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Merck
CN

S7010

Sigma-Aldrich

Span® 60

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别名:
山梨醇酐单硬脂酸酯, 硬脂山梨坦
CAS号:
EC 号:
MDL编号:
UNSPSC代码:
12161900
PubChem化学物质编号:
NACRES:
NA.25

描述

non-ionic

质量水平

分子量

430.63 g/mol

浓度

45-55% (GC)

SMILES字符串

CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O

InChI

1S/C24H46O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22(27)29-19-21(26)24-23(28)20(25)18-30-24/h20-21,23-26,28H,2-19H2,1H3/t20-,21?,23+,24+/m0/s1

InChI key

HVUMOYIDDBPOLL-XGKPLOKHSA-N

一般描述

Span® 60 是一种山梨醇单酯,用作非离子型洗涤剂。

应用

Span® 60曾在一项研究中用于评估阿霉素在囊泡中的包封,作为肿瘤靶向的一种途径。 也有研究用非离子型表面活性剂作为造影剂用于诊断超声。

其他说明

脂肪酸组成:硬脂酸 (C18:0) 约 50%;主要平衡棕榈酸 (C16:0)。

法律信息

Span is a registered trademark of Croda International PLC

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Preparation and properties of vesicles (niosomes) of sorbitan monoesters ([TM="Span"] 20, 40, 60 and 80) and a sorbitan triester ([TM="Span"] 85).
Yoshioka, T., et al.
International Journal of Pharmaceutics, 105, 1-1 (1994)
I F Uchegbu et al.
Pharmaceutical research, 12(7), 1019-1024 (1995-07-01)
Encapsulation of doxorubicin in niosomes was sought as a route to tumour targeting and improved tumoricidal through the alteration of doxorubicin pharmacokinetics and metabolism. Doxorubicin niosomes (10 mg kg-1 doxorubicin) prepared from sorbitan monostearate (Span 60), cholesterol and choleth-24 (a
Surfactant-stabilized microbubbles as ultrasound contrast agents: stability study of [TM="Span"] 60 and Tween 80 mixtures using a Langmuir trough
Singhal, S., et al.
Langmuir, 9, 2426-2426 (1993)
Isabel F Almeida et al.
International journal of pharmaceutics, 327(1-2), 73-77 (2006-09-26)
Oleogels are semisolid systems obtained with an organogelator and a hydrophobic liquid that have been investigated over the past few years and that could play an important role as dermatological bases. Recently, we have developed an oleogel of sorbitan monostearate
Ismail A Attia et al.
AAPS PharmSciTech, 8(4), E106-E106 (2008-01-10)
The purpose of this research was to prepare acyclovir niosomes in a trial to improve its poor and variable oral bioavailability. The nonionic surfactant vesicles were prepared by the conventional thin film hydration method. The lipid mixture consisted of cholesterol

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