推荐产品
生物源
plant (vegetable)
化驗
≥99%
形狀
powder
官能基
ester
脂質類型
saturated FAs
運輸包裝
ambient
儲存溫度
2-8°C
SMILES 字串
[Na+].CCCCCCCCCCCCCCCCCC([O-])=O
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
InChI 密鑰
RYYKJJJTJZKILX-UHFFFAOYSA-M
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應用
- 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).
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
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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
Kinetically stable propofol emulsions with reduced free drug concentration for intravenous delivery.
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
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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