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Key Documents

151114

Sigma-Aldrich

Cholesteryl acetate

97%

Synonym(s):

3β-Acetoxy-5-cholestene, 3β-Hydroxy-5-cholestene 3-acetate, 5-Cholesten-3β-ol 3-acetate

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$339.00

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25 G
$121.00
100 G
$339.00

About This Item

Empirical Formula (Hill Notation):
C29H48O2
CAS Number:
Molecular Weight:
428.69
Beilstein/REAXYS Number:
2064235
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

$121.00


Available to ship onMay 01, 2025Details


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Quality Level

assay

97%

form

liquid crystal

optical activity

[α]24/D −44°, c = 2 in chloroform

mp

112-114 °C (lit.)

SMILES string

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OC(C)=O

InChI

1S/C29H48O2/c1-19(2)8-7-9-20(3)25-12-13-26-24-11-10-22-18-23(31-21(4)30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-20,23-27H,7-9,11-18H2,1-6H3/t20-,23+,24+,25-,26+,27+,28+,29-/m1/s1

InChI key

XUGISPSHIFXEHZ-VEVYEIKRSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Dmitry A Aleksandrov et al.
The FEBS journal, 273(3), 548-557 (2006-01-20)
5-Lipoxygenase (5-LO) is the key enzyme in the biosynthesis of leukotrienes (LTs), biological mediators of host defense reactions and of inflammatory diseases. While the role of membrane binding in the regulation of 5-LO activity is well established, the effects of
P Ghosh et al.
Lipids, 32(9), 1011-1014 (1997-10-06)
Most work reporting the sterol composition of living organisms has not been done quantitatively, although good quantitative data are available for fatty acids and many other cellular components using an internal-standard method that compensates for errors during gas chromatographic analysis.
B Sjöström et al.
Journal of pharmaceutical sciences, 82(6), 584-589 (1993-06-01)
Small particles of two steroids, cholesteryl acetate and beta-sitosterol, were prepared by the following technique. The steroid was dissolved in an organic solvent, which was emulsified in water in the presence of surfactant, thus giving a water-continuous emulsion. As the
M Pelillo et al.
Rapid communications in mass spectrometry : RCM, 14(14), 1275-1279 (2000-08-05)
In this work, electron-impact mass spectroscopy (EI-MS) was employed on a wide range of sterol compounds in order to study their behaviour with regard to their functional groups. In particular, some specific mechanisms of fragmentation occurring in these substrates (i.e.
Nanostructured semiconductors templated by cholesteryl-oligo (ethylene oxide) amphiphiles
Rabatic, B. M., Pralle, M. U., Tew, G. N., & Stupp, S. I.
Chemistry of Materials, 15(6), 1249-1255 (2003)

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