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Merck

C4151

Sigma-Aldrich

癸酸钠

≥98%

别名:

Sodium caprate, 十烷酸 钠盐, 羊蜡酸 钠盐

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About This Item

线性分子式:
CH3(CH2)8COONa
CAS号:
分子量:
194.25
Beilstein:
3572742
EC號碼:
MDL號碼:
分類程式碼代碼:
12352211
PubChem物質ID:
NACRES:
NA.25

生物源

natural (organic)

品質等級

化驗

≥98%

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+].CCCCCCCCCC([O-])=O

InChI

1S/C10H20O2.Na/c1-2-3-4-5-6-7-8-9-10(11)12;/h2-9H2,1H3,(H,11,12);/q;+1/p-1

InChI 密鑰

FIWQZURFGYXCEO-UHFFFAOYSA-M

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應用


  • Neonatal intestinal mucus barrier changes in response to maturity, inflammation, and sodium decanoate supplementation.:研究癸酸钠如何影响新生肠道屏障,说明它增强黏膜免疫和肠道健康的营养干预作用(Ronholt et al., 2024)。

  • Effects of Sodium Salts of Fatty Acids and Their Derivatives on Skin Permeation of Cromolyn Sodium.:研究癸酸钠提高皮肤渗透性的作用,体现透皮给药应用潜力(Dinh et al., 2023)。

  • The Role of Paracellular Transport in the Intestinal Absorption and Biopharmaceutical Characterization of Minoxidil.:关注癸酸钠对肠道吸收机制的影响,为开发更多有效的口服药物制剂贡献力量(Dahan et al., 2022)。

  • Control of Escherichia coli Serotype O157:H7 Motility and Biofilm Formation by Salicylate and Decanoate:MarA/SoxS/Rob and pchE Interactions.:研究癸酸钠如何影响细菌行为,尤其是致病性和生物被膜形成,体现临床和环境应用价值(Ream et al., 2022)。

  • Sodium Decanoate Improves Intestinal Epithelial Barrier and Antioxidation via Activating G Protein-Coupled Receptor-43.:研究发现癸酸钠可增强肠道屏障和抗氧化性,有望成为治疗消化系统的候选药物(Ma et al., 2021)。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Ignacio Poblete-Castro et al.
Microbial cell factories, 11, 34-34 (2012-03-22)
Pseudomonas putida KT2442 is a natural producer of polyhydroxyalkanoates (PHAs), which can substitute petroleum-based non-renewable plastics and form the basis for the production of tailor-made biopolymers. However, despite the substantial body of work on PHA production by P. putida strains
C Roos et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 142, 387-395 (2019-07-16)
Oral administration of drug products is the preferred administration route. In recent decades there has been an increase in drug candidates with low solubility and/or low permeability. To increase the possibility of oral administration for the poorly permeating drugs, the
Ahmed Kassem et al.
International journal of food microbiology, 261, 19-24 (2017-09-11)
The aim of the current study was to assess the ability of a number of chemicals (acetic Acid (AA), citric acid (CA) lactic acid (LA), sodium decanoate (SD) and trisodium phosphate (TSP)) to reduce microbial populations (total viable count, Campylobacter
D Dahlgren et al.
International journal of pharmaceutics, 549(1-2), 239-248 (2018-07-29)
The small intestine mucosal barrier is physiologically regulated by the luminal conditions, where intestinal factors, such as diet and luminal tonicity, can affect mucosal permeability. The intestinal barrier may also be affected by absorption-modifying excipients (AME) in oral drug delivery
Wei Li et al.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 39(5), 639-647 (2018-04-13)
Entry of locally applied drugs into the inner ear can be enhanced by chemical manipulations. Perilymph drug concentrations achieved by intratympanic applications are well below the applied concentration due to limited entry through the round window (RW) membrane and stapes.

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