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S7010

Sigma-Aldrich

Span® 60

Sinonimo/i:

Sorbitan stearate, Sorbitane monostearate

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About This Item

Numero CAS:
1338-41-6
Numero CE:
215-664-9
Numero MDL:
MFCD00005366
Codice UNSPSC:
12161900
ID PubChem:
24899728
NACRES:
NA.25

Descrizione

non-ionic

PM

430.63 g/mol

Concentrazione

45-55% (GC)

Stringa SMILE

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
HVUMOYIDDBPOLL-XGKPLOKHSA-N

Categorie correlate

Descrizione generale

Span® 60 is a sorbitan monoester than is used as a non-ionic detergent.

Applicazioni

Span® 60 has been used in a study to assess encapsulation of doxorubicin in niosomes as a route to tumor targeting. It has also been used in a study to investigate the use of nonionic surfactants as contrast agents for use in diagnostic ultrasounds.

Altre note

Fatty acid composition: Stearic acid (C18:0) approx. 50%; balance primarily palmitic acid (C16:0).

Note legali

Span is a registered trademark of Croda International PLC

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Span® 85

Sigma-Aldrich

S7135

Span® 85

TWEEN® 40 viscous liquid

Sigma-Aldrich

P1504

TWEEN® 40

Span® 80 for synthesis

Sigma-Aldrich

8.40123

Span® 80

Span® 80 suitable for GC

Supelco

09569

Span® 80

Span® 85 for synthesis

Sigma-Aldrich

8.40124

Span® 85

TWEEN® 60 for synthesis

Sigma-Aldrich

8.22186

TWEEN® 60

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
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)
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)
Karimunnisa Sameer Shaikh et al.
Drug development and industrial pharmacy, 36(8), 946-953 (2010-03-04)
Niosomal delivery can prove an alternative to improve the poor skin penetration and residence of the topical antifungal drugs that account for the long treatment regimes in cutaneous mycosis. To investigate niosomes as carriers for dermal delivery of ciclopirox olamine
A Manosroi et al.
International journal of pharmaceutics, 356(1-2), 291-299 (2008-02-19)
Characteristics and physical stability of luciferase plasmid (pLuc) entrapped in cationic bilayer vesicles prepared from various molar ratios of amphiphiles (DPPC, Tween61 or Span60), cholesterol (Chol) and cationic charge lipid (DDAB) were investigated. The cationic liposomes were composed of DPPC/Chol/DDAB
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