robert Damitz et al.
International journal of pharmaceutics, 486(1-2), 232-241 (2015-04-04)
Intravenous injections of propofol emulsions are accompanied by pain likely due to the interaction of the dissolved drug with endothelial cells of the vasculature. It is commonly hypothesized that reducing the aqueous phase concentration of propofol could reduce pain. To
T Aikawa et al.
Biomaterials science, 3(6), 861-869 (2015-07-30)
In order for patients to avail of the therapeutic benefits of antioxidant drugs efficiently and conveniently, a robust oral delivery system needs to be developed. However, a common problem in oral drug delivery is ensuring that the drug remains functionally
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